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Author/Creator Rechavi, G

1. Co-existence of clonal expanded autologous and transplacental-acquired maternal T cells in recombination activating gene-deficient severe combined immunodeficiency. (24th April 2014)

Authors:
Lev, A; Simon, A J; Ben-Ari, J; Takagi, D; Stauber, T; Trakhtenbrot, L; Rosenthal, E; Rechavi, G; Amariglio, N; Somech, R
Journal:
Clinical and experimental immunology
Issue:
Volume 176:Number 3(2014:Jun.)
Page Start:
380
Record Type:
Journal Article
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2. DOP010 Activating PIK3CD mutations cause severe intestinal lymphonodular hyperplasia and an IBD-like phenotype. (16th January 2018)

Authors:
Farachi, S; Werner, L; Konnikova, L; Rea, F; Vardi, I; Romeo, E; Barel, O; De Angelis, P; Dall'Oglio, L; Rechavi, G; Snapper, S; Somech, R; Weiss, B; Cancrini, C; Shouval, D
Journal:
Journal of Crohn's and colitis
Issue:
Volume 12:Number 1(2018:Jan.)Supplement 1
Page Start:
S036
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation. Issue 3 (20th July 2005)

Authors:
Basel-Vanagaite, L; Attia, R; Yahav, M; Ferland, R J; Anteki, L; Walsh, C A; Olender, T; Straussberg, R; Magal, N; Taub, E; Drasinover, V; Alkelai, A; Bercovich, D; Rechavi, G; Simon, A J; Shohat, M
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 3(2006)
Page Start:
203
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