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The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
September 7, 2006
Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion
Sevgi Bagislar, Isik Ustuner, Bora Cengiz, et al.
Clinical Nutrition ESPEN
|
February 21, 2018
MaFOS-GDM trial: Maternal fish oil supplementation in women with gestational diabetes and cord blood DNA methylation at insulin like growth factor-1 (IGF-1) gene
Dilek Dilli, Nazan Neslihan Doğan, Mehmet Şah İpek, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 14, 2026
Carrier Frequency of Neurodegeneration with Brain Iron Accumulation (NBIA) Disorders in a Middle Eastern Clinical Cohort Based on Retrospective Genetic Testing Data
Hasan Ozturk, Hasan Bas, Zuhal Yapici, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
April 25, 2022
A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High <i>IGF-I</i> Values at Transition to Adult Care
Aslı Derya Kardelen, Esin Karakılıç Özturan, Şükran Poyrazoğlu, et al.
American Journal of Medical Genetics. Part A
|
January 26, 2020
Genotypes and estimated prevalence of phosphomannomutase 2 deficiency in Turkey differ significantly from those in Europe
Yılmaz Yıldız, Mutluay Arslan, Gökalp Çelik, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
December 17, 2015
Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing
Sebahat Yılmaz Ağladıoğlu, Zehra Aycan, Semra Çetinkaya, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
December 7, 2019
Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13
Melis Demir Köse, Mehtap Kagnici, Taha Reşit Özdemir, et al.
Journal of Clinical Immunology
|
October 15, 2024
Inborn Errors of Immunity in Pediatric Intensive Care: Prevalence, Characteristics, and Prognosis
Fatih Celmeli, Ayse Oz, Hasan Serdar Kihtir, et al.
Frontiers in Immunology
|
May 8, 2026
Clinical, immunological, treatment characteristics, and outcomes in 22 patients with major histocompatibility complex class II deficiency
Sule Haskologlu, Caner Aytekin, Candan Islamoglu, et al.
American Journal of Medical Genetics. Part A
|
July 17, 2010
Carmi syndrome with congenital heart defects
Mustafa Aydin, Aysegul Zenciroglu, Ayhan Yaman, et al.
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of 25
Search research articles
Search
Showing results (191-200 of 244) with videos related to
Sort By:
Page
of 25
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
September 7, 2006
Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion
Sevgi Bagislar, Isik Ustuner, Bora Cengiz, et al.
Clinical Nutrition ESPEN
|
February 21, 2018
MaFOS-GDM trial: Maternal fish oil supplementation in women with gestational diabetes and cord blood DNA methylation at insulin like growth factor-1 (IGF-1) gene
Dilek Dilli, Nazan Neslihan Doğan, Mehmet Şah İpek, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 14, 2026
Carrier Frequency of Neurodegeneration with Brain Iron Accumulation (NBIA) Disorders in a Middle Eastern Clinical Cohort Based on Retrospective Genetic Testing Data
Hasan Ozturk, Hasan Bas, Zuhal Yapici, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
April 25, 2022
A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High <i>IGF-I</i> Values at Transition to Adult Care
Aslı Derya Kardelen, Esin Karakılıç Özturan, Şükran Poyrazoğlu, et al.
American Journal of Medical Genetics. Part A
|
January 26, 2020
Genotypes and estimated prevalence of phosphomannomutase 2 deficiency in Turkey differ significantly from those in Europe
Yılmaz Yıldız, Mutluay Arslan, Gökalp Çelik, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
December 17, 2015
Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing
Sebahat Yılmaz Ağladıoğlu, Zehra Aycan, Semra Çetinkaya, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
December 7, 2019
Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13
Melis Demir Köse, Mehtap Kagnici, Taha Reşit Özdemir, et al.
Journal of Clinical Immunology
|
October 15, 2024
Inborn Errors of Immunity in Pediatric Intensive Care: Prevalence, Characteristics, and Prognosis
Fatih Celmeli, Ayse Oz, Hasan Serdar Kihtir, et al.
Frontiers in Immunology
|
May 8, 2026
Clinical, immunological, treatment characteristics, and outcomes in 22 patients with major histocompatibility complex class II deficiency
Sule Haskologlu, Caner Aytekin, Candan Islamoglu, et al.
American Journal of Medical Genetics. Part A
|
July 17, 2010
Carmi syndrome with congenital heart defects
Mustafa Aydin, Aysegul Zenciroglu, Ayhan Yaman, et al.
Page
of 25