Literature DB >> 33578072

Perry syndrome with progressive supranuclear palsy-like phenotype in a Portuguese family - Long-term clinical follow-up.

Rui Duarte Barreto1, Rita Rodrigues2, José Mário Roriz3, Isabel Alonso4, Marina Magalhães5.   

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Year:  2021        PMID： 33578072     DOI： 10.1016/j.parkreldis.2021.02.004

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN： 1353-8020            Impact factor:   4.891


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  3 in total

1.  DCTN1 mutation associated parkinsonism: case series of three new families with perry syndrome.

Authors:  Thomas B Stoker; Vaclav Dostal; Jeffrey Cochius; Caroline H Williams-Gray; Clemens R Scherzer; Junhao Wang; Ganqiang Liu; Ian Coyle-Gilchrist
Journal:  J Neurol       Date:  2022-07-27       Impact factor: 6.682

Review 2.  Differential Diagnosis of Rare Subtypes of Progressive Supranuclear Palsy and PSP-Like Syndromes-Infrequent Manifestations of the Most Common Form of Atypical Parkinsonism.

Authors:  Patrycja Krzosek; Natalia Madetko; Anna Migda; Bartosz Migda; Dominika Jaguś; Piotr Alster
Journal:  Front Aging Neurosci       Date:  2022-02-09       Impact factor: 5.750

Review 3.  Clinical, pathological and genetic characteristics of Perry disease-new cases and literature review.

Authors:  Jarosław Dulski; Catalina Cerquera-Cleves; Lukasz Milanowski; Alexa Kidd; Emilia J Sitek; Audrey Strongosky; Ana María Vanegas Monroy; Dennis W Dickson; Owen A Ross; Jolanta Pentela-Nowicka; Jarosław Sławek; Zbigniew K Wszolek
Journal:  Eur J Neurol       Date:  2021-08-26       Impact factor: 6.288
  3 in total

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