Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Resham Ejaz

Showing results (1-10 of 21) with videos related to

Pageof 3
Sort By:
Canadian Family Physician Medecin De Famille Canadien|February 3, 2015
Selective serotonin reuptake inhibitor discontinuation during pregnancy: at what risk?Resham Ejaz, Tom Leibson, Gideon Koren
BMJ Case Reports|January 3, 2023
Diagnosis and clinical presentation of two individuals with a rare <i>TCF20</i> pathogenic variantMichelle Robyn Schneeweiss, Breanne Dale, Resham Ejaz
Clinical Case Reports|April 22, 2016
The evolving features of Nicolaides-Baraitser syndrome - a clinical report of a 20-year follow-upResham Ejaz, Riyana Babul-Hirji, David Chitayat
Neurology. Genetics|August 13, 2021
Pathogenic <i>DNM1</i> Gene Variant Presenting With Unusually Nonsevere Neurodevelopmental Phenotype: A Case ReportElaine Choi, Breanne Dale, Rajesh RamachandranNair, et al.
Neurology. Genetics|December 17, 2025
<i>DEGS1</i>-Related Hypomyelinating Leukodystrophy: Four Individuals From Same Family and Review of LiteratureMark Grinberg, Breanne Dale, Rajesh Ramachandrannair, et al.
Neurology|November 23, 2016
Child Neurology: Diencephalic syndrome-like presentation of a cervicomedullary brainstem tumorMelanie Conway, Resham Ejaz, Elizabeth Kouzmitcheva, et al.
American Journal of Medical Genetics. Part A|December 2, 2017
Riboflavin transporter deficiency mimicking mitochondrial myopathy caused by complex II deficiencyGraeme A M Nimmo, Resham Ejaz, Dawn Cordeiro, et al.
Journal of Surgical Oncology|September 12, 2017
Primary mediastinal paraganglioma associated with a familial variant in the succinate dehydrogenase B subunit geneNardin Samuel, Resham Ejaz, Josh Silver, et al.
American Journal of Medical Genetics. Part A|November 4, 2025
Clinical Presentation of the Longest Reported Living Individual With Bent Bone Dysplasia-FGFR2-RelatedCheyenne Bates, Pardeep Gill, Matthew Choi, et al.
Genes|March 28, 2024
The Genetics of Tuberous Sclerosis Complex and Related mTORopathies: Current Understanding and Future DirectionsAlice Man, Matteo Di Scipio, Shan Grewal, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Canadian Family Physician Medecin De Famille Canadien|February 3, 2015
Selective serotonin reuptake inhibitor discontinuation during pregnancy: at what risk?Resham Ejaz, Tom Leibson, Gideon Koren
BMJ Case Reports|January 3, 2023
Diagnosis and clinical presentation of two individuals with a rare <i>TCF20</i> pathogenic variantMichelle Robyn Schneeweiss, Breanne Dale, Resham Ejaz
Clinical Case Reports|April 22, 2016
The evolving features of Nicolaides-Baraitser syndrome - a clinical report of a 20-year follow-upResham Ejaz, Riyana Babul-Hirji, David Chitayat
Neurology. Genetics|August 13, 2021
Pathogenic <i>DNM1</i> Gene Variant Presenting With Unusually Nonsevere Neurodevelopmental Phenotype: A Case ReportElaine Choi, Breanne Dale, Rajesh RamachandranNair, et al.
Neurology. Genetics|December 17, 2025
<i>DEGS1</i>-Related Hypomyelinating Leukodystrophy: Four Individuals From Same Family and Review of LiteratureMark Grinberg, Breanne Dale, Rajesh Ramachandrannair, et al.
Neurology|November 23, 2016
Child Neurology: Diencephalic syndrome-like presentation of a cervicomedullary brainstem tumorMelanie Conway, Resham Ejaz, Elizabeth Kouzmitcheva, et al.
American Journal of Medical Genetics. Part A|December 2, 2017
Riboflavin transporter deficiency mimicking mitochondrial myopathy caused by complex II deficiencyGraeme A M Nimmo, Resham Ejaz, Dawn Cordeiro, et al.
Journal of Surgical Oncology|September 12, 2017
Primary mediastinal paraganglioma associated with a familial variant in the succinate dehydrogenase B subunit geneNardin Samuel, Resham Ejaz, Josh Silver, et al.
American Journal of Medical Genetics. Part A|November 4, 2025
Clinical Presentation of the Longest Reported Living Individual With Bent Bone Dysplasia-FGFR2-RelatedCheyenne Bates, Pardeep Gill, Matthew Choi, et al.
Genes|March 28, 2024
The Genetics of Tuberous Sclerosis Complex and Related mTORopathies: Current Understanding and Future DirectionsAlice Man, Matteo Di Scipio, Shan Grewal, et al.
Pageof 3