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  1. Content type: Correction

    Following publication of the original article [1], the authors reported that the videos referred to in their article were not accessible to readers.

    Authors: Pichet Termsarasab, Thananan Thammongkolchai and Steven J. Frucht

    Citation: Journal of Clinical Movement Disorders 2018 5:8

    Published on:

    The original article was published in BMC Genomics 2018 19:686

  2. Content type: Research article

    Vitamin D (VitD) deficiency is common in Parkinson’s disease (PD) and has been raised as a possible PD risk factor. In the past decade, VitD supplementation for potential prevention of age related conditions h...

    Authors: Nijee S. Luthra, Soeun Kim, Yunxi Zhang and Chadwick W. Christine

    Citation: Journal of Clinical Movement Disorders 2018 5:7

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  3. Content type: Case report

    Spinocerebellar ataxia 2 (SCA2) is an autosomal dominant neurodegenerative disorder caused by CAG repeat expansions in ATXN2 on chromosome 12q24. Patients present with adult-onset progressive gait ataxia, slow sa...

    Authors: Nan Cheng, Heather M. Wied, James J. Gaul, Lauren E. Doyle and Stephen G. Reich

    Citation: Journal of Clinical Movement Disorders 2018 5:6

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  4. Content type: Research article

    Stiff person syndrome (SPS) is a progressive neurological disorder characterized by axial muscle rigidity and involuntary spasms. Autoimmune and neoplastic diseases are associated with SPS. Our study objective...

    Authors: James A. G. Crispo, Dylan P. Thibault, Yannick Fortin and Allison W. Willis

    Citation: Journal of Clinical Movement Disorders 2018 5:5

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  5. Content type: Research article

    Cervical dystonia is a heterogeneous disorder with several possible presentations, for which first-line therapy is often botulinum toxin (BoNT). In routine clinical practice the success of each BoNT injection ...

    Authors: Vijay P. Misra, Richard M. Trosch, Pascal Maisonobe and Savary Om

    Citation: Journal of Clinical Movement Disorders 2018 5:4

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  6. Content type: Research article

    Diagnosis of less common young-onset movement disorders is often challenging, requiring a broad spectrum of skills of clinicians regarding phenotyping, normal and abnormal development and the wide range of pos...

    Authors: Martje E. van Egmond, Hendriekje Eggink, Anouk Kuiper, Deborah A. Sival, Corien C. Verschuuren-Bemelmans, Marina A. J. Tijssen and Tom J. de Koning

    Citation: Journal of Clinical Movement Disorders 2018 5:3

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  7. Content type: Research article

    Striatal atrophy is detectable many years before the predicted onset of motor symptoms in premanifest Huntington’s disease (HD). However, the extent of these neurodegenerative changes at the actual time of con...

    Authors: Emma M. Coppen, Jeroen van der Grond and Raymund A. C. Roos

    Citation: Journal of Clinical Movement Disorders 2018 5:2

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  8. Content type: Case Report

    Cognitive fluctuations refer to alterations in cognition, attention, or arousal occurring over minutes to hours, most commonly in patients with dementias associated with advanced Lewy body pathology. Their pat...

    Authors: David E. Riley and Alberto J. Espay

    Citation: Journal of Clinical Movement Disorders 2018 5:1

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  9. Content type: Research article

    Although considerable research has focused on the etiology and symptomology of adductor focal laryngeal dystonia (AD-FLD), little is known about the correlation between clinicians’ ratings and patients’ percep...

    Authors: Celia Faye Stewart, Catherine F. Sinclair, Irene F. Kling, Beverly E. Diamond and Andrew Blitzer

    Citation: Journal of Clinical Movement Disorders 2017 4:20

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  10. Content type: Case Report

    Dopa-responsive dystonia (DRD) has largely been associated with autosomal dominant mutations in the GCH1 gene leading to GTP cyclohydrolase 1 deficiency. More recently, a deficiency in tyrosine hydroxylase (TH...

    Authors: Linn E. Katus and Steven J. Frucht

    Citation: Journal of Clinical Movement Disorders 2017 4:18

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  11. Content type: Letter to the Editor

    Here we discuss the report by Claassen and colleagues describing an indirect treatment comparison between tetrabenazine and deutetrabenazine for chorea in Huntington’s disease using individual patient data. We...

    Authors: Filipe B. Rodrigues, Gonçalo S. Duarte, João Costa, Joaquim J. Ferreira and Edward J. Wild

    Citation: Journal of Clinical Movement Disorders 2017 4:19

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  12. Content type: Case Report

    Primary progressive apraxia is a rare form of apraxia in the absence of dementia which develops insidiously and is slowly progressive. Most reports of patients with apraxia also describe coexisting aphasias or...

