Publications by authors named "Tiina Suominen"

20Publications

Myasthenic congenital myopathy from recessive mutations at a single residue in Na1.4.

Neurology 2019 03 1;92(13):e1405-e1415. Epub 2019 Mar 1.

From the Departments of Physiology (N.E., M.Q., S.C.C.) and Neurology (P.B.S.), David Geffen School of Medicine at UCLA; Molecular and Cellular Integrative Physiology Program at UCLA (N.E., S.C.C.), Los Angeles, CA; Tampere Neuromuscular Center (J.P., T.S., B.U.), Tampere University and University Hospital, Finland; MRC Centre for Neuromuscular Diseases (M.S.C., M.G.H., R.M.), Department of Neuromuscular Disease, UCL Institute of Neurology, London, UK; Folkhälsan Genetic Institute (B.U.), Helsinki; and Neurology Department (B.U.), Vasa Central Hospital, Finland.

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March 2019

Differential isoform expression and selective muscle involvement in muscular dystrophies.

Am J Pathol 2015 Oct 9;185(10):2833-42. Epub 2015 Aug 9.

Neuromuscular Research Center, Tampere University Hospital and University of Tampere, Tampere, Finland; Department of Medical Genetics, Folkhälsan Institute of Genetics, Haartman Institute, University of Helsinki, Helsinki, Finland; Department of Neurology, Vaasa Central Hospital, Vaasa, Finland.

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October 2015

Camptocormia as presenting sign in myofibrillar myopathy.

Neuromuscul Disord 2012 Nov 28;22(11):987-9. Epub 2012 Jun 28.

Department of Neurology, CHU Nîmes, Hôpital Caremeau, Place du Pr Debré, 30029 Nîmes Cedex 4, France.

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November 2012

Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish family.

Neuromuscul Disord 2011 Aug;21(8):551-5

Neuromuscular Research Unit, Department of Neurology, University Hospital and University of Tampere, Finland.

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August 2011

A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patient.

J Neurol 2011 Jun 30;258(6):1157-63. Epub 2011 Jan 30.

Centre de Référence des Maladies Neuromusculaires Paris-Est, Institut de Myologie, Groupe Hospitalier Pitié-Salpêtrière, Assistance Publique des Hôpitaux de Paris, Paris, France.

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June 2011

Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibers.

Acta Neuropathol 2010 Apr 28;119(4):495-500. Epub 2010 Jan 28.

Department of Neurology, Neuromuscular Molecular Pathology, University of Tampere, Biokatu 10, Finn-Medi 3, 33520 Tampere, Finland.

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April 2010

The first Italian family with tibial muscular dystrophy caused by a novel titin mutation.

J Neurol 2010 Apr 13;257(4):575-9. Epub 2009 Nov 13.

Medical Genetics, Department Molecular Biology, University of Siena, Policlinico Le Scotte, viale Bracci 2, 53100, Siena, Italy.

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April 2010