Neuroimaging and clinical features in type II (late-onset) Alexander diseaseGRAFF-RADFORD, Jonathan; SCHWARTZ, Kara; GAVRILOVA, Ralitza H et al.Neurology. 2014, Vol 82, Num 1, pp 49-56, issn 0028-3878, 8 p.Article

Une étiologie rare de scoliose neuromusculaire : la maladie d'Alexander = A rare cause of neuromuscular scoliosis : Alexander diseaseOZTURK, Cagatay; TEZER, Mehmet; KARATOPRAK, Omer et al.Revue du rhumatisme (Ed. française). 2009, Vol 76, Num 3, pp 297-300, issn 1169-8330, 4 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

Valproate-induced parkinsonism, glial cells and Alexander's diseasePIETRO SECHI, Gian; CONTI, Maurizio; SAU, Gian Franco et al.Progress in neuro-psychopharmacology & biological psychiatry. 2008, Vol 32, Num 5, pp 1351-1352, issn 0278-5846, 2 p.Article

Sleep Apnea Associated With Floppy Epiglottis in Adult-Onset Alexander Disease: A Case reportISHIKAWA, Masanori; SHIMOHATA, Takayoshi; ISHIHARA, Tomohiko et al.Movement disorders. 2010, Vol 25, Num 8, pp 1098-1100, issn 0885-3185, 3 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

Unraveling pathology in juvenile Alexander disease: serial quantitative MR imaging and spectroscopy of white matterVAN DER VOORN, J. Patrick; POUWELS, Petra J. W; SALOMONS, Gajja S et al.Neuroradiology (Berlin. Print). 2009, Vol 51, Num 10, pp 669-675, issn 0028-3940, 7 p.Article

Autophagy induced by Alexander disease-mutant GFAP accumulation is regulated by p38/MAPK and mTOR signaling pathwaysGUOMEI TANG; ZHENYU YUE; TALLOCZY, Zsolt et al.Human molecular genetics (Print). 2008, Vol 17, Num 11, pp 1540-1555, issn 0964-6906, 16 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

Stoffwechselstörungen mit typischen Veränderungen im MRT : MR-Spektroskopie im ZNS = Metabolic disorders with typical alterations in MRI : MR spectroscopy in the CNSWARMUTH-METZ, M.Der Radiologe (Berlin. Print). 2010, Vol 50, Num 9, pp 775-783, issn 0033-832X, 9 p.Article

Dual transgenic reporter mice as a tool for monitoring expression of glial fibrillary acidic proteinCHO, Woosung; HAGEMANN, Tracy L; JOHNSON, Delinda A et al.Journal of neurochemistry. 2009, Vol 110, Num 1, pp 343-351, issn 0022-3042, 9 p.Article

Can MR Imaging Diagnose Adult-Onset Alexander Disease?FARINA, L; PAREYSON, D; MINATI, L et al.American journal of neuroradiology. 2008, Vol 29, Num 6, pp 1190-1196, issn 0195-6108, 7 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

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

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

Adult-onset Alexander disease with an R66Q mutation in GFAP presented with severe vocal cord paralysis during sleepHIDA, Ayumi; ISHIURA, Hiroyuki; ARAI, Noritoshi et al.Journal of neurology. 2012, Vol 259, Num 10, pp 2234-2236, issn 0340-5354, 3 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

Magnetic Resonance Imaging Findings in Alexander DiseaseMATARESE, Christine A; RENAUD, Deborah L.Pediatric neurology. 2008, Vol 38, Num 5, pp 373-374, issn 0887-8994, 2 p.Article

Adult-Onset Alexander Disease with Progressive Ataxia and : Palatal TremorHOWARD, Katherine L; HALL, Deborah A; MOON, Michelle et al.Movement disorders. 2008, Vol 23, Num 1, pp 118-122, issn 0885-3185, 5 p.Article

Adult-onset Alexander disease : a series of eleven unrelated cases with review of the literaturePAREYSON, Davide; FANCELLU, Roberto; CECCHERINI, Isabella et al.Brain. 2008, Vol 131, pp 2321-2331, issn 0006-8950, 11 p., 9Article

Archetypal and New Families With Alexander Disease and Novel Mutations in GFAPMESSING, Albee; RONG LI; NAIDU, Sakkubai et al.Archives of neurology (Chicago). 2012, Vol 69, Num 2, pp 208-214, issn 0003-9942, 7 p.Article

GFAP mutations, age at onset, and clinical subtypes in Alexander diseasePRUST, M; WANG, J; ALBIN, R et al.Neurology. 2011, Vol 77, Num 13, pp 1287-1294, issn 0028-3878, 8 p.Article

Ceftriaxone has a therapeutic role in Alexander diseaseSECHI, Gianpietro; MATTA, Manuela; DEIANA, Giovanni A et al.Progress in neuro-psychopharmacology & biological psychiatry. 2010, Vol 34, Num 2, pp 416-417, issn 0278-5846, 2 p.Article

Suppression of GFAP toxicity by αB-crystallin in mouse models of Alexander diseaseHAGEMANN, Tracy L; BOELENS, Wilbert C; WAWROUSEK, Eric F et al.Human molecular genetics (Print). 2009, Vol 18, Num 7, pp 1190-1199, issn 0964-6906, 10 p.Article