Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Fatma İlknur VAROL"'
Publikováno v:
The Korean Journal of Gastroenterology, Vol 63, Iss 1, Pp 17-22 (2024)
Background/Aims: Solitary rectal ulcer syndrome (SRUS) can be overlooked, diagnosed late, or misdiagnosed, particularly in childhood. This study reviewed the 13-year experience of the authors’ institution to increase clinicians' awareness of SRUS i
Externí odkaz:
https://doaj.org/article/755358112c1e402c97eb747c632fb764
Autor:
İbrahim Umar Garzali, Abdirahman Sakulen Hargura, Volkan İnce, Fatma İlknur Varol, Brian I. Carr, Sezai Yılmaz
Publikováno v:
The Turkish Journal of Gastroenterology, Vol 34, Iss 12, Pp 1235-1239 (2023)
Externí odkaz:
https://doaj.org/article/a27142c2bb6048b0ba817681ebfd38a7
Publikováno v:
JCRPE, Vol 15, Iss 1, Pp 62-68 (2023)
INTRODUCTION: It has been reported that bone mineral density (BMD) is decreased in children with Celiac disease (CD) compared to their healthy peers. The aim of this study was to reveal possible risk factors for low BMD in Turkish children newly diag
Externí odkaz:
https://doaj.org/article/e153a41bafdf41c280c7e3a4bf48ab88
Publikováno v:
JCRPE, Vol 14, Iss 4, Pp 409-414 (2022)
INTRODUCTION: A close relationship has been suggested between Celiac disease (CD) and glandular autoimmunity. The aim of this study was to determine the predictive factors for autoimmune glandular disease (AGD) in children with CD. METHODS: The stud
Externí odkaz:
https://doaj.org/article/485cfeee11d743f98d4ef1463e6a3a72
Publikováno v:
Journal of Contemporary Medicine, Vol 11, Iss 2, Pp 147-150 (2021)
Aim: Gaucher disease is a rare lysosomal storage disease. Enzyme replacement therapy has proven to be very effective in reversing the risk of hepato-splenomegaly, cytopenia, osteopenia and reducing the risk of avasculer osteo necrosis, especially in
Externí odkaz:
https://doaj.org/article/9b1cd877b78a4e0e99e147e290210e9b
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 22, Iss 1, Pp 70-72 (2021)
While isotretinoin, a drug used for the treatment of severe nodulocystic acne, is known to be hepatotoxic, an association with autoimmune hepatitis (AIH) has not been suggested so far. A 17-year-old girl diagnosed with AIH following isotretinoin use
Externí odkaz:
https://doaj.org/article/8646a031226941b593585fb2261d4b33
Publikováno v:
Journal of Contemporary Medicine, Vol 10, Iss 3, Pp 471-472 (2020)
Sayın editör, Hatice Köse ve ark.nın[1] Cağdaş Tıp Dergisi’nin 2018 yılı ikinci sayısında (Cağdaş Tıp Dergisi 2018;8(2);165-167) yayımlanan“Erişkin bir visseral leishmaniazis olgusu:Tanı ve tedavi seçeneklerinin irdelenmesi: O
Externí odkaz:
https://doaj.org/article/57428e89bf874c2d86cee6b4c8a80542
Publikováno v:
Balkan Medical Journal, Vol 35, Iss 6, Pp 442-444 (2018)
Externí odkaz:
https://doaj.org/article/498a4af5e6d44360b2efb23f1751b567
Publikováno v:
São Paulo Medical Journal, Vol 136, Iss 4, Pp 304-309
ABSTRACT BACKGROUND: Wilson’s disease (WD) may present with different manifestations: from an asymptomatic state to liver cirrhosis. Here, we aimed to evaluate clinical presentations and laboratory findings and prognoses among WD cases. DESIGN AND
Externí odkaz:
https://doaj.org/article/3cb149a9390a4bf1991cbea20d7de262
Publikováno v:
Arab Journal of Gastroenterology. 22:310-315
Background and study aims Progressive familial intrahepatic cholestasis (PFIC) is an autosomal recessively inherited disease that causes intrahepatic-hepatocellular cholestasis. PFIC constitutes approximately 10–15% of cholestatic liver diseases in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0efaa8333b1d109916d237d7ecf6cc7a
https://doi.org/10.1016/j.ajg.2021.05.021
https://doi.org/10.1016/j.ajg.2021.05.021