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1.
Heterozygous SERPINA1 Defects and Their Impact on Clinical Manifestations of Patients with Predominantly Antibody Deficiencies.
Int J Mol Sci
; 25(10)2024 May 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-38791420
2.
A Nationwide Study of the Delayed Diagnosis and the Clinical Manifestations of Predominantly Antibody Deficiencies and CTLA4-Mediated Immune Dysregulation Syndrome in Greece.
Medicina (Kaunas)
; 60(5)2024 May 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-38792965
3.
TACI Mutations in Primary Antibody Deficiencies: A Nationwide Study in Greece.
Medicina (Kaunas)
; 57(8)2021 Aug 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-34441032
4.
Low Admission Immunoglobulin G Levels Predict Poor Outcome in Patients with Mild-to-Critical COVID-19: A Prospective, Single-Center Study.
J Epidemiol Glob Health
; 11(4): 338-343, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-34734379
5.
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia.
Blood
; 112(3): 814-21, 2008 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-18490517
6.
Mutation of the Wilms' tumor 1 gene is a poor prognostic factor associated with chemotherapy resistance in normal karyotype acute myeloid leukemia: the United Kingdom Medical Research Council Adult Leukaemia Working Party.
J Clin Oncol
; 26(33): 5429-35, 2008 Nov 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-18591546
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