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            <record>
              <language>eng</language>
              <publisher>Selçuk Üniversitesi Veteriner Fakültesi</publisher>
              <journalTitle>Eurasian Journal of Veterinary Sciences</journalTitle>
              <issn>1309-6958</issn>
              <eissn>2146-1953</eissn>
              <publicationDate>0000-00-00</publicationDate>
              <volume>29</volume>
              <issue>2</issue>
              <startPage>65</startPage>
              <endPage>69</endPage>
              <doi></doi>
              <publisherRecordId>989</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">The effect of 17&amp;#946; estradiol on the expression of enos and inos in ovariectomized rat uterus</title>
                <authors>
                              <author>
                                <name>Oktay  Yilmaz</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Artay Yagci</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Elmas Ulutas</name>
                                <affiliationId>3</affiliationId>
                              </author>
                              <author>
                                <name>Alper Sevimli</name>
                                <affiliationId>4</affiliationId>
                              </author>
                              <author>
                                <name>Korhan Altunbas</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Aziz Bulbul</name>
                                <affiliationId>3</affiliationId>
                              </author>
                              <author>
                                <name>Recep Aslan</name>
                                <affiliationId>3</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Obstetrics and Gynaecology, Faculty of Veterinary Medicine, Afyon Kocatepe University, ANS Campus, Afyonkarahisar, Turkey</affiliationName><affiliationName affiliationId="2">Department of Histology and Embryology, Faculty of Veterinary Medicine, Afyon Kocatepe University, ANS Campus, Afyonkarahisar, Turkey</affiliationName><affiliationName affiliationId="3">Department of Physiology, Faculty of Veterinary Medicine, Afyon Kocatepe University, ANS Campus, Afyonkarahisar, Turkey</affiliationName><affiliationName affiliationId="4">Department of Pathology, Faculty of Veterinary Medicine, Afyon Kocatepe University, ANS Campus, Afyonkarahisar, Turkey</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Aim:&lt;/b&gt; This study was design to describe the effect of 17&amp;#946; estradiol
on the dose-dependent expression patterns of endothelial nitric
oxide synthase (eNOS) and inducible NOS (iNOS) enzymes by
Western blotting in ovariectomized rat uterus.&lt;p&gt;
&lt;b&gt;Materials and Methods:&lt;/b&gt; Female, three months old,
ovariectomized, 40 Sprague&amp;#8211;Dawley rats were used. Rats in the
control group (n=10) received intramuscular injection of sesame
oil once daily for 3 days, whereas rats in the experimental groups
were treated with intramuscular injection of 17&amp;#946; estradiol 25
(n=10), 50 (n=10) and 100 (n=10) &amp;#956;g/rat/day. The rats were
killed by cervical dislocation at 18&lt;sup&gt;th&lt;/sup&gt; hour after the last injection.
Immediately after death, the uterine horns were removed. The
presence of eNOS and iNOS enzymes in uterine samples were
analysed by Western blot and the densitometry of each film were
performed.&lt;p&gt;
&lt;b&gt;Results:&lt;/b&gt; It was observed that the application of 25, 50 and
100 &amp;#956;g/rat/day 17&amp;#946; estradiol increased the eNOS expression
as compared to control group The relative density of eNOS
expressions in 25 and 50 &amp;#956;g/rat/day 17&amp;#946; estradiol groups
was higher than those in 100 &amp;#956;g/rat/day 17&amp;#946; estradiol group.
