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kw.\*:("Alexander disease")

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Maladie d'Alexander de l'adulte = Alexander's disease in an adultHABIB, M; HASSOUN, J; ALI-CHERIF, A et al.Revue neurologique (Paris). 1984, Vol 140, Num 3, pp 179-189, issn 0035-3787Article

DIE ASTROGLIALE DYSTROPHIE MIT ROSENTHALSCHEN FASERN. ZUR FRAGE DER ADULTEN FORM DER ALEXANDERSCHEN KRANKHEIT UND IHRER KLINISCHEN BEDEUTUNG = LA DYSTROPHIE ASTROGLIALE AVEC FIBRES DE ROSENTHAL. LE PROBLEME DE LA FORME ADULTE DE LA MALADE D'ALEXANDER ET DE SON IMPORTANCE CLINIQUEULE G; JACOB H.1983; NERVENARZT; ISSN 0028-2804; DEU; DA. 1983; VOL. 54; NO 2; PP. 69-73; BIBL. 28 REF.Article

ALEXANDER'S DISEASE: FURTHER LIGHT-, AND ELECTRON-MICROSCOPIC OBSERVATIONSTOWFIGHI J; YOUNG R; SASSANI J et al.1983; ACTA NEUROPATHOLOGICA; ISSN 0001-6322; DEU; DA. 1983; VOL. 61; NO 1; PP. 36-42; BIBL. 21 REF.Article

Fluoro-Jade : New fluorescent marker of Rosenthal fibersTANAKA, Kenji F; OCHI, Nobuhiko; HAYASHI, Toshiyuki et al.Neuroscience letters. 2006, Vol 407, Num 2, pp 127-130, issn 0304-3940, 4 p.Article

An adult form of Alexander disease : a novel mutation in glial fibrillary acidic proteinOHNARI, Keiko; YAMANO, Mitsuhiko; UOZUMI, Takenori et al.Journal of neurology. 2007, Vol 254, Num 10, pp 1390-1394, issn 0340-5354, 5 p.Article

Neurocognitive Decline in Alexander DiseaseRESTREPO, June; BERNARDIN, Linda; HAMMEKE, Thomas et al.Neuropsychology, development, and cognition. Section D, The clinical neuropsychologist. 2011, Vol 25, Num 7, pp 1266-1277, issn 1385-4046, 12 p.Article

Adult-onset Alexander disease : Report on a familyBALBI, Pietro; SERI, Marco; CECCHERINI, Isabella et al.Journal of neurology. 2008, Vol 255, Num 1, pp 24-30, issn 0340-5354, 7 p.Article

Increased levels of GFAP in the cerebrospinal fluid in three subtypes of genetically confirmed alexander diseaseKYLLERMAN, M; ROSENGREN, L; WIKLUND, L.-M et al.Neuropediatrics. 2005, Vol 36, Num 5, pp 319-323, issn 0174-304X, 5 p.Article

The clinical spectrum of late-onset Alexander disease: a systematic literature reviewBALBI, Pietro; SALVINI, Silvana; FUNDARO, Cira et al.Journal of neurology. 2010, Vol 257, Num 12, pp 1955-1962, issn 0340-5354, 8 p.Article

Late-onset Alexander disease with a V87L mutation in glial fibrillary acidic protein (GFAP) and calcifying lesions in the sub-cortex and cortexSUZUKI, Hidekazu; YOSHIDA, Tomokatsu; KITADA, Mari et al.Journal of neurology. 2012, Vol 259, Num 3, pp 457-461, issn 0340-5354, 5 p.Article

Alexander's disease with Rosenthal fibre formation in an adultWALLS, T. J; JONES, R. A; CARTLIDGE, N. E. F et al.Journal of neurology, neurosurgery and psychiatry. 1984, Vol 47, Num 4, pp 399-403, issn 0022-3050Article

Alexander's disease: cranial MRI and ultrasound findingsSCHUSTER, V; HORWITZ, A. E; KRETH, H. W et al.Pediatric radiology. 1991, Vol 21, Num 2, pp 133-134, issn 0301-0449Article

