Moeen Al-Sayed - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

Moeen Al-Sayed

Showing results (11-20 of 13) with videos related to

Pageof 2

Sort By:

You have reached the last page of results.This site can display upto 13 results.

American Journal of Medical Genetics. Part A|March 23, 2017

Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotypeRuqaiah Altassan, Haya Al Saud, Tariq Ahmad Masoodi, et al.

Blood Cells, Molecules & Diseases|December 15, 2010

Early access experience with VPRIV(®): recommendations for 'core data' collectionDerralynn A Hughes, Moeen Al-Sayed, Nadia Belmatoug, et al.

The Journal of Pediatrics|May 22, 2016

Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 DeficiencySunnie Yan-Wai Wong, Lesa J Beamer, Therese Gadomski, et al.

Pageof 2

Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

American Journal of Medical Genetics. Part A|March 23, 2017

Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotypeRuqaiah Altassan, Haya Al Saud, Tariq Ahmad Masoodi, et al.

Blood Cells, Molecules & Diseases|December 15, 2010

Early access experience with VPRIV(®): recommendations for 'core data' collectionDerralynn A Hughes, Moeen Al-Sayed, Nadia Belmatoug, et al.

The Journal of Pediatrics|May 22, 2016

Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 DeficiencySunnie Yan-Wai Wong, Lesa J Beamer, Therese Gadomski, et al.

Pageof 2