Comment on Akbar et al., "Valbenazine-induced parkinsonism".

Abstract:

:This letter to the editor acknowledges the contribution of Akbar et al. to the field of tardive dyskinesia (TD) and provides important regulatory information about the potential for parkinson-like symptoms in patients with TD who are treated with valbenazine.

authors

Shah C

doi

10.1016/j.parkreldis.2020.01.011

subject

Has Abstract

pub_date

2020-02-01 00:00:00

pages

35

eissn

1353-8020

issn

1873-5126

pii

S1353-8020(20)30021-3

journal_volume

71

pub_type

评论,信件
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    abstract:INTRODUCTION:Low body weight in Parkinson's disease (PD) is poorly understood despite the associated risks of malnutrition, fractures, and death. Sarcopenia (loss of muscle bulk and strength) and frailty are geriatric syndromes that are likewise associated with adverse health outcomes, yet have received scant attention...

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    authors: Tan AH,Hew YC,Lim SY,Ramli NM,Kamaruzzaman SB,Tan MP,Grossmann M,Ang BH,Tan JY,Manap MAAA,Tay TK,Tan SL,New RP,Fadzli F,Yee EJ,Moy FM,Mahadeva S,Lang AE

    更新日期:2018-11-01 00:00:00

  • Identification of a novel homozygous mutation Arg459Pro in SYNJ1 gene of an Indian family with autosomal recessive juvenile Parkinsonism.

    abstract:BACKGROUND:A novel homozygous missense mutation (c.773G > A, p.Arg258Gln) in Synaptojanin 1 (SYNJ1, 21q22.2) has recently been reported in two Italian and one Iranian consanguineous families with autosomal recessive juvenile Parkinsonism (ARJP). Contribution of this synaptic gene related to Parkinsonism phenotypes in o...

    journal_title:Parkinsonism & related disorders

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    doi:10.1016/j.parkreldis.2016.07.014

    authors: Kirola L,Behari M,Shishir C,Thelma BK

    更新日期:2016-10-01 00:00:00

  • High-dose treatment with pergolide in Parkinson's disease patients with motor fluctuations and dyskinesias.

    abstract::Motor complications arising after long-term treatment with levodopa remain one of the main challenges in the treatment of patients with Parkinson's disease (PD). Monotherapy with dopamine agonists may delay the onset of motor complications or reduce their severity when added to levodopa treatment. Here, we retrospecti...

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    pub_type: 杂志文章

    doi:10.1016/j.parkreldis.2005.03.005

    authors: Storch A,Trenkwalder C,Oehlwein C,Winkelmann J,Polzer U,Hundemer HP,Schwarz J

    更新日期:2005-09-01 00:00:00

  • Action observation improves sit-to-walk in patients with Parkinson's disease and freezing of gait. Biomechanical analysis of performance.

    abstract:INTRODUCTION:Freezing of gait (FoG) is one of the most disabling gait disorders in Parkinson's disease (PD), reflecting motor and cognitive impairments, mainly related to dopamine deficiency. Recent studies investigating kinematic and kinetic factors affecting gait in these patients showed a postural instability charac...

    journal_title:Parkinsonism & related disorders

    pub_type: 杂志文章

    doi:10.1016/j.parkreldis.2020.09.029

    authors: Mezzarobba S,Grassi M,Pellegrini L,Catalan M,Krüger B,Stragapede L,Manganotti P,Bernardis P

    更新日期:2020-11-01 00:00:00

  • Quality of sleep in young onset Parkinson's disease: Any difference from older onset Parkinson's disease.

    abstract:BACKGROUND:Sleep disorders occur commonly in Parkinson's disease and are often under-recognized and under treated in clinical practice. OBJECTIVES:To determine the quality of sleep in patients with Young onset Parkinson's disease (YOPD) and to note whether there is any difference in quality of sleep from those patient...

    journal_title:Parkinsonism & related disorders

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    doi:10.1016/j.parkreldis.2015.02.007

    authors: Mahale R,Yadav R,Pal PK

    更新日期:2015-05-01 00:00:00

  • Adult-onset primary focal foot dystonia.

