Literature DB >> 26712833

Pearls & Oy-sters: Spinocerebellar ataxia type 3 presenting with cervical dystonia without ataxia.

Jihad A Muglan1, Suresh Menon1, Mandar S Jog2.   

Abstract

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Mesh：

Year:  2016        PMID： 26712833      PMCID： PMC4731293          DOI： 10.1212/WNL.0000000000002232

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  10 in total

1.  Machado-Joseph disease presenting as severe generalised dystonia in a German patient.

Authors:  A Münchau; D Dressler; K P Bhatia; P Vogel; C Zühlke
Journal:  J Neurol       Date:  1999-09       Impact factor: 4.849

Review 2.  Movement disorders in spinocerebellar ataxias.

Authors:  Judith van Gaalen; Paola Giunti; Bart P van de Warrenburg
Journal:  Mov Disord       Date:  2011-03-02       Impact factor: 10.338

3.  Clinical criteria for diagnosis of Machado-Joseph disease: report of a non-Azorena Portuguese family.

Authors:  L Lima; P Coutinho
Journal:  Neurology       Date:  1980-03       Impact factor: 9.910

Review 4.  Machado-Joseph disease: an autosomal dominant motor system degeneration.

Authors:  R N Rosenberg
Journal:  Mov Disord       Date:  1992       Impact factor: 10.338

5.  Autosomal dominant spinocerebellar ataxias ad infinitum?

Authors:  S H Subramony; A Filla
Journal:  Neurology       Date:  2001-02-13       Impact factor: 9.910

6.  Focal dystonia as a presenting sign of spinocerebellar ataxia 17.

Authors:  Johann M Hagenah; Christine Zühlke; Yorck Hellenbroich; Wolfgang Heide; Christine Klein
Journal:  Mov Disord       Date:  2004-02       Impact factor: 10.338

7.  Homozygous inheritance of the Machado-Joseph disease gene.

Authors:  A E Lang; E A Rogaeva; T Tsuda; J Hutterer; P St George-Hyslop
Journal:  Ann Neurol       Date:  1994-09       Impact factor: 10.422

8.  Machado-Joseph disease in a Sicilian-American family.

Authors:  N D Suite; J Sequeiros; G M McKhann
Journal:  J Neurogenet       Date:  1986-05       Impact factor: 1.250

9.  Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions.

Authors:  P Coutinho; C Andrade
Journal:  Neurology       Date:  1978-07       Impact factor: 9.910

10.  Machado-Joseph disease: A proposal of spastic paraplegic subtype.

Authors:  T Sakai; H Kawakami
Journal:  Neurology       Date:  1996-03       Impact factor: 9.910
  10 in total
  4 in total

Review 1.  Dilemma of multiple system atrophy and spinocerebellar ataxias.

Authors:  Ming Li; Qianqian Ma; Xing Zhao; Can Wang; Huijie Wu; Jinyao Li; Wei Yang
Journal:  J Neurol       Date:  2018-04-26       Impact factor: 4.849

2.  A role for cerebellum in the hereditary dystonia DYT1.

Authors:  Rachel Fremont; Ambika Tewari; Chantal Angueyra; Kamran Khodakhah
Journal:  Elife       Date:  2017-02-15       Impact factor: 8.140

Review 3.  KCND3-Related Neurological Disorders: From Old to Emerging Clinical Phenotypes.

Authors:  Luca Pollini; Serena Galosi; Manuela Tolve; Caterina Caputi; Carla Carducci; Antonio Angeloni; Vincenzo Leuzzi
Journal:  Int J Mol Sci       Date:  2020-08-13       Impact factor: 5.923

4.  Dystonia in Patients with Spinocerebellar Ataxia 3 - Machado-Joseph disease: An Underestimated Diagnosis?

Authors:  Ligia Maria Perrucci Catai; Carlos Henrique Ferreira Camargo; Adriana Moro; Gustavo Ribas; Salmo Raskin; Hélio Afonso Ghizoni Teive
Journal:  Open Neurol J       Date:  2018-05-31
  4 in total

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