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Simon, Amos J.
482
results:
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Online (482)
Mediatypes
E-Books (5)
Articles (Online) (199)
Bookchapter (Online) (7)
OpenAccess-fulltext (271)
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1
Expanding the PRAAS spectrum: De novo mutations of immunopr..:
van der Made, Caspar I.
;
Kersten, Simone
;
Chorin, Odelia
...
The American Journal of Human Genetics. 111 (2024) 4 - p. 791-804 , 2024
Link:
https://doi.org/10.1016/..
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2
Helper T cell immunity in humans with inherited CD4 deficie..:
Guérin, Antoine
;
Moncada-Vélez, Marcela
;
Jackson, Katherine
...
Journal of Experimental Medicine. 221 (2024) 5 - p. , 2024
Link:
https://doi.org/10.1084/..
?
3
Combined Immunodeficiency Caused by a Novel Nonsense Mutati..:
Keller, Baerbel
;
Kfir-Erenfeld, Shlomit
;
Matusewicz, Paul
...
Journal of Clinical Immunology. 44 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1007/..
?
4
SLP76 Mutation Associated with Combined Immunodeficiency an..:
Lev, Atar
;
Asleh, Mahdi
;
Levy, Shiran
...
Journal of Clinical Immunology. 43 (2022) 3 - p. 625-635 , 2022
Link:
https://doi.org/10.1007/..
?
5
Genetic workup as a complementary tool for the diagnosis of..:
Shamriz, Oded
;
Simon, Amos J.
;
Frizinsky, Shirley
...
European Journal of Pediatrics. 181 (2022) 5 - p. 1997-2004 , 2022
Link:
https://doi.org/10.1007/..
?
6
Inadequate Activation of γδT- and B-cells in Patient with W..:
Palevski, Dahlia
;
Simon, Amos
;
Lev, Atar
..
Journal of Clinical Immunology. 43 (2022) 1 - p. 109-122 , 2022
Link:
https://doi.org/10.1007/..
?
7
B cell repertoire in patients with a novel BTK mutation: ex..:
Toker, Ori
;
Broides, Arnon
;
Lev, Atar
...
Immunologic Research. 70 (2022) 2 - p. 216-223 , 2022
Link:
https://doi.org/10.1007/..
?
8
Treatment options for DOCK8 deficiency‐related severe derma..:
Ollech, Ayelet
;
Mashiah, Jacob
;
Lev, Atar
...
The Journal of Dermatology. 48 (2021) 9 - p. 1386-1393 , 2021
Link:
https://doi.org/10.1111/..
?
9
A novel zeta-associated protein 70 homozygous mutation caus..:
Ling, Eduard
;
Broides, Arnon
;
Ling, Galina
...
Immunologic Research. 69 (2021) 1 - p. 100-106 , 2021
Link:
https://doi.org/10.1007/..
?
10
Presence of "ACKR1/DARC null" polymorphism in Arabs from Ji..:
Elhadad, Dana
;
Simon, Amos J.
;
Bronstein, Yotam
..
Pediatric Research. 91 (2021) 5 - p. 1012-1014 , 2021
Link:
https://doi.org/10.1038/..
?
11
Exploring genetic defects in adults who were clinically dia..:
Somekh, Ido
;
Lev, Atar
;
Barel, Ortal
...
Immunologic Research. 69 (2021) 2 - p. 145-152 , 2021
Link:
https://doi.org/10.1007/..
?
12
Chronic demodicosis in patients with immune dysregulation: ..:
Shamriz, Oded
;
Lev, Atar
;
Simon, Amos J
...
Clinical and Experimental Immunology. 206 (2021) 1 - p. 56-67 , 2021
Link:
https://doi.org/10.1111/..
?
13
Atypical immune phenotype in severe combined immunodeficien..:
Goldberg, Lior
;
Simon, Amos J.
;
Lev, Atar
...
Genes & Immunity. 21 (2020) 5 - p. 326-334 , 2020
Link:
https://doi.org/10.1038/..
?
14
Inherited SLP76 deficiency in humans causes severe combined..:
Lev, Atar
;
Lee, Yu Nee
;
Sun, Guangping
...
Journal of Experimental Medicine. 218 (2020) 3 - p. , 2020
Link:
https://doi.org/10.1084/..
?
15
Human FCHO1 deficiency reveals role for clathrin-mediated e..:
Łyszkiewicz, Marcin
;
Ziętara, Natalia
;
Frey, Laura
...
Nature Communications. 11 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
1-15