Grimbacher B - Search Results

1

Grimbacher B, Holland SM, Puck JM. Grimbacher B, et al. Immunol Rev. 2005 Feb;203:244-50. doi: 10.1111/j.0105-2896.2005.00228.x. Immunol Rev. 2005. PMID: 15661034 Review.

2

The interleukin-4 receptor variant Q576R in hyper-IgE syndrome.

Grimbacher B, Holland SM, Puck JM. Grimbacher B, et al. N Engl J Med. 1998 Apr 9;338(15):1073-4. doi: 10.1056/NEJM199804093381516. N Engl J Med. 1998. PMID: 9537881 No abstract available.

3

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder.

Grimbacher B, Holland SM, Gallin JI, Greenberg F, Hill SC, Malech HL, Miller JA, O'Connell AC, Puck JM. Grimbacher B, et al. N Engl J Med. 1999 Mar 4;340(9):692-702. doi: 10.1056/NEJM199903043400904. N Engl J Med. 1999. PMID: 10053178 Free article.

4

Genetic linkage of hyper-IgE syndrome to chromosome 4.

Grimbacher B, Schäffer AA, Holland SM, Davis J, Gallin JI, Malech HL, Atkinson TP, Belohradsky BH, Buckley RH, Cossu F, Español T, Garty BZ, Matamoros N, Myers LA, Nelson RP, Ochs HD, Renner ED, Wellinghausen N, Puck JM. Grimbacher B, et al. Am J Hum Genet. 1999 Sep;65(3):735-44. doi: 10.1086/302547. Am J Hum Genet. 1999. PMID: 10441580 Free PMC article.

5

Delayed eruption of permanent teeth in hyperimmunoglobulinemia E recurrent infection syndrome.

O'Connell AC, Puck JM, Grimbacher B, Facchetti F, Majorana A, Gallin JI, Malech HL, Holland SM. O'Connell AC, et al. Among authors: grimbacher b. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2000 Feb;89(2):177-85. doi: 10.1067/moe.2000.103129. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2000. PMID: 10673653

6

Analphoid marker chromosome in a patient with hyper-IgE syndrome, autism, and mild mental retardation.

Grimbacher B, Dutra AS, Holland SM, Fischer RE, Pao M, Gallin JI, Puck JM. Grimbacher B, et al. Genet Med. 1999 Jul-Aug;1(5):213-8. doi: 10.1097/00125817-199907000-00008. Genet Med. 1999. PMID: 11256675 Free article.

7

An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single family.

Atkinson TP, Schäffer AA, Grimbacher B, Schroeder HW Jr, Woellner C, Zerbe CS, Puck JM. Atkinson TP, et al. Among authors: grimbacher b. Am J Hum Genet. 2001 Oct;69(4):791-803. doi: 10.1086/323611. Epub 2001 Aug 21. Am J Hum Genet. 2001. PMID: 11517424 Free PMC article.

8

Immunoglobulin E in primary immunodeficiency diseases.

Grimbacher B, Belohradsky BH, Holland SM. Grimbacher B, et al. Allergy. 2002 Nov;57(11):995-1007. doi: 10.1034/j.1398-9995.2002.02168.x. Allergy. 2002. PMID: 12358995 Review. No abstract available.

9

Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity.

Renner ED, Puck JM, Holland SM, Schmitt M, Weiss M, Frosch M, Bergmann M, Davis J, Belohradsky BH, Grimbacher B. Renner ED, et al. Among authors: grimbacher b. J Pediatr. 2004 Jan;144(1):93-9. doi: 10.1016/S0022-3476(03)00449-9. J Pediatr. 2004. PMID: 14722525

10

The hyper IgE syndrome and mutations in TYK2.

Woellner C, Schäffer AA, Puck JM, Renner ED, Knebel C, Holland SM, Plebani A, Grimbacher B. Woellner C, et al. Among authors: grimbacher b. Immunity. 2007 May;26(5):535; author reply 536. doi: 10.1016/j.immuni.2007.05.007. Immunity. 2007. PMID: 17521577 Free article. No abstract available.

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