ライフサイエンスコーパス: hyper-IgM syndrome

コーパス検索結果 (１語後でソート)

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1 nitive therapeutic options for patients with hyper IgM syndrome.

2 detection and carrier detection in X-linked hyper IgM syndrome.

3 and are responsible for the X-linked form of hyper IgM syndrome.

4 ion that is absent in patients with X-linked hyper-IgM syndrome.

5 cy, immunoglobulin A deficiency, or X-linked hyper-IgM syndrome.

6 variants with truncated E5 in patients with hyper-IgM syndrome 2 and establish that AID, through the

7 d clinical feature of patients with X-linked hyper-IgM syndrome, an inherited immune deficiency disor

8 unistic infections in patients with X-linked hyper IgM syndrome and in patients with human immunodefi

9 ibed to cause atypical SCID, Omenn syndrome, Hyper IgM syndrome and inflammatory bowel disease-all wi

10 ed primary immunodeficiency characterized by hyper-IgM syndrome and hypohydrotic ectodermal dysplasia

11 hese findings now explain cases of autosomal hyper-IgM syndrome and reveal that critical components f

12 inguish X-linked disease from other forms of hyper IgM syndrome have been reported, nor are there tes

13 -linked anhidrotic ectodermal dysplasia with hyper-IgM syndrome (HED-ID) who have deficient expressio

14 cells from a patient (pt1) with non-X-linked hyper-IgM syndrome (HIGM) possess an atypical CD23(lo) p

15 initiate GC responses, patients with type 1 hyper-IgM syndrome (HIGM1) support populations of IgM(+)

16 Hyper-IgM syndrome (HIM) is a rare immunodeficiency diso

17 With genetic defects in the hyper IgM syndrome identified, it is possible to diagnos

18 To establish the underlying cause of hyper-IgM syndrome in one female patient, B cell functio

19 The hyper IgM syndrome is a rare, inherited immune deficienc

20 X-linked hyper-IgM syndrome is a rare immunodeficiency disorder r

21 ited deficiency of the CD40 ligand (X-linked hyper-IgM syndrome) is characterized by failure of immun

22 Hyper-IgM syndromes result from mutations in CD40 ligand

23 ts with common variable immunodeficiency and hyper IgM syndrome, suggests a potential narrow target f

24 Although hyper-IgM syndrome type 2 is rare, the 23 missense mutat

25 Hyper-IgM syndrome type 2 stems from mutations in activa

26 duced by bacterial products in patients with hyper-IgM syndrome who lack CD40 ligand expression and i

27 ical autoimmune complications; patients with hyper-IgM syndromes who are deficient in activation-indu

28 ne cases of X-linked hyper-immunoglobulin M (hyper-IgM) syndrome who, due to a mutation in CD40 ligan

29 aB essential modulator (NEMO) cause X-linked hyper-IgM syndrome with ectodermal dysplasia (XHM-ED).

30 Patients with X-linked hyper-IgM syndrome (X-HIGM) due to CD40 ligand (CD40L) m

31 Subjects with X-linked hyper-IgM syndrome (X-HIgM) have a markedly reduced freq

32 X-linked hyper-IgM syndrome (XHIGM) is a primary immunodeficiency

33 X-linked hyper IgM syndrome (XHIM) is a primary immunodeficiency

34 The X-linked hyper-IgM syndrome (XHIM) is a primary immunodeficiency

35 X-linked hyper-IgM syndrome (XHIM) results from mutations in the

36 ated, the clinical consequences are X-linked hyper-IgM syndrome (XHIM), a primary immunodeficiency di

37 Three patients with X-linked hyper-IgM syndrome (XHIM), who were all asymptomatic unt

38 X-linked hyper IgM syndrome (XHM) is a combined immune deficiency

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