Kaplan P - Search Results

1

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. J Pediatr. 1996 Jul;129(1):149-53. doi: 10.1016/s0022-3476(96)70203-2. J Pediatr. 1996. PMID: 8757576

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: kaplan p. 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

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: kaplan p. Arch Intern Med. 1998 Sep 14;158(16):1754-60. doi: 10.1001/archinte.158.16.1754. Arch Intern Med. 1998. PMID: 9738604 Review.

4

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: kaplan p. Am J Med. 2002 Aug 1;113(2):112-9. doi: 10.1016/s0002-9343(02)01150-6. Am J Med. 2002. PMID: 12133749

5

Pediatric non-neuronopathic Gaucher disease: presentation, diagnosis and assessment. Consensus statements.

Grabowski GA, Andria G, Baldellou A, Campbell PE, Charrow J, Cohen IJ, Harris CM, Kaplan P, Mengel E, Pocovi M, Vellodi A. Grabowski GA, et al. Among authors: kaplan p. Eur J Pediatr. 2004 Feb;163(2):58-66. doi: 10.1007/s00431-003-1362-0. Epub 2003 Dec 16. Eur J Pediatr. 2004. PMID: 14677061 Review.

6

Paediatric non-neuronopathic Gaucher disease: recommendations for treatment and monitoring.

Baldellou A, Andria G, Campbell PE, Charrow J, Cohen IJ, Grabowski GA, Harris CM, Kaplan P, McHugh K, Mengel E, Vellodi A. Baldellou A, et al. Among authors: kaplan p. Eur J Pediatr. 2004 Feb;163(2):67-75. doi: 10.1007/s00431-003-1363-z. Epub 2003 Dec 16. Eur J Pediatr. 2004. PMID: 14677062 Review.

7

The history and accomplishments of the ICGG Gaucher registry.

Weinreb NJ, Kaplan P. Weinreb NJ, et al. Among authors: kaplan p. Am J Hematol. 2015 Jul;90 Suppl 1:S2-5. doi: 10.1002/ajh.24054. Am J Hematol. 2015. PMID: 26096743 Free article. No abstract available.

8

Recommendations for the use of eliglustat in the treatment of adults with Gaucher disease type 1 in the United States.

Balwani M, Burrow TA, Charrow J, Goker-Alpan O, Kaplan P, Kishnani PS, Mistry P, Ruskin J, Weinreb N. Balwani M, et al. Among authors: kaplan p. Mol Genet Metab. 2016 Feb;117(2):95-103. doi: 10.1016/j.ymgme.2015.09.002. Epub 2015 Sep 7. Mol Genet Metab. 2016. PMID: 26387627 Free article. Review.

9

Transformation in pretreatment manifestations of Gaucher disease type 1 during two decades of alglucerase/imiglucerase enzyme replacement therapy in the International Collaborative Gaucher Group (ICGG) Gaucher Registry.

Mistry PK, Batista JL, Andersson HC, Balwani M, Burrow TA, Charrow J, Kaplan P, Khan A, Kishnani PS, Kolodny EH, Rosenbloom B, Scott CR, Weinreb N. Mistry PK, et al. Among authors: kaplan p. Am J Hematol. 2017 Sep;92(9):929-939. doi: 10.1002/ajh.24801. Epub 2017 Jul 7. Am J Hematol. 2017. PMID: 28569047 Free PMC article. Clinical Trial.

10

Intellectual outcome in children with maple syrup urine disease.

Kaplan P, Mazur A, Field M, Berlin JA, Berry GT, Heidenreich R, Yudkoff M, Segal S. Kaplan P, et al. J Pediatr. 1991 Jul;119(1 Pt 1):46-50. doi: 10.1016/s0022-3476(05)81037-6. J Pediatr. 1991. PMID: 2066858 Free article.

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