Literature DB >> 17450315

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

M P Rutgers, A Pielen, M Gille.   

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Year:  2007        PMID： 17450315     DOI： 10.1007/s00415-006-0507-2

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


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  9 in total

1.  Hereditary hemochromatosis and movement disorders: the still controversial relationship. Response to Russo et al. in J Neurol (2004) 251:849-852.

Authors:  G Demarquay; S Thobois; P Latour; Emmanuel Broussolle
Journal:  J Neurol       Date:  2005-08-17       Impact factor: 4.849

Review 2.  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

3.  The basal ganglia in haemochromatosis.

Authors:  D Berg; U Hoggenmüller; E Hofmann; R Fischer; M Kraus; M Scheurlen; G Becker
Journal:  Neuroradiology       Date:  2000-01       Impact factor: 2.804

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

5.  [Extrapyramidal syndrome in idiopathic hemochromatosis. Significance of laboratory chemical, neurophysiologic and imaging procedures (CCT, MRT)].

Authors:  J Schröder; J Haan
Journal:  Nervenarzt       Date:  1987-09       Impact factor: 1.214

6.  Heterozygosity for the C282Y mutation in the hemochromatosis gene is associated with increased serum iron, transferrin saturation, and hemoglobin in young women: a protective role against iron deficiency?

Authors:  C Datz; T Haas; H Rinner; F Sandhofer; W Patsch; B Paulweber
Journal:  Clin Chem       Date:  1998-12       Impact factor: 8.327

7.  Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs.

Authors:  H R Jones; E T Hedley-Whyte
Journal:  Neurology       Date:  1983-11       Impact factor: 9.910

8.  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

9.  Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome.

Authors:  J E Nielsen; L N Jensen; K Krabbe
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-09       Impact factor: 10.154
  9 in total
  5 in total

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

Authors:  Massimiliano Di Filippo; Piero Floridi; Vera Rossi; Emanuele Mattucci; Aroldo Rossi; Paolo Calabresi; Nicola Tambasco
Journal:  J Neurol       Date:  2009-10-14       Impact factor: 4.849

2.  Does thiamine protect the brain from iron overload and alcohol-related dementia?

Authors:  Stephan Listabarth; Daniel König; Benjamin Vyssoki; Simon Hametner
Journal:  Alzheimers Dement       Date:  2020-08-18       Impact factor: 21.566

Review 3.  Iron uptake and transport across physiological barriers.

Authors:  Kari A Duck; James R Connor
Journal:  Biometals       Date:  2016-07-25       Impact factor: 2.949

Review 4.  Hepcidin, an emerging and important player in brain iron homeostasis.

Authors:  Driton Vela
Journal:  J Transl Med       Date:  2018-02-07       Impact factor: 5.531

Review 5.  The Dual Role of Hepcidin in Brain Iron Load and Inflammation.

Authors:  Driton Vela
Journal:  Front Neurosci       Date:  2018-10-15       Impact factor: 4.677
  5 in total

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