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H Pihko

Showing results (91-100 of 98) with videos related to

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Neurology|August 25, 2004
Five new cases of a recently described leukoencephalopathy with high brain lactateT Linnankivi, N Lundbom, T Autti, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB lociB Talim, A Ferreiro, B Cormand, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|April 1, 1996
Quality of life in early adolescence: a sixteen-dimensional health-related measure (16D)M Apajasalo, H Sintonen, C Holmberg, et al.
Muscle & Nerve|March 1, 2005
Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patientsP Hackman, V Juvonen, J Sarparanta, et al.
Journal of Medical Genetics|July 14, 2009
DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosisP Isohanni, T Linnankivi, J Buzkova, et al.
Neurology|September 1, 2006
Cerebroretinal microangiopathy with calcifications and cystsT Linnankivi, L Valanne, A Paetau, et al.
Neurology|March 2, 2011
POLG1 manifestations in childhoodP Isohanni, A H Hakonen, L Euro, et al.
Neurology|April 26, 2001
Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain diseaseB Cormand, H Pihko, M Bayés, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
Neurology|August 25, 2004
Five new cases of a recently described leukoencephalopathy with high brain lactateT Linnankivi, N Lundbom, T Autti, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB lociB Talim, A Ferreiro, B Cormand, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|April 1, 1996
Quality of life in early adolescence: a sixteen-dimensional health-related measure (16D)M Apajasalo, H Sintonen, C Holmberg, et al.
Muscle & Nerve|March 1, 2005
Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patientsP Hackman, V Juvonen, J Sarparanta, et al.
Journal of Medical Genetics|July 14, 2009
DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosisP Isohanni, T Linnankivi, J Buzkova, et al.
Neurology|September 1, 2006
Cerebroretinal microangiopathy with calcifications and cystsT Linnankivi, L Valanne, A Paetau, et al.
Neurology|March 2, 2011
POLG1 manifestations in childhoodP Isohanni, A H Hakonen, L Euro, et al.
Neurology|April 26, 2001
Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain diseaseB Cormand, H Pihko, M Bayés, et al.
Pageof 10