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kw.\*:("Enfermedad canaván")

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A radiometric assay for aspartoacylase activity in human fibroblasts : application for the diagnosis of Canavan's diseaseBARASH, V; FLHOR, D; MORAG, B et al.Clinica chimica acta. 1991, Vol 201, Num 3, pp 175-181, issn 0009-8981Article

Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan disease. ReplyDIVRY, P; MATHIEU, M; MATALON, R et al.American journal of medical genetics. 1989, Vol 32, Num 4, pp 550-551, issn 0148-7299Article

N-acetylaspartic aciduria in young ageELPELEG, O. N.Neuropediatrics. 1992, Vol 23, Num 2, issn 0174-304X, p. 112Article

A review of phylogenetic and metabolic relationships between the acylamino acids, N-acetyl-L-aspartic acid and N-acetyl-L-histidine, in the vertebrate nervous systemBASLOW, M. H.Journal of neurochemistry. 1997, Vol 68, Num 4, pp 1335-1344, issn 0022-3042Article

Proton NMR spectroscopy of Canavan's diseaseBARKER, P. B; BRYAN, R. N; KUMAR, A. J et al.Neuropediatrics. 1992, Vol 23, Num 5, pp 263-267, issn 0174-304XArticle

Variable course of canavan disease in two boys with early infantile aspartoacylase deficiencyMOERS, A; SPERNER, J; MICHAEL, T et al.Developmental medicine and child neurology (Print). 1991, Vol 33, Num 9, pp 824-828, issn 0012-1622Article

Intracerebral distribution of mitochondrial abnormalities in 21 cases of infantile spongy dystrophyPAULUS, W; PEIFFER, J.Journal of the neurological sciences. 1990, Vol 95, Num 1, pp 49-62, issn 0022-510XArticle

Canavan disease : findings in four new casesMICHELAKAKIS, H; GIOUROUKOS, S; DIVRY, P et al.Journal of inherited metabolic disease. 1991, Vol 14, Num 2, pp 267-268, issn 0141-8955, 2 p.Article

Canavan disease : neuromorphological and biochemical analysis of a brain biopsy specimenDE COO, I. F. M; GABREËLS, F. J. M; RENIER, W. O et al.Clinical neuropathology. 1991, Vol 10, Num 2, pp 73-78, issn 0722-5091Article

Prolonged survival in canavan diseaseFEIGELMAN, T; SHIH, V. E; BUYSE, M. L et al.Dysmorphology and clinical genetics. 1991, Vol 5, Num 4, pp 107-110, issn 0893-6633Article

Localized 1H NMR spectroscopy in Canavan's disease : a report of two casesAUSTIN, S. J; CONNELLY, A; GADIAN, D. G et al.Magnetic resonance in medicine. 1991, Vol 19, Num 2, pp 439-445, issn 0740-3194Article

Infantile CNS spongy degeneration : 14 cases : clinical updateCASCON, G. G; OZAND, P. T; MAHDI, A et al.Neurology. 1990, Vol 40, Num 12, pp 1876-1882, issn 0028-3878, 7 p.Article

Spongy degeneration of the neuraxis (Canavan-van Bogaert disease) and N-acetylaspartic aciduriaECHENNE, B; DIVRY, P; VIANEY-LIAUD, C et al.Neuropediatrics. 1989, Vol 20, Num 2, pp 79-81, issn 0174-304X, 3 p.Article

Rapid and sensitive screening for and chemical diagnosis of Canavan disease by gas chromatography-mass spectrometryINOUE, Y; KUHARA, T.Journal of chromatography. B. 2004, Vol 806, Num 1, pp 33-39, issn 1570-0232, 7 p.Conference Paper

Identification and expression of eight novel mutations among non-Jewish patients with Canavan diseaseKAUL, R; GAO, G. P; MATALON, R et al.American journal of human genetics. 1996, Vol 59, Num 1, pp 95-102, issn 0002-9297Article

Identification and distribution of aspartoacylase in the postnatal rat brainKLUGMANN, Matthias; SYMES, C. Wymond; KLAUSSNER, Bettina K et al.Neuroreport (Oxford). 2003, Vol 14, Num 14, pp 1837-1840, issn 0959-4965, 4 p.Article

Biochemical diagnosis of Canavan diseaseBARTALINI, G; MARGOLLICCI, M; BALESTRI, P et al.Child's nervous system (Print). 1992, Vol 8, Num 8, pp 468-470, issn 0256-7040Article

Prenatal diagnosis of canavan diseaseMATALON, R; MICHALS, K; GASHKOFF, P et al.Journal of inherited metabolic disease. 1992, Vol 15, Num 3, pp 392-394, issn 0141-8955Conference Paper

Cas précoce de dystrophie spongieuse héréditaire (van Bogaert-Bertrand) = A case of early hereditary spongiform dystrophy (von Bogart-Bertrand)GUILLEMIN, P; PIZZOLATO, G.-P; MEGRET, M et al.Schweizer Archiv für Neurologie und Psychiatrie (1985). 1989, Vol 140, Num 4, pp 345-364, issn 0258-7661Article

Aspartoacylase deficiency: the enzyme defect in Canavan diseaseMATALON, R; KAUL, R; CASANOVA, J et al.Journal of inherited metabolic disease. 1989, Vol 12, pp 329-331, issn 0141-8955, suppl. 2Article

Quantification of N-acetyl-L-aspartic acid in urine by isotope dilution gas chromatography-mass spectrometryKELLEY, R. I; STAMAS, J. N.Journal of inherited metabolic disease. 1992, Vol 15, Num 1, pp 97-104, issn 0141-8955Article

Aspartoacylase deficiency and canavan disease in Saudi ArabiaOZAND, P. T; GASCON, G. G; MOHAMMED DHALLA et al.American journal of medical genetics. 1990, Vol 35, Num 2, pp 266-268, issn 0148-7299Article

CT and MT imaging of Canavan diseasePAGE MCADAMS, H; GEYER, C. A; DONE, S. L et al.American journal of neuroradiology. 1990, Vol 11, Num 2, pp 397-399, issn 0195-6108Conference Paper

Sonographic and computed tomographic findings in Canavan's diseasePATEL, P. J; KOLAWOLE, T. M; MAHDI, A. H et al.British journal of radiology. 1986, Vol 59, Num 708, pp 1226-1228, issn 0007-1285Article

Prenatal diagnosis of Canavan diseaseMATALON, R; MICHALS-MATALON, K.Prenatal diagnosis. 1999, Vol 19, Num 7, pp 669-670, issn 0197-3851Article

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