Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Güngör T.Tümay"'
Autor:
S. Sökücü, Tülay Erkan, Beyhan Tüysüz, Tufan Kutlu, Nihan Erginel-Unaltuna, A. Dursun, Ö. Süoğlu, Naci Cine, Güngör T.Tümay
Publikováno v:
Tissue Antigens. 57:540-542
The prevalence of the HLA-DQA1 and DQB1 alleles in 55 Turkish children with celiac disease and 50 control subjects was investigated by using an allele-specific DNA-based polymerase chain reaction-sequence-specific primer (PCR-SSP) method. The frequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa4c906907b62249cd1f24f9aa0e20f3
https://doi.org/10.1034/j.1399-0039.2001.057006540.x
https://doi.org/10.1034/j.1399-0039.2001.057006540.x
Autor:
Kaypmaz A, Ahmet Arvas, Ethem Erginöz, Fügen Çullu, Güngör T.Tümay, Tufan Kutlu, Yücel Taştan, Mujgan Alikasifoglu
Publikováno v:
Journal of Tropical Pediatrics. 47:60-62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f098bd0567f1285597bd3f03d29415e1
https://doi.org/10.1093/tropej/47.1.60
https://doi.org/10.1093/tropej/47.1.60
Publikováno v:
Archives de Pédiatrie. 5:1344-1346
Resume Le syndrome de Hennekam est caracterise par des lymphangiectasies intestinales, une dysmorphie faciale et une deficience mentale moderee. Huit cas ont ete rapportes a ce jour. Observation Une fillette âgee de 17 mois a consulte pour des odeme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6af63ed16445694d85b5319d6ace389b
https://doi.org/10.1016/s0929-693x(99)80054-2
https://doi.org/10.1016/s0929-693x(99)80054-2
Autor:
M.K. Gumustas, Vida Shams, Hafize Kaya, Seval Aydin, Güngör T.Tümay, Tülay Erkan, Fügen Çullu, Tufan Kutlu
Publikováno v:
Journal of tropical pediatrics. 49(1)
The hyperdynamic circulation of cirrhosis and portal hypertension has been postulated to be due to the vasodilatory effects of nitric oxide. However, there have been conflicting results in adults and no studies in children. We aimed to measure the ni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3951d927a424a04f9ae9fc17cb5c4c79
https://pubmed.ncbi.nlm.nih.gov/12630718
https://pubmed.ncbi.nlm.nih.gov/12630718
Autor:
Tül.A.Y. Erkan, Füg.E.N. Çullu, Enver Gülcan, Hilmi Apak, Güngör T.Tümay, Tufan Kutlu, Ç.I.G.D.E.M. Aktuglu
Publikováno v:
The Journal of adolescent health : official publication of the Society for Adolescent Medicine. 31(4)
Wilson disease (WD), referred to as hepatolenticulardegeneration and occurring primarily as neurologi-cal and liver disease, is an inherited disorder that hasvarious clinical presentations [1–3]. The altered geneis localized on the long arm of chro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4636673884fd3856dcc26936c930c49
https://pubmed.ncbi.nlm.nih.gov/12359384
https://pubmed.ncbi.nlm.nih.gov/12359384
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 87(9)
We present a case of hepatitis A infection in a 2.5-month-old male who became icteric after 18 d of birth. The diagnosis of hepatitis A was made by compatible clinical symptoms, laboratory results and liver biopsy showing evidence of hepatitis, and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::465e5d66c9806ad9fac214e09a032283
https://pubmed.ncbi.nlm.nih.gov/9764900
https://pubmed.ncbi.nlm.nih.gov/9764900
Publikováno v:
Archives de Pédiatrie. 5:233
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ef5443e4cdd69e448303eab9c5ac155
https://doi.org/10.1016/s0929-693x(97)86909-6
https://doi.org/10.1016/s0929-693x(97)86909-6