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

J Massaad

Showing results (41-50 of 73) with videos related to

Pageof 8
Sort By:
The Journal of Allergy and Clinical Immunology|August 18, 2023
The opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunityRana Mansour, Rana El-Hassan, Youmna El-Orfali, et al.
The Journal of Allergy and Clinical Immunology|June 23, 2012
LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiencyAbdullah Alangari, Abdulrahman Alsultan, Nouran Adly, et al.
Journal of Clinical Immunology|October 24, 2017
DOCK8 Deficiency Presenting as an IPEX-Like DisorderFayhan J Alroqi, Louis-Marie Charbonnier, Sevgi Keles, et al.
The Journal of Allergy and Clinical Immunology|February 14, 2015
A novel mutation in ICOS presenting as hypogammaglobulinemia with susceptibility to opportunistic pathogensJanet Chou, Michel J Massaad, Brittney Cangemi, et al.
The Journal of Allergy and Clinical Immunology|October 19, 2015
Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal associationChristina S Yee, Michel J Massaad, Wayne Bainter, et al.
The Journal of Allergy and Clinical Immunology|August 29, 2016
Epidermodysplasia verruciformis as a manifestation of ARTEMIS deficiency in a young adultAzzedine Tahiat, Yousef R Badran, Janet Chou, et al.
Clinical Immunology (Orlando, Fla.)|January 3, 2013
Intronic SH2D1A mutation with impaired SAP expression and agammaglobulinemiaMike Recher, Ari J Fried, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|April 5, 2014
Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiencySung-Yun Pai, Helen de Boer, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|July 31, 2012
A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndromeJanet Chou, Rima Hanna-Wakim, Irit Tirosh, et al.
Clinical Immunology (Orlando, Fla.)|September 9, 2017
DOCK8 and STAT3 dependent inhibition of IgE isotype switching by TLR9 ligation in human B cellsMichel J Massaad, Brittney Cangemi, Waleed Al-Herz, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
The Journal of Allergy and Clinical Immunology|August 18, 2023
The opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunityRana Mansour, Rana El-Hassan, Youmna El-Orfali, et al.
The Journal of Allergy and Clinical Immunology|June 23, 2012
LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiencyAbdullah Alangari, Abdulrahman Alsultan, Nouran Adly, et al.
Journal of Clinical Immunology|October 24, 2017
DOCK8 Deficiency Presenting as an IPEX-Like DisorderFayhan J Alroqi, Louis-Marie Charbonnier, Sevgi Keles, et al.
The Journal of Allergy and Clinical Immunology|February 14, 2015
A novel mutation in ICOS presenting as hypogammaglobulinemia with susceptibility to opportunistic pathogensJanet Chou, Michel J Massaad, Brittney Cangemi, et al.
The Journal of Allergy and Clinical Immunology|October 19, 2015
Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal associationChristina S Yee, Michel J Massaad, Wayne Bainter, et al.
The Journal of Allergy and Clinical Immunology|August 29, 2016
Epidermodysplasia verruciformis as a manifestation of ARTEMIS deficiency in a young adultAzzedine Tahiat, Yousef R Badran, Janet Chou, et al.
Clinical Immunology (Orlando, Fla.)|January 3, 2013
Intronic SH2D1A mutation with impaired SAP expression and agammaglobulinemiaMike Recher, Ari J Fried, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|April 5, 2014
Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiencySung-Yun Pai, Helen de Boer, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|July 31, 2012
A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndromeJanet Chou, Rima Hanna-Wakim, Irit Tirosh, et al.
Clinical Immunology (Orlando, Fla.)|September 9, 2017
DOCK8 and STAT3 dependent inhibition of IgE isotype switching by TLR9 ligation in human B cellsMichel J Massaad, Brittney Cangemi, Waleed Al-Herz, et al.
Pageof 8