    Authors: Yeva M. Fernandez and Steven J. Frucht

    Citation: Journal of Clinical Movement Disorders 2017 4:17

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  13. Content type: Case Report

    Pure akinesia with gait freezing is a rare syndrome with few autopsied cases. Severe freezing of gait occurs in the absence of bradykinesia and rigidity. Most autopsies have revealed progressive supranuclear p...

    Authors: Ahmad Elkouzi, Esther N. Bit-Ivan and Rodger J. Elble

    Citation: Journal of Clinical Movement Disorders 2017 4:15

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  14. Content type: Case report

    Parkinson’s disease (PD) is predominantly recognized for its motor symptoms, but patients struggle from a morbid and heterogeneous collection of non-motor symptoms (NMS-PD) that can affect their quality of lif...

    Authors: Andre Y. Son, Alberto Cucca, Shashank Agarwal, Anli Liu, Alessandro Di Rocco and Milton C. Biagioni

    Citation: Journal of Clinical Movement Disorders 2017 4:14

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  15. Content type: Research article

    Parkinson disease (PD) is associated with a high prevalence of insomnia, affecting up to 88% of patients. Pharmacotherapy studies in the literature addressing insomnia in PD reveal disappointing and inconsiste...

    Authors: Shnehal Patel, Oluwadamilola Ojo, Gencer Genc, Srivadee Oravivattanakul, Yang Huo, Tanaporn Rasameesoraj, Lu Wang, James Bena, Michelle Drerup, Nancy Foldvary-Schaefer, Anwar Ahmed and Hubert H. Fernandez

    Citation: Journal of Clinical Movement Disorders 2017 4:16

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  16. Content type: Research article

    Writer’s cramp (WC) is a task-specific focal dystonia which manifests itself as abnormal postures interfering with motor performance. As the spread of motor symptoms remains controversial and non-motor symptom...

    Authors: Ali Amouzandeh, Michael Grossbach, Joachim Hermsdörfer and Eckart Altenmüller

    Citation: Journal of Clinical Movement Disorders 2017 4:13

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  17. Content type: Research article

    Quality of life (QoL) is the sense of well-being perceived by people. The improvement of parkinsonian patient’s QoL is a crucial goal for clinicians involved in rehabilitative care. In order to provide an appr...

    Authors: Paola Ortelli, Roberto Maestri, Marianna Zarucchi, Veronica Cian, Elisa Urso, Francesca Giacomello, Davide Ferrazzoli and Giuseppe Frazzitta

    Citation: Journal of Clinical Movement Disorders 2017 4:12

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  18. Content type: Research article

    Proprioceptive deficits have been largely documented in PD patients, thus external sensory signals (peripheral sensory feedback) are often used to compensate the abnormalities of proprioceptive integration.

    Authors: Daniele Volpe, Elisa Pelosin, Leila Bakdounes, Stefano Masiero, Giannettore Bertagnoni, Chiara Sorbera and Maria Giulia Giantin

    Citation: Journal of Clinical Movement Disorders 2017 4:11

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  19. Content type: Review

    Chorea is a hyperkinetic movement disorder consisting of involuntary irregular, flowing movements of the trunk, neck or face. Although Huntington’s disease is the most common cause of chorea in adults, chorea ...

    Authors: Debra J. Ehrlich and Ruth H. Walker

    Citation: Journal of Clinical Movement Disorders 2017 4:8

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  20. Content type: Review

    The aim of this study was to examine the efficacy, safety and dosing practices of rimabotulinumtoxinB (BoNT-B) for the treatment of patients with sialorrhea based on a systematic review of clinical trials.

    Authors: Khashayar Dashtipour, Roongroj Bhidayasiri, Jack J. Chen, Bahman Jabbari, Mark Lew and Diego Torres-Russotto

    Citation: Journal of Clinical Movement Disorders 2017 4:9

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  21. Content type: Case Report

    Gaucher disease (GD) is an inborn error of metabolism caused by mutations in the gene (GBA) coding for glucocerebrosidase (GCase), inherited in an autosomal recessive pattern. GD patients have up to 9% risk of de...

    Authors: Federico Rodriguez-Porcel, Alberto J. Espay and Miryam Carecchio

    Citation: Journal of Clinical Movement Disorders 2017 4:7

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  22. Content type: Review

    Dystonic storm is a frightening hyperkinetic movement disorder emergency. Marked, rapid exacerbation of dystonia requires prompt intervention and admission to the intensive care unit. Clinical features of dyst...