A case of leucodystrophy presenting as hydrocephalusMAITI, B; ROY, I; SAHA, P et al.Journal of the Indian Medical Association. 1986, Vol 84, Num 10, pp 311-313, issn 0019-5847Article

MEGALENCEPHALIE PROGRESSIVE CHEZ L'ENFANT. A PROPOS D'UN CAS DE MALADIE D'ALEXANDER ET TROIS CAS DE DEGENERESCENCE SPONGIEUSE DU NEVRAXECHAUVEAU JEAN MICHEL.sd; FRA; DA. S.D.; 236; 145-XII P.-ILL.; 30 CM; BIBL. 73 P.; TH.: MED./PARIS 5/1978Thesis

A LARGE HEAD IN A 2-YEAR-OLD BOY.BECKER LE; ARMSTRONG JB; MELOFF KL et al.1977; J. PEDIATR.; U.S.A.; DA. 1977; VOL. 91; NO 3; PP. 499-502; BIBL. 5 REF.Article

ALEXANDER'S DISEASE: CASE REPORT INCLUDING HISTOPATHOLOGICAL AND ELECTRON MICROSCOPIC FEATURESCOLE G; DE VILLIERS F; PROCTOR NSF et al.1979; J. NEUROL. NEUROSURG. PSYCHIATRY; GBR; DA. 1979; VOL. 42; NO 7; PP. 619-624; BIBL. 8 REF.Article

NONINVASIVE CT DIAGNOSIS OF INFANTILE ALEXANDER DISEASE: PATHOLOGIC CORRELATIONTROMMER BL; NAIDICH TP; DAL CANTO MC et al.1983; JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY; ISSN 0363-8715; USA; DA. 1983; VOL. 7; NO 3; PP. 509-516; BIBL. 25 REF.Article

COMPUTED TOMOGRAPHY IN ALEXANDER'S DISEASEHOLLAND IM; KENDALL BE.1980; NEURORADIOLOGY; ISSN 0028-3940; DEU; DA. 1980; VOL. 20; NO 2; PP. 103-106; BIBL. 8 REF.Article

Novel mutations in exon 6 of the GFAP gene affecta highly conserved IF motif in the rod domain 2B and are associated with early onset infantile alexander diseaseHARTMANN, H; NERCHENBACH, J; STEPHANI, U et al.Neuropediatrics. 2007, Vol 38, Num 3, pp 143-147, issn 0174-304X, 5 p.Article

Alexander Disease Mutant Glial Fibrillary Acidic Protein Compromises Glutamate Transport in AstrocytesRUJIN TIAN; XIAOPING WU; HAGEMANN, Tracy L et al.Journal of neuropathology and experimental neurology. 2010, Vol 69, Num 4, pp 335-345, issn 0022-3069, 11 p.Article

A case of adult-onset Alexander disease with Arg416Trp human glial fibrillary acidic protein gene mutationKINOSHITA, Takashi; IMAIZUMI, Toshihiro; MIURA, Yumiko et al.Neuroscience letters. 2003, Vol 350, Num 3, pp 169-172, issn 0304-3940, 4 p.Article

Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosisYOSHIDA, Tomokatsu; SASAKI, Masayuki; YOSHIDA, Mari et al.Journal of neurology. 2011, Vol 258, Num 11, pp 1998-2008, issn 0340-5354, 11 p.Article

Mild functional effects of a novel GFAP mutant allele identified in a familial case of adult-onset Alexander diseaseBACHETTI, Tiziana; CAROLI, Francesco; CECCHERINI, Isabella et al.European journal of human genetics. 2008, Vol 16, Num 4, pp 462-470, issn 1018-4813, 9 p.Article

Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79LSHIROMA, Naohide; KANAZAWA, Naomi; SUGAI, Kenji et al.Brain & development (Tokyo. 1979). 2003, Vol 25, Num 2, pp 116-121, issn 0387-7604, 6 p.Article

Glial fibrillary acidic protein mutations in adult-onset Alexander disease: clinical features observed in 12 Japanese patientsYOSHIDA, T; SASAYAMA, H; OKUDA, S et al.Acta neurologica scandinavica. 2011, Vol 124, Num 2, pp 104-108, issn 0001-6314, 5 p.Article

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