Similarly to eNOS, 25 and 50 &amp;#956;g/rat/day 17&amp;#946; estradiol groups
showed higher iNOS expression as compared to control and 100
&amp;#956;g/rat/day 17&amp;#946; estradiol groups.&lt;p&gt;
&lt;b&gt;Conclusion:&lt;/b&gt; Estrogen may mediate the NOS/NO activity in
ovariectomized rat uterus.</abstract>
              <fullTextUrl format="pdf">http://eurasianjvetsci.org/pdf.php3?id=989</fullTextUrl>
              <keywords><keyword>17&amp;#946; estradiol</keyword><keyword>eNOS</keyword><keyword>iNOS</keyword><keyword>rat uterus</keyword><keyword>ovariectomy</keyword>
                  </keywords>
            </record>

            <record>
              <language>eng</language>
              <publisher>Selçuk Üniversitesi Veteriner Fakültesi</publisher>
              <journalTitle>Eurasian Journal of Veterinary Sciences</journalTitle>
              <issn>1309-6958</issn>
              <eissn>2146-1953</eissn>
              <publicationDate>0000-00-00</publicationDate>
              <volume>29</volume>
              <issue>2</issue>
              <startPage>70</startPage>
              <endPage>75</endPage>
              <doi></doi>
              <publisherRecordId>990</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Determination of growth performance of the saanen kids reared in north-west mediterranean condition</title>
                <authors>
                              <author>
                                <name>Aykut Asım Akbaş</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Mehmet Çolak</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Özkan Elmaz</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Mustafa Saatcı</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Mehmet Akif Ersoy Üniversitesi, Veteriner Fakültesi, Zootekni Anabilim Dalı, Burdur, Türkiye</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Aim:&lt;/b&gt; The aim of this study was to determine the growth
and some body measurements of Saanen kids reared on the
northwest Mediterranean until 90&lt;sup&gt;th&lt;/sup&gt; days.&lt;p&gt;
&lt;b&gt;Materials and Methods:&lt;/b&gt; The research has been carried out
on 136 Saanen kids which were born in 2010 and 2011. Birth
weights of the kids were recorded using 50 g-sensitive precision
scales within 12 hours following the birth. Kids live weights were
taken from birth up to 90&lt;sup&gt;th&lt;/sup&gt; days by 15 days intervals. Height at
withers, rump height, body length and heart girth of kids were
detected in the same period.&lt;p&gt;
&lt;b&gt;Results:&lt;/b&gt; The average live weights of Saanen male and female
kids on birth, 30&lt;sup&gt;th&lt;/sup&gt;, 60&lt;sup&gt;th&lt;/sup&gt; and 90&lt;sup&gt;th&lt;/sup&gt; days were determined to be 3.42
kg and 3.16 kg, 7.92 kg and 7.86 kg, 11.39 kg and 10.82 kg, 15.35
kg and 14.60 kg, respectively. The average of zoometrical body
measurements such as height at withers, rump height, body
length and heart girth were detected as 52.46 cm and 51.58 cm,
52.95 cm and 52.07 cm, 52.15 cm and 51.72 cm, 51.78 cm and
51.05 cm, respectively. While birth year had an important effect
on all the growth periods, sex and the birth type affected 90th
day value. Also, positive and high correlations were detected
between live weight and body measurements until the age that
were followed up to growth.&lt;p&gt;
&lt;b&gt;Conclusion:&lt;/b&gt; Consistent results can be obtained by determination
of correlations between live weights and body parts measured
easily. Also these correlations can be used as a criteria for early
selection studies.</abstract>
              <fullTextUrl format="pdf">http://eurasianjvetsci.org/pdf.php3?id=990</fullTextUrl>
              <keywords><keyword>Saanen</keyword><keyword>kid</keyword><keyword>live weight</keyword><keyword>body measurements</keyword>
                  </keywords>
            </record>

            <record>
              <language>eng</language>
              <publisher>Selçuk Üniversitesi Veteriner Fakültesi</publisher>
              <journalTitle>Eurasian Journal of Veterinary Sciences</journalTitle>
              <issn>1309-6958</issn>
              <eissn>2146-1953</eissn>
              <publicationDate>0000-00-00</publicationDate>
              <volume>29</volume>
              <issue>2</issue>
              <startPage>76</startPage>
              <endPage>81</endPage>
              <doi></doi>
              <publisherRecordId>991</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Investigation of mycoplasma gallisepticum infection in layer flocks by rapid serum agglutination, culture and polymerase chain reaction methods</title>
                <authors>
                              <author>
                                <name>Kamile  Kesler</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Leyla Güler</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Gülşen Orhan</name>
