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Jaime Vengoechea

Showing results (1-10 of 34) with videos related to

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American Journal of Medical Genetics. Part A|November 14, 2017
In reply to "Mast Cell Disorders in Ehlers-Danlos Syndrome"Jaime Vengoechea
American Journal of Medical Genetics. Part A|March 24, 2020
A case of Singleton-Merten syndrome without cardiac involvement harboring a novel IFIH1 variantJaime Vengoechea, Janette DiMonda
American Journal of Medical Genetics. Part A|April 14, 2015
Gnathodiaphyseal dysplasia presenting as polyostotic fibrous dysplasiaJaime Vengoechea, Lori Carpenter
Journal of Medical Genetics|July 30, 2017
A germline deletion of 9p21.3 presenting as familial melanoma, astrocytoma and breast cancer: clinical and genetic counselling challengesJaime Vengoechea, Christine Tallo
American Journal of Medical Genetics. Part A|November 14, 2023
Isolated cardiomyopathy in a pathogenic X-linked in frame hemizygous DMD exon 49 deletion: A rare presentation with normal creatine kinase levels and absence of musculoskeletal symptomsRana Aljaberi, Jaime Vengoechea
The Journal of the Arkansas Medical Society|May 22, 2015
Cholesterol and family history: when genetics mattersJaime Vengoechea, Kent D McKelvey
The Journal of the Arkansas Medical Society|May 23, 2013
Genetics and cardiovascular disease: the impact of molecular diagnosisJaime Vengoechea, Kent D McKelvey
Journal of Medical Genetics|August 1, 2019
Segregation of two variants suggests the presence of autosomal dominant and recessive forms of <i>WFS1</i>-related disease within the same family: expanding the phenotypic spectrum of Wolfram SyndromeLaina Lusk, Emily Black, Jaime Vengoechea
Developing World Bioethics|December 3, 2008
Misconduct in medical studentsJaime Vengoechea, Socorro Moreno, Alvaro Ruiz
Movement Disorders Clinical Practice|October 9, 2025
Ataxia As New Presentation of Likely Combined Oxidative Phosphorylation Deficiency 54 (COXPD54): A Case Report and Literature ReviewAbdalmalik Bin Khunayfir, Jaime Vengoechea, Richa Tripathi
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics. Part A|November 14, 2017
In reply to "Mast Cell Disorders in Ehlers-Danlos Syndrome"Jaime Vengoechea
American Journal of Medical Genetics. Part A|March 24, 2020
A case of Singleton-Merten syndrome without cardiac involvement harboring a novel IFIH1 variantJaime Vengoechea, Janette DiMonda
American Journal of Medical Genetics. Part A|April 14, 2015
Gnathodiaphyseal dysplasia presenting as polyostotic fibrous dysplasiaJaime Vengoechea, Lori Carpenter
Journal of Medical Genetics|July 30, 2017
A germline deletion of 9p21.3 presenting as familial melanoma, astrocytoma and breast cancer: clinical and genetic counselling challengesJaime Vengoechea, Christine Tallo
American Journal of Medical Genetics. Part A|November 14, 2023
Isolated cardiomyopathy in a pathogenic X-linked in frame hemizygous DMD exon 49 deletion: A rare presentation with normal creatine kinase levels and absence of musculoskeletal symptomsRana Aljaberi, Jaime Vengoechea
The Journal of the Arkansas Medical Society|May 22, 2015
Cholesterol and family history: when genetics mattersJaime Vengoechea, Kent D McKelvey
The Journal of the Arkansas Medical Society|May 23, 2013
Genetics and cardiovascular disease: the impact of molecular diagnosisJaime Vengoechea, Kent D McKelvey
Journal of Medical Genetics|August 1, 2019
Segregation of two variants suggests the presence of autosomal dominant and recessive forms of <i>WFS1</i>-related disease within the same family: expanding the phenotypic spectrum of Wolfram SyndromeLaina Lusk, Emily Black, Jaime Vengoechea
Developing World Bioethics|December 3, 2008
Misconduct in medical studentsJaime Vengoechea, Socorro Moreno, Alvaro Ruiz
Movement Disorders Clinical Practice|October 9, 2025
Ataxia As New Presentation of Likely Combined Oxidative Phosphorylation Deficiency 54 (COXPD54): A Case Report and Literature ReviewAbdalmalik Bin Khunayfir, Jaime Vengoechea, Richa Tripathi
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