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  1. Musician’s Dystonia (MD) by impaired or complete loss of fine motor control in extensively trained movements at the instrument. In pianists, it frequently leads to involuntary flexion or extension of one or mo...

    Authors: Julius Gründahl, Michael Großbach and Eckart Altenmüller
    Citation: Journal of Clinical Movement Disorders 2022 7(Suppl 1):10
    Content type: Research article Published on:

    This article is part of a Supplement: Volume 7 Supplement 1

  2. Subthalamic Deep Brain Stimulation (DBS) have demonstrated in the last decades to determine an important clinical improvement in advanced and selected Parkinson’s disease (PD) patients. However, only a minorit...

    Authors: Francesca Spagnolo, Francesco Romeo, Piermassimo Proto, Augusto Maria Rini, Emanuela Leopizzi, Andrea Tedesco, Marco Frizzi and Bruno Passarella
    Citation: Journal of Clinical Movement Disorders 2021 7(Suppl 1):9
    Content type: Case report Published on:

    This article is part of a Supplement: Volume 7 Supplement 1

  3. Cervical dystonia (CD), the most common focal dystonia, is a chronic neurological movement disorder characterized by sustained involuntary contractions of the neck muscles, leading to abnormal postures. Abobot...

    Authors: Khashayar Dashtipour, Stefan Wietek, Bruce Rubin, Pascal Maisonobe, Laxman Bahroo and Richard Trosch
    Citation: Journal of Clinical Movement Disorders 2020 7:8
    Content type: Research article Published on:

  4. COVID-19 has made itself known to health care providers and families across the world in a matter of months. While primarily a respiratory disorder, it has also been shown to cause neurological symptoms, which...

    Authors: Ali Elbeddini, Anthony To, Yasamin Tayefehchamani and Cindy Wen
    Citation: Journal of Clinical Movement Disorders 2020 7:7
    Content type: Commentary Published on:

  5. An amendment to this paper has been published and can be accessed via the original article.

    Authors: V. P. Misra, N. Danchenko, P. Maisonobe, J. Lundkvist and M. Hunger
    Citation: Journal of Clinical Movement Disorders 2020 7:6
    Content type: Correction Published on:

    The original article was published in Journal of Clinical Movement Disorders 2020 7:2

  6. The Personal KinetiGraph® (PKG®) Movement Recording System provides continuous, objective, ambulatory movement data during routine daily activities and provides information on medication compliance, motor fluc...

    Authors: Rajesh Pahwa, Filip Bergquist, Malcolm Horne and Michael E. Minshall
    Citation: Journal of Clinical Movement Disorders 2020 7:5
    Content type: Research article Published on:

  7. To quantify pharmacological effects on tremor in patients with essential tremor (ET) or Parkinson’s Disease (PD), laboratory-grade accelerometers have previously been used. Over the last years, consumer produc...

    Authors: Emilie M. J. van Brummelen, Dimitrios Ziagkos, Wadim M. I. de Boon, Ellen P. Hart, Robert J. Doll, Teppo Huttunen, Petteri Kolehmainen and Geert Jan Groeneveld
    Citation: Journal of Clinical Movement Disorders 2020 7:4
    Content type: Research article Published on:

  8. Vitamin B12 deficiency causes a number of neurological features including cognitive and psychiatric disturbances, gait instability, neuropathy, and autonomic dysfunction. Clinical recognition of B12 deficiency...

    Authors: Nijee S. Luthra, Ariane H. Marcus, Nancy K. Hills and Chadwick W. Christine
    Citation: Journal of Clinical Movement Disorders 2020 7:3
    Content type: Research article Published on:

  9. Botulinum neurotoxins type A (BoNT-As) are commonly used treatments for cervical dystonia (CD). Clinical trials have demonstrated the benefits of them in these patients, but data from real-life clinical practi...

    Authors: V. P. Misra, N. Danchenko, P. Maisonobe, J. Lundkvist and M. Hunger
    Citation: Journal of Clinical Movement Disorders 2020 7:2
    Content type: Research article Published on:

    The Correction to this article has been published in Journal of Clinical Movement Disorders 2020 7:6

  10. Kernicterus Spectrum Disorder (KSD) is the result of prolonged bilirubin toxicity resulting in widespread neurological injury. Once the bilirubin levels are normalized the encephalopathy becomes static, howeve...

