Literature DB >> 21714005

Expanding the phenomenology of benign hereditary chorea: evolution from chorea to myoclonus and dystonia.

Melissa J Armstrong, Binit B Shah, Robert Chen, Michael J Angel, Anthony E Lang.   

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Year:  2011        PMID： 21714005     DOI： 10.1002/mds.23822

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


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  6 in total

Review 1.  Recent advances in genetics of chorea.

Authors:  Niccolò E Mencacci; Miryam Carecchio
Journal:  Curr Opin Neurol       Date:  2016-08       Impact factor: 5.710

2.  Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency.

Authors:  Maria Stamelou; Niccolo E Mencacci; Carla Cordivari; Amit Batla; Nick W Wood; Henry Houlden; John Hardy; Kailash P Bhatia
Journal:  Neurology       Date:  2012-07-18       Impact factor: 9.910

3.  The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician.

Authors:  Davide Martino; Maria Stamelou; Kailash P Bhatia
Journal:  J Neurol Neurosurg Psychiatry       Date:  2012-09-19       Impact factor: 10.154

4.  ADCY5 mutations are another cause of benign hereditary chorea.

Authors:  Niccolo E Mencacci; Roberto Erro; Sarah Wiethoff; Joshua Hersheson; Mina Ryten; Bettina Balint; Christos Ganos; Maria Stamelou; Niall Quinn; Henry Houlden; Nicholas W Wood; Kailash P Bhatia
Journal:  Neurology       Date:  2015-06-17       Impact factor: 9.910

5.  Benign hereditary chorea related to NKX2-1 with ataxia and dystonia.

Authors:  Claudio M de Gusmao; Fernando Kok; Erasmo Barbante Casella; Jeff L Waugh
Journal:  Neurol Genet       Date:  2015-12-22

6.  Benign hereditary chorea, not only chorea: a family case presentation.

Authors:  Jeanette Koht; Sven Olav Løstegaard; Iselin Wedding; Marie Vidailhet; Malek Louha; Chantal Me Tallaksen
Journal:  Cerebellum Ataxias       Date:  2016-02-02
  6 in total

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