    Authors: Pichet Termsarasab and Steven J. Frucht

    Citation: Journal of Clinical Movement Disorders 2017 4:10

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  23. Content type: Research article

    AbobotulinumtoxinA (Dysport®) was distributed for many years in vials containing 500MU (D500). Recently a new 300MU vial (D300) was additionally introduced (introduction). We wanted to explore whether more dif...

    Authors: Dirk Dressler and Fereshte Adib Saberi

    Citation: Journal of Clinical Movement Disorders 2017 4:6

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  24. Content type: Research article

    In high-income countries patients with Huntington disease (HD) typically present to healthcare providers after developing involuntary movements, or for pre-symptomatic genetic testing if at familial risk. A po...

    Authors: Jarmal Charles, Lindyann Lessey, Jennifer Rooney, Ingmar Prokop, Katherine Yearwood, Hazel Da Breo, Patrick Rooney, Ruth H. Walker and Andrew K. Sobering

    Citation: Journal of Clinical Movement Disorders 2017 4:4

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  25. Content type: Review

    Disruption of the frontal lobes and its associated networks are a common consequence of neurodegenerative disorders. Given the wide range of cognitive, behavioral and motor processes in which the frontal lobes...

    Authors: Russell P. Sawyer, Federico Rodriguez-Porcel, Matthew Hagen, Rhonna Shatz and Alberto J. Espay

    Citation: Journal of Clinical Movement Disorders 2017 4:2

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  26. Content type: Research article

    Vesicular monoamine transporter 2 (VMAT2) inhibitors can improve hyperkinetic movements, and are effective treatment options for chorea of Huntington disease (HD). Tetrabenazine was assessed for treating chore...

    Authors: Daniel O. Claassen, Benjamin Carroll, Lisa M. De Boer, Eric Wu, Rajeev Ayyagari, Sanjay Gandhi and David Stamler

    Citation: Journal of Clinical Movement Disorders 2017 4:3

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  27. Content type: Case report

    Primary orthostatic tremor is a rare disorder that is still under-diagnosed or misdiagnosed. Motor symptoms are fairly characteristics but the real impact on the patient’s every day life and quality of life is...

    Authors: Marie Vidailhet, Emmanuel Roze, Lucie Maugest and Cécile Gallea

    Citation: Journal of Clinical Movement Disorders 2017 4:1

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  28. Content type: Review

    Therapeutic strategies in dystonia have evolved considerably in the past few decades. Three major treatment modalities include oral medications, botulinum toxin injections and surgical therapies, particularly ...

    Authors: Pichet Termsarasab, Thananan Thammongkolchai and Steven J. Frucht

    Citation: Journal of Clinical Movement Disorders 2016 3:19

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  29. Content type: Commentary

    Mutations in six genes are known to cause Parkinson’s disease (PD) (autosomal dominant: alpha-synuclein, LRRK2, VPS35 and autosomal recessive: Parkin, PINK1 and DJ1) and number of other genes are implicated. I...

    Authors: Diana A. Olszewska, Conor Fearon and Tim Lynch

    Citation: Journal of Clinical Movement Disorders 2016 3:17

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  30. Content type: Case report

    Compulsive movements, complex tics and stereotypies are frequent, especially among patients with autism or psychomotor retardation. These movements can be difficult to characterize and can mimic other conditio...

    Authors: A. Kuiper, M.E. van Egmond, M.P.M. Harms, M.D. Oosterhoff, B. van Harten, D.A. Sival, T.J. de Koning and M.A.J. Tijssen

    Citation: Journal of Clinical Movement Disorders 2016 3:16

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  31. Content type: Research article

    Focal dystonia is the most common type of adult-onset dystonia; however, it infrequently affects truncal musculature. Although commonly attributed to secondary etiologies such as a neurodegenerative illness or...

    Authors: Debra J. Ehrlich and Steven J. Frucht

    Citation: Journal of Clinical Movement Disorders 2016 3:15

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  32. Content type: Review

    Physicians are usually at the forefront when the issue of driving ability is raised by Parkinson’s disease (PD) patients or their family members, even though few have been formally trained in this area.

    Authors: Onanong Jitkritsadakul and Roongroj Bhidayasiri

    Citation: Journal of Clinical Movement Disorders 2016 3:14

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  33. Content type: Case report

    In the absence of visual feedback, humans depend upon proprioceptive information for reaching movements and coordination. Use of sensory information in order to assist movement is impaired in patients with ear...

