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1 r hematopoietic stem cell transplantation in primary immunodeficiency disease.
2 is and management of patients with suspected primary immunodeficiency diseases.
3 nostic evaluation of patients with suspected primary immunodeficiency diseases.
4 t studies to determine optimal therapies for primary immunodeficiency diseases.
5  that study the treatment of rare and severe primary immunodeficiency diseases.
6 pplications for the domain of immunology and primary immunodeficiency diseases.
7 ws for emergence of many autosomal recessive primary immunodeficiency diseases.
8 he cornerstone of treatment in patients with primary immunodeficiency diseases affecting the humoral
9 We have therefore identified the cause for a primary immunodeficiency disease and determined the mech
10 s progress in the study of rare variants and primary immunodeficiency diseases arising from whole-exo
11 globulin is used as a replacement therapy in primary immunodeficiency diseases as well as an immunomo
12    Activated PI3K Delta Syndrome (APDS) is a primary immunodeficiency disease caused by activating mu
13 is (WHIM) syndrome is an ultra-rare combined primary immunodeficiency disease caused by heterozygous
14       X-linked agammaglobulinemia (XLA) is a primary immunodeficiency disease caused by mutations of
15 f B-lineage acute lymphoblastic leukemia and primary immunodeficiency diseases characterized by agamm
16 ciency disorders (CVID) represent a group of primary immunodeficiency diseases characterized by hypog
17 ommon variable immune deficiency (CVID) is a primary immunodeficiency disease, characterized by hypog
18 ican Academy of Allergy, Asthma & Immunology Primary Immunodeficiency Diseases Committee established
19 y in Japan is reaching out regionally to the primary immunodeficiency disease community and internati
20                                              Primary immunodeficiency diseases comprise a group of he
21 ic studies implicate STATs in autoimmune and primary immunodeficiency diseases in humans.
22                         We present PIDO, the primary immunodeficiency disease ontology.
23                                Children with primary immunodeficiency diseases, particularly those le
24  Hem-1 have recently been found to result in primary immunodeficiency disease (PID) in humans, charac
25  and malignancies-are known to exist in many primary immunodeficiency diseases (PID) and to participa
26                                     Over 500 primary immunodeficiency diseases (PID) have been descri
27                                 The field of primary immunodeficiency disease (PIDD) has expanded rem
28 pecific incidence of cancer in subjects with primary immunodeficiency diseases (PIDD) enrolled in the
29                                              Primary immunodeficiency diseases (PIDDs) are clinically
30                                              Primary immunodeficiency diseases (PIDDs) are inherited
31 ideration of many patients suspected to have primary immunodeficiency diseases (PIDDs) is the applica
32  REVIEW: Neutropenia is a feature of several primary immunodeficiency diseases (PIDDs).
33                                              Primary immunodeficiency diseases (PIDs) are a rapidly g
34                                              Primary immunodeficiency diseases (PIDs) are characteriz
35                                              Primary immunodeficiency diseases (PIDs) are Mendelian c
36  been reported occasionally in patients with primary immunodeficiency diseases (PIDs) since the early
37           Analyses of other genes mutated in primary immunodeficiency diseases (PIDs) where reversion
38      The rapid increases in newly recognized primary immunodeficiency diseases (PIDs), including thei
39 hniques are an essential diagnostic tool for primary immunodeficiency diseases (PIDs).
40 d the genetic characterization of many human primary immunodeficiency diseases (PIDs).
41 here is urgent need for the establishment of primary immunodeficiency disease registries, stem cell t
42      Identification of the genetic causes of primary immunodeficiency diseases revealed that Th17 cel
43                            The most profound primary immunodeficiency disease, severe combined immuno
44 n infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease
45          Physicians caring for patients with primary immunodeficiency diseases were identified throug
46 side other symptoms in patients with various primary immunodeficiency diseases with diverse genetic d