BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 3827224)

  • 1. Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease.
    Koeppen AH; Ronca NA; Greenfield EA; Hans MB
    Ann Neurol; 1987 Feb; 21(2):159-70. PubMed ID: 3827224
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Pelizaeus-Merzbacher disease].
    Koetsveld-Baart JC; Glaudemans-van Gelderen IE; Valk J; Barth PG
    Ned Tijdschr Geneeskd; 1993 Nov; 137(48):2494-8. PubMed ID: 8272126
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pelizaeus-Merzbacher disease: an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid protein.
    Gencic S; Abuelo D; Ambler M; Hudson LD
    Am J Hum Genet; 1989 Sep; 45(3):435-42. PubMed ID: 2773936
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher disease.
    Carango P; Funanage VL; QuirĂ³s RE; Debruyn CS; Marks HG
    Ann Neurol; 1995 Oct; 38(4):610-7. PubMed ID: 7574457
    [TBL] [Abstract][Full Text] [Related]  

  • 5. X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus.
    Saugier-Veber P; Munnich A; Bonneau D; Rozet JM; Le Merrer M; Gil R; Boespflug-Tanguy O
    Nat Genet; 1994 Mar; 6(3):257-62. PubMed ID: 8012387
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comparative immunocytochemistry of Pelizaeus-Merzbacher disease, the jimpy mouse, and the myelin-deficient rat.
    Koeppen AH; Barron KD; Csiza CK; Greenfield EA
    J Neurol Sci; 1988 Apr; 84(2-3):315-27. PubMed ID: 2454299
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Jimpy(msd) mouse mutation and connatal Pelizaeus-Merzbacher disease.
    Yamamoto T; Nanba E; Zhang H; Sasaki M; Komaki H; Takeshita K
    Am J Med Genet; 1998 Feb; 75(4):439-40. PubMed ID: 9482656
    [No Abstract]   [Full Text] [Related]  

  • 8. Pelizaeus-Merzbacher disease presenting as spinal muscular atrophy: clinical and molecular studies.
    Kaye EM; Doll RF; Natowicz MR; Smith FI
    Ann Neurol; 1994 Dec; 36(6):916-9. PubMed ID: 7998780
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease.
    Pratt VM; Trofatter JA; Schinzel A; Dlouhy SR; Conneally PM; Hodes ME
    Am J Med Genet; 1991 Jan; 38(1):136-9. PubMed ID: 1707231
    [TBL] [Abstract][Full Text] [Related]  

  • 10. In-frame deletion in the proteolipid protein gene of a family with Pelizaeus-Merzbacher disease.
    Kleindorfer DO; Dlouhy SR; Pratt VM; Jones MC; Trofatter JA; Hodes ME
    Am J Med Genet; 1995 Feb; 55(4):405-7. PubMed ID: 7539213
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Family with Pelizaeus-Merzbacher disease/X-linked spastic paraplegia and a nonsense mutation in exon 6 of the proteolipid protein gene.
    Bond C; Si X; Crisp M; Wong P; Paulson GW; Boesel CP; Dlouhy SR; Hodes ME
    Am J Med Genet; 1997 Aug; 71(3):357-60. PubMed ID: 9268109
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease.
    Ellis D; Malcolm S
    Nat Genet; 1994 Apr; 6(4):333-4. PubMed ID: 7519941
    [No Abstract]   [Full Text] [Related]  

  • 14. Pelizaeus-Merzbacher disease in a family of Portuguese origin caused by a point mutation in exon 5 of the proteolipid protein gene.
    Pratt VM; Boyadjiev S; Dlouhy SR; Silver K; Der Kaloustian VM; Hodes ME
    Am J Med Genet; 1995 Feb; 55(4):402-4. PubMed ID: 7539212
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Girl with signs of Pelizaeus-Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene.
    Hodes ME; DeMyer WE; Pratt VM; Edwards MK; Dlouhy SR
    Am J Med Genet; 1995 Feb; 55(4):397-401. PubMed ID: 7539211
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Absence of cerebral myelin sheaths in a case of presumed Pelizaeus-Merzbacher disease. Electron microscopic and biochemical studies.
    Watanabe I; McCaman R; Dyken P; Zeman W
    J Neuropathol Exp Neurol; 1969 Apr; 28(2):243-56. PubMed ID: 5787430
    [No Abstract]   [Full Text] [Related]  

  • 17. Pelizaeus-Merzbacher disease: biochemical analysis of isolated myelin (electron-microscopy; protein, lipid and unsubstituted fatty acids analysis).
    Bourre JM; Jacque C; Nguyen-Legros J; Bornhofen JH; Araoz CA; Daudu O; Baumann NA
    Eur Neurol; 1978; 17(6):317-26. PubMed ID: 744198
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lipophilin (PLP) gene in X-linked myelin disorders.
    Fahim S; Riordan JR
    J Neurosci Res; 1986; 16(1):303-10. PubMed ID: 3746948
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New variant in exon 3 of the proteolipid protein (PLP) gene in a family with Pelizaeus-Merzbacher disease.
    Pratt VM; Trofatter JA; Larsen MB; Hodes ME; Dlouhy SR
    Am J Med Genet; 1992 Jun; 43(3):642-6. PubMed ID: 1376553
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Anatomo-clinical and neurochemical aspects of Pelizaeus-Merzbacher disease].
    Leclercq JP; Andersson JC; Davy JP; Lorteau P; Poilpre E
    Encephale; 1982; 8(3):377-88. PubMed ID: 7186459
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.