Wappner RS - Search Results

1

Gaucher disease: recommendations on diagnosis, evaluation, and monitoring.

Charrow J, Esplin JA, Gribble TJ, Kaplan P, Kolodny EH, Pastores GM, Scott CR, Wappner RS, Weinreb NJ, Wisch JS. Charrow J, et al. Among authors: wappner rs. Arch Intern Med. 1998 Sep 14;158(16):1754-60. doi: 10.1001/archinte.158.16.1754. Arch Intern Med. 1998. PMID: 9738604 Review.

2

Enzyme replacement therapy and monitoring for children with type 1 Gaucher disease: consensus recommendations.

Charrow J, Andersson HC, Kaplan P, Kolodny EH, Mistry P, Pastores G, Prakash-Cheng A, Rosenbloom BE, Scott CR, Wappner RS, Weinreb NJ. Charrow J, et al. Among authors: wappner rs. J Pediatr. 2004 Jan;144(1):112-20. doi: 10.1016/j.jpeds.2003.10.067. J Pediatr. 2004. PMID: 14722528 Review. No abstract available.

3

Acceleration of retarded growth in children with Gaucher disease after treatment with alglucerase.

Kaplan P, Mazur A, Manor O, Charrow J, Esplin J, Gribble TJ, Wappner RS, Wisch JS, Weinreb NJ. Kaplan P, et al. Among authors: wappner rs. J Pediatr. 1996 Jul;129(1):149-53. doi: 10.1016/s0022-3476(96)70203-2. J Pediatr. 1996. PMID: 8757576

4

The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease.

Charrow J, Andersson HC, Kaplan P, Kolodny EH, Mistry P, Pastores G, Rosenbloom BE, Scott CR, Wappner RS, Weinreb NJ, Zimran A. Charrow J, et al. Among authors: wappner rs. Arch Intern Med. 2000 Oct 9;160(18):2835-43. doi: 10.1001/archinte.160.18.2835. Arch Intern Med. 2000. PMID: 11025794

5

Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry.

Weinreb NJ, Charrow J, Andersson HC, Kaplan P, Kolodny EH, Mistry P, Pastores G, Rosenbloom BE, Scott CR, Wappner RS, Zimran A. Weinreb NJ, et al. Among authors: wappner rs. Am J Med. 2002 Aug 1;113(2):112-9. doi: 10.1016/s0002-9343(02)01150-6. Am J Med. 2002. PMID: 12133749

6

Gaucher disease type 1: revised recommendations on evaluations and monitoring for adult patients.

Weinreb NJ, Aggio MC, Andersson HC, Andria G, Charrow J, Clarke JT, Erikson A, Giraldo P, Goldblatt J, Hollak C, Ida H, Kaplan P, Kolodny EH, Mistry P, Pastores GM, Pires R, Prakash-Cheng A, Rosenbloom BE, Scott CR, Sobreira E, Tylki-Szymańska A, Vellodi A, vom Dahl S, Wappner RS, Zimran A; International Collaborative Gaucher Group (ICGG). Weinreb NJ, et al. Among authors: wappner rs. Semin Hematol. 2004 Oct;41(4 Suppl 5):15-22. doi: 10.1053/j.seminhematol.2004.07.010. Semin Hematol. 2004. PMID: 15468046

7

Individualization of long-term enzyme replacement therapy for Gaucher disease.

Andersson HC, Charrow J, Kaplan P, Mistry P, Pastores GM, Prakash-Cheng A, Rosenbloom BE, Scott CR, Wappner RS, Weinreb NJ; International Collaborative Gaucher Group U.S. Regional Coordinators. Andersson HC, et al. Among authors: wappner rs. Genet Med. 2005 Feb;7(2):105-10. doi: 10.1097/01.gim.0000153660.88672.3c. Genet Med. 2005. PMID: 15714077 Free article. Review.

8

Development of guidelines for treatment of children with phenylketonuria: report of a meeting at the National Institute of Child Health and Human Development held August 15, 1995, National Institutes of Health, Bethesda, Maryland.

Seashore MR, Wappner R, Cho S, de La Cruz F. Seashore MR, et al. Pediatrics. 1999 Dec;104(6):e67. doi: 10.1542/peds.104.6.e67. Pediatrics. 1999. PMID: 10586001

9

Management of phenylketonuria for optimal outcome: a review of guidelines for phenylketonuria management and a report of surveys of parents, patients, and clinic directors.

Wappner R, Cho S, Kronmal RA, Schuett V, Seashore MR. Wappner R, et al. Pediatrics. 1999 Dec;104(6):e68. doi: 10.1542/peds.104.6.e68. Pediatrics. 1999. PMID: 10586002

10

Lactation and phenylketonuria.

Bradburn NC, Wappner RS, Lemons JA, Meyer BA, Roberts RS. Bradburn NC, et al. Among authors: wappner rs. Am J Perinatol. 1985 Apr;2(2):138-41. doi: 10.1055/s-2007-999931. Am J Perinatol. 1985. PMID: 4096753

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