                                <affiliationId>3</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Konya Veteriner Kontrol Enstitüsü Müdürlüğü, Meram, Konya, Türkiye</affiliationName><affiliationName affiliationId="2">Mehmet Akif Ersoy Üniversitesi, Veteriner Fakültesi, Mikrobiyoloji Anabilim Dalı, Burdur, Türkiye</affiliationName><affiliationName affiliationId="3">Ceren Veterinerlik ve Laboratuvar Hizmetleri, Konya, Türkiye</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Aim:&lt;/b&gt; Chronic respiratory disease of chickens caused by Mycoplasma
gallisepticum (MG) causes significant economic losses to poultry
industry due to decreased meat and egg production. In this study
MG infection in layer flocks was investigated by rapid serum
agglutination (RSA), culture and polymerase chain reaction (PCR)
methods.&lt;p&gt;
&lt;b&gt;Materials and Methods:&lt;/b&gt; A total of 375 chicken sera from 15
commercial layer flocks older than 24 weeks, 25 sera per flocks,
were tested by RSA. Tracheal (before and after necropsy), air sac and
lung swabs of 292 samples collected from 73 chickens were tested
for MG isolation. Culture broths of 292 samples and 73 tracheal
swabs directly from live chickens were tested by PCR.&lt;p&gt;
&lt;b&gt;Results:&lt;/b&gt; In 13 (86.6%) of 15 flocks a seropositivity rate between 12
to 100% was detected by RSA while all sera from 2 (13.3%) of flocks
were found negative. MG was isolated from 3 of 73 chickens belong
to 3 (20%) flocks. In 292 culture broths, 9 of 73 chickens from 7
(46.6%) flocks and in 2 of 73 tracheal swabs of live chickens from 2
(13.3%) flocks were PCR positive. Although serology was positive in
majority of flocks, detection rate of microorganism or DNA was low.
When evaluated with clinical findings the results indicate a presence
of chronic infection in these flocks.&lt;p&gt;
&lt;b&gt;Conclusion:&lt;/b&gt; In the diagnosis of MG infection of chickens, serological
tests are not sufficient alone because antibodies remain for a long
time after infection. Therefore, for the diagnosis of clinical infection
and therapy decisions in commercial flocks, serological findings in
the flock should be supported by PCR and/or culture.</abstract>
              <fullTextUrl format="pdf">http://eurasianjvetsci.org/pdf.php3?id=991</fullTextUrl>
              <keywords><keyword>Chicken</keyword><keyword>Mycoplasma gallisepticum</keyword><keyword>isolation</keyword><keyword>RSA</keyword><keyword>PCR</keyword>
                  </keywords>
            </record>

            <record>
              <language>eng</language>
              <publisher>Selçuk Üniversitesi Veteriner Fakültesi</publisher>
              <journalTitle>Eurasian Journal of Veterinary Sciences</journalTitle>
              <issn>1309-6958</issn>
              <eissn>2146-1953</eissn>
              <publicationDate>0000-00-00</publicationDate>
              <volume>29</volume>
              <issue>2</issue>
              <startPage>82</startPage>
              <endPage>86</endPage>
              <doi></doi>
              <publisherRecordId>992</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Investigation of bovine herpesvirus-1, bovine viral diarrhea virus and bovine herpesvirus-4 in a dairy herd with naturally infected in konya</title>
                <authors>
                              <author>
                                <name>Oğuzhan  Avcı</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Sibel Yavru</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Selçuk Üniversitesi, Veteriner Fakültesi, Viroloji Anabilim Dalı, Konya, Türkiye</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Aim:&lt;/b&gt; The research was aimed to determine the presence of Bovine
Herpesvirus-1 (BHV-1), Bovine Viral Diarrhea Virus (BVDV) and
Bovine Herpesvirus-4 (BHV-4) infections in a dairy herd with
abortion problem in Konya and to determine their possible roles for
abortions.&lt;p&gt;
&lt;b&gt;Materials and Methods:&lt;/b&gt; Blood serum and leukocyte samples
were collected from cattle (450) in herd. Blood sera samples were
investigated for antibodies to three infections by indirect Enzyme
Linked Immunosorbent Assay (ELISA). Also, leukocyte samples were
investigated for the presence of BVDV antigen by direct ELISA.&lt;p&gt;
&lt;b&gt;Results:&lt;/b&gt; Of the 450 samples tested, 72.88%, 46.22% and 20.22%
were determined to be seropositive for BHV-1, BVDV and BHV-
4 antibodies, respectively. BVDV antigen was not detected in any
leukocyte samples.&lt;p&gt;
&lt;b&gt;Conclusion:&lt;/b&gt; All herds with abortion problem should be examined
for viral agents that cause abortion.</abstract>
              <fullTextUrl format="pdf">http://eurasianjvetsci.org/pdf.php3?id=992</fullTextUrl>
              <keywords><keyword>BHV-1</keyword><keyword>BVDV</keyword><keyword>BHV-4</keyword><keyword>abort</keyword><keyword>cattle</keyword>
                  </keywords>
            </record>

            <record>
              <language>eng</language>
