Research output per year
Research output per year
- 15 results
Search results
-
2022
Treatment of cerebral adrenoleukodystrophy: allogeneic transplantation and lentiviral gene therapy
Gupta, A. O., Raymond, G., Pierpont, E. I., Kemp, S., McIvor, R. S., Rayannavar, A., Miller, B., Lund, T. C. & Orchard, P. J., 2022, In: Expert Opinion on Biological Therapy. 22, 9, p. 1151-1162 12 p.Research output: Contribution to journal › Review article › peer-review
Open Access -
2016
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines
Braverman, N. E., Raymond, G. V., Rizzo, W. B., Moser, A. B., Wilkinson, M. E., Stone, E. M., Steinberg, S. J., Wangler, M. F., Rush, E. T., Hacia, J. G. & Bose, M., Mar 1 2016, In: Molecular genetics and metabolism. 117, 3, p. 313-321 9 p.Research output: Contribution to journal › Review article › peer-review
Open Access101 Scopus citations -
2012
Adrenoleukodystrophy in female heterozygotes: Underrecognized and undertreated
Jangouk, P., Zackowski, K. M., Naidu, S. & Raymond, G. V., Feb 2012, In: Molecular genetics and metabolism. 105, 2, p. 180-185 6 p.Research output: Contribution to journal › Review article › peer-review
32 Scopus citations -
2011
Research challenges in central nervous system manifestations of inborn errors of metabolism
Dickson, P. I., Pariser, A. R., Groft, S. C., Ishihara, R. W., McNeil, D. E., Tagle, D., Griebel, D. J., Kaler, S. G., Mink, J. W., Shapiro, E. G., Bjoraker, K. J., Krivitzky, L., Provenzale, J. M., Gropman, A., Orchard, P., Raymond, G., Cohen, B. H., Steiner, R. D., Goldkind, S. F., Nelson, R. M., & 2 others, Mar 2011, In: Molecular genetics and metabolism. 102, 3, p. 326-338 13 p.Research output: Contribution to journal › Review article › peer-review
Open Access16 Scopus citations -
2010
Metachromatic leukodystrophy: A case of triplets with the late infantile variant and a systematic review of the literature
Mahmood, A., Berry, J., Wenger, D. A., Escolar, M., Sobeih, M., Raymond, G. & Eichler, F. S., May 2010, In: Journal of child neurology. 25, 5, p. 572-580 9 p.Research output: Contribution to journal › Review article › peer-review
19 Scopus citations -
2007
Immunopathogenesis of adrenoleukodystrophy: Current understanding
Hudspeth, M. P. & Raymond, G. V., Jan 2007, In: Journal of Neuroimmunology. 182, 1-2, p. 5-12 8 p.Research output: Contribution to journal › Review article › peer-review
25 Scopus citations -
"Lorenzo's oil" therapy for X-linked adrenoleukodystrophy: Rationale and current assessment of efficacy
Moser, H. W., Moser, A. B., Hollandsworth, K., Brereton, N. H. & Raymond, G. V., Sep 2007, In: Journal of Molecular Neuroscience. 33, 1, p. 105-113 9 p.Research output: Contribution to journal › Review article › peer-review
44 Scopus citations -
Newborn screening for adrenoleukodystrophy: Implications for therapy
Raymond, G. V., Jones, R. O. & Moser, A. B., 2007, In: Molecular Diagnosis and Therapy. 11, 6, p. 381-384 4 p.Research output: Contribution to journal › Review article › peer-review
24 Scopus citations -
X-linked adrenoleukodystrophy
Moser, H. W., Mahmood, A. & Raymond, G. V., Mar 2007, In: Nature Clinical Practice Neurology. 3, 3, p. 140-151 12 p.Research output: Contribution to journal › Review article › peer-review
227 Scopus citations -
2006
Peroxisome biogenesis disorders
Steinberg, S. J., Dodt, G., Raymond, G. V., Braverman, N. E., Moser, A. B. & Moser, H. W., Dec 2006, In: Biochimica et Biophysica Acta - Molecular Cell Research. 1763, 12, p. 1733-1748 16 p.Research output: Contribution to journal › Review article › peer-review
Open Access354 Scopus citations -
2005
A novel MGP mutation in a consanguineous family: Review of the clinical and molecular characteristics of Keutel syndrome
Hur, D. J., Raymond, G. V., Kahler, S. G., Riegert-Johnson, D. L., Cohen, B. A. & Boyadjiev, S. A., May 15 2005, In: American Journal of Medical Genetics. 135 A, 1, p. 36-40 5 p.Research output: Contribution to journal › Review article › peer-review
77 Scopus citations -
2004
Evaluation of therapy of X-linked adrenoleukodystrophy
Moser, H. W., Fatemi, A., Zackowski, K. M., Smith, S., Golay, X., Muenz, L. & Raymond, G., May 1 2004, In: Neurochemical Research. 29, 5, p. 1003-1016 14 p.Research output: Contribution to journal › Review article › peer-review
14 Scopus citations -
2001
ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations
Kemp, S., Pujol, A., Waterham, H. R., Van Geel, B. M., Boehm, C. D., Raymond, G. V., Cutting, G. R., Wanders, R. J. A. & Moser, H. W., 2001, In: Human mutation. 18, 6, p. 499-515 17 p.Research output: Contribution to journal › Review article › peer-review
Open Access187 Scopus citations -
Peroxisomal disorders
Raymond, G. V., Dec 1 2001, In: Current opinion in neurology. 14, 6, p. 783-787 5 p.Research output: Contribution to journal › Review article › peer-review
8 Scopus citations -
1999
X-Linked adrenoleukodystrophy in children: Review of genetic, clinical, and MR imaging characteristics
Melhem, E. R., Barker, P. B., Raymond, G. V. & Moser, H. W., Dec 1999, In: American Journal of Roentgenology. 173, 6, p. 1575-1581 7 p.Research output: Contribution to journal › Review article › peer-review
22 Scopus citations