Spongy degeneration of the CNS in infancyYI LUO; KEWEI HUANG.Archives of neurology (Chicago). 1984, Vol 41, Num 2, pp 164-170, issn 0003-9942Article

N-acetylaspartate in the vertebrate brain: Metabolism and functionBASLOW, Morris H.Neurochemical research. 2003, Vol 28, Num 6, pp 941-953, issn 0364-3190, 13 p.Article

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

RICHTUNGWEISENDE SYMPTOMENKONSTELLATION BEI MORBUS CANAVAN-VAN-BOGAERT-BERTRAND = CONSTELLATION DE SYMPTOMES EVOCATEURS DANS LA MALADIE DE CANAVAN-VAN BOGAERT-BERTRANDKOTLAREK F; SCHUTZ E; ZEUMER H et al.1982; ROEFO, FORSCHR. GEB. ROENTGENSTR. NUKLEARMED.; ISSN 0340-1618; DEU; DA. 1982; VOL. 137; NO 5; PP. 608-610; BIBL. 9 REF.Article

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

Die spongiöse Hirndystrophie von Bogaert-Bertrand = La dégénérescence spongieuse cérébrale de von Bogaert-Bertrand = Canavan diseaseSTROMPEN, W; DIEKMANN, L.Klinische Pädiatrie. 1984, Vol 196, Num 2, pp 111-114, issn 0300-8630Article

SPONGY DEGENERATION OF THE BRAIN IN ISRAEL: A RETROSPECTIVE STUDYUNGAR M; GOODMAN RM.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 1; PP. 23-29; BIBL. 13 REF.Article

Possible genotype-phenotype correlations in children with mild clinical course of canavan diseaseTACKE, U; OLBRICH, H; VARGIAMI, E et al.Neuropediatrics. 2005, Vol 36, Num 4, pp 252-255, issn 0174-304X, 4 p.Article

Ultrasound findings in follow-up investigations in a case of aspartoacylase deficiency (Canavan disease)BREITBACH-FALLER, N; SCHRADER, K; RATING, D et al.Neuropediatrics. 2003, Vol 34, Num 2, pp 96-99, issn 0174-304X, 4 p.Article

Radiological Clue to Diagnosis of Canavan DiseaseSREENIVASAN, Priya; PURUSHOTHAMAN, K. K.Indian journal of pediatrics. 2013, Vol 80, Num 1, pp 75-77, issn 0019-5456, 3 p.Article

Preimplantation genetic diagnosis of canavan diseaseYARON, Yuval; SCHWARTZ, Tamar; MEY-RAZ, Nava et al.Fetal diagnosis and therapy. 2005, Vol 20, Num 5, pp 465-468, issn 1015-3837, 4 p.Article

Characterisation of the ¹H and ¹³C NMR spectra of N-acetylaspartylglutamate and its detection in urine from patients with Canavan diseaseKRAWCZYK, Hanna; GRADOWSKA, Wanda.Journal of pharmaceutical and biomedical analysis. 2003, Vol 31, Num 3, pp 455-463, issn 0731-7085, 9 p.Article

Aspartoacylase supports oxidative energy metabolism during myelinationFRANCIS, Jeremy S; STRANDE, Louise; MARKOV, Vladamir et al.Journal of cerebral blood flow and metabolism. 2012, Vol 32, Num 9, pp 1725-1736, issn 0271-678X, 12 p.Article

Natural history of canavan disease revealed by proton magnetic resonance spectroscopy (¹H-MRS) and diffusion-weighted MRIJANSON, C. G; MCPHEE, S. W. J; LEONE, P et al.Neuropediatrics. 2006, Vol 37, Num 4, pp 209-221, issn 0174-304X, 13 p.Article

Aspartoacylase gene knockout in the mouse : Impact on reproductionSURENDRAN, Sankar; SZUCS, Sylvia; TYRING, Stephen K et al.Reproductive toxicology (Elmsford, NY). 2005, Vol 20, Num 2, pp 283-285, issn 0890-6238, 3 p.Article

Atypical MRI findings in canavan disease : A patient with a mild courseYALCINKAYA, C; BENBIR, G; SALOMONS, G. S et al.Neuropediatrics. 2005, Vol 36, Num 5, pp 336-339, issn 0174-304X, 4 p.Article

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

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

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