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Harefuah
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June 23, 2022
[SURGICAL PALLIATION FOR PANCREATIC CANCER]
Ido Ashbell, Nadav Agam, Yoel Chocron, et al.
Heliyon
|
May 19, 2023
Laser tissue soldering of the gastrointestinal tract: A systematic review LTS of the gastrointestinal tract
Ido Ashbell, Nadav Agam, Abraham Katzir, et al.
The Canadian Journal of Cardiology
|
January 29, 2025
Mitral Valve Prolapse Caused by TLL1 Gain-of-Function Mutation
Nadav Agam, Vadim Dolgin, Artyom Star, et al.
American Journal of Medical Genetics. Part A
|
August 24, 2023
Partial penetrance and phenotypic variability of aplasia of lacrimal and salivary glands caused by a novel FGF10 donor splice-site mutation
Ofek Freund, Baker Elsana, Nadav Agam, et al.
Clinical Genetics
|
November 25, 2024
Novel BRAT1 Deep Intronic Variant Affects Splicing Regulatory Elements Causing Cerebellar Hypoplasia Syndrome: Genotypic and Phenotypic Expansion
Tomer Poleg, Regina Proskorovski-Ohayon, Vadim Dolgin, et al.
Clinical Genetics
|
April 20, 2022
A syndrome of severe intellectual disability, hypotonia, failure to thrive, dysmorphism, and thinning of corpus callosum maps to chromosome 7q21.13-q21.3
Daniel Halperin, Nadav Agam, Maher Hallak, et al.
Harefuah
|
December 25, 2025
[Monogenic Kidney Diseases in Children - Five Years of Experience from a Dedicated Nephrogenetic Clinic in Southern Israel]
Ruth Schreiber, Rebbeka Kebesch, Vadim Dolgin, et al.
NPJ Genomic Medicine
|
March 14, 2025
Unraveling MECP2 structural variants in previously elusive Rett syndrome cases through IGV interpretation
Tomer Poleg, Noam Hadar, Gali Heimer, et al.
Journal of Cardiovascular Translational Research
|
November 16, 2023
Compound Heterozygosity for Late-Onset Cardiomyopathy-Causative ALPK3 Coding Variant and Novel Intronic Variant Cause Infantile Hypertrophic Cardiomyopathy
Tomer Poleg, Marina Eskin-Schwartz, Regina Proskorovski-Ohayon, et al.
Journal of Inherited Metabolic Disease
|
January 25, 2023
Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation
Amit Safran, Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, et al.
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Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Harefuah
|
June 23, 2022
[SURGICAL PALLIATION FOR PANCREATIC CANCER]
Ido Ashbell, Nadav Agam, Yoel Chocron, et al.
Heliyon
|
May 19, 2023
Laser tissue soldering of the gastrointestinal tract: A systematic review LTS of the gastrointestinal tract
Ido Ashbell, Nadav Agam, Abraham Katzir, et al.
The Canadian Journal of Cardiology
|
January 29, 2025
Mitral Valve Prolapse Caused by TLL1 Gain-of-Function Mutation
Nadav Agam, Vadim Dolgin, Artyom Star, et al.
American Journal of Medical Genetics. Part A
|
August 24, 2023
Partial penetrance and phenotypic variability of aplasia of lacrimal and salivary glands caused by a novel FGF10 donor splice-site mutation
Ofek Freund, Baker Elsana, Nadav Agam, et al.
Clinical Genetics
|
November 25, 2024
Novel BRAT1 Deep Intronic Variant Affects Splicing Regulatory Elements Causing Cerebellar Hypoplasia Syndrome: Genotypic and Phenotypic Expansion
Tomer Poleg, Regina Proskorovski-Ohayon, Vadim Dolgin, et al.
Clinical Genetics
|
April 20, 2022
A syndrome of severe intellectual disability, hypotonia, failure to thrive, dysmorphism, and thinning of corpus callosum maps to chromosome 7q21.13-q21.3
Daniel Halperin, Nadav Agam, Maher Hallak, et al.
Harefuah
|
December 25, 2025
[Monogenic Kidney Diseases in Children - Five Years of Experience from a Dedicated Nephrogenetic Clinic in Southern Israel]
Ruth Schreiber, Rebbeka Kebesch, Vadim Dolgin, et al.
NPJ Genomic Medicine
|
March 14, 2025
Unraveling MECP2 structural variants in previously elusive Rett syndrome cases through IGV interpretation
Tomer Poleg, Noam Hadar, Gali Heimer, et al.
Journal of Cardiovascular Translational Research
|
November 16, 2023
Compound Heterozygosity for Late-Onset Cardiomyopathy-Causative ALPK3 Coding Variant and Novel Intronic Variant Cause Infantile Hypertrophic Cardiomyopathy
Tomer Poleg, Marina Eskin-Schwartz, Regina Proskorovski-Ohayon, et al.
Journal of Inherited Metabolic Disease
|
January 25, 2023
Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation
Amit Safran, Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, et al.
Page
of 2