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

Rowida Almomani

Showing results (11-20 of 34) with videos related to

Pageof 4
Sort By:
Journal of Skin Cancer|August 6, 2019
Erratum to "Basal Cell Carcinoma Pathology Requests and Reports Are Lacking Important Information"Firas Al-Qarqaz, Khaldon Bodoor, Awad Al-Tarawneh, et al.
Plos One|September 12, 2025
Gene expression alterations in testicular biopsies from males with spermatogenesis arrest identified by transcriptome analysisOsamah Batiha, Esra'a Al-Zoubi, Rowida Almomani, et al.
Journal of Skin Cancer|February 6, 2019
Basal Cell Carcinoma Pathology Requests and Reports Are Lacking Important InformationFiras Al-Qarqaz, Khaldon Bodoor, Awad Al-Tarawneh, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|September 27, 2019
Evaluation of Patched-1 Protein Expression Level in Low Risk and High Risk Basal Cell Carcinoma SubtypesRowida Almomani, Mariam Khanfar, Khaldon Bodoor, et al.
Journal of Neurophysiology|July 29, 2021
A novel gain-of-function sodium channel β2 subunit mutation in idiopathic small fiber neuropathyMatthew Alsaloum, Julie I R Labau, Daniel Sosniak, et al.
Molecular Pain|May 2, 2019
A gain-of-function sodium channel β2-subunit mutation in painful diabetic neuropathyMatthew Alsaloum, Mark Estacion, Rowida Almomani, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
GPSM2 and Chudley-McCullough syndrome: a Dutch founder variant brought to North AmericaRowida Almomani, Yu Sun, Emmelien Aten, et al.
International Journal of Molecular Sciences|November 26, 2022
Peripheral Ion Channel Genes Screening in Painful Small Fiber NeuropathyMilena Ślęczkowska, Rowida Almomani, Margherita Marchi, et al.
American Journal of Human Genetics|July 6, 2010
Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA geneYu Sun, Rowida Almomani, Emmelien Aten, et al.
Human Mutation|April 10, 2013
Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnosticsBirgit Sikkema-Raddatz, Lennart F Johansson, Eddy N de Boer, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Journal of Skin Cancer|August 6, 2019
Erratum to "Basal Cell Carcinoma Pathology Requests and Reports Are Lacking Important Information"Firas Al-Qarqaz, Khaldon Bodoor, Awad Al-Tarawneh, et al.
Plos One|September 12, 2025
Gene expression alterations in testicular biopsies from males with spermatogenesis arrest identified by transcriptome analysisOsamah Batiha, Esra'a Al-Zoubi, Rowida Almomani, et al.
Journal of Skin Cancer|February 6, 2019
Basal Cell Carcinoma Pathology Requests and Reports Are Lacking Important InformationFiras Al-Qarqaz, Khaldon Bodoor, Awad Al-Tarawneh, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|September 27, 2019
Evaluation of Patched-1 Protein Expression Level in Low Risk and High Risk Basal Cell Carcinoma SubtypesRowida Almomani, Mariam Khanfar, Khaldon Bodoor, et al.
Journal of Neurophysiology|July 29, 2021
A novel gain-of-function sodium channel β2 subunit mutation in idiopathic small fiber neuropathyMatthew Alsaloum, Julie I R Labau, Daniel Sosniak, et al.
Molecular Pain|May 2, 2019
A gain-of-function sodium channel β2-subunit mutation in painful diabetic neuropathyMatthew Alsaloum, Mark Estacion, Rowida Almomani, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
GPSM2 and Chudley-McCullough syndrome: a Dutch founder variant brought to North AmericaRowida Almomani, Yu Sun, Emmelien Aten, et al.
International Journal of Molecular Sciences|November 26, 2022
Peripheral Ion Channel Genes Screening in Painful Small Fiber NeuropathyMilena Ślęczkowska, Rowida Almomani, Margherita Marchi, et al.
American Journal of Human Genetics|July 6, 2010
Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA geneYu Sun, Rowida Almomani, Emmelien Aten, et al.
Human Mutation|April 10, 2013
Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnosticsBirgit Sikkema-Raddatz, Lennart F Johansson, Eddy N de Boer, et al.
Pageof 4