Raymond GV - Search Results

1

Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines.

Braverman NE, Raymond GV, Rizzo WB, Moser AB, Wilkinson ME, Stone EM, Steinberg SJ, Wangler MF, Rush ET, Hacia JG, Bose M. Braverman NE, et al. Among authors: raymond gv. Mol Genet Metab. 2016 Mar;117(3):313-21. doi: 10.1016/j.ymgme.2015.12.009. Epub 2015 Dec 23. Mol Genet Metab. 2016. PMID: 26750748 Free PMC article. Review.

2

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups.

Moser AB, Rasmussen M, Naidu S, Watkins PA, McGuinness M, Hajra AK, Chen G, Raymond G, Liu A, Gordon D, et al. Moser AB, et al. J Pediatr. 1995 Jul;127(1):13-22. doi: 10.1016/s0022-3476(95)70250-4. J Pediatr. 1995. PMID: 7541833

3

Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies.

Watkins PA, McGuinness MC, Raymond GV, Hicks BA, Sisk JM, Moser AB, Moser HW. Watkins PA, et al. Among authors: raymond gv. Ann Neurol. 1995 Sep;38(3):472-7. doi: 10.1002/ana.410380322. Ann Neurol. 1995. PMID: 7668838

4

Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls.

Moser AB, Kreiter N, Bezman L, Lu S, Raymond GV, Naidu S, Moser HW. Moser AB, et al. Among authors: raymond gv. Ann Neurol. 1999 Jan;45(1):100-10. doi: 10.1002/1531-8249(199901)45:1<100::aid-art16>3.0.co;2-u. Ann Neurol. 1999. PMID: 9894883

5

Plasma and red blood cell fatty acids in peroxisomal disorders.

Moser AB, Jones DS, Raymond GV, Moser HW. Moser AB, et al. Among authors: raymond gv. Neurochem Res. 1999 Feb;24(2):187-97. doi: 10.1023/a:1022549618333. Neurochem Res. 1999. PMID: 9972864

6

Peroxisomal disorders.

Raymond GV. Raymond GV. Curr Opin Pediatr. 1999 Dec;11(6):572-6. doi: 10.1097/00008480-199912000-00017. Curr Opin Pediatr. 1999. PMID: 10590918 Review.

7

Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening.

Bezman L, Moser AB, Raymond GV, Rinaldo P, Watkins PA, Smith KD, Kass NE, Moser HW. Bezman L, et al. Among authors: raymond gv. Ann Neurol. 2001 Apr;49(4):512-7. Ann Neurol. 2001. PMID: 11310629

8

Peroxisomal disorders.

Raymond GV. Raymond GV. Curr Opin Neurol. 2001 Dec;14(6):783-7. doi: 10.1097/00019052-200112000-00017. Curr Opin Neurol. 2001. PMID: 11723389

9

Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.

Corzo D, Gibson W, Johnson K, Mitchell G, LePage G, Cox GF, Casey R, Zeiss C, Tyson H, Cutting GR, Raymond GV, Smith KD, Watkins PA, Moser AB, Moser HW, Steinberg SJ. Corzo D, et al. Among authors: raymond gv. Am J Hum Genet. 2002 Jun;70(6):1520-31. doi: 10.1086/340849. Epub 2002 Apr 29. Am J Hum Genet. 2002. PMID: 11992258 Free PMC article.

10

MRI and proton MRSI in women heterozygous for X-linked adrenoleukodystrophy.

Fatemi A, Barker PB, Uluğ AM, Nagae-Poetscher LM, Beauchamp NJ, Moser AB, Raymond GV, Moser HW, Naidu S. Fatemi A, et al. Among authors: raymond gv. Neurology. 2003 Apr 22;60(8):1301-7. doi: 10.1212/01.wnl.0000059546.15529.cb. Neurology. 2003. PMID: 12707433

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