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1.
Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene.
Clin Mol Allergy
; 19(1): 3, 2021 Apr 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-33827715
2.
Nijmegen breakage syndrome in two half sibs with peripheral T-cell lymphoma and cortical T-cell acute lymphoid leukemia.
Cent Eur J Immunol
; 45(4): 507-510, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33658897
3.
Novel biallelic ATM mutations coexist with a mosaic form of triple X syndrome in an 11-year-old girl at remission after T cell acute leukemia.
Immunogenetics
; 70(9): 613-617, 2018 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-29492593
4.
Novel Mutations in SH2D1A Gene in X-linked Lymphoproliferative Syndrome, Diagnosed After B-Cell Non-Hodgkin Lymphoma.
J Pediatr Hematol Oncol
; 39(4): e203-e206, 2017 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28267077
5.
Next generation sequencing revealed DNA ligase IV deficiency in a "developmentally normal" patient with massive brain Epstein-Barr virus-positive diffuse large B-cell lymphoma.
Clin Immunol
; 163: 108-10, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26774591
6.
Molecular Characteristics, Clinical and Immunologic Manifestations of 11 Children with Omenn Syndrome in East Slavs (Russia, Belarus, Ukraine).
J Clin Immunol
; 36(1): 46-55, 2016 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-26596586
7.
Novel LRBA Mutation and Possible Germinal Mosaicism in a Slavic Family.
J Clin Immunol
; 38(4): 471-474, 2018 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29804237
8.
Late-onset combined immune deficiency associated to skin granuloma due to heterozygous compound mutations in RAG1 gene in a 14 years old male.
Hum Immunol
; 74(1): 18-22, 2013 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-23085344
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