Büyükgebiz, Atilla
38  Ergebnisse:
Personensuche X
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5

Homozygous Loss-of-function Mutations inSOHLH1in Patients W..:

Bayram, Yavuz ; Gulsuner, Suleyman ; Guran, Tulay...
The Journal of Clinical Endocrinology & Metabolism.  100 (2015)  5 - p. E808-E814 , 2015
 
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6

Isolated hyperthyrotropinemia in childhood obesity and its ..:

Ünüvar, Tolga ; Anık, Ahmet ; Çatlı, Gönül...
Journal of Endocrinological Investigation.  37 (2014)  9 - p. 799-804 , 2014
 
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7

Clinical and diagnostic characteristics of hyperprolactinem..:

Catli, Gonul ; Abaci, Ayhan ; Bober, Ece.
Journal of Pediatric Endocrinology and Metabolism.  26 (2013)  1-2 - p. 1-11 , 2013
 
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8

Hyperprolactinemia in children: clinical features and long-..:

Catli, Gonul ; Abaci, Ayhan ; Altincik, Ayca...
Journal of Pediatric Endocrinology and Metabolism.  25 (2012)  11-12 - p. , 2012
 
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9

Clinical profile and etiologies of children with central di..:

Catli, Gonul ; Abaci, Ayhan ; Demir, Korcan...
Journal of Pediatric Endocrinology and Metabolism.  25 (2012)  5-6 - p. , 2012
 
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10

Hepatic glycogenosis: a rare cause of hepatomegaly in Type ..:

Abaci, Ayhan ; Bekem, Ozlem ; Unuvar, Tolga...
Journal of Diabetes and its Complications.  22 (2008)  5 - p. 325-328 , 2008
 
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11

Clinical Significance of the Parental Origin of the X Chrom..:

Sagi, Liora ; Zuckerman-Levin, Nehama ; Gawlik, Aneta...
The Journal of Clinical Endocrinology & Metabolism.  92 (2007)  3 - p. 846-852 , 2007
 
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13

Newborn Screening, Hypothyroidism in Infants, Children and ..:

, In: Diseases of the Thyroid in Childhood and Adolescence; Pediatric and Adolescent Medicine,
Büyükgebiz, Atilla - p. 128-141 , 2006
 
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15

New Autosomal Recessive Mutation of the TSH-β Subunit Gene ..:

Vuissoz, Jean-Marc ; Deladoëy, Johnny ; Buyukgebiz, Atilla...
The Journal of Clinical Endocrinology & Metabolism.  86 (2001)  9 - p. 4468-4471 , 2001
 
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