              <publisher>Selçuk Üniversitesi Veteriner Fakültesi</publisher>
              <journalTitle>Eurasian Journal of Veterinary Sciences</journalTitle>
              <issn>1309-6958</issn>
              <eissn>2146-1953</eissn>
              <publicationDate>0000-00-00</publicationDate>
              <volume>29</volume>
              <issue>2</issue>
              <startPage>87</startPage>
              <endPage>91</endPage>
              <doi></doi>
              <publisherRecordId>993</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Investigation of canine parainfluenza virus type 2 in dogs by immunofluorescence</title>
                <authors>
                              <author>
                                <name>Oğuzhan  Avcı</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Oya Bulut</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Orhan Yapıcı</name>
                                <affiliationId>1</affiliationId>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Atilla Şimşek</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Sibel Hasırcıoğlu</name>
                                <affiliationId>3</affiliationId>
                              </author>
                              <author>
                                <name>Sibel Yavru</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Mehmet Kale</name>
                                <affiliationId>3</affiliationId>
                              </author>
                              <author>
                                <name>Irmak Dik</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Kamil Atlı</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Selçuk Üniversitesi, Veteriner Fakültesi, Viroloji Anabilim Dalı, Konya, Türkiye</affiliationName><affiliationName affiliationId="2">Kırgızistan-Türkiye Manas Üniversitesi, Veteriner Fakültesi, Viroloji Anabilim Dalı, Bişkek, Kırgızistan</affiliationName><affiliationName affiliationId="3">Mehmet Akif Ersoy Üniversitesi, Veteriner Fakültesi, Viroloji Anabilim Dalı, Burdur, Türkiye</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Aim:&lt;/b&gt; It was aimed to determine the Canine Parainfluenza Virus
Type 2 (CPIV-2) in dogs by immunofluorescence (IF).&lt;p&gt;
&lt;b&gt;Materials and Methods:&lt;/b&gt; In this study nasal and conjunctival
swab samples were obtained from 61 pet dogs with clinical signs
of respiratory system. Swab samples (total 132) were passaged
on Madin-Darby Canine Kidney (MDCK) cell cultures for three
times. Cell culture supernatant obtained from last passage was
tested for CPIV-2 by IF.&lt;p&gt;
&lt;b&gt;Results:&lt;/b&gt; Swab samples were inoculated onto MDCK cell cultures
and subjected to three passages and no CPE was observed. All
cell culture supernatants were analyzed by IF but no positive
results to be determined.&lt;p&gt;
&lt;b&gt;Conclusion:&lt;/b&gt; Although all of the samples were determined
as negative, CPIV-2 dogs showing clinical signs of respiratory
system should be examined for the presence of both CPIV and
other respiratoric viral agents.</abstract>
              <fullTextUrl format="pdf">http://eurasianjvetsci.org/pdf.php3?id=993</fullTextUrl>
              <keywords><keyword>CPIV-2</keyword><keyword>dog</keyword><keyword>MDCK</keyword><keyword>immunofluorescence</keyword>
                  </keywords>
            </record>

            <record>
              <language>eng</language>
              <publisher>Selçuk Üniversitesi Veteriner Fakültesi</publisher>
              <journalTitle>Eurasian Journal of Veterinary Sciences</journalTitle>
              <issn>1309-6958</issn>
              <eissn>2146-1953</eissn>
              <publicationDate>0000-00-00</publicationDate>
              <volume>29</volume>
              <issue>2</issue>
              <startPage>92</startPage>
              <endPage>96</endPage>
              <doi></doi>
              <publisherRecordId>994</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Comparison of various techniques used for diagnosis of rabies in cats</title>
                <authors>
                              <author>
                                <name>Mugale Madhav Nilakanth</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Bhupinder Singh Sandhu</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Beigh Akeel</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Gupta Kuldeep</name>
                                <affiliationId>3</affiliationId>
                              </author>
                              <author>
                                <name>Sood Naresh Kumar</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Charan Kamal Singh</name>
                                <affiliationId>2</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Veterinary Pathology, Madras Veterinary College, Vepary, Chennai, Tamilnadu</affiliationName><affiliationName affiliationId="2">Department of Veterinary Pathology, GADVASU, (PAU campus) Ludhiana, Punjab, India</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Aim:&lt;/b&gt; Objectives of this study was to compare and evaluate the
