Zobrazeno 1 - 10
of 220
pro vyhledávání: '"Tinaztepe K"'
Autor:
Mithat Büyükçelik, Bulent Gogebakan, Mesut Parlak, Sibel Oguzkan Balci, Ayse Balat, Nilgün Çöl, Tinaztepe K, Seval Kul
Publikováno v:
The Turkish Journal of Pediatrics. 62:208
BACKGROUND AND OBJECTIVES There are controversial results in the literature regarding urinary electrolytes, especially potassium, in enuretic children. KCNJ10 channel protein, a member of the Kir 4.1 family is expressed in renal distal tubules and ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8c32bb92b8db05fbaa2416a4538d987
https://doi.org/10.24953/turkjped.2020.02.006
https://doi.org/10.24953/turkjped.2020.02.006
Autor:
Tinaztepe K, Nesrin Besbas, Hanan Gur, Eldad Ben-Chetrit, Meral Calguneri, Tekin Akpolat, Seza Ozen, Aydin Turkmen, Ilkser Akpolat, Aysin Bakkaloglu, Cetin Turgan, Murat Danaci
Publikováno v:
Seminars in Arthritis and Rheumatism. 30:281-287
Background: Familial Mediterranean Fever (FMF) is caused by mutations in the gene encoding pyrin and is characterized by self-limited, recurrent attacks of fever and serositis. Vasculitis has been increasingly reported in FMF. A study evaluating the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2db8295c3dffb045ad242d1c5e7d094
https://doi.org/10.1053/sarh.2001.19958
https://doi.org/10.1053/sarh.2001.19958
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 27:86-89
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36eef7884f8dbd34b2940560a2224d6a
https://doi.org/10.1097/00005176-199807000-00015
https://doi.org/10.1097/00005176-199807000-00015
Publikováno v:
International Urology and Nephrology. 29:711-716
Membranoproliferative glomerulonephritis (MPGN) is a distinctive form of chronic glomerulonephritis. We present the results of our 96 paediatric patients with MPGN, reporting the survival and factors affecting prognosis in these patients. There were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9233a464c7bd9bc5604d7916f421ab80
https://doi.org/10.1007/bf02552190
https://doi.org/10.1007/bf02552190
Autor:
Meral Özgüç, Tinaztepe K, Nesrin Besbas, Rezan Topaloglu, Engin Yilmaz, Safak Gucer, Seza Ozen, Banu Balci, Aysin Bakkaloglu
Publikováno v:
Scopus-Elsevier
Background Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurring attacks of fever and serositis. The definition of the mutated gene has allowed molecular diagnosis of the disease. The most important complicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4c974e20deedb7e3c83f084de19df56
https://pubmed.ncbi.nlm.nih.gov/12401847
https://pubmed.ncbi.nlm.nih.gov/12401847
Autor:
Seza Ozen, Aysin Bakkaloglu, Nesrin Besbas, Tinaztepe K, A Gur-Guven, Ozgur Kasapcopur, E Baskin
Publikováno v:
Archives of disease in childhood. 85(5)
AIMS To describe the distribution and features of classic polyarteritis nodosa (PAN) and microscopic polyarteritis (MPA) and the importance of antineutrophil cytoplasmic antibody (ANCA) in childhood PAN. METHODS Classic PAN was diagnosed in 15 patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68d72786124e9c2b4034fe141ebb9550
https://pubmed.ncbi.nlm.nih.gov/11668111
https://pubmed.ncbi.nlm.nih.gov/11668111
WOS: 000167127700006 PubMed: 11182028 Background: Familial Mediterranean fever (FMF) is caused by mutations in the gene encoding pyrin and is characterized by self-limited, recurrent attacks of fever and serositis. Vasculitis has been increasingly re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9773::f201fca611029b96184abbd285377eff
https://hdl.handle.net/20.500.12712/22221
https://hdl.handle.net/20.500.12712/22221
Publikováno v:
Pediatric nephrology (Berlin, Germany). 14(4)
Renal involvement is common in childhood polyarteritis nodosa (PAN). We report a retrospective analysis of the presentation and clinical course of 26 patients with PAN and renal involvement. The mean age was 9.3 years (range 1–14 years) and there w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6f3360146ce38ac8ed07b386781f7a2
https://pubmed.ncbi.nlm.nih.gov/10775079
https://pubmed.ncbi.nlm.nih.gov/10775079
Autor:
Tinaztepe K, Seza Ozen
Publikováno v:
Nephron. 72(2)
Clinical and pathological findings in four Turkish infants with isolated diffuse mesangial sclerosis (DMS) are presented. All the patients were offsprings of consanguineous marriages and two had similarly affected sibs indicating an autosomal recessi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0706758c070f80de6314c76d306e20e5
https://pubmed.ncbi.nlm.nih.gov/8684541
https://pubmed.ncbi.nlm.nih.gov/8684541
Publikováno v:
Pediatric nephrology (Berlin, Germany). 9(1)
Twelve patients with Henoch-Schonlein purpura, aged 6-14 years (mean 10.3 years), presenting with rapidly progressive glomerulonephritis (RPGN) were investigated prospectively. Analysis of the initial clinical features revealed: oedema (8 patients),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::965d9da695d0da041559ddec6db8f5f4
https://pubmed.ncbi.nlm.nih.gov/7742225
https://pubmed.ncbi.nlm.nih.gov/7742225