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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1960 1
1964 1
1968 3
1969 2
1970 2
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1985 1
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2021 1
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Page 1
Clinical and Radiologic Features, Pathology, and Treatment of Balo Concentric Sclerosis.
Jolliffe EA, Guo Y, Hardy TA, Morris PP, Flanagan EP, Lucchinetti CF, Tobin WO. Jolliffe EA, et al. Neurology. 2021 Jul 27;97(4):e414-e422. doi: 10.1212/WNL.0000000000012230. Epub 2021 May 19. Neurology. 2021. PMID: 34011576 Free PMC article.
METHODS: Retrospective review of BCS cases from US and Australian tertiary care centers. RESULTS: We identified 40 BCS cases with 38 available MRIs. ...CONCLUSIONS: BCS may be a distinct subtype of multiple sclerosis characterized by pattern III immunopathology....
METHODS: Retrospective review of BCS cases from US and Australian tertiary care centers. RESULTS: We identified 40 BCS cases with 38 …
Adrenoleukodystrophy: biochemical procedures in diagnosis, prevention and treatment.
Watkins PA, Naidu S, Moser HW. Watkins PA, et al. J Inherit Metab Dis. 1987;10 Suppl 1:46-53. doi: 10.1007/BF01812846. J Inherit Metab Dis. 1987. PMID: 3119941 Review.
Thus, such studies can supplement very long chain fatty acid concentrations in heterozygote detection. Therapeutic interventions for adrenoleukodystrophy, such as dietary restriction of very long chain fatty acids, administration of clofibrate or carnitine, immunosuppressi …
Thus, such studies can supplement very long chain fatty acid concentrations in heterozygote detection. Therapeutic interventions for …
Prenatal genetic diagnosis (second of three parts).
Milunsky A, Littlefield JW, Kanfer JN, Kolodny EH, Shih VE, Atkins L. Milunsky A, et al. N Engl J Med. 1970 Dec 24;283(26):1441-7. doi: 10.1056/NEJM197012242832605. N Engl J Med. 1970. PMID: 4098222 Review. No abstract available.
Adrenoleukodystrophy: a fatal disorder with new opportunities for prevention and treatment.
O'Donnell-O'Toole S. O'Donnell-O'Toole S. J Neurosurg Nurs. 1985 Feb;17(1):53-60. J Neurosurg Nurs. 1985. PMID: 3844443
Adrenoleukodystrophy is an X-linked disorder characterized by adrenal insufficiency and progressive demyelination of the cerebral white matter. Young boys usually become symptomatic during pre- or primary school years and follow a time-variable, downhill, terminal c …
Adrenoleukodystrophy is an X-linked disorder characterized by adrenal insufficiency and progressive demyelination of the cerebral …
The effect of genotype on the natural history of eIF2B-related leukodystrophies.
Fogli A, Schiffmann R, Bertini E, Ughetto S, Combes P, Eymard-Pierre E, Kaneski CR, Pineda M, Troncoso M, Uziel G, Surtees R, Pugin D, Chaunu MP, Rodriguez D, Boespflug-Tanguy O. Fogli A, et al. Neurology. 2004 May 11;62(9):1509-17. doi: 10.1212/01.wnl.0000123259.67815.db. Neurology. 2004. PMID: 15136673
Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2).
Hodes ME, Zimmerman AW, Aydanian A, Naidu S, Miller NR, Garcia Oller JL, Barker B, Aleck KA, Hurley TD, Dlouhy SR. Hodes ME, et al. Am J Med Genet. 1999 Jan 15;82(2):132-9. doi: 10.1002/(sici)1096-8628(19990115)82:2<132::aid-ajmg6>3.0.co;2-4. Am J Med Genet. 1999. PMID: 9934976
20 results