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Shlomo Almashanu

Showing results (11-20 of 43) with videos related to

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Genes|August 27, 2021
Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin TribeOrna 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 UsageGil 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 pregnancyZohar Steinberg Ben-Zeev, Marina Peniakov, Clari Felszer, et al.
American Journal of Human Genetics|January 22, 2005
Functional consequences of PRODH missense mutationsHans-Ulrich Bender, Shlomo Almashanu, Gary Steel, et al.
Immunologic Research|August 8, 2018
MHC II deficient infant identified by newborn screening program for SCIDNufar 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 StudyDor 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 studyOrian 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 InfantsAviv 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 StudyEyal 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 rescueAlina Kurolap, Dalit Barel, Nava Shaul Lotan, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Genes|August 27, 2021
Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin TribeOrna 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 UsageGil 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 pregnancyZohar Steinberg Ben-Zeev, Marina Peniakov, Clari Felszer, et al.
American Journal of Human Genetics|January 22, 2005
Functional consequences of PRODH missense mutationsHans-Ulrich Bender, Shlomo Almashanu, Gary Steel, et al.
Immunologic Research|August 8, 2018
MHC II deficient infant identified by newborn screening program for SCIDNufar 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 StudyDor 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 studyOrian 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 InfantsAviv 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 StudyEyal 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 rescueAlina Kurolap, Dalit Barel, Nava Shaul Lotan, et al.
Pageof 5