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O Boespflug

Showing results (31-40 of 64) with videos related to

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Journal of Computer Assisted Tomography|December 23, 1999
Doppler ultrasonography of peripheral vascular disease: the potential for ultrasound contrast agentsJ M Correas, O Boespflug, K Hamida, et al.
International Surgery|July 1, 1981
Carotid artery surgery in patients over 70 years of ageA C Benhamou, E Kieffer, J F Tricot, et al.
AJNR. American Journal of Neuroradiology|April 27, 2019
<i>GJA1</i> Variants Cause Spastic Paraplegia Associated with Cerebral HypomyelinationL Saint-Val, T Courtin, P Charles, et al.
Nature Genetics|March 1, 1994
X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locusP Saugier-Veber, A Munnich, D Bonneau, et al.
Revista De Neurologia|December 10, 1999
[Early diagnosis of a serious form of Pelizaeus-Merzbacher's disease confirmed by molecular analysis of the gene for proto-lipoproteins]J López-Pisón, M Muñoz-Albillos, M Moros-Peña, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating DiseaseF Cailloux, F Gauthier-Barichard, C Mimault, et al.
Human Molecular Genetics|April 1, 1993
Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid geneD Pham-Dinh, O Boespflug-Tanguy, C Mimault, et al.
American Journal of Human Genetics|September 1, 1994
Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical GroupO Boespflug-Tanguy, C Mimault, J Melki, et al.
Journal Francais D'Ophtalmologie|March 27, 2002
[A familial case of chronic progressive external ophthalmoplegia associated with mitochondrial disease]M Patte, H Dalens, P Sole, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1991
Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipidD Pham-Dinh, J L Popot, O Boespflug-Tanguy, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Journal of Computer Assisted Tomography|December 23, 1999
Doppler ultrasonography of peripheral vascular disease: the potential for ultrasound contrast agentsJ M Correas, O Boespflug, K Hamida, et al.
International Surgery|July 1, 1981
Carotid artery surgery in patients over 70 years of ageA C Benhamou, E Kieffer, J F Tricot, et al.
AJNR. American Journal of Neuroradiology|April 27, 2019
<i>GJA1</i> Variants Cause Spastic Paraplegia Associated with Cerebral HypomyelinationL Saint-Val, T Courtin, P Charles, et al.
Nature Genetics|March 1, 1994
X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locusP Saugier-Veber, A Munnich, D Bonneau, et al.
Revista De Neurologia|December 10, 1999
[Early diagnosis of a serious form of Pelizaeus-Merzbacher's disease confirmed by molecular analysis of the gene for proto-lipoproteins]J López-Pisón, M Muñoz-Albillos, M Moros-Peña, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating DiseaseF Cailloux, F Gauthier-Barichard, C Mimault, et al.
Human Molecular Genetics|April 1, 1993
Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid geneD Pham-Dinh, O Boespflug-Tanguy, C Mimault, et al.
American Journal of Human Genetics|September 1, 1994
Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical GroupO Boespflug-Tanguy, C Mimault, J Melki, et al.
Journal Francais D'Ophtalmologie|March 27, 2002
[A familial case of chronic progressive external ophthalmoplegia associated with mitochondrial disease]M Patte, H Dalens, P Sole, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1991
Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipidD Pham-Dinh, J L Popot, O Boespflug-Tanguy, et al.
Pageof 7