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I F de Coo

Showing results (11-20 of 18) with videos related to

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Annals of Neurology|July 1, 1997
Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalitiesM S van der Knaap, L M Smit, P G Barth, et al.
Journal of Medical Genetics|August 19, 2005
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephalyG Breedveld, I F de Coo, M H Lequin, et al.
Clinical Neuropathology|March 1, 1991
Canavan disease: neuromorphological and biochemical analysis of a brain biopsy specimenI F de Coo, F J Gabreëls, W O Renier, et al.
Neurology|January 27, 1998
A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesI F de Coo, E A Sistermans, I J de Wijs, et al.
Journal of Medical Genetics|July 7, 2009
The unfolding clinical spectrum of POLG mutationsM J Blok, B J van den Bosch, E Jongen, et al.
Mitochondrion|November 21, 2012
A multi-center comparison of diagnostic methods for the biochemical evaluation of suspected mitochondrial disordersR J T Rodenburg, G C Schoonderwoerd, V Tiranti, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
COL4A2 mutation associated with familial porencephaly and small-vessel diseaseElly Verbeek, Marije E C Meuwissen, Frans W Verheijen, et al.
European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM Snoeck, B G M van Engelen, B Küsters, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Annals of Neurology|July 1, 1997
Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalitiesM S van der Knaap, L M Smit, P G Barth, et al.
Journal of Medical Genetics|August 19, 2005
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephalyG Breedveld, I F de Coo, M H Lequin, et al.
Clinical Neuropathology|March 1, 1991
Canavan disease: neuromorphological and biochemical analysis of a brain biopsy specimenI F de Coo, F J Gabreëls, W O Renier, et al.
Neurology|January 27, 1998
A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesI F de Coo, E A Sistermans, I J de Wijs, et al.
Journal of Medical Genetics|July 7, 2009
The unfolding clinical spectrum of POLG mutationsM J Blok, B J van den Bosch, E Jongen, et al.
Mitochondrion|November 21, 2012
A multi-center comparison of diagnostic methods for the biochemical evaluation of suspected mitochondrial disordersR J T Rodenburg, G C Schoonderwoerd, V Tiranti, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
COL4A2 mutation associated with familial porencephaly and small-vessel diseaseElly Verbeek, Marije E C Meuwissen, Frans W Verheijen, et al.
European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM Snoeck, B G M van Engelen, B Küsters, et al.
Pageof 2