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    doi:10.1016/j.parkreldis.2005.07.004

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    更新日期:2006-01-01 00:00:00

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    更新日期:2015-04-01 00:00:00

  • Survival in Parkinson's disease in relation to striatal dopamine transporter binding.

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    doi:10.1016/j.parkreldis.2017.06.013

    authors: Mäkinen E,Joutsa J,Vahlberg T,Kaasinen V

    更新日期:2017-09-01 00:00:00

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    更新日期:2019-09-01 00:00:00

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    doi:10.1016/j.parkreldis.2019.02.001

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    更新日期:2019-05-01 00:00:00

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    doi:10.1016/s1353-8020(03)00109-3

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    更新日期:2003-12-01 00:00:00

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    更新日期:2016-01-01 00:00:00

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    更新日期:2018-10-01 00:00:00

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    更新日期:2014-07-01 00:00:00

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    更新日期:2017-11-01 00:00:00

  • Prescribing medications in Parkinson's disease (PD) patients during acute admissions to a District General Hospital.

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    pub_type: 临床试验,杂志文章

    doi:10.1016/j.parkreldis.2006.11.006

    authors: Magdalinou KN,Martin A,Kessel B

    更新日期:2007-12-01 00:00:00

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    abstract::White matter lesions (WML) and epilepsy have been occasionally seen in Wilson's disease. No cases of generalized myoclonus have been reported so far. We present a patient with psychiatric symptoms starting at age 16, followed by tremor, generalized dystonia and severe generalized myoclonus. In addition to classical fi...

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    doi:10.1016/j.parkreldis.2006.03.012

    authors: Barbosa ER,Silveira-Moriyama L,Machado AC,Bacheschi LA,Rosemberg S,Scaff M

    更新日期:2007-04-01 00:00:00

  • alpha-Synuclein multiplication analysis in Italian familial Parkinson disease.

    abstract::The alpha-synuclein gene (SNCA) multiplication causes autosomal dominant Parkinson Disease (PD): triplication is associated with early-onset rapidly progressing parkinsonism with a strong likelihood of developing dementia, while duplication is associated with a less severe phenotype similar to idiopathic PD. We tested...

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    doi:10.1016/j.parkreldis.2009.09.008

    authors: Sironi F,Trotta L,Antonini A,Zini M,Ciccone R,Della Mina E,Meucci N,Sacilotto G,Primignani P,Brambilla T,Coviello DA,Pezzoli G,Goldwurm S

    更新日期:2010-03-01 00:00:00

  • Prevalence survey of movement disorders, epilepsy, hypertension and smoking habit in Vejer de la Frontera, Southern Spain-I. Methodology.

    abstract::A prevalence survey of movement disorders, epilepsy, hypertension and smoking was undertaken in Vejer de la Frontera, Southern Spain in 1988. A validated screening instrument designed for door-to-door tracing of specific disorders was used. Neurological diagnoses were based on: (1) direct anamnesis and examination by ...

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    doi:10.1016/s1353-8020(96)00021-1

    authors: Acosta-Varo J,De Pedro-Cuesta J

    更新日期:1996-10-01 00:00:00

  • Nationwide prevalence of primary dystonia, progressive ataxia and hereditary spastic paraplegia.

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    doi:10.1016/j.parkreldis.2019.10.028

    authors: Hellberg C,Alinder E,Jaraj D,Puschmann A

    更新日期:2019-12-01 00:00:00

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    doi:10.1016/j.parkreldis.2019.04.014

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    authors: Dobričić V,Kresojević N,Žarković M,Tomić A,Marjanović A,Westenberger A,Cvetković D,Svetel M,Novaković I,Kostić VS

    更新日期:2015-10-01 00:00:00

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    pub_type: 杂志文章,评审

    doi:10.1016/j.parkreldis.2008.02.003

    authors: Lee MS,Lam P,Ernst E

    更新日期:2008-12-01 00:00:00

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    authors: Imbriani P,D'Angelo V,Platania P,Di Lazzaro G,Scalise S,Salimei C,El Atiallah I,Colona VL,Mercuri NB,Bonsi P,Pisani A,Schirinzi T,Martella G

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    authors: Thompson PD

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    更新日期:2015-05-01 00:00:00