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Journal of Clinical Research in Pediatric Endocrinology
|
November 7, 2018
Comparison of Treatment Regimens in Management of Severe Hypercalcemia Due to Vitamin D Intoxication in Children
Korcan Demir, Hakan Döneray, Cengiz Kara, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
April 18, 2019
Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study
Ayşehan Akıncı, Doğa Türkkahraman, İbrahim Tekedereli, et al.
The Turkish Journal of Gastroenterology : the Official Journal of Turkish Society of Gastroenterology
|
September 11, 2020
Magnetic resonance spectroscopy to assess hepatic steatosis in patients with lipodystrophy
Canan Altay, Mustafa Seçil, Süleyman Cem Adıyaman, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
March 15, 2024
Adherence to Growth Hormone Treatment in Children During the COVID-19 Pandemic
Erdal Eren, Semra Çetinkaya, Yasemin Denkboy Öngen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 18, 2014
Loss-of-function mutations in PNPLA6 encoding neuropathy target esterase underlie pubertal failure and neurological deficits in Gordon Holmes syndrome
A Kemal Topaloglu, Alejandro Lomniczi, Doris Kretzschmar, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis
Hakan Cangul, Zehra Aycan, Halil Saglam, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 12, 2016
The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study
Zeynep Atay, Ediz Yesilkaya, Senay Savas Erdeve, et al.
Clinical Endocrinology
|
August 20, 2010
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism
Hakan Cangul, Neil V Morgan, Julia R Forman, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
July 12, 2021
Molecular Diagnosis of Monogenic Diabetes and Their Clinical/Laboratory Features in Turkish Children
Damla Gökşen, Ediz Yeşilkaya, Samim Özen, et al.
JCI Insight
|
October 19, 2018
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
Hakan Cangul, Xiao-Hui Liao, Erik Schoenmakers, et al.
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Search research articles
Search
Showing results (61-70 of 79) with videos related to
Sort By:
Page
of 8
Journal of Clinical Research in Pediatric Endocrinology
|
November 7, 2018
Comparison of Treatment Regimens in Management of Severe Hypercalcemia Due to Vitamin D Intoxication in Children
Korcan Demir, Hakan Döneray, Cengiz Kara, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
April 18, 2019
Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study
Ayşehan Akıncı, Doğa Türkkahraman, İbrahim Tekedereli, et al.
The Turkish Journal of Gastroenterology : the Official Journal of Turkish Society of Gastroenterology
|
September 11, 2020
Magnetic resonance spectroscopy to assess hepatic steatosis in patients with lipodystrophy
Canan Altay, Mustafa Seçil, Süleyman Cem Adıyaman, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
March 15, 2024
Adherence to Growth Hormone Treatment in Children During the COVID-19 Pandemic
Erdal Eren, Semra Çetinkaya, Yasemin Denkboy Öngen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 18, 2014
Loss-of-function mutations in PNPLA6 encoding neuropathy target esterase underlie pubertal failure and neurological deficits in Gordon Holmes syndrome
A Kemal Topaloglu, Alejandro Lomniczi, Doris Kretzschmar, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis
Hakan Cangul, Zehra Aycan, Halil Saglam, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 12, 2016
The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study
Zeynep Atay, Ediz Yesilkaya, Senay Savas Erdeve, et al.
Clinical Endocrinology
|
August 20, 2010
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism
Hakan Cangul, Neil V Morgan, Julia R Forman, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
July 12, 2021
Molecular Diagnosis of Monogenic Diabetes and Their Clinical/Laboratory Features in Turkish Children
Damla Gökşen, Ediz Yeşilkaya, Samim Özen, et al.
JCI Insight
|
October 19, 2018
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
Hakan Cangul, Xiao-Hui Liao, Erik Schoenmakers, et al.
Page
of 8