Raymond G - Search Results

1

Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly.

Gonzaga-Jauregui C, Lotze T, Jamal L, Penney S, Campbell IM, Pehlivan D, Hunter JV, Woodbury SL, Raymond G, Adesina AM, Jhangiani SN, Reid JG, Muzny DM, Boerwinkle E, Lupski JR, Gibbs RA, Wiszniewski W. Gonzaga-Jauregui C, et al. Among authors: raymond g. JAMA Neurol. 2013 Dec;70(12):1491-8. doi: 10.1001/jamaneurol.2013.4598. JAMA Neurol. 2013. PMID: 24126608 Free PMC article.

2

Antioxidant Capacity and Superoxide Dismutase Activity in Adrenoleukodystrophy.

Turk BR, Theisen BE, Nemeth CL, Marx JS, Shi X, Rosen M, Jones RO, Moser AB, Watkins PA, Raymond GV, Tiffany C, Fatemi A. Turk BR, et al. JAMA Neurol. 2017 May 1;74(5):519-524. doi: 10.1001/jamaneurol.2016.5715. JAMA Neurol. 2017. PMID: 28288261 Free PMC article.

3

Neurocognitive Trajectory of Boys Who Received a Hematopoietic Stem Cell Transplant at an Early Stage of Childhood Cerebral Adrenoleukodystrophy.

Pierpont EI, Eisengart JB, Shanley R, Nascene D, Raymond GV, Shapiro EG, Ziegler RS, Orchard PJ, Miller WP. Pierpont EI, et al. Among authors: raymond gv. JAMA Neurol. 2017 Jun 1;74(6):710-717. doi: 10.1001/jamaneurol.2017.0013. JAMA Neurol. 2017. PMID: 28418523 Free PMC article.

4

Evolution of phenotypes in adult male patients with X-linked adrenoleukodystrophy.

van Geel BM, Bezman L, Loes DJ, Moser HW, Raymond GV. van Geel BM, et al. Among authors: raymond gv. Ann Neurol. 2001 Feb;49(2):186-94. doi: 10.1002/1531-8249(20010201)49:2<186::aid-ana38>3.0.co;2-r. Ann Neurol. 2001. PMID: 11220738

5

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

6

Proton MR spectroscopic imaging predicts lesion progression on MRI in X-linked adrenoleukodystrophy.

Eichler FS, Barker PB, Cox C, Edwin D, Ulug AM, Moser HW, Raymond GV. Eichler FS, et al. Among authors: raymond gv. Neurology. 2002 Mar 26;58(6):901-7. doi: 10.1212/wnl.58.6.901. Neurology. 2002. PMID: 11914405

7

Molecular findings in symptomatic and pre-symptomatic Alexander disease patients.

Gorospe JR, Naidu S, Johnson AB, Puri V, Raymond GV, Jenkins SD, Pedersen RC, Lewis D, Knowles P, Fernandez R, De Vivo D, van der Knaap MS, Messing A, Brenner M, Hoffman EP. Gorospe JR, et al. Among authors: raymond gv. Neurology. 2002 May 28;58(10):1494-500. doi: 10.1212/wnl.58.10.1494. Neurology. 2002. PMID: 12034785

8

Spectroscopic evidence of cerebral axonopathy in patients with "pure" adrenomyeloneuropathy.

Dubey P, Fatemi A, Barker PB, Degaonkar M, Troeger M, Zackowski K, Bastian A, Smith SA, Pomper MG, Moser HW, Raymond GV. Dubey P, et al. Among authors: raymond gv. Neurology. 2005 Jan 25;64(2):304-10. doi: 10.1212/01.WNL.0000149514.13580.84. Neurology. 2005. PMID: 15668429

9

Magnetization transfer MRI demonstrates spinal cord abnormalities in adrenomyeloneuropathy.

Fatemi A, Smith SA, Dubey P, Zackowski KM, Bastian AJ, van Zijl PC, Moser HW, Raymond GV, Golay X. Fatemi A, et al. Among authors: raymond gv. Neurology. 2005 May 24;64(10):1739-45. doi: 10.1212/01.WNL.0000164458.02141.06. Neurology. 2005. PMID: 15911801

10

Adrenoleukodystrophy: new approaches to a neurodegenerative disease.

Moser HW, Raymond GV, Dubey P. Moser HW, et al. JAMA. 2005 Dec 28;294(24):3131-4. doi: 10.1001/jama.294.24.3131. JAMA. 2005. PMID: 16380594

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