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The Cerebellum
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3.41
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Papers 1295
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Published on 2019in The Cerebellum3.41
Bernardo Machado Dias Domingues (UFPR: Federal University of Paraná), Fábio A. Nascimento6
Estimated H-index: 6
(BCM: Baylor College of Medicine)
+ 4 AuthorsHélio A.G. Teive25
Estimated H-index: 25
(UFPR: Federal University of Paraná)
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder in which patients have a slowly progressive cerebellar ataxia, with dysarthria, dysphagia, and epilepsy. The aims of this study were to characterize the phenotypic expression of SCA10 and to examine its genotype-phenotype relationships. Ninety-one Brazilian patients with SCA10 from 16 families were selected. Clinical and epidemiological data were assessed by a standardized protocol, and severity of disease was measured by t...
Published on Aug 22, 2019in The Cerebellum3.41
Christian Hohenfeld2
Estimated H-index: 2
(RWTH Aachen University),
Imis Dogan14
Estimated H-index: 14
(RWTH Aachen University)
+ 8 AuthorsRalf Reilmann29
Estimated H-index: 29
(University of Tübingen)
Friedreich’s ataxia (FRDA) is a rare autosomal-recessive slowly progressive neurodegenerative disorder. As common clinical measures for this devastating disease lack sensitivity, we explored whether (a) the quantitative motor assessments of the Q-Motor battery can enhance clinical characterisation of FRDA; (b) clinical measures can predict Q-Motor outcomes and (c) Q-Motor is sensitive to longitudinal change. At baseline 29 patients and 23 controls and in a 1-year follow-up 14 patients and 6 cont...
Published on Aug 30, 2019in The Cerebellum3.41
Alberto Ranavolo15
Estimated H-index: 15
,
Mariano Serrao22
Estimated H-index: 22
(Sapienza University of Rome)
+ 8 AuthorsSergio Iavicoli23
Estimated H-index: 23
The aim of the present study was to characterize and analyze the most important individual and organizational variables associated with job accommodation in subjects with degenerative cerebellar ataxia by administering a series of international and validated work activity-related scales. Twenty-four workers (W) and 58 non-workers (NW) were recruited: 34 with autosomal dominant ataxia and 48 with autosomal recessive ataxia (27 with Friedreich ataxia and 21 with sporadic adult-onset ataxia of unkn...
Published on 2019in The Cerebellum3.41
Xueyan Jiang (German Center for Neurodegenerative Diseases), Jennifer Faber10
Estimated H-index: 10
(University Hospital Bonn)
+ 7 AuthorsFrank Jessen61
Estimated H-index: 61
(University of Cologne)
Published on 2019in The Cerebellum3.41
Helen Hartley1
Estimated H-index: 1
,
Elizabeth Cassidy (International University, Cambodia)+ 4 AuthorsBernie Carter23
Estimated H-index: 23
(Edge Hill University)
The effectiveness of exercise and physical therapy for children with ataxia is poorly understood. The aim of this systematic review was to critically evaluate the range, scope and methodological quality of studies investigating the effectiveness of exercise and physical therapy interventions for children with ataxia. The following databases were searched: AMED, CENTRAL, CDSR, CINAHL, ClinicalTrials.gov, EMBASE, Ovid MEDLINE, PEDro and Web of Science. No limits were placed on language, type of st...
Published on 2019in The Cerebellum3.41
Matteo Bologna21
Estimated H-index: 21
(Sapienza University of Rome),
Isabella Berardelli10
Estimated H-index: 10
(Sapienza University of Rome)
+ 5 AuthorsAlfredo Berardelli72
Estimated H-index: 72
(Sapienza University of Rome)
In addition to having postural and kinetic tremor of the upper limbs, some patients with essential tremor (ET) may have head tremor as well as cognitive and psychiatric disorders. We aimed to investigate whether the variable clinical presentation in ET patients, including motor and non-motor symptoms, differs in patients with and without head tremor. We consecutively enrolled 70 patients with a diagnosis of ET. Tremor severity was assessed by means of clinical rating scales. Patients also underw...
Published on Aug 29, 2019in The Cerebellum3.41
Alberto Vogrig2
Estimated H-index: 2
,
Andrea Bernardini (University of Udine)+ 6 AuthorsMariarosaria Valente18
Estimated H-index: 18
(Misericordia University)
Paraneoplastic cerebellar degeneration (PCD) is usually thought to have a subacute progression over several weeks. We report herein incidence and clinical features of hyperacute onset PCD, a vertebrobasilar stroke mimic. We performed a retrospective analysis of all suspected PCD cases referred to the Udine University Hospital between 2009 and 2017. Our center provides the only neuroimmunology laboratory for three provinces of the Friuli-Venezia Giulia region, Italy (983,190 people as of January ...
Published on 2019in The Cerebellum3.41
Narjes Ahmadian (UU: Utrecht University), Kirsten M van Baarsen (UU: Utrecht University)+ 1 AuthorsPierre A. Robe1
Estimated H-index: 1
(UU: Utrecht University)
The cerebellar cognitive affective syndrome (CCAS) was first described by Schmahmann and Sherman in 1998. Despite their clear depiction of the syndrome, it is our experience that the CCAS has not yet found solid ground as a disease entity in routine clinical practice. This made us question the dimension of the CCAS in cerebellar patients. We performed a systematic review of the literature according to the PRISMA guidelines, in order to answer the question whether patients with acquired isolated ...
Published on Jul 24, 2019in The Cerebellum3.41
Diego Veliz-Otani3
Estimated H-index: 3
,
Miguel Inca-Martinez3
Estimated H-index: 3
+ 5 AuthorsMario Cornejo-Olivas5
Estimated H-index: 5
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