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Hagit Baris

Showing results (31-40 of 96) with videos related to

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The New England Journal of Medicine|November 1, 2023
Corin and Left Atrial Cardiomyopathy, Hypertension, Arrhythmia, and FibrosisHagit Baris Feldman, Chofit Chai Gadot, David Zahler, et al.
Scientific Reports|May 21, 2020
ERK Activity in Immature Leukemic Cells Drives Clonal Selection during Induction Therapy for Acute Myeloid LeukemiaMichal Hayun, Maria Zaatra, Chen Itzkovich, et al.
Human Genetics|March 22, 2022
CD55-deficiency in Jews of Bukharan descent is caused by the Cromer blood type Dr(a-) variantAlina Kurolap, David Hagin, Tal Freund, et al.
Familial Cancer|December 23, 2008
Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type IHelen Toledano, Yael Goldberg, Inbal Kedar-Barnes, et al.
Journal of Human Genetics|March 24, 2019
A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4Tova Hershkovitz, Alina Kurolap, Claudia Gonzaga-Jauregui, et al.
British Journal of Haematology|July 6, 2021
Experts' views on COVID-19 vaccination and the impact of the pandemic on patients with Gaucher diseaseUri Hamiel, Alina Kurolap, Ian J Cohen, et al.
Frontiers in Immunology|July 12, 2021
A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case ReportShirley Pollack, Israel Eisenstein, Adi Mory, et al.
American Journal of Medical Genetics. Part A|December 28, 2018
Clinical diversity of MYH7-related cardiomyopathies: Insights into genotype-phenotype correlationsTova Hershkovitz, Alina Kurolap, Noa Ruhrman-Shahar, et al.
Molecular Genetics and Metabolism Reports|January 18, 2021
A recurring <i>NFS1</i> pathogenic variant causes a mitochondrial disorder with variable intra-familial patient outcomesTova Hershkovitz, Alina Kurolap, Galit Tal, et al.
European Journal of Pediatrics|July 10, 2012
Revised recommendations for the management of Gaucher disease in childrenPaige Kaplan, Hagit Baris, Linda De Meirleir, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
The New England Journal of Medicine|November 1, 2023
Corin and Left Atrial Cardiomyopathy, Hypertension, Arrhythmia, and FibrosisHagit Baris Feldman, Chofit Chai Gadot, David Zahler, et al.
Scientific Reports|May 21, 2020
ERK Activity in Immature Leukemic Cells Drives Clonal Selection during Induction Therapy for Acute Myeloid LeukemiaMichal Hayun, Maria Zaatra, Chen Itzkovich, et al.
Human Genetics|March 22, 2022
CD55-deficiency in Jews of Bukharan descent is caused by the Cromer blood type Dr(a-) variantAlina Kurolap, David Hagin, Tal Freund, et al.
Familial Cancer|December 23, 2008
Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type IHelen Toledano, Yael Goldberg, Inbal Kedar-Barnes, et al.
Journal of Human Genetics|March 24, 2019
A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4Tova Hershkovitz, Alina Kurolap, Claudia Gonzaga-Jauregui, et al.
British Journal of Haematology|July 6, 2021
Experts' views on COVID-19 vaccination and the impact of the pandemic on patients with Gaucher diseaseUri Hamiel, Alina Kurolap, Ian J Cohen, et al.
Frontiers in Immunology|July 12, 2021
A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case ReportShirley Pollack, Israel Eisenstein, Adi Mory, et al.
American Journal of Medical Genetics. Part A|December 28, 2018
Clinical diversity of MYH7-related cardiomyopathies: Insights into genotype-phenotype correlationsTova Hershkovitz, Alina Kurolap, Noa Ruhrman-Shahar, et al.
Molecular Genetics and Metabolism Reports|January 18, 2021
A recurring <i>NFS1</i> pathogenic variant causes a mitochondrial disorder with variable intra-familial patient outcomesTova Hershkovitz, Alina Kurolap, Galit Tal, et al.
European Journal of Pediatrics|July 10, 2012
Revised recommendations for the management of Gaucher disease in childrenPaige Kaplan, Hagit Baris, Linda De Meirleir, et al.
Pageof 10