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1        One case occurred in a patient with a congenital immunodeficiency.
2  cancer treatment, organ transplant, HIV, or congenital immunodeficiency.
3 nts a potential mechanism underlying a human congenital immunodeficiency.
4  is a highly successful treatment for severe congenital immunodeficiencies.
5 seases such as breast cancer, leukemias, and congenital immunodeficiencies.
6 ients without hematopoietic cell transplant, congenital immunodeficiency (adjusted odds ratio, 1.90;
7 justed odds ratio, 3.15; 95% CI, 2.09-4.74), congenital immunodeficiency (adjusted odds ratio, 6.94;
8 e, liver disease, chromosomal abnormalities, congenital immunodeficiencies, and inborn errors of meta
9 herapy for patients with hemoglobinopathies, congenital immunodeficiencies, and other conditions, pos
10 nancies, hemophagocytic lymphohistiocytosis, congenital immunodeficiency, and hematopoietic cell tran
11          Patients with WHIM syndrome, a rare congenital immunodeficiency caused by mutations that pre
12    Leukocyte adhesion deficiency or LAD is a congenital immunodeficiency disease characterized by rec
13 ining the nature of immune reconstitution in congenital immunodeficiency diseases, in bone marrow tra
14                      WHIM syndrome is a rare congenital immunodeficiency disorder characterized by wa
15                              The spectrum of congenital immunodeficiency disorders recognized to deve
16                     Studies of patients with congenital immunodeficiency due to mutation of the NF-ka
17 velopment that give rise to certain types of congenital immunodeficiency, leukemia/lymphoma, and auto
18 the context of a broader genetically defined congenital immunodeficiency, of which there are more tha
19  and myelokathexis (WHIM) syndrome is a rare congenital immunodeficiency often caused by mutations in
20 nifestations, NP-C1 also resembles long-term congenital immunodeficiencies that arise from impairment
21 ukemia gene but also as a cause of a complex congenital immunodeficiency that evolves over decades an
22 inked lymphoproliferative disease (XLP) is a congenital immunodeficiency that is characterized by an
23  lymphoproliferative disease (XLP) is a rare congenital immunodeficiency that leads to an extreme, us