    Authors: Diana A. Olszewska, Conor Fearon and Tim Lynch

    Citation: Journal of Clinical Movement Disorders 2016 3:12

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  34. Content type: Research article

    Embarrassment can be a considerable problem for patients with essential tremor (ET) and is a major motivator for treatment. Depression is also a common feature of ET; as many as 35 % of patients report moderat...

    Authors: Elan D. Louis, Stephanie Cosentino and Edward D. Huey

    Citation: Journal of Clinical Movement Disorders 2016 3:11

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  35. Content type: Case report

    A 45–year-old woman reported automatic behaviors and communication whilst she was being treated with pramipexole. These episodes vanished after the medication was tapered and she was started on levodopa/carbid...

    Authors: Ruth H. Walker

    Citation: Journal of Clinical Movement Disorders 2016 3:9

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  36. Content type: Research article

    Embouchure dystonia is an unusual focal task-specific dystonia affecting the muscles that control the flow of air into the mouthpiece of a brass or woodwind instrument. The complexity of the embouchure and the...

    Authors: Steven J Frucht

    Citation: Journal of Clinical Movement Disorders 2016 3:10

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  37. Content type: Letter to the Editor

    Most Parkinson’s disease (PD) patients present without known family history and without a diagnosed prodromal phase, underscoring the difficulty of employing primary (neuroprevention) and secondary (neuroprote...

    Authors: Leonard L. Sokol, Michael J. Young, Alberto J. Espay and Ronald B. Postuma

    Citation: Journal of Clinical Movement Disorders 2016 3:7

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  38. Content type: Research article

    The modulation of levodopa transport across the blood brain barrier by large neutral amino acids is well documented. Protein limitation and protein redistribution diets may improve motor fluctuations in patien...

    Authors: Tuhin Virmani, Sirinan Tazan, Pietro Mazzoni, Blair Ford and Paul E. Greene

    Citation: Journal of Clinical Movement Disorders 2016 3:8

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  39. Content type: Case report

    A patient with right-side-predominant Parkinson’s disease presented visual artwork which improved in resemblance to the model which he was copying with increasing doses of levodopa. I propose that increased do...

    Authors: Ruth H. Walker

    Citation: Journal of Clinical Movement Disorders 2016 3:6

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  40. Content type: Research article

    Parkinson’s disease patients are at an elevated risk of developing cognitive impairment. Although cognitive impairment is one of the strongest predictors of quality of life, dopaminergic anti-parkinsonian medi...

    Authors: Clara Warden, Jaclyn Hwang, Anisa Marshall, Michelle Fenesy and Kathleen L. Poston

    Citation: Journal of Clinical Movement Disorders 2016 3:5

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  41. Content type: Research article

    This paper describes the use of real-time magnetic resonance imaging in visualizing and quantifying oral cavity motor strategies employed by 6 healthy, elite horn players and 5 horn players with embouchure dys...

    Authors: Peter W. Iltis, Jens Frahm, Dirk Voit, Arun Joseph, Erwin Schoonderwaldt and Eckart Altenmüller

    Citation: Journal of Clinical Movement Disorders 2016 2:15

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  42. Content type: Case Report

    Freezing of gait (FoG) is a debilitating feature of Parkinson’s disease and other parkinsonian disorders. This case demonstrates a variant of freezing of gait in a non-parkinsonian patient with a lesion of the...

    Authors: Marian L. Dale, Martina Mancini, Carolin Curtze, Fay B. Horak and Brett W. Fling

    Citation: Journal of Clinical Movement Disorders 2016 3:2

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  43. Content type: Research article

    Various postural deformities appear during progression of Parkinson’s disease (PD), but the underlying pathophysiology of these deformities is not well understood. The angle abnormalities seen in individual pa...

    Authors: Fumihito Yoshii, Yusuke Moriya, Tomohide Ohnuki, Masafuchi Ryo and Wakoh Takahashi

    Citation: Journal of Clinical Movement Disorders 2016 3:1

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  44. Content type: Review

    Spinal-generated movement disorders (SGMDs) include spinal segmental myoclonus, propriospinal myoclonus, orthostatic tremor, secondary paroxysmal dyskinesias, stiff person syndrome and its variants, movements ...

    Authors: Pichet Termsarasab, Thananan Thammongkolchai and Steven J. Frucht

    Citation: Journal of Clinical Movement Disorders 2015 2:18

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    The Publisher’s Erratum to this article has been published in Journal of Clinical Movement Disorders 2016 3:18

2017 Journal Metrics

  • Speed
    67 days to first decision for reviewed manuscripts only
    64 days to first decision for all manuscripts
    144 days from submission to acceptance
    20 days from acceptance to publication

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