Holland SM - Search Results

1

Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee.

Tangye SG, Al-Herz W, Bousfiha A, Cunningham-Rundles C, Franco JL, Holland SM, Klein C, Morio T, Oksenhendler E, Picard C, Puel A, Puck J, Seppänen MRJ, Somech R, Su HC, Sullivan KE, Torgerson TR, Meyts I. Tangye SG, et al. Among authors: holland sm. J Clin Immunol. 2022 Oct;42(7):1473-1507. doi: 10.1007/s10875-022-01289-3. Epub 2022 Jun 24. J Clin Immunol. 2022. PMID: 35748970 Free PMC article.

2

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.

3

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

4

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.

5

High levels of interferon gamma in the plasma of children with complete interferon gamma receptor deficiency.

Fieschi C, Dupuis S, Picard C, Smith CI, Holland SM, Casanova JL. Fieschi C, et al. Among authors: holland sm. Pediatrics. 2001 Apr;107(4):E48. doi: 10.1542/peds.107.4.e48. Pediatrics. 2001. PMID: 11335769

6

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

7

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

8

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.

9

Hyper-IgE syndromes.

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

10

The chronicles of chronic granulomatous disease.

Holland S, Seger R, Sullivan KE. Holland S, et al. Clin Immunol. 2005 Aug;116(2):99-100. doi: 10.1016/j.clim.2005.04.001. Clin Immunol. 2005. PMID: 15914086 No abstract available.

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