    Authors: Jessie Mann, Dory A. Wallace and Stephanie DeLuca
    Citation: Journal of Clinical Movement Disorders 2020 7:1
    Content type: Case report Published on:

  12. Reliable detection of slowed vertical saccades may help discriminate progressive supranuclear palsy (PSP) from the subset of Parkinson’s disease patients who lack tremor (akinetic-rigid or PD-postural instabil...

    Authors: Marian L. Dale, Emmi P. Scott, Saher Khalid, Andrew S. Eiseman and Travis H. Turner
    Citation: Journal of Clinical Movement Disorders 2019 6:6
    Content type: Research article Published on:

  13. The embouchure of trumpet players is of utmost importance for tone production and quality of playing. It requires skilled coordination of lips, facial muscles, tongue, oral cavity, larynx and breathing and has...

    Authors: Soenke J. Hellwig, Peter W. Iltis, Arun A. Joseph, Dirk Voit, Jens Frahm, Erwin Schoonderwaldt and Eckart Altenmüller
    Citation: Journal of Clinical Movement Disorders 2019 6:5
    Content type: Research article Published on:

  15. Huntington’s disease (HD) is an autosomal dominant, neurodegenerative disorder. Associated cognitive deficits including impulsivity and disinhibition are the same factors that also predispose to forensic risk....

    Authors: Elvina May-Yin Chu, Mari O’Neill, Debasish Das Purkayastha and Caroline Knight
    Citation: Journal of Clinical Movement Disorders 2019 6:3
    Content type: Case report Published on:

  16. Telemedicine is a convenient health service delivery modality for patients with movement disorders, including Parkinson’s disease (PD), but is currently underutilized in the management of associated psychiatri...

    Authors: Andreea L. Seritan, Melissa Heiry, Ana-Maria Iosif, Michael Dodge and Jill L. Ostrem
    Citation: Journal of Clinical Movement Disorders 2019 6:2
    Content type: Research article Published on:

    The Publisher Correction to this article has been published in Journal of Clinical Movement Disorders 2019 6:4

  17. Dystonia is a debilitating disease that causes abnormal, often repetitive, movements, postures or both. The pathophysiology is unknown but related to loss of neuronal inhibition, aberrant sensorimotor integrat...

    Authors: Kush Sharma, Alberto Cucca, Andrea Lee, Shashank Agarwal, Steven Joel Frucht and Milton Cesar Biagioni
    Citation: Journal of Clinical Movement Disorders 2019 6:1
    Content type: Case report Published on:

  18. 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
    Content type: Correction Published on:

    The original article was published in Journal of Clinical Movement Disorders 2016 3:19

  19. 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
    Content type: Research article Published on:

  20. 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
    Content type: Case report Published on:

  21. 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
    Content type: Research article Published on:

  22. 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
    Content type: Research article Published on:

  23. 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
    Content type: Research article Published on:

  24. 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
    Content type: Research article Published on:

  25. 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
    Content type: Case Report Published on:

  26. 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
    Content type: Research article Published on:

  27. 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
    Content type: Case Report Published on:

  28. 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
    Content type: Letter to the Editor Published on:

  29. 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
    Content type: Case Report Published on:

  30. 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
    Content type: Case Report Published on:

  31. 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
    Content type: Case report Published on:

  32. 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
    Content type: Research article Published on:

  33. 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
    Content type: Research article Published on:

  34. 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
    Content type: Research article Published on:

  35. 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
    Content type: Research article Published on:

  36. 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
    Content type: Review Published on:

  37. 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
    Content type: Review Published on:

  38. 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
    Content type: Case Report Published on:

  40. 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
    Content type: Review Published on:

  41. 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
    Content type: Research article Published on:

  42. 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
    Content type: Research article Published on:

  43. 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
    Content type: Review Published on:

  44. 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
    Content type: Research article Published on:

  45. 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
    Content type: Case report Published on:

  46. 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
    Content type: Review Published on:

    The Correction to this article has been published in Journal of Clinical Movement Disorders 2018 5:8

  48. 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
    Content type: Commentary Published on:

  49. 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
    Content type: Case report Published on:

  50. 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
    Content type: Research article Published on:

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Journal of Clinical Movement Disorders

ISSN: 2054-7072

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