Literature DB >> 29443213

Characteristic abnormal signals in medulla oblongata-"eye spot" sign: Four cases of elderly-onset Alexander disease.

Tomokatsu Yoshida1, Ikuko Mizuta1, Kozo Saito1, Yasuyoshi Kimura1, Kwiyoung Park1, Yasuo Ito1, Shotaro Haji1, Masanori Nakagawa1, Toshiki Mizuno1.   

Abstract

Entities:  

Year:  2015        PMID： 29443213      PMCID： PMC5764465          DOI： 10.1212/CPJ.0000000000000124

Source DB:  PubMed          Journal:  Neurol Clin Pract        ISSN： 2163-0402


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  7 in total

1.  Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant.

Authors:  W S ALEXANDER
Journal:  Brain       Date:  1949-09       Impact factor: 13.501

2.  Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis.

Authors:  Tomokatsu Yoshida; Masayuki Sasaki; Mari Yoshida; Michito Namekawa; Yuji Okamoto; Seiichi Tsujino; Hiroshi Sasayama; Ikuko Mizuta; Masanori Nakagawa
Journal:  J Neurol       Date:  2011-05-01       Impact factor: 4.849

3.  Can MR imaging diagnose adult-onset Alexander disease?

Authors:  L Farina; D Pareyson; L Minati; I Ceccherini; L Chiapparini; S Romano; P Gambaro; R Fancellu; M Savoiardo
Journal:  AJNR Am J Neuroradiol       Date:  2008-04-03       Impact factor: 3.825

Review 4.  Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature.

Authors:  Michito Namekawa; Yoshihisa Takiyama; Junko Honda; Haruo Shimazaki; Kumi Sakoe; Imaharu Nakano
Journal:  BMC Neurol       Date:  2010-04-01       Impact factor: 2.474

5.  Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease.

Authors:  Michito Namekawa; Yoshihisa Takiyama; Yoko Aoki; Norio Takayashiki; Kumi Sakoe; Haruo Shimazaki; Tomohiro Taguchi; Yasufumi Tanaka; Masatoyo Nishizawa; Ken Saito; Yoichi Matsubara; Imaharu Nakano
Journal:  Ann Neurol       Date:  2002-12       Impact factor: 10.422

6.  Neuroimaging and clinical features in type II (late-onset) Alexander disease.

Authors:  Jonathan Graff-Radford; Kara Schwartz; Ralitza H Gavrilova; Daniel H Lachance; Neeraj Kumar
Journal:  Neurology       Date:  2013-12-04       Impact factor: 9.910

7.  Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease.

Authors:  M Brenner; A B Johnson; O Boespflug-Tanguy; D Rodriguez; J E Goldman; A Messing
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330
  7 in total
  3 in total

1.  A novel three-base duplication, E243dup, of GFAP identified in a patient with Alexander disease.

Authors:  Rei Yasuda; Tomokatsu Yoshida; Ikuko Mizuta; Masanori Nakagawa; Toshiki Mizuno
Journal:  Hum Genome Var       Date:  2017-07-06

2.  Towards genomic database of Alexander disease to identify variations modifying disease phenotype.

Authors:  Rei Yasuda; Masakazu Nakano; Tomokatsu Yoshida; Ryuichi Sato; Hiroko Adachi; Yuichi Tokuda; Ikuko Mizuta; Kozo Saito; Jun Matsuura; Masanori Nakagawa; Kei Tashiro; Toshiki Mizuno
Journal:  Sci Rep       Date:  2019-10-14       Impact factor: 4.379

Review 3.  Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing.

Authors:  Katayoun Heshmatzad; Niloofar Naderi; Tannaz Masoumi; Hamidreza Pouraliakbar; Samira Kalayinia
Journal:  Eur J Med Res       Date:  2022-09-10       Impact factor: 4.981
  3 in total

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