Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Feride Tahmiscioğlu Bucak"'
Autor:
Elif Söbü, Gül Demet Kaya Özçora, Elif Yılmaz Güleç, Bahtiyar Şahinoğlu, Feride Tahmiscioğlu Bucak
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 344-350 (2024)
Microcephaly, epilepsy and diabetes syndrome 1 (MEDS1) is a rare autosomal recessive disorder caused by defects in the immediate early response 3 interacting protein 1 (IER3IP1) gene. Only nine cases have been described in the literature. MEDS1 manif
Externí odkaz:
https://doaj.org/article/bd9f2857a6604e8f9587537dbd9bc503
Autor:
Bahar Özcabi, Gürkan Tarçın, Esma Şengenç, Feride Tahmiscioğlu Bucak, Oya Ercan, İbrahim Murat Bolayırlı, Olcay Evliyaoğlu
Publikováno v:
JCRPE, Vol 13, Iss 2, Pp 152-159 (2021)
Objective:Obesity is known to affect thyroid function. Recently, waist-height ratio (WHtR) has been considered as a useful marker of subclinical hypothyroidism in obese cases, but its relation with thyroid autoimmunity still remains unclear. We evalu
Externí odkaz:
https://doaj.org/article/5546171652294e2a813f38685e6fbd87
Autor:
Elif, Söbü, Gül Demet, Kaya Özçora, Elif, Yılmaz Güleç, Bahtiyar, Şahinoğlu, Feride, Tahmiscioğlu Bucak
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.
Microcephaly, Epilepsy, and Diabetes Syndrome 1 (MEDS1) is a rare autosomal recessive disorder and caused by defects in the IER3IP1 (Immediate Early Response 3 Interacting Protein 1) gene. Only 9 cases have been described in the literature. MEDS1 man
Autor:
Bahar Özcabı, Feride Tahmiscioğlu Bucak, Serdar Ceylaner, Rahşan Özcan, Cenk Büyükünal, Oya Ercan, Beyhan Tüysüz, Olcay Evliyaoğlu
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 7:242-248
Testotoxicosis is a rare disorder which presents as isosexual peripheral precocious puberty in males. Despite the pattern of autosomal dominant inheritance, sporadic cases also may occur. Due to activating mutation in luteinizing hormone (LH))/chorio