HD10981/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1981	1
1982	1
1985	1
1986	6
1988	2
1989	3
1990	2
1991	5
1992	2
1993	1
1994	1
1995	7
1996	3
1997	2
1998	3
1999	14
2000	11
2001	4
2002	5
2003	2
2004	2
2005	3
2006	2
2007	2
2012	2
2024	0

1

ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations.

Kemp S, Pujol A, Waterham HR, van Geel BM, Boehm CD, Raymond GV, Cutting GR, Wanders RJ, Moser HW. Kemp S, et al. Hum Mutat. 2001 Dec;18(6):499-515. doi: 10.1002/humu.1227. Hum Mutat. 2001. PMID: 11748843 Review.

2

Adrenoleukodystrophy.

Moser HW, Bergin A, Naidu S, Ladenson PW. Moser HW, et al. Endocrinol Metab Clin North Am. 1991 Jun;20(2):297-318. Endocrinol Metab Clin North Am. 1991. PMID: 1879401 Review.

3

Disorders of peroxisome biogenesis.

Braverman N, Dodt G, Gould SJ, Valle D. Braverman N, et al. Hum Mol Genet. 1995;4 Spec No:1791-8. doi: 10.1093/hmg/4.suppl_1.1791. Hum Mol Genet. 1995. PMID: 8541879 Review.

4

The evolution of alloimmunity and the genesis of adaptive immunity.

Gould SJ, Hildreth JE, Booth AM. Gould SJ, et al. Q Rev Biol. 2004 Dec;79(4):359-82. doi: 10.1086/426088. Q Rev Biol. 2004. PMID: 15669770 Review.

5

Clinical aspects of adrenoleukodystrophy and adrenomyeloneuropathy.

Moser HW, Moser AB, Naidu S, Bergin A. Moser HW, et al. Dev Neurosci. 1991;13(4-5):254-61. doi: 10.1159/000112170. Dev Neurosci. 1991. PMID: 1817030 Review.

6

Visualization and purification of yeast peroxisomes.

Erdmann R, Gould SJ. Erdmann R, et al. Methods Enzymol. 2002;351:365-81. doi: 10.1016/s0076-6879(02)51858-9. Methods Enzymol. 2002. PMID: 12073357 Review. No abstract available.

7

Adrenoleukodystrophy: phenotypic variability and implications for therapy.

Moser HW, Moser AB, Smith KD, Bergin A, Borel J, Shankroff J, Stine OC, Merette C, Ott J, Krivit W, et al. Moser HW, et al. J Inherit Metab Dis. 1992;15(4):645-64. doi: 10.1007/BF01799621. J Inherit Metab Dis. 1992. PMID: 1528023 Review.

8

MR findings in adult-onset adrenoleukodystrophy.

Kumar AJ, Köhler W, Kruse B, Naidu S, Bergin A, Edwin D, Moser HW. Kumar AJ, et al. AJNR Am J Neuroradiol. 1995 Jun-Jul;16(6):1227-37. AJNR Am J Neuroradiol. 1995. PMID: 7677014 Free PMC article.

9

Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes.

Kelley RI, Datta NS, Dobyns WB, Hajra AK, Moser AB, Noetzel MJ, Zackai EH, Moser HW. Kelley RI, et al. Am J Med Genet. 1986 Apr;23(4):869-901. doi: 10.1002/ajmg.1320230404. Am J Med Genet. 1986. PMID: 3515938 Review.

10

Peroxisome biogenesis disorders: genetics and cell biology.

Gould SJ, Valle D. Gould SJ, et al. Trends Genet. 2000 Aug;16(8):340-5. doi: 10.1016/s0168-9525(00)02056-4. Trends Genet. 2000. PMID: 10904262 Free article. Review.

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