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kw.\*:("Leucodystrophie Pelizaeus-Merzbacher")

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DIE MAUS-MUTANTE "JIMPY". TIERMODELL EINER LEUKODYSTROPHIE. = LA SOURIS MUTANTE "JIMPY", UN MODELE ANIMAL D'UNE LEUCODYSTROPHIEMEIER C.1977; FORTSCHR. D. MED.; DTSCH.; DA. 1977; VOL. 95; NO 43; PP. 2623-2626; ABS. ANGL.; BIBL. 18 REF.Article

MICROCEPHALY WITH PECULIAR DEMYELINATION MIMICKING PELIZAEUS-MERZBACHER DISEASE.KAMOSHITA S; IGARASHI M; KOHNO R et al.1977; ACTA NEUROPATOL.; ALLEM.; DA. 1977; VOL. 40; NO 1; PP. 95-98; BIBL. 10 REF.Article

CONNATAL PELIZAEUS-MERZBACHER DISEASE WITH CONGENITAL STRIDOR IN TWO MATERNAL COUSINSRENIER WO; GABREELS FJM; HUSTINX TWJ et al.1981; ACTA NEUROPATHOL.; ISSN 0001-6322; DEU; DA. 1981; VOL. 54; NO 1; PP. 11-17; BIBL. 33 REF.Article

PELIZAEUS-MERZBACHER DISEASE: BRAIN LIPID AND FATTY ACID COMPOSITIONBOURRE JM; BORNHOFEN JH; ARAOZ CA et al.1978; J. NEUROCHEM.; GBR; DA. 1978; VOL. 30; NO 4; PP. 719-727; BIBL. 56 REF.Article

Magnetic resonance imaging in Pelizaeus-Merzbacher diseaseJOURNEL, H; ROUSSEY, M; GANDON, Y et al.Neuroradiology (Berlin. Print). 1987, Vol 29, Num 4, pp 403-405, issn 0028-3940Article

Pelizaeus-Merzbacher disease in a brother and sisterPAMPHLETT, R; SILBERSTEIN, P.Acta neuropathologica. 1986, Vol 69, Num 3-4, pp 343-346, issn 0001-6322Article

Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher diseaseKOEPPEN, A. H; RONCA, N. A; GREENFIELD, E. A et al.Annals of neurology. 1987, Vol 21, Num 2, pp 159-170, issn 0364-5134Article

COMPUTED TOMOGRAPHY IN PELIZAEUS-MERZBACHER DISEASESTATZ A; BOLTSHAUSER E; SCHINZEL A et al.1981; NEURORADIOLOGY; ISSN 0028-3940; DEU; DA. 1981; VOL. 22; NO 2; PP. 103-105; BIBL. 11 REF.Article

CEREBELLAR ATAXIA. CLINICAL AND CT FINDINGS IN TWO CASES OF RARE ETIOLOGYZEUMER H; KOTLAREK F; BLANKENNAGEL A et al.1980; J. NEUROL.; DEU; DA. 1980; VOL. 224; NO 1; PP. 47-51; ABS. GER; BIBL. 14 REF.Article

ELECTROPHYSIOLOGIC OBSERVATIONS IN THE CLASSICAL FORM OF PELIZAEUS-MERZBACHER DISEASE.WILKUS RJ; FARRELL DF.1976; NEUROLOGY; U.S.A.; DA. 1976; VOL. 26; NO 11; PP. 1042-1045; BIBL. 15 REF.Article

LES MALADIES DEMYELINISANTES HEREDITAIRES (LEUCODYSTROPHIES)FRANCOIS J.1979; J. GENET. HUM.; CHE; DA. 1979; VOL. 27; NO 2; PP. 123-130; ABS. ENG; BIBL. 44 REF.Article

