M01-RR00071/RR/NCRR NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1989	1
1990	1
1992	4
1993	3
1994	1
1995	8
1996	9
1997	12
1998	10
1999	16
2000	11
2001	17
2002	11
2003	15
2004	17
2005	11
2006	14
2007	21
2008	11
2009	18
2010	12
2011	6
2012	4
2013	5
2014	4
2015	1
2016	1
2024	0

1

Agalsidase-beta therapy for advanced Fabry disease: a randomized trial.

Banikazemi M, Bultas J, Waldek S, Wilcox WR, Whitley CB, McDonald M, Finkel R, Packman S, Bichet DG, Warnock DG, Desnick RJ; Fabry Disease Clinical Trial Study Group. Banikazemi M, et al. Ann Intern Med. 2007 Jan 16;146(2):77-86. doi: 10.7326/0003-4819-146-2-200701160-00148. Epub 2006 Dec 18. Ann Intern Med. 2007. PMID: 17179052 Free article. Clinical Trial.

2

Impulsivity.

Hollander E, Rosen J. Hollander E, et al. J Psychopharmacol. 2000;14(2 Suppl 1):S39-44. doi: 10.1177/02698811000142S106. J Psychopharmacol. 2000. PMID: 10888030 Review.

3

High incidence of later-onset fabry disease revealed by newborn screening.

Spada M, Pagliardini S, Yasuda M, Tukel T, Thiagarajan G, Sakuraba H, Ponzone A, Desnick RJ. Spada M, et al. Am J Hum Genet. 2006 Jul;79(1):31-40. doi: 10.1086/504601. Epub 2006 Apr 28. Am J Hum Genet. 2006. PMID: 16773563 Free PMC article.

4

HIV-associated nephropathy.

Winston J, Klotman PE. Winston J, et al. Mt Sinai J Med. 1998 Jan;65(1):27-32. Mt Sinai J Med. 1998. PMID: 9458681 Review.

5

Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease.

Eng CM, Guffon N, Wilcox WR, Germain DP, Lee P, Waldek S, Caplan L, Linthorst GE, Desnick RJ; International Collaborative Fabry Disease Study Group. Eng CM, et al. N Engl J Med. 2001 Jul 5;345(1):9-16. doi: 10.1056/NEJM200107053450102. N Engl J Med. 2001. PMID: 11439963 Free article. Clinical Trial.

6

The demographics and distribution of type B Niemann-Pick disease: novel mutations lead to new genotype/phenotype correlations.

Simonaro CM, Desnick RJ, McGovern MM, Wasserstein MP, Schuchman EH. Simonaro CM, et al. Am J Hum Genet. 2002 Dec;71(6):1413-9. doi: 10.1086/345074. Epub 2002 Oct 4. Am J Hum Genet. 2002. PMID: 12369017 Free PMC article.

7

Enzyme replacement and beyond.

Desnick RJ. Desnick RJ. J Inherit Metab Dis. 2001 Apr;24(2):251-65. doi: 10.1023/a:1010331404448. J Inherit Metab Dis. 2001. PMID: 11405344 Review.

8

Enzyme replacement and enhancement therapies for lysosomal diseases.

Desnick RJ. Desnick RJ. J Inherit Metab Dis. 2004;27(3):385-410. doi: 10.1023/B:BOLI.0000031101.12838.c6. J Inherit Metab Dis. 2004. PMID: 15190196 Review.

9

Recommendations for the diagnosis and treatment of the acute porphyrias.

Anderson KE, Bloomer JR, Bonkovsky HL, Kushner JP, Pierach CA, Pimstone NR, Desnick RJ. Anderson KE, et al. Ann Intern Med. 2005 Mar 15;142(6):439-50. doi: 10.7326/0003-4819-142-6-200503150-00010. Ann Intern Med. 2005. PMID: 15767622 Review.

10

Prenatal genetic screening in the Ashkenazi Jewish population.

Zinberg RE, Kornreich R, Edelmann L, Desnick RJ. Zinberg RE, et al. Clin Perinatol. 2001 Jun;28(2):367-82. doi: 10.1016/s0095-5108(05)70089-0. Clin Perinatol. 2001. PMID: 11499058 Review.

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