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Yael Goldberg

Showing results (81-90 of 116) with videos related to

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Pediatric Blood & Cancer|November 7, 2015
Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and ConsanguinityHagit N Baris, Inbal Barnes-Kedar, Helen Toledano, et al.
Journal of Medical Genetics|November 12, 2018
Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancyManon Suerink, Tim Ripperger, Ludwine Messiaen, et al.
Journal of Medical Genetics|April 17, 2014
Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD)Katharina Wimmer, Christian P Kratz, Hans F A Vasen, et al.
Human Mutation|February 18, 2021
Re-evaluating the pathogenicity of the c.783+2T>C BAP1 germline variantYael Goldberg, Yael Laitman, Merav Ben David, et al.
Clinical Genetics|July 20, 2020
COG6-CDG: Expanding the phenotype with emphasis on glycosylation defects involved in the causation of male disorders of sex developmentHanna Mandel, Nehama Cohen Kfir, Ayalla Fedida, et al.
Oncotargets and Therapy|November 25, 2020
Clinical Characteristics and Prognosis of Gastric Cancer Patients with <i>BRCA 1/2</i> Germline Mutations: Report of Ten Cases and a Literature ReviewNaama Halpern, Albert Grinshpun, Ben Boursi, et al.
Medicine|May 18, 2017
Treatment inferred from mutations identified using massive parallel sequencing leads to clinical benefit in some heavily pretreated cancer patientsAviad Zick, Tamar Peretz, Michal Lotem, et al.
Gastroenterology|March 1, 2017
Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and SurveillanceSari Lieberman, Tom Walsh, Menachem Schechter, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|February 5, 2023
High prevalence of MUTYH associated polyposis among minority populations in Israel, due to rare founder pathogenic variantsGili Reznick Levi, Yael Goldberg, Hanna Segev, et al.
Canadian Geriatrics Journal : CGJ|March 7, 2025
The Canadian Coalition for Seniors' Mental Health Canadian Clinical Practice Guidelines for Assessing and Managing Behavioural and Psychological Symptoms of Dementia (BPSD)Stacey Hatch, Dallas P Seitz, Marie-Andrée Bruneau, et al.
Pageof 12

Showing results (81-90 of 116) with videos related to

Sort By:
Pageof 12
Pediatric Blood & Cancer|November 7, 2015
Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and ConsanguinityHagit N Baris, Inbal Barnes-Kedar, Helen Toledano, et al.
Journal of Medical Genetics|November 12, 2018
Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancyManon Suerink, Tim Ripperger, Ludwine Messiaen, et al.
Journal of Medical Genetics|April 17, 2014
Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD)Katharina Wimmer, Christian P Kratz, Hans F A Vasen, et al.
Human Mutation|February 18, 2021
Re-evaluating the pathogenicity of the c.783+2T>C BAP1 germline variantYael Goldberg, Yael Laitman, Merav Ben David, et al.
Clinical Genetics|July 20, 2020
COG6-CDG: Expanding the phenotype with emphasis on glycosylation defects involved in the causation of male disorders of sex developmentHanna Mandel, Nehama Cohen Kfir, Ayalla Fedida, et al.
Oncotargets and Therapy|November 25, 2020
Clinical Characteristics and Prognosis of Gastric Cancer Patients with <i>BRCA 1/2</i> Germline Mutations: Report of Ten Cases and a Literature ReviewNaama Halpern, Albert Grinshpun, Ben Boursi, et al.
Medicine|May 18, 2017
Treatment inferred from mutations identified using massive parallel sequencing leads to clinical benefit in some heavily pretreated cancer patientsAviad Zick, Tamar Peretz, Michal Lotem, et al.
Gastroenterology|March 1, 2017
Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and SurveillanceSari Lieberman, Tom Walsh, Menachem Schechter, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|February 5, 2023
High prevalence of MUTYH associated polyposis among minority populations in Israel, due to rare founder pathogenic variantsGili Reznick Levi, Yael Goldberg, Hanna Segev, et al.
Canadian Geriatrics Journal : CGJ|March 7, 2025
The Canadian Coalition for Seniors' Mental Health Canadian Clinical Practice Guidelines for Assessing and Managing Behavioural and Psychological Symptoms of Dementia (BPSD)Stacey Hatch, Dallas P Seitz, Marie-Andrée Bruneau, et al.
Pageof 12