Kristin Orstavik

Nydalen, Norway

Last Updated: 09/26/2026

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Found 57 publications

Exploring the experiences of physical activity in people with Charcot-Marie-Tooth disease: a qualitative study.

Exploring the experiences of physical activity in people with Charcot-Marie-Tooth disease: a qualitative study.

Journal: Disability and rehabilitation
Published: April 30, 2026

The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway - A Description of Demographic, Medical, and Neurological Findings.

The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway - A Description of Demographic, Medical, and Neurological Findings.

Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: January 21, 2026

Living and coping with adult-onset myotonic dystrophy type 1 from the perspectives of caregivers.

Living and coping with adult-onset myotonic dystrophy type 1 from the perspectives of caregivers.

Journal: Disability and rehabilitation
Published: August 22, 2025

Psychometric Properties of MFM32 in Myotonic Dystrophy Type 1.

Psychometric Properties of MFM32 in Myotonic Dystrophy Type 1.

Journal: Archives of physical medicine and rehabilitation
Published: June 16, 2025

Exploring self-management of diet and physical activity in CACNA1S-related hypokalemic periodic paralysis: A qualitative interview study.

Exploring self-management of diet and physical activity in CACNA1S-related hypokalemic periodic paralysis: A qualitative interview study.

Journal: Journal of neuromuscular diseases
Published: May 21, 2025

Gastrointestinal symptoms in adults with Fabry disease and their associations with physical and mental health.

Gastrointestinal symptoms in adults with Fabry disease and their associations with physical and mental health.

Journal: BMC gastroenterology
Published: May 19, 2025

Rehabilitation technology in assessment and treatment of arm and hand function in myotonic dystrophy type 1: A single subject experimental design study.

Rehabilitation technology in assessment and treatment of arm and hand function in myotonic dystrophy type 1: A single subject experimental design study.

Journal: Journal of neuromuscular diseases
Published: February 20, 2025

Type 1 spinal muscular atrophy treated with nusinersen in Norway, a five-year follow-up.

Type 1 spinal muscular atrophy treated with nusinersen in Norway, a five-year follow-up.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: July 04, 2024

Correction: Myotonic dystrophy type 1 – a multiorgan disorder

Correction: Myotonic dystrophy type 1 – a multiorgan disorder

Journal: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke
Published: May 13, 2024

Myotonic dystrophy type 1 - a multiorgan disorder.

Myotonic dystrophy type 1 - a multiorgan disorder.

Journal: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke
Published: April 23, 2024

Small and large fiber neuropathy in adults with myotonic dystrophy type 1.

Small and large fiber neuropathy in adults with myotonic dystrophy type 1.

Journal: Frontiers in neurology
Published: January 23, 2024

Multidisciplinary management and care in rare neuromuscular disorders: A call for action.

Multidisciplinary management and care in rare neuromuscular disorders: A call for action.

Journal: European journal of neurology
Published: November 20, 2023
Showing 1-12 of 57

Last Updated: 09/26/2026