Literature DB >> 19826858

A young patient with type C multiple system atrophy and hereditary hemochromatosis.

Massimiliano Di Filippo, Piero Floridi, Vera Rossi, Emanuele Mattucci, Aroldo Rossi, Paolo Calabresi, Nicola Tambasco.   

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Year:  2009        PMID： 19826858     DOI： 10.1007/s00415-009-5345-6

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  7 in total

Review 1.  Iron metabolism in Parkinsonian syndromes.

Authors:  Daniela Berg; Helmine Hochstrasser
Journal:  Mov Disord       Date:  2006-09       Impact factor: 10.338

2.  Chronic cerebellar ataxia and hereditary hemochromatosis: causal or coincidental association?

Authors:  M P Rutgers; A Pielen; M Gille
Journal:  J Neurol       Date:  2007-04-21       Impact factor: 4.849

Review 3.  Clinical report of three patients with hereditary hemochromatosis and movement disorders.

Authors:  G Demarquay; A Setiey; Y Morel; C Trepo; G Chazot; E Broussolle
Journal:  Mov Disord       Date:  2000-11       Impact factor: 10.338

Review 4.  Hereditary haemochromatosis is unlikely to cause movement disorders--a critical review.

Authors:  Noemi Russo; Mark Edwards; Thomasin Andrews; Michael O'Brien; Kailash P Bhatia
Journal:  J Neurol       Date:  2004-07       Impact factor: 4.849

Review 5.  Haemochromatosis.

Authors:  Paul C Adams; James C Barton
Journal:  Lancet       Date:  2007-12-01       Impact factor: 79.321

6.  Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series.

Authors:  D J Costello; S L Walsh; H J Harrington; C H Walsh
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-04       Impact factor: 10.154

7.  Second consensus statement on the diagnosis of multiple system atrophy.

Authors:  S Gilman; G K Wenning; P A Low; D J Brooks; C J Mathias; J Q Trojanowski; N W Wood; C Colosimo; A Dürr; C J Fowler; H Kaufmann; T Klockgether; A Lees; W Poewe; N Quinn; T Revesz; D Robertson; P Sandroni; K Seppi; M Vidailhet
Journal:  Neurology       Date:  2008-08-26       Impact factor: 9.910
  7 in total
  1 in total

1.  A parkinsonian movement disorder with brain iron deposition and a haemochromatosis mutation.

Authors:  Stefan Williams; Maruthi Ravi Vinjam; Azzam Ismail; Ahamad Hassan
Journal:  J Neurol       Date:  2013-06-23       Impact factor: 4.849
  1 in total

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