Literature DB >> 25060649

PARK2 presenting as a disabling peripheral axonal neuropathy.

Joana Domingos1, Teresa Coelho, Ricardo Taipa, Jorge P Basto, Manuel Melo-Pires, Marina J Magalhães.   

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Year:  2014        PMID： 25060649     DOI： 10.1007/s10072-014-1898-y

Source DB:  PubMed          Journal:  Neurol Sci        ISSN： 1590-1874            Impact factor:   3.307


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  5 in total

1.  Does parkin play a role in the peripheral nervous system? A family report.

Authors:  Giovanni Abbruzzese; Simona Pigullo; Angelo Schenone; Emilia Bellone; Roberta Marchese; Emilio Di Maria; Luana Benedetti; Paola Ciotti; Lucilla Nobbio; Vincenzo Bonifati; Franco Ajmar; Paola Mandich
Journal:  Mov Disord       Date:  2004-08       Impact factor: 10.338

2.  Reduced amplitude of the sural nerve sensory action potential in PARK2 patients.

Authors:  Y Ohsawa; K Kurokawa; M Sonoo; H Yamada; S Hemmi; K Iwatsuki; H Hagiwara; T Murakami; T Shirabe; T Shimizu; Y Sunada
Journal:  Neurology       Date:  2005-08-09       Impact factor: 9.910

3.  Molecular cloning, gene expression, and identification of a splicing variant of the mouse parkin gene.

Authors:  T Kitada; S Asakawa; S Minoshima; Y Mizuno; N Shimizu
Journal:  Mamm Genome       Date:  2000-06       Impact factor: 2.957

4.  Sensory neuropathy in autosomal recessive juvenile parkinsonism (PARK2).

Authors:  Yasuyuki Okuma; Nobutaka Hattori; Yoshikuni Mizuno
Journal:  Parkinsonism Relat Disord       Date:  2003-06       Impact factor: 4.891

5.  Parkin disease: a phenotypic study of a large case series.

Authors:  Naheed L Khan; Elizabeth Graham; Peter Critchley; Anette E Schrag; Nicholas W Wood; Andrew J Lees; Kailash P Bhatia; Niall Quinn
Journal:  Brain       Date:  2003-06       Impact factor: 13.501
  5 in total
  2 in total

Review 1.  Movement disorders and neuropathies: overlaps and mimics in clinical practice.

Authors:  Francesco Gentile; Alessandro Bertini; Alberto Priori; Tommaso Bocci
Journal:  J Neurol       Date:  2022-06-03       Impact factor: 6.682

2.  Parkin Pleiotropy: Extremely Atypical Phenotypes in Patients With Compound Heterozygous Mutations.

Authors:  Patricio Millar Vernetti; Malco Rossi; Marcelo Merello
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2020-08-13
  2 in total

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