Related references
Note: Only part of the references are listed.LRRK2 in Parkinson disease: challenges of clinical trials
Eduardo Tolosa et al.
NATURE REVIEWS NEUROLOGY (2020)
Disease modification and biomarker development in Parkinson disease: Revision or reconstruction?
Alberto J. Espay et al.
NEUROLOGY (2020)
New generation genetic testing entering the clinic
Sorina Gorcenco et al.
PARKINSONISM & RELATED DISORDERS (2020)
Opinions and clinical practices related to diagnosing and managing functional (psychogenic) movement disorders: changes in the last decade
K. LaFaver et al.
EUROPEAN JOURNAL OF NEUROLOGY (2020)
Management of rare movement disorders in Europe: outcome of surveys of the European Reference Network for Rare Neurological Diseases
C. Painous et al.
EUROPEAN JOURNAL OF NEUROLOGY (2020)
Clinical application of next-generation sequencing to the practice of neurology
Jessica Rexach et al.
LANCET NEUROLOGY (2019)
Will genotype drive treatment options?
Norbert Brueggemann et al.
MOVEMENT DISORDERS (2019)
Targeting Huntingtin Expression in Patients with Huntington's Disease
Sarah J. Tabrizi et al.
NEW ENGLAND JOURNAL OF MEDICINE (2019)
Treatable Inherited Rare Movement Disorders
H. A. Jinnah et al.
MOVEMENT DISORDERS (2018)
Addressing challenges in the diagnosis and treatment of rare genetic diseases
Kym M. Boycott et al.
NATURE REVIEWS DRUG DISCOVERY (2018)
Genetics of Movement Disorders and the Practicing Clinician; Who and What to Test for?
Alessio Di Fonzo et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2018)
Informed consent and ethics committee approval in laboratory medicine
Ana Borovecki et al.
BIOCHEMIA MEDICA (2018)
Workload measurement for molecular genetics laboratory: A survey study
Enrico Tagliafico et al.
PLOS ONE (2018)
MDSGene: Closing Data Gaps in Genotype-Phenotype Correlations of Monogenic Parkinson's Disease
Christine Klein et al.
JOURNAL OF PARKINSONS DISEASE (2018)
Physician-Reported Benefits and Barriers to Clinical Implementation of Genomic Medicine: A Multi-Site IGNITE-Network Survey
Aniwaa Owusu Obeng et al.
JOURNAL OF PERSONALIZED MEDICINE (2018)
The value of genetic testing: beyond clinical utility
Barbara Lerner et al.
GENETICS IN MEDICINE (2017)
Neurology Individualized Medicine: When to Use Next-Generation Sequencing Panels
Christopher J. Klein et al.
MAYO CLINIC PROCEEDINGS (2017)
Molecular diagnostic experience of whole-exome sequencing in adult patients
Jennifer E. Posey et al.
GENETICS IN MEDICINE (2016)
Genetics of movement disorders in the next-generation sequencing era
Simone Olgiati et al.
MOVEMENT DISORDERS (2016)
Launching the movement disorders society genetic mutation database (MDSGene)
Christina M. Lill et al.
MOVEMENT DISORDERS (2016)
Next generation sequencing for neurological diseases: New hope or new hype?
M. J. Keogh et al.
CLINICAL NEUROLOGY AND NEUROSURGERY (2013)
A Comparison of Web-Based and Paper-Based Survey Methods Testing Assumptions of Survey Mode and Response Cost
Corey Greenlaw et al.
EVALUATION REVIEW (2009)