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Richard Sidlow

Showing results (1-10 of 35) with videos related to

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Cureus|November 24, 2025
Hereditary Hyperferritinemia-Cataract Syndrome: A Pediatric Case Without Congenital CataractAnusha Hemanna, Richard Sidlow
Cureus|September 29, 2025
Atypical Presentation in X-linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus (EBV) Infection, and Neoplasia (XMEN) Disease: A Case Report and Review of Emerging TherapiesMicah Madsen, Richard Sidlow
Cureus|May 14, 2024
A Case of Beta-Propeller Protein-Associated Neurodegeneration With a Unique Truncating Variant in the WDR45 Gene and Uncommon Clinical and Radiologic FindingsSimon Esbit, Richard Sidlow
American Journal of Medical Genetics. Part A|April 20, 2016
A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathyOmri David Soffer, Richard Sidlow
Cureus|August 21, 2025
A Loss-of-Function Variant Causing Primary Autosomal Recessive Hypertrophic OsteoarthropathyDevanshi N Patel, Richard Sidlow
Urology Case Reports|March 24, 2017
Juvenile Granulosa Cell Tumor of the Testicle - Report of a Neonatal Case with Positive Alpha-fetoprotein Immunohistochemical StainingMelissa Dundas, Mark Horowitz, Richard Sidlow
Cureus|March 20, 2026
CAPRIN1 (Cell Cycle-Associated Protein 1)-Related Neurodevelopmental Disorder: A Novel Mutation With AtaxiaRebecca A Civan, Jessica Kottmeier, Richard Sidlow
Cureus|June 20, 2023
Homozygous EXOSC3 c.395A>C Variants in Pontocerebellar Hypoplasia Type 1B: A Sibling Pair With Childhood Lethal Presentation and Literature ReviewChun Ho Szeto, Sarina Rubin, Richard Sidlow
Iscience|September 2, 2025
Conifer metabolite pisiferic acid restores activity in human Kv1.2 potassium channels carrying pathogenic sequence variantsRían W Manville, Richard Sidlow, Geoffrey W Abbott
Case Reports in Psychiatry|July 5, 2018
Camptocormia in an Adolescent: A Case Report and Review of the LiteratureLaura Kaplan, Erik Aurigemma, Timothy Sullivan, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Cureus|November 24, 2025
Hereditary Hyperferritinemia-Cataract Syndrome: A Pediatric Case Without Congenital CataractAnusha Hemanna, Richard Sidlow
Cureus|September 29, 2025
Atypical Presentation in X-linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus (EBV) Infection, and Neoplasia (XMEN) Disease: A Case Report and Review of Emerging TherapiesMicah Madsen, Richard Sidlow
Cureus|May 14, 2024
A Case of Beta-Propeller Protein-Associated Neurodegeneration With a Unique Truncating Variant in the WDR45 Gene and Uncommon Clinical and Radiologic FindingsSimon Esbit, Richard Sidlow
American Journal of Medical Genetics. Part A|April 20, 2016
A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathyOmri David Soffer, Richard Sidlow
Cureus|August 21, 2025
A Loss-of-Function Variant Causing Primary Autosomal Recessive Hypertrophic OsteoarthropathyDevanshi N Patel, Richard Sidlow
Urology Case Reports|March 24, 2017
Juvenile Granulosa Cell Tumor of the Testicle - Report of a Neonatal Case with Positive Alpha-fetoprotein Immunohistochemical StainingMelissa Dundas, Mark Horowitz, Richard Sidlow
Cureus|March 20, 2026
CAPRIN1 (Cell Cycle-Associated Protein 1)-Related Neurodevelopmental Disorder: A Novel Mutation With AtaxiaRebecca A Civan, Jessica Kottmeier, Richard Sidlow
Cureus|June 20, 2023
Homozygous EXOSC3 c.395A>C Variants in Pontocerebellar Hypoplasia Type 1B: A Sibling Pair With Childhood Lethal Presentation and Literature ReviewChun Ho Szeto, Sarina Rubin, Richard Sidlow
Iscience|September 2, 2025
Conifer metabolite pisiferic acid restores activity in human Kv1.2 potassium channels carrying pathogenic sequence variantsRían W Manville, Richard Sidlow, Geoffrey W Abbott
Case Reports in Psychiatry|July 5, 2018
Camptocormia in an Adolescent: A Case Report and Review of the LiteratureLaura Kaplan, Erik Aurigemma, Timothy Sullivan, et al.
Pageof 4