best method for diagnosis of rabies in cats.&lt;p&gt;
&lt;b&gt;Materials and Methods:&lt;/b&gt; Antemortem examination of 5
suspected cats were evaluated. Brains were collected from
the suspected cats. Direct Fluorescent Antibody Test (dFAT),
Hematoxylin and Eosin (H &amp; E) and Immunohistochemistry
(IHC) histopathological diagnostic tests were applied.&lt;p&gt;
&lt;b&gt;Results:&lt;/b&gt; The dFAT test was conducted on the saliva and fresh
brain impression smear of all cats, among that 4 cats showed
positive for rabies virus. After death of cats, Hematoxylin &amp;
Eosin (H&amp;E) and Immunohistochemistry (IHC) techniques were
carried out. One case showed meningitis and remaining showed
Negri bodies. Viral antigen depositions were observed by
counting 100 cells each region of hippocampus and cerebellum
by H&amp;E and IHC. Hippocampus pyramidal cell showed 87% and
cerebellum Purkinje cells showed 69% of rabies viral antigen
deposition.&lt;p&gt;
&lt;b&gt;Conclusion:&lt;/b&gt; The IHC can be used as reliable diagnostic
technique in addition to dFAT. IHC shows positivity in mildly
infected cases and having immense value for retrospective
studies. It also minimizes the risk of public health hazard during
shipping of rabid positive brain samples.</abstract>
              <fullTextUrl format="pdf">http://eurasianjvetsci.org/pdf.php3?id=994</fullTextUrl>
              <keywords><keyword>Brain</keyword><keyword>direct fluorescent antibody test</keyword><keyword>histopathology</keyword><keyword>immunohistochemistry</keyword><keyword>rabies</keyword>
                  </keywords>
            </record>

            <record>
              <language>eng</language>
              <publisher>Selçuk Üniversitesi Veteriner Fakültesi</publisher>
              <journalTitle>Eurasian Journal of Veterinary Sciences</journalTitle>
              <issn>1309-6958</issn>
              <eissn>2146-1953</eissn>
              <publicationDate>0000-00-00</publicationDate>
              <volume>29</volume>
              <issue>2</issue>
              <startPage>97</startPage>
              <endPage>102</endPage>
              <doi></doi>
              <publisherRecordId>995</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Detection of bovine viral diarrhea virus antibodies in blood and milk serum in dairy cattle by elisa</title>
                <authors>
                              <author>
                                <name>Sibel  Yavru</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Atilla Şimşek</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Mehmet Kale</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Oya Bulut</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Orhan Yapıcı</name>
                                <affiliationId>1</affiliationId>
                                <affiliationId>3</affiliationId>
                              </author>
                              <author>
                                <name>Oğuzhan Avcı</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Irmak Dik</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Selçuk Üniversitesi, Veteriner Fakültesi, Viroloji ABD, Konya, Türkiye</affiliationName><affiliationName affiliationId="2">Mehmet Akif Ersoy Üniversitesi, Veteriner Fakültesi, Viroloji ABD, Burdur, Türkiye</affiliationName><affiliationName affiliationId="3">Türkiye-Kırgızistan Manas Üniversitesi, Veteriner Fakültesi, Bişkek, Kırgızistan</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Aim:&lt;/b&gt; The aim of this study was to detection of Bovine Viral
Diarrhea Virus (BVDV) antigens and determine of antibodies
against BVDV in blood and milk serum.&lt;p&gt;
&lt;b&gt;Materials and Methods:&lt;/b&gt; Totally 202 cattle blood and milk sera
samples were used. Samples obtained from herds were analyzed
for the detection of BVDV antigens by direct Enyzme Linked
Immunosorbent Assay (ELISA) and for determine the presence
of antibodies against BVDV by indirect ELISA.&lt;p&gt;
&lt;b&gt;Results:&lt;/b&gt; While 167 of blood serum (82.6%) were positive for
the presence of BVDV antibodies, 160 of milk serum samples
(79.2%) were positive. In this study, 148 (73.2%) both blood
and milk serum samples of same cattle were positive for BVDV
antibodies. Only 19 (9.4%) blood serum of cattle was detected
positive for BVDV, while only 12 (5.94%) milk serum was
seropositive. No positive result to be determined for BVDV
antigens in any blood or milk serum samples.&lt;p&gt;
&lt;b&gt;Conclusion:&lt;/b&gt; Determined similar indirect ELISA results of blood
and milk sera (P&gt;0.05) may be suggest that milk sera can be
used in determine of serological diagnosis of BVDV instead of
blood sera. Further research is needed in order to achieve using
blood and/or milk serum samples presence of BVDV antigens
