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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.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.Military Medicine|November 3, 2005
Myotonias and army personnel: symptoms and effects on service fitnessJyrki P Mäkelä, Hannu SomerDuodecim; Laaketieteellinen Aikakauskirja|October 29, 2009
[Bent spine straightens up--a case of camptocormia]Ibrahim Mahjneh, Birgitta Edström, Gunilla SandströmNeuromuscular Disorders : NMD|August 14, 2012
DOK7 limb-girdle myasthenic syndrome mimicking congenital muscular dystrophyIbrahim Mahjneh, Hanns Lochmüller, Francesco Muntoni, et al.Conference Proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference|October 20, 2007
Human balance estimation using a wireless 3D acceleration sensor networkHeidi Similä, Jouni Kaartinen, Mikko Lindholm, et al.Journal of Neurology|May 28, 2004
Muscle computed tomography patterns in patients with the mitochondrial DNA mutation 3243A>GMikko Kärppä, Ibrahim Mahjneh, Ari Karttunen, 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.Journal of Neurology|July 12, 2002
Axial myopathy--an unrecognised entityIbrahim Mahjneh, G Marconi, A Paetau, et al.Nature Genetics|November 12, 2005
The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperoneAnna-Kaisa Anttonen, Ibrahim Mahjneh, Riikka H Hämäläinen, et al.Pageof 3