Consanguinity rate and delay in diagnosis in Turkish patients with combined immunodeficiencies: a single-center study.
about
The value of family history in diagnosing primary immunodeficiency disordersCombined immunodeficiencies: twenty years experience from a single center in TurkeyCombined immunodeficiency in the United States and Kuwait: Comparison of patients' characteristics and molecular diagnosis.The spread of the J Project.Patterns of Primary Immunodeficiency Disorders Among a Highly Consanguineous Population: Cairo University Pediatric Hospital's 5-Year Experience.Intracranial hemorrhage in children with congenital factor deficiencies.In vitro T lymphocyte proliferation by carboxyfluorescein diacetate succinimidyl ester method is helpful in diagnosing and managing primary immunodeficiencies.Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency.
P2860
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P2860
Consanguinity rate and delay in diagnosis in Turkish patients with combined immunodeficiencies: a single-center study.
description
2010 nî lūn-bûn
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name
Consanguinity rate and delay i ...... encies: a single-center study.
@en
Consanguinity rate and delay i ...... encies: a single-center study.
@nl
type
label
Consanguinity rate and delay i ...... encies: a single-center study.
@en
Consanguinity rate and delay i ...... encies: a single-center study.
@nl
prefLabel
Consanguinity rate and delay i ...... encies: a single-center study.
@en
Consanguinity rate and delay i ...... encies: a single-center study.
@nl
P2093
P2860
P1476
Consanguinity rate and delay i ...... encies: a single-center study.
@en
P2093
Elif Azarsiz
Necil Kutukculer
Neslihan Edeer Karaca
Nesrin Gulez
P2860
P2888
P304
P356
10.1007/S10875-010-9472-8
P50
P577
2010-10-06T00:00:00Z