Literature DB >> 33567051

Parkinson-related neuropathy.

Josef Finsterer1, Fúlvio Alexandre Scorza2, Carla Alessandra Scorza2, Ana Claudia Fiorini3,4.   

Abstract

Entities:  

Mesh：

Year:  2021        PMID： 33567051      PMCID： PMC7847250          DOI： 10.6061/clinics/2021/e2675

Source DB:  PubMed          Journal:  Clinics (Sao Paulo)        ISSN： 1807-5932            Impact factor:   2.365


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  28 in total

1.  A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy.

Authors:  D Thyagarajan; S Bressman; C Bruno; S Przedborski; S Shanske; T Lynch; S Fahn; S DiMauro
Journal:  Ann Neurol       Date:  2000-11       Impact factor: 10.422

2.  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

3.  SLC25A46 mutations in patients with Parkinson's Disease and optic atrophy.

Authors:  Giacomo Bitetto; Maria Chiara Malaguti; Roberto Ceravolo; Edoardo Monfrini; Letizia Straniero; Alberto Morini; Raffaella Di Giacopo; Daniela Frosini; Giovanni Palermo; Fabio Biella; Dario Ronchi; Stefano Duga; Franco Taroni; Stefania Corti; Giacomo P Comi; Nereo Bresolin; Bruno Giometto; Alessio Di Fonzo
Journal:  Parkinsonism Relat Disord       Date:  2020-04-02       Impact factor: 4.891

Review 4.  Spinocerebellar ataxia type 48: last but not least.

Authors:  Giovanna De Michele; Daniele Galatolo; Melissa Barghigiani; Diletta Dello Iacovo; Rosanna Trovato; Alessandra Tessa; Elena Salvatore; Alessandro Filla; Giuseppe De Michele; Filippo M Santorelli
Journal:  Neurol Sci       Date:  2020-04-27       Impact factor: 3.307

5.  Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9).

Authors:  H Eiberg; L Hansen; L Korbo; I M Nielsen; K Svenstrup; S Bech; L H Pinborg; L Friberg; L E Hjermind; O R Olsen; J E Nielsen
Journal:  Clin Genet       Date:  2011-07-18       Impact factor: 4.438

6.  FIG4 mutations leading to parkinsonism and a phenotypical continuum between CMT4J and Yunis Varón syndrome.

Authors:  Milan Zimmermann; Stefanie Schuster; Sylvia Boesch; G Christoph Korenke; Julia Mohr; Jennifer Reichbauer; Christoph Kernstock; Dieter Kotzot; Veronika Spahlinger; Rebecca Schüle-Freyer; Ludger Schöls
Journal:  Parkinsonism Relat Disord       Date:  2020-03-28       Impact factor: 4.891

7.  Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of Walworth.

Authors:  P Giunti; M G Sweeney; A E Harding
Journal:  Brain       Date:  1995-10       Impact factor: 13.501

8.  Peripheral neuropathy associated with levodopa-carbidopa intestinal infusion: a long-term prospective assessment.

Authors:  A Merola; A Romagnolo; M Zibetti; A Bernardini; D Cocito; L Lopiano
Journal:  Eur J Neurol       Date:  2015-10-25       Impact factor: 6.089

9.  Bi-allelic variants in PNPLA6 possibly associated with Parkinsonian features in addition to spastic paraplegia phenotype.

Authors:  Kuntal Sen; Melesilika Finau; Pritha Ghosh
Journal:  J Neurol       Date:  2020-07-04       Impact factor: 4.849

10.  Large-Fiber Neuropathy in Parkinson's Disease: Clinical, Biological, and Electroneurographic Assessment of a Romanian Cohort.

Authors:  Oana Maria Vanta; Nicoleta Tohanean; Sebastian Pintea; Lacramioara Perju-Dumbrava
Journal:  J Clin Med       Date:  2019-09-24       Impact factor: 4.241
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  1 in total

1.  Neuropathy in Parkinson's Disease: Risk Determinants and Impact on Quality of Life.

Authors:  Ravi Soumiya; Birinder S Paul; Riya Aggarwal; Gunchan Paul
Journal:  Ann Indian Acad Neurol       Date:  2022-06-24       Impact factor: 1.714
  1 in total

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