Tiina Suominen

C-terminal extension of HSPB6 in a family with myopathy and cataract.

Journal: Human molecular genetics

Published: April 25, 2025

Myasthenic congenital myopathy from recessive mutations at a single residue in NaV1.4.

Journal: Neurology

Published: August 10, 2018

TIA1 variant drives myodegeneration in multisystem proteinopathy with SQSTM1 mutations.

Journal: The Journal of clinical investigation

Published: August 29, 2017

Homozygosity of the Dominant Myotilin c.179C>T (p.Ser60Phe) Mutation Causes a More Severe and Proximal Muscular Dystrophy.

Journal: Journal of neuromuscular diseases

Published: November 18, 2016

Distal myopathies in Finnish patients.

Journal: Duodecim; laaketieteellinen aikakauskirja

Published: January 01, 2016

Differential isoform expression and selective muscle involvement in muscular dystrophies.

Journal: The American journal of pathology

Published: July 15, 2014

The expanding spectrum of LGMD--recently discovered disease genes are important also in Finnish patients

Journal: Duodecim; laaketieteellinen aikakauskirja

Published: November 14, 2013

Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy.

Journal: Human mutation

Published: November 12, 2013

Atypical phenotypes in titinopathies explained by second titin mutations.

Journal: Annals of neurology

Published: October 22, 2013

New immunohistochemical method for improved myotonia and chloride channel mutation diagnostics.

Journal: Neurology

Published: November 16, 2012

TARDBP mutations are not a frequent cause of ALS in Finnish patients.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology

C-terminal extension of HSPB6 in a family with myopathy and cataract.

C-terminal extension of HSPB6 in a family with myopathy and cataract.

Myasthenic congenital myopathy from recessive mutations at a single residue in NaV1.4.

Myasthenic congenital myopathy from recessive mutations at a single residue in NaV1.4.

TIA1 variant drives myodegeneration in multisystem proteinopathy with SQSTM1 mutations.

TIA1 variant drives myodegeneration in multisystem proteinopathy with SQSTM1 mutations.

Homozygosity of the Dominant Myotilin c.179C>T (p.Ser60Phe) Mutation Causes a More Severe and Proximal Muscular Dystrophy.

Homozygosity of the Dominant Myotilin c.179C>T (p.Ser60Phe) Mutation Causes a More Severe and Proximal Muscular Dystrophy.

Distal myopathies in Finnish patients.

Distal myopathies in Finnish patients.

Differential isoform expression and selective muscle involvement in muscular dystrophies.

Differential isoform expression and selective muscle involvement in muscular dystrophies.

The expanding spectrum of LGMD--recently discovered disease genes are important also in Finnish patients

The expanding spectrum of LGMD--recently discovered disease genes are important also in Finnish patients

Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy.

Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy.

Atypical phenotypes in titinopathies explained by second titin mutations.

Atypical phenotypes in titinopathies explained by second titin mutations.

New immunohistochemical method for improved myotonia and chloride channel mutation diagnostics.

New immunohistochemical method for improved myotonia and chloride channel mutation diagnostics.

TARDBP mutations are not a frequent cause of ALS in Finnish patients.

TARDBP mutations are not a frequent cause of ALS in Finnish patients.

Camptocormia as presenting sign in myofibrillar myopathy.

Camptocormia as presenting sign in myofibrillar myopathy.