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Waleed Al-Herz
Waleed Al-Herz
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Human inborn errors of immunity: 2019 update on the classification from the International Union of Immunological Societies Expert Committee
SG Tangye, W Al-Herz, A Bousfiha, T Chatila, C Cunningham-Rundles, ...
Journal of clinical immunology 40, 24-64, 2020
17032020
International union of immunological societies: 2017 primary immunodeficiency diseases committee report on inborn errors of immunity
C Picard, H Bobby Gaspar, W Al-Herz, A Bousfiha, JL Casanova, ...
Journal of clinical immunology 38, 96-128, 2018
9212018
Primary immunodeficiency diseases: an update on the classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015
C Picard, W Al-Herz, A Bousfiha, JL Casanova, T Chatila, ME Conley, ...
Journal of clinical immunology 35, 696-726, 2015
8572015
Human inborn errors of immunity: 2019 update of the IUIS phenotypical classification
A Bousfiha, L Jeddane, C Picard, W Al-Herz, F Ailal, T Chatila, ...
Journal of clinical immunology 40, 66-81, 2020
7222020
Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency
W Al-Herz, A Bousfiha, JL Casanova, T Chatila, ME Conley, ...
Frontiers in immunology 5, 162, 2014
6872014
Gene therapy for Wiskott-Aldrich syndrome—long-term efficacy and genotoxicity
CJ Braun, K Boztug, A Paruzynski, M Witzel, A Schwarzer, M Rothe, ...
Science translational medicine 6 (227), 227ra33-227ra33, 2014
6182014
The 2017 IUIS phenotypic classification for primary immunodeficiencies
A Bousfiha, L Jeddane, C Picard, F Ailal, H Bobby Gaspar, W Al-Herz, ...
Journal of clinical immunology 38, 129-143, 2018
6132018
Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency
W Al-Herz, A Bousfiha, JL Casanova, H Chapel, ME Conley, ...
Frontiers in immunology 2, 54, 2011
5622011
Loss of interleukin-10 signaling and infantile inflammatory bowel disease: implications for diagnosis and therapy
D Kotlarz, R Beier, D Murugan, J Diestelhorst, O Jensen, K Boztug, ...
Gastroenterology 143 (2), 347-355, 2012
5262012
The 2015 IUIS phenotypic classification for primary immunodeficiencies
A Bousfiha, L Jeddane, W Al-Herz, F Ailal, JL Casanova, T Chatila, ...
Journal of clinical immunology 35, 727-738, 2015
3032015
DOCK8 deficiency: clinical and immunological phenotype and treatment options-a review of 136 patients
SE Aydin, SS Kilic, C Aytekin, A Kumar, O Porras, L Kainulainen, ...
Journal of clinical immunology 35, 189-198, 2015
2902015
BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies
BE Marciano, CY Huang, G Joshi, N Rezaei, BC Carvalho, Z Allwood, ...
Journal of allergy and clinical immunology 133 (4), 1134-1141, 2014
2702014
Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia
B Boisson, E Laplantine, K Dobbs, A Cobat, N Tarantino, M Hazen, ...
Journal of Experimental Medicine 212 (6), 939-951, 2015
2512015
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation
HH Jabara, DR McDonald, E Janssen, MJ Massaad, N Ramesh, ...
Nature immunology 13 (6), 612-620, 2012
2412012
The 2022 update of IUIS phenotypical classification for human inborn errors of immunity
A Bousfiha, A Moundir, SG Tangye, C Picard, L Jeddane, W Al-Herz, ...
Journal of clinical immunology 42 (7), 1508-1520, 2022
2252022
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency
HH Jabara, SE Boyden, J Chou, N Ramesh, MJ Massaad, H Benson, ...
Nature genetics 48 (1), 74-78, 2016
2162016
The ever-increasing array of novel inborn errors of immunity: an interim update by the IUIS committee
SG Tangye, W Al-Herz, A Bousfiha, C Cunningham-Rundles, JL Franco, ...
Journal of clinical immunology 41, 666-679, 2021
2132021
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
KR Engelhardt, ME Gertz, S Keles, AA Schäffer, EC Sigmund, C Glocker, ...
Journal of Allergy and Clinical Immunology 136 (2), 402-412, 2015
1952015
Inherited DOCK2 deficiency in patients with early-onset invasive infections
K Dobbs, C Domínguez Conde, SY Zhang, S Parolini, M Audry, J Chou, ...
New England Journal of Medicine 372 (25), 2409-2422, 2015
1912015
Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis
IK Chinn, OS Eckstein, EC Peckham-Gregory, BR Goldberg, LR Forbes, ...
Blood, The Journal of the American Society of Hematology 132 (1), 89-100, 2018
1752018
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