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European Journal of Neurology
|
January 29, 2025
Hereditary Transthyretin Amyloidosis in Israel: Genetic Landscape and Clinical Characteristics
Amir Dori, Odelia Chorin, Noa Ruhrman-Shahar, et al.
Heart Rhythm
|
November 29, 2024
Describing cardiac anatomy: The truth is staring us in the face
Travis D Richardson, Zachi Itzhak Attia, Ehud Chorin, et al.
BMJ Supportive & Palliative Care
|
November 12, 2020
Nutrition and physical activity: French intergroup clinical practice guidelines for diagnosis, treatment and follow-up (SNFGE, FFCD, GERCOR, UNICANCER, SFCD, SFED, SFRO, ACHBT, AFC, SFP-APA, SFNCM, AFSOS)
Cindy Neuzillet, Amélie Anota, Aude-Marie Foucaut, et al.
Orphanet Journal of Rare Diseases
|
March 19, 2025
Clinical profiling and medical management of Israeli individuals with Phelan McDermid syndrome
Odelia Chorin, Lior Greenbaum, Shelly Lev-Hochberg, et al.
Journal of Medical Genetics
|
July 3, 2021
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects
Yoav Bolkier, Ortal Barel, Dina Marek-Yagel, et al.
Frontiers in Genetics
|
January 26, 2023
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders
Maayan Kagan, Rotem Semo-Oz, Yishay Ben Moshe, et al.
European Journal of Neurology
|
June 23, 2026
A Practice Framework for Genetic Testing in Asymptomatic Relatives of Patients With Creutzfeldt-Jakob Disease: Experience and Insights From Israel
Dror Shir, Noa Bregman, Aya Bar David, et al.
Parkinsonism & Related Disorders
|
July 5, 2025
Genetic testing for Parkinson's disease in Israel: Insights from the Rostock Parkinson's Disease (ROPAD) study
Saar Anis, Caroline Weill, Penina Ponger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 22, 2024
Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly
Yue Huang, Kristy L Jay, Alden Yen-Wen Huang, et al.
Frontiers in Digital Health
|
October 24, 2025
Digital home-based multimodal prehabilitation of colorectal cancer patients prior to surgery (the dHOPE study): a non-inferiority clinical trial protocol
Guro Kleve, Chiara Dalla Santa, Felicia Kristiansen, et al.
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Search research articles
Search
Showing results (181-190 of 203) with videos related to
Sort By:
Page
of 21
European Journal of Neurology
|
January 29, 2025
Hereditary Transthyretin Amyloidosis in Israel: Genetic Landscape and Clinical Characteristics
Amir Dori, Odelia Chorin, Noa Ruhrman-Shahar, et al.
Heart Rhythm
|
November 29, 2024
Describing cardiac anatomy: The truth is staring us in the face
Travis D Richardson, Zachi Itzhak Attia, Ehud Chorin, et al.
BMJ Supportive & Palliative Care
|
November 12, 2020
Nutrition and physical activity: French intergroup clinical practice guidelines for diagnosis, treatment and follow-up (SNFGE, FFCD, GERCOR, UNICANCER, SFCD, SFED, SFRO, ACHBT, AFC, SFP-APA, SFNCM, AFSOS)
Cindy Neuzillet, Amélie Anota, Aude-Marie Foucaut, et al.
Orphanet Journal of Rare Diseases
|
March 19, 2025
Clinical profiling and medical management of Israeli individuals with Phelan McDermid syndrome
Odelia Chorin, Lior Greenbaum, Shelly Lev-Hochberg, et al.
Journal of Medical Genetics
|
July 3, 2021
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects
Yoav Bolkier, Ortal Barel, Dina Marek-Yagel, et al.
Frontiers in Genetics
|
January 26, 2023
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders
Maayan Kagan, Rotem Semo-Oz, Yishay Ben Moshe, et al.
European Journal of Neurology
|
June 23, 2026
A Practice Framework for Genetic Testing in Asymptomatic Relatives of Patients With Creutzfeldt-Jakob Disease: Experience and Insights From Israel
Dror Shir, Noa Bregman, Aya Bar David, et al.
Parkinsonism & Related Disorders
|
July 5, 2025
Genetic testing for Parkinson's disease in Israel: Insights from the Rostock Parkinson's Disease (ROPAD) study
Saar Anis, Caroline Weill, Penina Ponger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 22, 2024
Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly
Yue Huang, Kristy L Jay, Alden Yen-Wen Huang, et al.
Frontiers in Digital Health
|
October 24, 2025
Digital home-based multimodal prehabilitation of colorectal cancer patients prior to surgery (the dHOPE study): a non-inferiority clinical trial protocol
Guro Kleve, Chiara Dalla Santa, Felicia Kristiansen, et al.
Page
of 21