instead of leukocytes samples in routine diagnosis, even though
not detect the presence of BVDV antigen in blood and milk serum
samples in this study.</abstract>
              <fullTextUrl format="pdf">http://eurasianjvetsci.org/pdf.php3?id=995</fullTextUrl>
              <keywords><keyword>Blood</keyword><keyword>milk</keyword><keyword>serum</keyword><keyword>BVDV</keyword><keyword>ELISA</keyword>
                  </keywords>
            </record>

            <record>
              <language>eng</language>
              <publisher>Selçuk Üniversitesi Veteriner Fakültesi</publisher>
              <journalTitle>Eurasian Journal of Veterinary Sciences</journalTitle>
              <issn>1309-6958</issn>
              <eissn>2146-1953</eissn>
              <publicationDate>0000-00-00</publicationDate>
              <volume>29</volume>
              <issue>2</issue>
              <startPage>103</startPage>
              <endPage>105</endPage>
              <doi></doi>
              <publisherRecordId>996</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Helminthosis of rural poultry in quetta, pakistan</title>
                <authors>
                              <author>
                                <name>Faizullah  Faizullah</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Sher Ahmed</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Shakeel Babar</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Syed Khurram Fareed</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Muhammad Azam Kakar</name>
                                <affiliationId>3</affiliationId>
                              </author>
                              <author>
                                <name>Ziaulhaq</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Saadullah Jan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Center for Advanced Studies in Vaccinology and Biotechnology, University of Balochistan, Quetta</affiliationName><affiliationName affiliationId="2">Federal Government Degree College, Madrissa Road, Quetta</affiliationName><affiliationName affiliationId="3">Faculty of Veterinary and Animal Sciences, Lasbella University of Agriculture, Water and Marine Sciences, Uthal, Pakistan</affiliationName></affiliationsList><abstract language="eng">Helminth parasites were studied in 120 rural chickens in
Quetta, showing overall infection to be 75.8%. Prevalence was
higher in winter (81.6%) than in summer (70%). Five cestodes
were found, i.e., Raillietina tetragona (48.3%), followed by
Choanotaenia spp. (20%), R. echinobothrida (19.2%), Cotugnia
spp. (1.7%) and R. cesticillus (0.8%). The nematode, Ascaridia
galli was more prevalent (10.8%) than Allodapa suctoria (0.8%).
Infection of one host with single species of helminth was seen
at most occasions (53.3%), followed by double, triple and
quadruple infections (20, 1.7 and 0.8%), respectively. Mixed
infection with both nematodes and cestodes was seen in 5.8% of
chickens. In conclusion, anthelmintic treatments should be done
routinely in the rural poultry.</abstract>
              <fullTextUrl format="pdf">http://eurasianjvetsci.org/pdf.php3?id=996</fullTextUrl>
              <keywords><keyword>Helminth</keyword><keyword>rural poultry</keyword><keyword>Pakistan</keyword>
                  </keywords>
            </record>

            <record>
              <language>eng</language>
              <publisher>Selçuk Üniversitesi Veteriner Fakültesi</publisher>
              <journalTitle>Eurasian Journal of Veterinary Sciences</journalTitle>
              <issn>1309-6958</issn>
              <eissn>2146-1953</eissn>
              <publicationDate>0000-00-00</publicationDate>
              <volume>29</volume>
              <issue>2</issue>
              <startPage>106</startPage>
              <endPage>109</endPage>
              <doi></doi>
              <publisherRecordId>997</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">An incidence of acute nitrate-nitrite poisoning in a guinea pig (cavia porcellus) colony</title>
                <authors>
                              <author>
                                <name>Nakulan Valsala Rajesh</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Veluchamy Kumar</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Palanisamy Ganapathi</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Marudhai Thangapandiyan</name>
                                <affiliationId>2</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Institute of Veterinary Preventive Medicine, Ranipet, Tamilnadu</affiliationName><affiliationName affiliationId="2">Department of Veterinary Pathology, Madras Veterinary College, Chennai, India</affiliationName></affiliationsList><abstract language="eng">We present an incidence of acute nitrate-nitrite poisoning in
a guinea pig (Cavia porcellus) colony which resulted in the
substantial and spontaneous death of 28 out of 88 guinea pigs.
