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1 . Academic Journal
Lessons Learned From Five Years of Newborn Screening for Severe Combined Immunodeficiency in Israel
저자
by
Lev, Atar
;
Sharir, Idan
;
Simon, Amos J.
;
Levy, Shiran
;
Lee, Yu Nee
, et al.
소스
In
The Journal of Allergy and Clinical Immunology: In Practice
October 2022 10(10):2722-2731
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7 . Academic Journal
Phenotypic variability in patients with unique double homozygous mutations causing variant ataxia telangiectasia
저자
by
Bistritzer, Jacob
;
Mijalovsky, Analia
;
Nissenkorn, Andreea
;
Flusser, Hagit
;
Levy, Jacov
, et al.
소스
In
European Journal of Paediatric Neurology
May 2021 32:36-39
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7 . Academic Journal
124 Neutropenia in X-linked agammaglobulinemia patients, is possibly the most common presenting sign
저자
by
Mandelblit, Nufar Marcus
;
Kryshtal, Eyal
;
Soffair, Niv Niv
;
Toker, Ori
;
Nahum, Amit
, et al.
소스
In
Clinical Immunology
May 2024 262 Supplement
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7 . Academic Journal
Fatal combined immunodeficiency associated with heterozygous mutation in STAT1
저자
by
Sharfe, Nigel
;
Nahum, Amit
;
Newell, Andrea
;
Dadi, Harjit
;
Ngan, Bo
, et al.
소스
In
The Journal of Allergy and Clinical Immunology
March 2014 133(3):807-817
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7 . Periodical
X-linked C1GALT1C1mutation causes atypical hemolytic uremic syndrome
저자
by
Hadar, Noam
;
Schreiber, Ruth
;
Eskin-Schwartz, Marina
;
Kristal, Eyal
;
Shubinsky, George
, et al.
소스
European Journal of Human Genetics: EJHG; October 2023, Vol. 31 Issue: 10 p1101-1107, 7p
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7 . Academic Journal
Characterization of ζ-associated protein, 70 kd (ZAP70)–deficient human lymphocytes
저자
by
Roifman, Chaim M.
;
Dadi, Harjit
;
Somech, Raz
;
Nahum, Amit
;
Sharfe, Nigel
.
소스
In
The Journal of Allergy and Clinical Immunology
December 2010 126(6):1226-1233
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7 . Academic Journal
SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related Lymphoma.
저자
by
Lev, Atar
;
Asleh, Mahdi
;
Levy, Shiran
;
Lee, Yu Nee
;
Simon, Amos J.
, et al.
소스
Journal of Clinical Immunology
. Apr2023, Vol. 43 Issue 3, p625-635. 11p.
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7 . Academic Journal
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome
저자
by
Hadar, Noam
;
Schreiber, Ruth
;
Eskin-Schwartz, Marina
;
Kristal, Eyal
;
Shubinsky, George
, et al.
소스
European Journal of Human Genetics
. 31(10):1101-1107
Web of Science
Scopus
JCR 저널정보
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7 . Academic Journal
Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene: IgG hypergammaglobulinemia with IgA and IgE deficiency
저자
by
Nahum, Amit
;
Somech, Raz
;
Shubinsky, George
;
Levy, Jacov
;
Broides, Arnon
.
소스
In
Clinical Immunology
April 2020 213
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7 . Academic Journal
Toll-like receptor 3 (TLR3) variant and NLRP12 mutation confer susceptibility to a complex clinical presentation
저자
by
Tal, Yuval
;
Ribak, Yaarit
;
Khalaila, Aya
;
Shamriz, Oded
;
Marcus, Nofar
, et al.
소스
In
Clinical Immunology
March 2020 212
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