Publications by authors named "Mayke Oosterloo"

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The clinical phenotype of carriers of intermediate alleles in the huntingtin gene: A scoping review.
Anna van Hofslot, Mayke Oosterloo, Joost J A de Jong, Ruben L Andriessen, Susanne T de Bot

J Huntingtons Dis· December 2025

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Navigating Life With Parkinson's Disease: A Focus Group Study on Coping Strategies and Considerations for Self-Management Support.
Maud M J Daemen, Bouke A A G De Bruijn-Heijligers, Colin Van Der Heijden, Lizzy M M Boots, Mayke Oosterloo

J Adv Nurs· April 2025

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Improving the Clinical Diagnostic Criteria for Genetically Confirmed Adult-Onset Huntington Disease: Considering Nonmotor Presentations.
Ciaran M Considine, Clare M Eddy, Samuel A Frank, Sandra K Kostyk, Mayke Oosterloo

Neurol Clin Pract· April 2025

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Pharmacological Treatment of Neuropsychiatric Symptoms in Huntington's Disease: A Systematic Review.
Ruben L Andriessen, Mayke Oosterloo, Jory Molema, Maud M J Daemen, David E J Linden

Mov Disord Clin Pract· April 2025

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Through their eyes: A retrospective mixed-methods study on the experiences and support needs of children growing up with a parent with Huntington's disease.
Maud Mj Daemen, Annelien A Duits, Lucienne B van der Meer, Ruben L Andriessen, Ruth B Veenhuizen, Mayke Oosterloo

J Huntingtons Dis· February 2025

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Evaluating the web-based 'Partner in Balance' program for informal caregivers of people with Huntington's disease: A pilot study.
Maud M J Daemen, Lizzy M M Boots, Mayke Oosterloo, Marjolein E de Vugt, Annelien A Duits

Internet Interv· December 2024

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Quality of care through the eyes of residents with Huntington's disease living in a nursing home: A qualitative explorative study.
Joyce Cf Heffels, Mayke Oosterloo, Bram de Boer, Raymund Ac Roos, Jos Mga Schols

J Huntingtons Dis· November 2024

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Preferences for genetic interventions for SCA and Huntington's disease: results of a discrete choice experiment among patients.
Nienke J H van Os, Mayke Oosterloo, Janneke P C Grutters, Brigitte A B Essers, Bart P C van de Warrenburg

Orphanet J Rare Dis· October 2024

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Genetic Interventions for Spinocerebellar Ataxia and Huntington's Disease: A Qualitative Study of the Patient Perspective.
Nienke J H van Os, Mayke Oosterloo, Brigitte A B Essers, Janneke P C Grutters, Bart P C van de Warrenburg

J Huntingtons Dis· September 2024

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A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder.
Teije H van Prooije, Maartje Pennings, Lucille Dorresteijn, Thatjana Gardeitchik, Vincent J J Odekerken, Mayke Oosterloo

Mov Disord· September 2024

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Clinical Review of Juvenile Huntington's Disease.
Mayke Oosterloo, Alexiane Touze, Lauren M Byrne, Jannis Achenbach, Hande Aksoy

J Huntingtons Dis· July 2024

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High Levels of Mutant Huntingtin Protein in Tear Fluid From Huntington's Disease Gene Expansion Carriers.
Marlies Gijs, Nynke Jorna, Nicole Datson, Chantal Beekman, Cira Dansokho, Mayke Oosterloo

J Mov Disord· April 2024

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Facilitators and barriers in caring for a person with Huntington's disease: input for a remote support program.
Maud M J Daemen, Lizzy M M Boots, Mayke Oosterloo, Marjolein E de Vugt, Annelien A Duits

Aging Ment Health· January 2024

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Dystonia in Pediatric Huntington's Disease; Prominent and Possibly Painful.
Marjolein M A Ketels, Oliver William Quarrell, Mayke Oosterloo

Mov Disord Clin Pract· October 2023

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Psychotropic medication use in Huntington's disease: A retrospective cohort study.
Ruben L Andriessen, Mayke Oosterloo, Angelique Hollands, David E J Linden, Bianca T A de Greef

Parkinsonism Relat Disord· December 2022

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The cross-sectional area of the vagus nerve is not reduced in Parkinson's disease patients.
Laura C J Sijben, Werner H Mess, Uwe Walter, A Miranda L Janssen, Mark L Kuijf, Mayke Oosterloo

eNeurologicalSci· June 2022

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Reader Response: Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease.
Thomas D Bird, Herwig Lange, Travis Cruickshank, Matthias Dose, Clare Eddy, Mayke Oosterloo

Neurology· March 2022

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Teaching Video NeuroImage: Improvement in Motor Development After Start of Levodopa in Tyrosine Hydroxylase Deficiency.
Etienne Janssen, Mayke Oosterloo, Estela Rubio-Gozalbo, Koen van Gassen, Joost Nicolai

Neurology· August 2021

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Disease Onset in Huntington's Disease: When Is the Conversion?
Mayke Oosterloo, Bianca T A de Greef, Emilia K Bijlsma, Alexandra Durr, Sarah J Tabrizi

Mov Disord Clin Pract· April 2021

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Predictive genetic testing in Huntington's disease: should a neurologist be involved?
Mayke Oosterloo, Emilia K Bijlsma, Corien C Verschuuren-Bemelmans, Meyke I Schouten, Christine de Die-Smulders

Eur J Hum Genet· September 2020

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De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability.
Iris G M Wijnen, Hermine E Veenstra-Knol, Fleur Vansenne, Erica H Gerkes, Tom de Koning, Mayke Oosterloo

Eur J Hum Genet· June 2020

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Obsessive-Compulsive and Perseverative Behaviors in Huntington's Disease.
Mayke Oosterloo, David Craufurd, Hanneke Nijsten, Erik van Duijn

J Huntingtons Dis· March 2020

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Diagnosing Juvenile Huntington's Disease: An Explorative Study among Caregivers of Affected Children.
Mayke Oosterloo, Emilia K Bijlsma, Christine de Die-Smulders, Raymund A C Roos

Brain Sci· March 2020

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Measuring the quality of care in nursing home residents with early-onset neurodegenerative diseases: a scoping review.
Joyce C F Heffels, Irma H J Everink, Mayke Oosterloo, Raymund A C Roos, Jos M G A Schols

BMC Palliat Care· February 2020

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Defining pediatric huntington disease: Time to abandon the term Juvenile Huntington Disease?
Oliver W J Quarrell, Martha A Nance, Peg Nopoulos, Ralf Reilmann, Mayke Oosterloo

Mov Disord· April 2019

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