Sonja Strang-Karlsson

University of Helsinki

Finland

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Articles (7)

Year:

2025

Year:

2024

Year:

2023

Year:

2022

Year:

2021

Year:

2021

Year:

2020

Collaborators (3)

Tomasz Stokłosa

POLAND

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Hans Ehrencrona

Head of Clinical Genetics

Skåne University Hospital

SWEDEN

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Lauren Charlotte Phillips

University of Oxford

UNITED KINGDOM

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Sonja Strang-Karlsson

Research Interests

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Articles (7)

Nutritional status of patients with nemaline myopathy and related congenital myopathies in Finland: A pilot study

Genetic counselling legislation and practice in cancer in EU Member States

Self-reported functioning among patients with ultra-rare nemaline myopathy or a related disorder in Finland: a pilot study

Multi‐exon COL5A1 deletion in a child with classical Ehlers–Danlos syndrome: A case report expanding the allelic spectrum and showing evidence of parental gonosomal mosaicism

A novel MPLKIP-variant in three Finnish patients with non-photosensitive trichothiodystrophy type 4

Migraine in children and adults born preterm: A nationwide register linkage study

Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness.

Collaborators (3)

Tomasz Stokłosa

Hans Ehrencrona

Lauren Charlotte Phillips

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