Weemaes CM - Search Results

1

[Immunology in medical practice. XXXV. Screening of suspected immunodeficiency: diagnostic protocols for patients with opportunistic or recurrent severe infections, wasting and failure to thrive].

de Vries E, Kuijpers TW, van Tol MJ, van der Meer JW, Weemaes CM, van Dongen JJ. de Vries E, et al. Among authors: weemaes cm. Ned Tijdschr Geneeskd. 2000 Nov 11;144(46):2197-203. Ned Tijdschr Geneeskd. 2000. PMID: 11103256 Review. Dutch.

2

[Immunology in medical practice. XXXIV. Screening for suspected immunodeficiency: Introduction].

de Vries E, Kuijpers TW, van Tol MJ, van der Meer JW, Weemaes CM, van Dongen JJ. de Vries E, et al. Among authors: weemaes cm. Ned Tijdschr Geneeskd. 2000 Nov 11;144(46):2192-6. Ned Tijdschr Geneeskd. 2000. PMID: 11103255 Review. Dutch.

3

[Diagnostic image (9). Chronic mucocutaneous candidiasis].

van der Meer JW, Weemaes CM. van der Meer JW, et al. Among authors: weemaes cm. Ned Tijdschr Geneeskd. 2000 Oct 28;144(44):2103. Ned Tijdschr Geneeskd. 2000. PMID: 11103671 Dutch.

4

[Immunodeficiency in The Netherlands: clinical and immunological survey, 1970-1983. Interfacultaire werkgroep Immunodeficiëntie].

Zegers BJ, Weemaes CM, Weening RS, van der Meer JW, Vossen JM. Zegers BJ, et al. Among authors: weemaes cm. Ned Tijdschr Geneeskd. 1994 Feb 12;138(7):354-9. Ned Tijdschr Geneeskd. 1994. PMID: 8121525 Dutch.

5

Immunodeficiency in a child with partial trisomy 6p.

Bart IY, Weemaes CM, Schuitema-Dijkstra AR, Smeets D, de Vries E. Bart IY, et al. Among authors: weemaes cm. Acta Paediatr. 2011 Aug;100(8):e92-4. doi: 10.1111/j.1651-2227.2011.02202.x. Epub 2011 Mar 2. Acta Paediatr. 2011. PMID: 21299612

6

Common variable immunodeficiency (CVID) in a family: an autosomal dominant mode of inheritance.

Nijenhuis T, Klasen I, Weemaes CM, Preijers F, de Vries E, van der Meer JW. Nijenhuis T, et al. Among authors: weemaes cm. Neth J Med. 2001 Sep;59(3):134-9. doi: 10.1016/s0300-2977(01)00151-6. Neth J Med. 2001. PMID: 11583829

7

Genetic variation in ICF syndrome: evidence for genetic heterogeneity.

Wijmenga C, Hansen RS, Gimelli G, Björck EJ, Davies EG, Valentine D, Belohradsky BH, van Dongen JJ, Smeets DF, van den Heuvel LP, Luyten JA, Strengman E, Weemaes C, Pearson PL. Wijmenga C, et al. Hum Mutat. 2000 Dec;16(6):509-17. doi: 10.1002/1098-1004(200012)16:6<509::AID-HUMU8>3.0.CO;2-V. Hum Mutat. 2000. PMID: 11102980 Review.

8

Critical aneurysmal dilatation of the thoracic aorta in young adolescents with variant hyperimmunoglobulin E syndrome.

van der meer JW, Weemaes CM, van Krieken JH, Blomjous CE, van Die CE, Netea MG, Bredie SJ. van der meer JW, et al. Among authors: weemaes cm. J Intern Med. 2006 Jun;259(6):615-8. doi: 10.1111/j.1365-2796.2006.01653.x. J Intern Med. 2006. PMID: 16704563 Free article.

9

B-cell recovery after stem cell transplantation of Artemis-deficient SCID requires elimination of autologous bone marrow precursor-B-cells.

van der Burg M, Weemaes CM, Preijers F, Brons P, Barendregt BH, van Tol MJ, Hoogerbrugge P, van Dongen JJ. van der Burg M, et al. Among authors: weemaes cm. Haematologica. 2006 Dec;91(12):1705-9. Haematologica. 2006. PMID: 17145611

10

Hyper-immunoglobulin A in the hyperimmunoglobulinemia D syndrome.

Klasen IS, Göertz JH, van de Wiel GA, Weemaes CM, van der Meer JW, Drenth JP. Klasen IS, et al. Among authors: weemaes cm. Clin Diagn Lab Immunol. 2001 Jan;8(1):58-61. doi: 10.1128/CDLI.8.1.58-61.2001. Clin Diagn Lab Immunol. 2001. PMID: 11139196 Free PMC article.

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