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European Journal of Medical Genetics
|
November 19, 2021
Broadening the phenotype of LRRK1 mutations - Features of malignant osteopetrosis and optic nerve atrophy with intrafamilial variable expressivity
Odelia Chorin, Guy Chowers, Rawan Agbariah, et al.
Journal of Neuroscience Methods
|
February 8, 2006
Synaptic release of zinc from brain slices: factors governing release, imaging, and accurate calculation of concentration
Christopher J Frederickson, Leonard J Giblin, Rengarajan V Balaji, et al.
American Journal of Medical Genetics. Part A
|
October 8, 2022
PPP2R1A neurodevelopmental disorder is associated with congenital heart defects
Elizabeth K Baker, Beulah Solivio, Ben Pode-Shakked, et al.
Heart Rhythm
|
May 11, 2019
Grapefruit juice prolongs the QT interval of healthy volunteers and patients with long QT syndrome
Ehud Chorin, Aviram Hochstadt, Yoav Granot, et al.
Heart Rhythm
|
May 15, 2020
QT interval prolongation and torsade de pointes in patients with COVID-19 treated with hydroxychloroquine/azithromycin
Ehud Chorin, Lalit Wadhwani, Silvia Magnani, et al.
Journal of the American College of Cardiology
|
January 11, 2023
Regional Antibiotic Delivery for Implanted Cardiovascular Electronic Device Infections
Moris Topaz, Ehud Chorin, Arie Lorin Schwartz, et al.
Frontiers in Genetics
|
October 7, 2022
Vici syndrome in Israel: Clinical and molecular insights
Odelia Chorin, Yoel Hirsch, Rachel Rock, et al.
Lupus
|
August 11, 2020
Soluble ST2 and CXCL-10 may serve as biomarkers of subclinical diastolic dysfunction in SLE and correlate with disease activity and damage
Ehud Chorin, Aviram Hochstadt, Uri Arad, et al.
Journal of the Neurological Sciences
|
July 5, 2024
The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world setting
Noga Lempel, Shahar Shelly, Odelia Chorin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 1, 2026
De novo rare EMX2 variants lead to idiopathic hypogonadotropic hypogonadism
Maria Stamou, Miranda Tompkins, Hannah Bow, et al.
Page
of 21
Search research articles
Search
Showing results (171-180 of 203) with videos related to
Sort By:
Page
of 21
European Journal of Medical Genetics
|
November 19, 2021
Broadening the phenotype of LRRK1 mutations - Features of malignant osteopetrosis and optic nerve atrophy with intrafamilial variable expressivity
Odelia Chorin, Guy Chowers, Rawan Agbariah, et al.
Journal of Neuroscience Methods
|
February 8, 2006
Synaptic release of zinc from brain slices: factors governing release, imaging, and accurate calculation of concentration
Christopher J Frederickson, Leonard J Giblin, Rengarajan V Balaji, et al.
American Journal of Medical Genetics. Part A
|
October 8, 2022
PPP2R1A neurodevelopmental disorder is associated with congenital heart defects
Elizabeth K Baker, Beulah Solivio, Ben Pode-Shakked, et al.
Heart Rhythm
|
May 11, 2019
Grapefruit juice prolongs the QT interval of healthy volunteers and patients with long QT syndrome
Ehud Chorin, Aviram Hochstadt, Yoav Granot, et al.
Heart Rhythm
|
May 15, 2020
QT interval prolongation and torsade de pointes in patients with COVID-19 treated with hydroxychloroquine/azithromycin
Ehud Chorin, Lalit Wadhwani, Silvia Magnani, et al.
Journal of the American College of Cardiology
|
January 11, 2023
Regional Antibiotic Delivery for Implanted Cardiovascular Electronic Device Infections
Moris Topaz, Ehud Chorin, Arie Lorin Schwartz, et al.
Frontiers in Genetics
|
October 7, 2022
Vici syndrome in Israel: Clinical and molecular insights
Odelia Chorin, Yoel Hirsch, Rachel Rock, et al.
Lupus
|
August 11, 2020
Soluble ST2 and CXCL-10 may serve as biomarkers of subclinical diastolic dysfunction in SLE and correlate with disease activity and damage
Ehud Chorin, Aviram Hochstadt, Uri Arad, et al.
Journal of the Neurological Sciences
|
July 5, 2024
The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world setting
Noga Lempel, Shahar Shelly, Odelia Chorin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 1, 2026
De novo rare EMX2 variants lead to idiopathic hypogonadotropic hypogonadism
Maria Stamou, Miranda Tompkins, Hannah Bow, et al.
Page
of 21