Search research articles
Contact Us
Filters
Showing results (21-30 of 43) with videos related to
Page
of 5
Sort By:
Thyroid : Official Journal of the American Thyroid Association
|
January 6, 2015
Long-term outcome of loss-of-function mutations in thyrotropin receptor gene
Yardena Tenenbaum-Rakover, Shlomo Almashanu, Ora Hess, et al.
Endocrine Connections
|
October 16, 2024
The natural course of newborns with transient congenital hypothyroidism
Tal Almagor, Shlomo Almashanu, Ghadir Elias-Assad, et al.
American Journal of Perinatology
|
December 10, 2021
Preterm Singleton Birth Rate during the COVID-19 Lockdown: A Population-Based Study
Leah Leibovitch, Brian Reichman, Francis Mimouni, et al.
The Israel Medical Association Journal : IMAJ
|
October 2, 2013
Newborn screening for severe T and B cell immunodeficiency in Israel: a pilot study
Raz Somech, Atar Lev, Amos J Simon, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 23, 2017
Risk Factors for the Development of Delayed TSH Elevation in Neonatal Intensive Care Unit Newborns
Amnon Zung, Rachel Bier Palmon, Agneta Golan, et al.
Archives of Gynecology and Obstetrics
|
October 2, 2021
Maternal iodine deficiency: a newborns' overweight risk factor? A prospective study
Yaniv S Ovadia, Shmuel Zangen, Shani R Rosen, et al.
American Journal of Human Genetics
|
September 11, 2004
Isolated 3-methylcrotonyl-CoA carboxylase deficiency: evidence for an allele-specific dominant negative effect and responsiveness to biotin therapy
Matthias R Baumgartner, M Fernanda Dantas, Terttu Suormala, et al.
Journal of Inherited Metabolic Disease
|
November 15, 2015
Primary and maternal 3-methylcrotonyl-CoA carboxylase deficiency: insights from the Israel newborn screening program
Jonathan Rips, Shlomo Almashanu, Hanna Mandel, et al.
European Thyroid Journal
|
June 28, 2021
High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism
Tal Almagor, Shoshana Rath, Dan Nachtigal, et al.
Journal of Inherited Metabolic Disease
|
July 23, 2024
The natural history of dihydrolipoamide dehydrogenase deficiency in Israel
Ben Pode-Shakked, Yuval E Landau, Nava Shaul Lotan, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 43) with videos related to
Sort By:
Page
of 5
Thyroid : Official Journal of the American Thyroid Association
|
January 6, 2015
Long-term outcome of loss-of-function mutations in thyrotropin receptor gene
Yardena Tenenbaum-Rakover, Shlomo Almashanu, Ora Hess, et al.
Endocrine Connections
|
October 16, 2024
The natural course of newborns with transient congenital hypothyroidism
Tal Almagor, Shlomo Almashanu, Ghadir Elias-Assad, et al.
American Journal of Perinatology
|
December 10, 2021
Preterm Singleton Birth Rate during the COVID-19 Lockdown: A Population-Based Study
Leah Leibovitch, Brian Reichman, Francis Mimouni, et al.
The Israel Medical Association Journal : IMAJ
|
October 2, 2013
Newborn screening for severe T and B cell immunodeficiency in Israel: a pilot study
Raz Somech, Atar Lev, Amos J Simon, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 23, 2017
Risk Factors for the Development of Delayed TSH Elevation in Neonatal Intensive Care Unit Newborns
Amnon Zung, Rachel Bier Palmon, Agneta Golan, et al.
Archives of Gynecology and Obstetrics
|
October 2, 2021
Maternal iodine deficiency: a newborns' overweight risk factor? A prospective study
Yaniv S Ovadia, Shmuel Zangen, Shani R Rosen, et al.
American Journal of Human Genetics
|
September 11, 2004
Isolated 3-methylcrotonyl-CoA carboxylase deficiency: evidence for an allele-specific dominant negative effect and responsiveness to biotin therapy
Matthias R Baumgartner, M Fernanda Dantas, Terttu Suormala, et al.
Journal of Inherited Metabolic Disease
|
November 15, 2015
Primary and maternal 3-methylcrotonyl-CoA carboxylase deficiency: insights from the Israel newborn screening program
Jonathan Rips, Shlomo Almashanu, Hanna Mandel, et al.
European Thyroid Journal
|
June 28, 2021
High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism
Tal Almagor, Shoshana Rath, Dan Nachtigal, et al.
Journal of Inherited Metabolic Disease
|
July 23, 2024
The natural history of dihydrolipoamide dehydrogenase deficiency in Israel
Ben Pode-Shakked, Yuval E Landau, Nava Shaul Lotan, et al.
Page
of 5