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Iranian Journal of Allergy, Asthma, and Immunology
|
May 7, 2022
Scales of Magt1 Gene: Novel Mutations, Different Presentations
Sule Haskologlu, Kubra Baskin, Caner Aytekin, et al.
Prenatal Diagnosis
|
February 14, 2006
Postmortem evaluation of 220 prenatally diagnosed fetuses with neural tube defects: detection of associated anomalies in a Turkish population
Serdar Ceylaner, Gülay Ceylaner, Ilker Günyeli, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
March 26, 2024
Exploring Multiple Endocrinological Issues and Dysautonomia in a Rare Case: Hypoparathyroidism in MIRAGE Syndrome
Sirmen Kızılcan Çetin, Elif Özsu, Zeynep Şıklar, et al.
Molecular Syndromology
|
May 20, 2021
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey
Rabia Miray Kisla Ekinci, Sibel Balci, Haldun Dogan, et al.
Congenital Anomalies
|
November 28, 2012
Novel CRLF1 gene mutation in a newborn infant diagnosed with Crisponi syndrome
Nilay Hakan, Fatma Tuba Eminoglu, Mustafa Aydin, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 25, 2021
Glycogen storage disease type XII; an ultra rare cause of hemolytic anemia and rhabdomyolysis: one new case report
Esra Kara, Deniz Kor, Fatma Derya Bulut, et al.
Indian Journal of Pediatrics
|
January 15, 2020
Cardiac Tamponade in Gorham-Stout Syndrome Associated with GATA2 Mutation
Melahat Melek Oguz, Berna Oguz, Vehbi Dogan, et al.
JIMD Reports
|
July 12, 2018
The Second Case of Saposin A Deficiency and Altered Autophagy
Melis Kose, Secil Akyildiz Demir, Gulcin Akinci, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
June 17, 2020
Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in <i>CYP11B2</i>
Hande Turan, Aydilek Dağdeviren Çakır, Yavuz Özer, et al.
Balkan Medical Journal
|
August 27, 2019
The Prevalence of Fabry Disease Among Turkish Patients with Non-Obstructive Hypertrophic Cardiomyopathy: Insights from a Screening Study
Hasan Ali Barman, Barış İkitimur, Burçak Kılıçkıran Avcı, et al.
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of 25
Search research articles
Search
Showing results (171-180 of 244) with videos related to
Sort By:
Page
of 25
Iranian Journal of Allergy, Asthma, and Immunology
|
May 7, 2022
Scales of Magt1 Gene: Novel Mutations, Different Presentations
Sule Haskologlu, Kubra Baskin, Caner Aytekin, et al.
Prenatal Diagnosis
|
February 14, 2006
Postmortem evaluation of 220 prenatally diagnosed fetuses with neural tube defects: detection of associated anomalies in a Turkish population
Serdar Ceylaner, Gülay Ceylaner, Ilker Günyeli, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
March 26, 2024
Exploring Multiple Endocrinological Issues and Dysautonomia in a Rare Case: Hypoparathyroidism in MIRAGE Syndrome
Sirmen Kızılcan Çetin, Elif Özsu, Zeynep Şıklar, et al.
Molecular Syndromology
|
May 20, 2021
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey
Rabia Miray Kisla Ekinci, Sibel Balci, Haldun Dogan, et al.
Congenital Anomalies
|
November 28, 2012
Novel CRLF1 gene mutation in a newborn infant diagnosed with Crisponi syndrome
Nilay Hakan, Fatma Tuba Eminoglu, Mustafa Aydin, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 25, 2021
Glycogen storage disease type XII; an ultra rare cause of hemolytic anemia and rhabdomyolysis: one new case report
Esra Kara, Deniz Kor, Fatma Derya Bulut, et al.
Indian Journal of Pediatrics
|
January 15, 2020
Cardiac Tamponade in Gorham-Stout Syndrome Associated with GATA2 Mutation
Melahat Melek Oguz, Berna Oguz, Vehbi Dogan, et al.
JIMD Reports
|
July 12, 2018
The Second Case of Saposin A Deficiency and Altered Autophagy
Melis Kose, Secil Akyildiz Demir, Gulcin Akinci, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
June 17, 2020
Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in <i>CYP11B2</i>
Hande Turan, Aydilek Dağdeviren Çakır, Yavuz Özer, et al.
Balkan Medical Journal
|
August 27, 2019
The Prevalence of Fabry Disease Among Turkish Patients with Non-Obstructive Hypertrophic Cardiomyopathy: Insights from a Screening Study
Hasan Ali Barman, Barış İkitimur, Burçak Kılıçkıran Avcı, et al.
Page
of 25