PELIZAEUS-MERZBACHER DISEASE: BIOCHEMICAL ANALYSIS OF ISOLATED MYELIN (ELECTRON-MICROSCOPY; PROTEIN, LIPID AND UNSUBSTITUTED FATTY ACIDS ANALYSIS)BOURRE JM; JACQUE C; NGUYEN LEGROS J et al.1978; EUROP. NEUROL.; CHE; DA. 1978; VOL. 17; NO 6; PP. 317-326; BIBL. 2 P.Article

CONGENITAL RETARDED MYELINIZATION IN A NEW-BORN CHILD WITH INFANTILE SPASMS.DE WEERDT CJ; HOOGHWINKEL GJM.1976; CLIN. NEUROL. NEUROSURG.; NETHERL.; DA. 1976; VOL. 79; NO 2; PP. 143-150; BIBL. 13 REF.Article

Mild pelizaeus-merzbacher disease caused by a point mutation affecting correct splicing of PLP1 mRNAHÜBNER, C. A; SENNING, A; ORTH, U et al.Neuroscience. 2005, Vol 132, Num 3, pp 697-701, issn 0306-4522, 5 p.Article

A brief history of Pelizaeus-Merzbacher disease and proteolipid protein : The science of myelinKOEPPEN, Amulf H.Journal of the neurological sciences. 2005, Vol 228, Num 2, pp 198-200, issn 0022-510X, 3 p.Conference Paper

Pelizaeus-Merzbacher disease: pathogenic mechanisms and insights into the roles of proteolipid protein 1 in the nervous system : The science of myelinGARBERN, James Y.Journal of the neurological sciences. 2005, Vol 228, Num 2, pp 201-203, issn 0022-510X, 3 p.Conference Paper

Dinucleotide repeat polymorphism in the proteolipoprotein (PLP) geneMIMAULT, C; CAILLOUX, F; GIRAUD, G et al.Human genetics. 1995, Vol 96, Num 2, issn 0340-6717, p. 236Article

Pelizaeus-Merzbacher disease : cellular hypersensitivity to ultraviolet lightSUGITA, K; ISHII, M; TAKANASHI, J. I et al.Brain & development (Tokyo. 1979). 1992, Vol 14, Num 1, pp 44-47, issn 0387-7604Article

Pelizaeus-Merzbacher disease : a point mutation in exon 6 of the proteolipid protein (PLP) genePRATT, V. M; DLOUHY, S. R; HODES, M. E et al.Clinical genetics. 1995, Vol 47, Num 2, pp 99-100, issn 0009-9163Article

Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anonymous DNA polymorphisms and the proteolipid protein (PLP) gene cDNABRIDGE, P. J; MACLEOD, P. M; LILLICRAP, D. P et al.American journal of medical genetics. 1991, Vol 38, Num 4, pp 616-621, issn 0148-7299Article

MR imaging of the brain in five members of a family with Pelizaeus-Merzbacher diseaseSILVERSTEIN, A. M; HIRSH, D. K; TROBE, J. D et al.American journal of neuroradiology. 1990, Vol 11, Num 3, pp 495-499, issn 0195-6108, 5 p.Article

Magnetic resonance imaging and computed tomography in Pelizaeus-Merzbacher diseaseCARO, P. A; MARKS, H. G.Magnetic resonance imaging. 1990, Vol 8, Num 6, pp 791-796, issn 0730-725XArticle

Prenatal diagnosis of Pelizaeus-Merzbacher disease using RFLP analysisMAENPAA, J; LINDAHL, E; AULA, P et al.Clinical genetics. 1990, Vol 37, Num 2, pp 141-147, issn 0009-9163Article

The reflection of histology in MR imaging of Pelizaeus-Merzbacher diseaseVAN DER KNAAP, M. S; VALK, J.American journal of neuroradiology. 1989, Vol 10, Num 1, pp 99-103, issn 0195-6108Article

Pelizaeus-Merzbacher disease: identification of heterozygotes with magnetic resonance imaging?BOLTSHAUSER, E; SCHINZEL, A; WICHMANN, W et al.Human genetics. 1988, Vol 80, Num 4, pp 393-394, issn 0340-6717Article

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