Holland SM - Search Results

1

Brain abnormalities in patients with hyperimmunoglobulin E syndrome.

Freeman AF, Collura-Burke CJ, Patronas NJ, Ilcus LS, Darnell D, Davis J, Puck JM, Holland SM. Freeman AF, et al. Among authors: holland sm. Pediatrics. 2007 May;119(5):e1121-5. doi: 10.1542/peds.2006-2649. Epub 2007 Apr 16. Pediatrics. 2007. PMID: 17438082

2

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

Grimbacher B, Holland SM, Puck JM. Grimbacher B, et al. Among authors: holland sm. 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. Among authors: holland sm. 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. Among authors: holland sm. 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: holland sm. 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. Among authors: holland sm. Genet Med. 1999 Jul-Aug;1(5):213-8. doi: 10.1097/00125817-199907000-00008. Genet Med. 1999. PMID: 11256675 Free article.

7

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: holland sm. J Pediatr. 2004 Jan;144(1):93-9. doi: 10.1016/S0022-3476(03)00449-9. J Pediatr. 2004. PMID: 14722525

8

Familial immunodeficiency with cutaneous vasculitis, myoclonus, and cognitive impairment.

Hay BN, Martin JE, Karp B, Davis J, Darnell D, Solomon B, Turner M, Holland SM, Puck JM. Hay BN, et al. Among authors: holland sm. Am J Med Genet A. 2004 Mar 1;125A(2):145-51. doi: 10.1002/ajmg.a.20595. Am J Med Genet A. 2004. PMID: 14981714

9

A man with distinctive facial features and recurrent pyoderma, pneumonia, and skeletal fractures.

Tock CL, Holland SM, Puck JM, Turner ML. Tock CL, et al. Among authors: holland sm. J Am Acad Dermatol. 2004 Apr;50(4):627-9. doi: 10.1016/j.jaad.2003.09.003. J Am Acad Dermatol. 2004. PMID: 15034515 No abstract available.

10

Gastrointestinal involvement in chronic granulomatous disease.

Marciano BE, Rosenzweig SD, Kleiner DE, Anderson VL, Darnell DN, Anaya-O'Brien S, Hilligoss DM, Malech HL, Gallin JI, Holland SM. Marciano BE, et al. Among authors: holland sm. Pediatrics. 2004 Aug;114(2):462-8. doi: 10.1542/peds.114.2.462. Pediatrics. 2004. PMID: 15286231

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