The cause of death was traced to nitrate-nitrite toxicity from
ingestion of the green leaves of overfertilized Cichorium intybus.
The predominant symptoms in the 28 guinea pigs were chocolate
brown bloody discharge from all natural orifices, cyanotic
mucous membrane, mydriasis, and bloated abdomen. Necropsy
of all the 28 animals showed hemorrhage in all visceral organs
grossly, and tubular nephrosis of the kidney, lymphoid depletion
in the spleen, hydropic changes and necrosis in hepatocytes,
and hemorrhages in the intestine and lungs histopathologically.
Nitrate-nitrite toxicity was confirmed spectrophotometrically.
The toxicological analysis of the feed samples of C. intybus
revealed 2.1 g% nitrate, 1.0 g% nitrite, and 80 ppb citrinin. The
intestinal loop had 10 ppm of nitrate and 1 ppm of nitrite. To the
best of our knowledge, this is the first report of acute nitratenitrite
poisoning in guinea pigs owing to the ingestion of the
green leaves of overfertilized C. intybus.</abstract>
              <fullTextUrl format="pdf">http://eurasianjvetsci.org/pdf.php3?id=997</fullTextUrl>
              <keywords><keyword>Nitrate-nitrite poisoning</keyword><keyword>Cichorium intybus</keyword><keyword>guinea pig</keyword>
                  </keywords>
            </record>

            <record>
              <language>eng</language>
              <publisher>Selçuk Üniversitesi Veteriner Fakültesi</publisher>
              <journalTitle>Eurasian Journal of Veterinary Sciences</journalTitle>
              <issn>1309-6958</issn>
              <eissn>2146-1953</eissn>
              <publicationDate>0000-00-00</publicationDate>
              <volume>29</volume>
              <issue>2</issue>
              <startPage>110</startPage>
              <endPage>113</endPage>
              <doi></doi>
              <publisherRecordId>998</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Congenital meningoencephalocele in a brown swiss calf: a case report</title>
                <authors>
                              <author>
                                <name>Turan  Yaman</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Serkan Erdoğan</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Funda Terzi</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Zafer Özyıldız</name>
                                <affiliationId>3</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Pathology, Faculty of Veterinary Medicine, Dicle University, Diyarbakır, Turkey</affiliationName><affiliationName affiliationId="2">Department of Anatomy, Faculty of Veterinary Medicine, Dicle University, Diyarbakır, Turkey</affiliationName><affiliationName affiliationId="3">Department of Pathology, Faculty of Veterinary Medicine, Harran University, Şanlıurfa, Turkey</affiliationName></affiliationsList><abstract language="eng">After inspection and radiological examinations, meningocele
was suspected on a 2-day old Brown swiss male calf which
was brought dead to the Department of Pathology, Faculty
of Veterinary Medicine in Dicle University. As a result of the
anatomopathologic analysis, a saclike protrusion that was 17x15
cm sized fluctuant and covered with a hairy skin was observed
on frontal squama. In the pouch, approximately 200 mL serous
fluid mixed with blood were seen. The brain was also protrused
with meninges rostro-dorsal to frontal region. Ethmoid bone was
formed rudimentary, so ethmoid labyrinths was not detected in
this region. On the other hand, absences of nasal bone, nasal
part of frontal bone, nasal conchae and rostral half of hard
palate were detected. Cerebral hypoplasia with macrogyria was
evident. In conclusion, rarely observed meningoencephalocele
case was firstly identified as anatomopathologically in a calf in
Diyarbakır province.</abstract>
              <fullTextUrl format="pdf">http://eurasianjvetsci.org/pdf.php3?id=998</fullTextUrl>
              <keywords><keyword>Calf</keyword><keyword>congenital meningoencephalocele</keyword>
                  </keywords>
            </record></records>