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I Mahjneh

Showing results (1-10 of 18) with videos related to

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European Journal of Neurology|April 18, 2007
Episodic muscle pain, stiffness, and weakness associated with tubular aggregates and myoedemaI Mahjneh, A Lamminen, H Tuominen
Acta Neurologica Scandinavica|September 12, 2001
Muscle CT in peripheral neuropathiesG Marconi, I Mahjneh, A Pizzi
Acta Neurologica Scandinavica|March 21, 2002
Familial carpal tunnel syndrome: a report of a Finnish familyI Mahjneh, A Saarinen, J Siivola
European Journal of Neurology|June 26, 2003
Pure quadriceps myopathy in two sistersI Mahjneh, H Somer, A Paetau, et al.
Neuromuscular Disorders : NMD|January 1, 1992
A large inbred Palestinian family with two forms of muscular dystrophyI Mahjneh, G Vannelli, K Bushby, et al.
Acta Neurologica Scandinavica|September 1, 1996
Limb-girdle muscular dystrophy: a follow-up study of 79 patientsI Mahjneh, K Bushby, A Pizzi, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutationsI Mahjneh, G Marconi, K Bushby, et al.
European Journal of Neurology|July 20, 2013
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1DS M Sandell, I Mahjneh, J Palmio, et al.
Neurology|July 9, 2003
A distinct phenotype of distal myopathy in a large Finnish familyI Mahjneh, H Haravuori, A Paetau, et al.
Human Molecular Genetics|March 1, 1994
A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2pR Bashir, T Strachan, S Keers, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
European Journal of Neurology|April 18, 2007
Episodic muscle pain, stiffness, and weakness associated with tubular aggregates and myoedemaI Mahjneh, A Lamminen, H Tuominen
Acta Neurologica Scandinavica|September 12, 2001
Muscle CT in peripheral neuropathiesG Marconi, I Mahjneh, A Pizzi
Acta Neurologica Scandinavica|March 21, 2002
Familial carpal tunnel syndrome: a report of a Finnish familyI Mahjneh, A Saarinen, J Siivola
European Journal of Neurology|June 26, 2003
Pure quadriceps myopathy in two sistersI Mahjneh, H Somer, A Paetau, et al.
Neuromuscular Disorders : NMD|January 1, 1992
A large inbred Palestinian family with two forms of muscular dystrophyI Mahjneh, G Vannelli, K Bushby, et al.
Acta Neurologica Scandinavica|September 1, 1996
Limb-girdle muscular dystrophy: a follow-up study of 79 patientsI Mahjneh, K Bushby, A Pizzi, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutationsI Mahjneh, G Marconi, K Bushby, et al.
European Journal of Neurology|July 20, 2013
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1DS M Sandell, I Mahjneh, J Palmio, et al.
Neurology|July 9, 2003
A distinct phenotype of distal myopathy in a large Finnish familyI Mahjneh, H Haravuori, A Paetau, et al.
Human Molecular Genetics|March 1, 1994
A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2pR Bashir, T Strachan, S Keers, et al.
Pageof 2