Search research articles
Contact Us
Filters
Showing results (11-20 of 43) with videos related to
Page
of 5
Sort By:
Genes
|
August 27, 2021
Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin Tribe
Orna Staretz-Chacham, Shirly Amar, Shlomo Almashanu, et al.
Thyroid : Official Journal of the American Thyroid Association
|
October 7, 2021
Congenital Hypothyroidism Can Dictate the Mode of Delivery and Intra-Labor Medication Usage
Gil Rosen, Anat Lavie, Michal Yackobovitch-Gavan, et al.
European Thyroid Journal
|
May 25, 2022
Usefulness of thyroid function assessment in infants born to mothers with thyroid dysfunction during pregnancy
Zohar Steinberg Ben-Zeev, Marina Peniakov, Clari Felszer, et al.
American Journal of Human Genetics
|
January 22, 2005
Functional consequences of PRODH missense mutations
Hans-Ulrich Bender, Shlomo Almashanu, Gary Steel, et al.
Immunologic Research
|
August 8, 2018
MHC II deficient infant identified by newborn screening program for SCID
Nufar Marcus, Tali Stauber, Atar Lev, et al.
Endocrine Connections
|
September 1, 2025
Gestational Diabetes Mellitus and Its Association with Newborn Thyroid Screening: A Population-Based Study
Dor Shoshan, Avivit Brener, Eyal Cohen-Sela, et al.
BMC Pediatrics
|
January 29, 2025
The association between gestational selective serotonin reuptake inhibitor (SSRI) treatment and newborn thyroid screen: a large-scale cohort study
Orian Raviv, Yael Lebenthal, Michal Yackobovitch-Gavan, et al.
Neonatology
|
June 9, 2026
Early Metabolic Alterations are Associated with Intraventricular Hemorrhage and Its Complications in Very Preterm Infants
Aviv Schupper, Brian Reichman, Inna Zaslavsky-Paltiel, et al.
Thyroid : Official Journal of the American Thyroid Association
|
November 27, 2023
Outcomes in Maternal Graves' Disease: A Population-Based Mother-Infant Dyad Cohort Study
Eyal Cohen-Sela, Avivit Brener, Orian Raviv, et al.
Molecular Genetics and Metabolism
|
September 30, 2023
A common benign intronic deletion masking a pathogenic deep intronic PCCB variant - genome sequencing and RNA studies to the rescue
Alina Kurolap, Dalit Barel, Nava Shaul Lotan, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 43) with videos related to
Sort By:
Page
of 5
Genes
|
August 27, 2021
Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin Tribe
Orna Staretz-Chacham, Shirly Amar, Shlomo Almashanu, et al.
Thyroid : Official Journal of the American Thyroid Association
|
October 7, 2021
Congenital Hypothyroidism Can Dictate the Mode of Delivery and Intra-Labor Medication Usage
Gil Rosen, Anat Lavie, Michal Yackobovitch-Gavan, et al.
European Thyroid Journal
|
May 25, 2022
Usefulness of thyroid function assessment in infants born to mothers with thyroid dysfunction during pregnancy
Zohar Steinberg Ben-Zeev, Marina Peniakov, Clari Felszer, et al.
American Journal of Human Genetics
|
January 22, 2005
Functional consequences of PRODH missense mutations
Hans-Ulrich Bender, Shlomo Almashanu, Gary Steel, et al.
Immunologic Research
|
August 8, 2018
MHC II deficient infant identified by newborn screening program for SCID
Nufar Marcus, Tali Stauber, Atar Lev, et al.
Endocrine Connections
|
September 1, 2025
Gestational Diabetes Mellitus and Its Association with Newborn Thyroid Screening: A Population-Based Study
Dor Shoshan, Avivit Brener, Eyal Cohen-Sela, et al.
BMC Pediatrics
|
January 29, 2025
The association between gestational selective serotonin reuptake inhibitor (SSRI) treatment and newborn thyroid screen: a large-scale cohort study
Orian Raviv, Yael Lebenthal, Michal Yackobovitch-Gavan, et al.
Neonatology
|
June 9, 2026
Early Metabolic Alterations are Associated with Intraventricular Hemorrhage and Its Complications in Very Preterm Infants
Aviv Schupper, Brian Reichman, Inna Zaslavsky-Paltiel, et al.
Thyroid : Official Journal of the American Thyroid Association
|
November 27, 2023
Outcomes in Maternal Graves' Disease: A Population-Based Mother-Infant Dyad Cohort Study
Eyal Cohen-Sela, Avivit Brener, Orian Raviv, et al.
Molecular Genetics and Metabolism
|
September 30, 2023
A common benign intronic deletion masking a pathogenic deep intronic PCCB variant - genome sequencing and RNA studies to the rescue
Alina Kurolap, Dalit Barel, Nava Shaul Lotan, et al.
Page
of 5