Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Şahika Baysun"'
Publikováno v:
Turkderm Turkish Archives of Dermatology and Venereology, Vol 58, Iss 3, Pp 83-86 (2024)
Gardner-Diamond syndrome (GDS) is a condition characterized by the appearance of unexplained ecchymosis on the skin. Other common symptoms include gastrointestinal complaints, such as abdominal pain and vomiting, as well as complaints about the nervo
Externí odkaz:
https://doaj.org/article/bb886d4ef86049288950a4a0085f31ac
Autor:
Filiz Başak Cengiz Ergin, Mustafa Tekin, Meltem Güneş, Begüm Güneş, Şahika Baysun, Nejat Akar
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-4 (2022)
Abstract Background Incontinentia pigmenti (IP) is a rare X-linked dominant disorder affecting the skin and other ectodermal tissues that is caused by a mutation of the IKBKG/NEMO gene. Case presentation We describe a Turkish family with IP. Sanger s
Externí odkaz:
https://doaj.org/article/b66aae0061e142da8eca1958aeb48c4c
Autor:
Ozlem Erdogan, Ayşegül Oksal, Gülay Demircin, Ayse Oner, Leyla Memiş, Kenan Bek, Mehmet Bülbül, Şahika Baysun, Ali Delibaş
Publikováno v:
International Urology and Nephrology. 41:933-939
In this study we evaluated the indications, complications, and the spectrum of histopathological results of percutaneous renal needle biopsy (PRNB) performed in our clinic. Between June 1990 and December 2006, 679 PRNBs were performed on native kidne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77e92b4aa8de2e6bf9aae02af2dd177b
https://doi.org/10.1007/s11255-008-9433-9
https://doi.org/10.1007/s11255-008-9433-9
Publikováno v:
Pediatrics International. 52:e164-e166
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97343606d982ee93eadbb5d453670c0b
https://doi.org/10.1111/j.1442-200x.2010.03076.x
https://doi.org/10.1111/j.1442-200x.2010.03076.x
Publikováno v:
Pediatric Nephrology. 23:1235-1237
A 14-year-old girl was diagnosed with familial Mediterrenean fever (FMF) with homozygous for M694V mutation of the MEFV gene and was started on colchicine therapy 4 years before admission to our hospital. She was uncompliant to therapy and was admitt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::136bd6d7b58c52acad428070677c6b40
https://doi.org/10.1007/s00467-007-0680-2
https://doi.org/10.1007/s00467-007-0680-2
Autor:
Ozlem Erdogan, Ayşegül Oksal, Ayşe Öner, Kenan Bek, Şahika Baysun, Ali Delibaş, Mehmet Bülbül, Giilay Demircin
Publikováno v:
Renal failure. 30(6)
BEK, KENAN/0000-0002-1005-2379 WOS: 000258002700004 PubMed: 18661410 In this study, we evaluated the frequency, clinical presentation, treatment protocols, prognostic factors, and outcome in children with diffuse proliferative lupus nephritis (DPLN).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d854c7164293a4a302c77861fc6c66
https://pubmed.ncbi.nlm.nih.gov/18661410
https://pubmed.ncbi.nlm.nih.gov/18661410
Autor:
Kenan Bek, Mehmet Bülbül, Gülay Demircin, Ayse Oner, Ali Delibaş, Ozlem Erdogan, Şahika Baysun, Engin Yilmaz, Banu Balci
Publikováno v:
American journal of nephrology. 25(5)
BEK, KENAN/0000-0002-1005-2379; YILMAZ, Engin/0000-0001-8873-7645 WOS: 000232490000003 PubMed: 16118480 Background/ Aims: Evaluation of the risk factors, and phenotype- genotype correlation of familial Mediterranean fever ( FMF) gene ( MEFV) and seru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21c557173562a338b625f2c0f02f0936
https://pubmed.ncbi.nlm.nih.gov/16118480
https://pubmed.ncbi.nlm.nih.gov/16118480
Autor:
Ayse Oner, Şahika Baysun, Φzlem Erdogan, Mehmet Bülbül, Gülay Demircin, Nilüfer Arda, Tuba Eren
Publikováno v:
Pediatrics. 121:S144-S145
INTRODUCTION: The long-term prognosis in Henoch-Schönlein purpura is determined principally by the development of progressive glomerulonephritis (>10% progress to end-stage renal failure). OBJECTIVE: In this study we aimed to investigate the long-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c416482d79108633596663bb33788a1
https://doi.org/10.1542/peds.2007-2022vvvvv
https://doi.org/10.1542/peds.2007-2022vvvvv
Autor:
Gülay Demircin, Ali Delibaş, Mehmet Bülbül, Ozlem Erdogan, Kenan Bek, Şahika Baysun, Ayse Oner
Publikováno v:
Annals of Paediatric Rheumatology. 1:65
Objective: Juvenile dermatomyositis (JDM) is a rare disease of childhood characterized by nonsuppurative inflammation of striated muscle and skin and calcinosis is one of the most important sequelae of the disease. Methods: In this study we investiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8c8ae6423ccdcafd95c153d96ee96c9
https://doi.org/10.5455/apr.110520111313
https://doi.org/10.5455/apr.110520111313
Publikováno v:
Pediatric Nephrology. 23:1233-1233
A 14-year-old girl was diagnosed with familial Mediterranean fever (FMF) with homozygous for M694V mutation of the MEFV gene and was started on colchicine therapy 4 years before admission to our hospital. She was uncompliant to therapy and was admitt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d94a46967212995de0c7861804461554
https://doi.org/10.1007/s00467-007-0677-x
https://doi.org/10.1007/s00467-007-0677-x