Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tarkan Kalkan"'
Autor:
Ayşehan Akıncı, Doğa Türkkahraman, İbrahim Tekedereli, Leyla Özer, Bahri Evren, İbrahim Şahin, Tarkan Kalkan, Yusuf Çürek, Emine Çamtosun, Esra Döğer, Aysun Bideci, Ayla Güven, Erdal Eren, Özlem Sangün, Atilla Çayır, Pelin Bilir, Ayça Törel Ergür, Oya Ercan
Publikováno v:
JCRPE, Vol 11, Iss 4, Pp 341-349 (2019)
Objective:Non syndromic monogenic obesity is a rare cause of early onset severe obesity in the childhood period. This form may not be distinguishable from other forms of severe obesity without genetic analysis, particularly if patients do not exibit
Externí odkaz:
https://doaj.org/article/becf95a4d1e646db81c94a832df61196
Publikováno v:
Haseki Tıp Bülteni, Vol 55, Iss 1, Pp 82-84 (2017)
Touraine-Solente-Gole syndrome, also known as pachydermoperiostosis, is transmitted as an autosomal recessive trait. It is characterized by enlargement of fingers and toes, pachyderma, excessive sweating, and pain. In this paper, we present a 9-year-
Externí odkaz:
https://doaj.org/article/1bc233b7ee1f422f84ea9bdcaeb2efac
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::042868f4913349b018de791cba19b8a2
https://doi.org/10.4274/jcrpe.galenos.2023.2022-9-14
https://doi.org/10.4274/jcrpe.galenos.2023.2022-9-14
Autor:
Doga Turkkahraman, Tarkan Kalkan, Pelin Bilir, Esra Döğer, Leyla Özer, Emine Çamtosun, Bahri Evren, Ayla Güven, Atilla Cayir, Özlem Sangün, Ayşehan Akıncı, Yusuf Çürek, Oya Ercan, Ayça Törel Ergür, İbrahim Tekedereli, Aysun Bideci, Ibrahim Sahin, Erdal Eren
Publikováno v:
JCRPE, Vol 11, Iss 4, Pp 341-349 (2019)
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology
Eren, Erdal/0000-0002-1684-1053; Ercan, Oya/0000-0001-7397-2837; camtosun, emine/0000-0002-8144-4409; Turkkahraman, Doga/0000-0002-7472-5712 WOS:000498876500002 PubMed ID: 30991789 Objective: Non syndromic monogenic obesity is a rare cause of early o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::043e25de3612584245b0e03ddd3406c1
https://avesis.gazi.edu.tr/publication/details/3c4fb91c-5f67-4112-a7b9-7ec6b83137a3/oai
https://avesis.gazi.edu.tr/publication/details/3c4fb91c-5f67-4112-a7b9-7ec6b83137a3/oai
Publikováno v:
SiSli Etfal Hastanesi Tip Bulteni / The Medical Bulletin of Sisli Hospital. :243-6
Objective: Mucopolysaccharidoses, develop with genetic transmission which cause destructive changes in various organs as a result of glycasoaminoglycans deposition in lysosomes. Herein, we are presenting a case with Morquio syndrome so as to attract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::255902926b3b7643fafdecc782f753be
https://doi.org/10.5350/semb.20160611123415
https://doi.org/10.5350/semb.20160611123415
Autor:
Lale Şatiroğlu Tufan, C. Nur Semerci, Tarkan Kalkan, Gülseren Bağci, Metin Eser, Özkan Öztürk, G. Ozan Çetin
A 30-year-old male patient referred to our clinic for unraveling the underlying etiology of the azoospermia. He had no unusual medical history. At physical examination, obesity, short neck and gynecomastia were noted. All hormone levels were normal e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3be8da31bd14f4c6733f5c9b47fe9db3
https://doi.org/10.5336/medsci.2011-23453
https://doi.org/10.5336/medsci.2011-23453