J
Jacov Levy
Researcher at Ben-Gurion University of the Negev
Publications - 70
Citations - 3083
Jacov Levy is an academic researcher from Ben-Gurion University of the Negev. The author has contributed to research in topics: Congenital insensitivity to pain with anhidrosis & Congenital insensitivity to pain. The author has an hindex of 25, co-authored 70 publications receiving 2856 citations. Previous affiliations of Jacov Levy include Barzilai Medical Center & Soroka Medical Center.
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Journal Article
Clinical features of candidiasis in patients with interleukin-12 receptor b1 deficiency
J. C. Rodriguez-Gallego,Monia Ouederni,Stéphanie Boisson-Dupuis,Anne Puel,Capucine Picard,Ithaisa Sologuren,Jacinta Bustamante,Arina Samarina,Estefanía Herrera-Ramos,M. Lopez-Rodriguez,Figen Dogu,Gönül Tanır,Aydan Ikinciogullari,Özden Sanal,S Pedraza,Elena Colino,Melike Keser,Chris Nieuwhof,Dinakantha S. Kumararatne,Anthony W. Segal,Jacov Levy,Necil Kutukculer,Neslihan Edeer Karaca,Ridha Barbouche,Mohamed Bejaoui,S Kachboura,Jose Luis Lezana-Fernández,M Bobadilla-Del Valle,Caner Aytekin,Laurent Abel,Jean-Laurent Casanova +30 more
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Reply to the letter to the editor by Toscano and Andria—“congenital insensitivity to pain with anhidrosis: An NGF/TrkA‐related disorder”
Journal ArticleDOI
Phenotypic variability in patients with unique double homozygous mutations causing variant ataxia telangiectasia.
Jacob Bistritzer,Analia Mijalovsky,Andreea Nissenkorn,Hagit Flusser,Jacov Levy,Amit Nahum,Arnon Broides +6 more
TL;DR: In this paper, a retrospective study of 15 patients with variant A-T, all double homozygous for the same mutations was conducted, and the age of first symptom ranged from 4-180 months, including truncal ataxia at <18 months of age in 9 patients, ataxias and instability only during fever in one patient, dystonia in one patients, and malignancy in 4 patients.
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MHC class 2 deficiency and X-linked agammaglobulinaemia in a consanguineous extended family.
Arnon Broides,George Shubinsky,Ruti Parvari,Bodo Grimbacher,Raz Somech,Raz Somech,Ben-Zion Garty,Jacov Levy +7 more
TL;DR: A consanguineous extended family where four patients have immunodeficiency, three have X‐linked agammaglobulinaemia and one has major histocompatibility complex class 2 deficiency is reported.
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Variation of muscular structure in congenital insensitivity to pain and anhidrosis.
TL;DR: It is assumed that the variable histological findings in the muscle biopsies of these patients reflect a variation in congenital insensitivity to pain with anhidrosis patients that is not related to their genetic mutation.