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Hannu Somer

Showing results (1-10 of 14) with videos related to

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Duodecim; Laaketieteellinen Aikakauskirja|October 10, 2002
[Axial myopathy--an unrecognized back disease]Ibrahim Mahjneh, Hannu Somer
Military Medicine|November 3, 2005
Myotonias and army personnel: symptoms and effects on service fitnessJyrki P Mäkelä, Hannu Somer
Duodecim; Laaketieteellinen Aikakauskirja|September 26, 2002
[Hyperkalemic periodic paralysis]Riitta Pirilä, Saara Lehmus, Hannu Somer, et al.
Clinical Physiology and Functional Imaging|April 2, 2004
Abnormal blood lactate accumulation after exercise in patients with multiple mitochondrial DNA deletions and minor muscular symptomsHarri Lindholm, Mervi Löfberg, Hannu Somer, et al.
Neuromuscular Disorders : NMD|July 16, 2002
Welander distal myopathy outside the Swedish population: phenotype and genotypeDésirée von Tell, Hannu Somer, Bjarne Udd, et al.
Journal of Neuropathology and Experimental Neurology|June 20, 2002
Neuromuscular pathology in hereditary gelsolin amyloidosisSari Kiuru-Enari, Hannu Somer, Anna-Maria Seppäläinen, et al.
Journal of Neurology|September 10, 2005
Myopathy is a prominent feature in Marinesco-Sjögren syndrome: A muscle computed tomography studyIbrahim Mahjneh, Anna-Kaisa Anttonen, Mirja Somer, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 27, 2009
Severe ataxia with neuropathy in hereditary gelsolin amyloidosisMaarit Tanskanen, Anders Paetau, Oili Salonen, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 25, 2007
Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: a case reportMaarit Tanskanen, Anders Paetau, Oili Salonen, et al.
Neuromuscular Disorders : NMD|March 24, 2004
Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3)Henna Haravuori, H Annika Siitonen, Ibrahim Mahjneh, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Duodecim; Laaketieteellinen Aikakauskirja|October 10, 2002
[Axial myopathy--an unrecognized back disease]Ibrahim Mahjneh, Hannu Somer
Military Medicine|November 3, 2005
Myotonias and army personnel: symptoms and effects on service fitnessJyrki P Mäkelä, Hannu Somer
Duodecim; Laaketieteellinen Aikakauskirja|September 26, 2002
[Hyperkalemic periodic paralysis]Riitta Pirilä, Saara Lehmus, Hannu Somer, et al.
Clinical Physiology and Functional Imaging|April 2, 2004
Abnormal blood lactate accumulation after exercise in patients with multiple mitochondrial DNA deletions and minor muscular symptomsHarri Lindholm, Mervi Löfberg, Hannu Somer, et al.
Neuromuscular Disorders : NMD|July 16, 2002
Welander distal myopathy outside the Swedish population: phenotype and genotypeDésirée von Tell, Hannu Somer, Bjarne Udd, et al.
Journal of Neuropathology and Experimental Neurology|June 20, 2002
Neuromuscular pathology in hereditary gelsolin amyloidosisSari Kiuru-Enari, Hannu Somer, Anna-Maria Seppäläinen, et al.
Journal of Neurology|September 10, 2005
Myopathy is a prominent feature in Marinesco-Sjögren syndrome: A muscle computed tomography studyIbrahim Mahjneh, Anna-Kaisa Anttonen, Mirja Somer, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 27, 2009
Severe ataxia with neuropathy in hereditary gelsolin amyloidosisMaarit Tanskanen, Anders Paetau, Oili Salonen, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 25, 2007
Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: a case reportMaarit Tanskanen, Anders Paetau, Oili Salonen, et al.
Neuromuscular Disorders : NMD|March 24, 2004
Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3)Henna Haravuori, H Annika Siitonen, Ibrahim Mahjneh, et al.
Pageof 2