229 related articles for article (PubMed ID: 9482656)
41. A new missense mutation in exon 6 of the proteolipid protein gene in a patient with Pelizaeus-Merzbacher disease.
Kawanishi C; Osaka H; Owa K; Inoue K; Miyakawa T; Onishi H; Yamada Y; Suzuki K; Kimura S; Kosaka K
Hum Mutat; 1997; 9(5):475-6. PubMed ID: 9143933
[No Abstract] [Full Text] [Related]
42. Pelizaeus-Merzbacher-like disease: exclusion of the proteolipid protein locus and documentation of a new locus on Xq.
Lazzarini A; Schwarz KO; Jiang S; Stenroos ES; Lehner T; Johnson WG
Neurology; 1997 Sep; 49(3):824-32. PubMed ID: 9305348
[TBL] [Abstract][Full Text] [Related]
43. Molecular pathways of oligodendrocyte apoptosis revealed by mutations in the proteolipid protein gene.
Southwood C; Gow A
Microsc Res Tech; 2001 Mar; 52(6):700-8. PubMed ID: 11276122
[TBL] [Abstract][Full Text] [Related]
44. Variable expression of a novel PLP1 mutation in members of a family with Pelizaeus-Merzbacher disease.
Fattal-Valevski A; DiMaio MS; Hisama FM; Hobson GM; Davis-Williams A; Garbern JY; Mahoney MJ; Kolodny EH; Pastores GM
J Child Neurol; 2009 May; 24(5):618-24. PubMed ID: 19151366
[TBL] [Abstract][Full Text] [Related]
45. Pelizaeus-Merzbacher disease: pathogenic mechanisms and insights into the roles of proteolipid protein 1 in the nervous system.
Garbern JY
J Neurol Sci; 2005 Feb; 228(2):201-3. PubMed ID: 15694206
[No Abstract] [Full Text] [Related]
46. A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch family.
Sistermans EA; de Wijs IJ; de Coo RF; Smit LM; Menko FH; van Oost BA
Hum Genet; 1996 Mar; 97(3):337-9. PubMed ID: 8786077
[TBL] [Abstract][Full Text] [Related]
47. Hypomyelinated pt mutant rabbit as a new model of Pelizeaus-Merzbacher disease.
Sypecka J; DomaĆska-Janik K
Neurol Neurochir Pol; 1996; 30 Suppl 2():43-7. PubMed ID: 9100242
[No Abstract] [Full Text] [Related]
48. Autosomal recessive form of connatal Pelizaeus-Merzbacher disease.
Begleiter ML; Harris DJ
Am J Med Genet; 1989 Jul; 33(3):311-3. PubMed ID: 2679088
[TBL] [Abstract][Full Text] [Related]
49. Processing of PLP in a model of Pelizaeus-Merzbacher disease/SPG2 due to the rumpshaker mutation.
McLaughlin M; Barrie JA; Karim S; Montague P; Edgar JM; Kirkham D; Thomson CE; Griffiths IR
Glia; 2006 May; 53(7):715-22. PubMed ID: 16506223
[TBL] [Abstract][Full Text] [Related]
50. A brief history of Pelizaeus-Merzbacher disease and proteolipid protein.
Koeppen AH
J Neurol Sci; 2005 Feb; 228(2):198-200. PubMed ID: 15694205
[No Abstract] [Full Text] [Related]
51. Jimpy-4J mouse has a missense mutation in exon 2 of the Plp gene.
Pearsall GB; Nadon NL; Wolf MK; Billings-Gagliardi S
Dev Neurosci; 1997; 19(4):337-41. PubMed ID: 9215879
[TBL] [Abstract][Full Text] [Related]
52. [Female autopsy case of Seitelberger's connatal form of Pelizaeus-Merzbacher disease].
Shimizu Y; Shioda K; Takada K; Minagawa M; Isshiki T
No To Hattatsu; 1997 Nov; 29(6):507-13. PubMed ID: 9394608
[TBL] [Abstract][Full Text] [Related]
53. Tissue culture analysis of the inherited defect of central nervous system myelination in jimpy mice.
Wolf MK; Holden AB
J Neuropathol Exp Neurol; 1969 Apr; 28(2):195-213. PubMed ID: 5787429
[No Abstract] [Full Text] [Related]
54. Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant.
Trofatter JA; Dlouhy SR; DeMyer W; Conneally PM; Hodes ME
Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9427-30. PubMed ID: 2480601
[TBL] [Abstract][Full Text] [Related]
55. Trafficking of PLP/DM20 and cAMP signaling in immortalized jimpy oligodendrocytes.
Ghandour MS; Feutz AC; Jalabi W; Taleb O; Bessert D; Cypher M; Carlock L; Skoff RP
Glia; 2002 Dec; 40(3):300-11. PubMed ID: 12420310
[TBL] [Abstract][Full Text] [Related]
56. Clinical and molecular evaluation of Italian patients affected by Pelizaeus-Merzbacher disease.
Terregino C; Cardona F; Barbetti F; Antonozzi I; Carducci C
J Inherit Metab Dis; 1996; 19(2):197-200. PubMed ID: 8739964
[No Abstract] [Full Text] [Related]
57. A point mutation at the X-chromosomal proteolipid protein locus in Pelizaeus-Merzbacher disease leads to disruption of myelinogenesis.
Weimbs T; Dick T; Stoffel W; Boltshauser E
Biol Chem Hoppe Seyler; 1990 Dec; 371(12):1175-83. PubMed ID: 1708672
[TBL] [Abstract][Full Text] [Related]
58. The molecular and cellular defects underlying Pelizaeus-Merzbacher disease.
Woodward KJ
Expert Rev Mol Med; 2008 May; 10():e14. PubMed ID: 18485258
[TBL] [Abstract][Full Text] [Related]
59. Seitelberger's connatal form of Pelizaeus-Merzbacher Disease. Case report, clinical, pathological and biochemical findings.
Ulrich J; Herschkowitz N
Acta Neuropathol; 1977 Oct; 40(2):129-36. PubMed ID: 201145
[TBL] [Abstract][Full Text] [Related]
60. Primary progressive multiple sclerosis as a phenotype of a PLP1 gene mutation.
Warshawsky I; Rudick RA; Staugaitis SM; Natowicz MR
Ann Neurol; 2005 Sep; 58(3):470-3. PubMed ID: 16130097
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]