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Journal Francais D'Ophtalmologie
|
February 24, 2007
[A novel mutation of the OPA1 gene responsible for isolated autosomal dominant optic atrophy in two brothers]
R Macarez, P Amati-Bonneau, X Burelle, et al.
Nature Genetics
|
February 1, 1995
An autosomal locus predisposing to deletions of mitochondrial DNA
A Suomalainen, J Kaukonen, P Amati, et al.
Revue Neurologique
|
November 9, 2010
[Hereditary optic atrophies]
C Scherer, V Procaccio, M Ferre, et al.
American Journal of Medical Genetics
|
September 24, 1999
Splenogonadal fusion limb defect syndrome: report of five new cases and review
D Bonneau, J Roume, M Gonzalez, et al.
Molecular and Cellular Probes
|
September 4, 1998
Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome gene
L Bisceglia, L d'Ambrosio, M R Piemontese, et al.
Oncogene
|
May 18, 1999
Medullary thyroid carcinomas in transgenic mice expressing a Polyoma carboxyl-terminal truncated middle-T and wild type small-T antigens
A Felici, M Giorgio, N Krauzewicz, et al.
Rivista Di Neurologia
|
July 1, 1991
[Expression of a defect in the respiratory chain in cultured human cells]
G Meola, G Rotondo, M Velicogna, et al.
American Journal of Human Genetics
|
December 1, 1990
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease
M Zeviani, N Bresolin, C Gellera, et al.
American Journal of Human Genetics
|
December 5, 1998
A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2
F Canzian, P Amati, H R Harach, et al.
Revue Neurologique
|
May 6, 2014
Perspectives of drug-based neuroprotection targeting mitochondria
V Procaccio, C Bris, J M Chao de la Barca, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 79) with videos related to
Sort By:
Page
of 8
Journal Francais D'Ophtalmologie
|
February 24, 2007
[A novel mutation of the OPA1 gene responsible for isolated autosomal dominant optic atrophy in two brothers]
R Macarez, P Amati-Bonneau, X Burelle, et al.
Nature Genetics
|
February 1, 1995
An autosomal locus predisposing to deletions of mitochondrial DNA
A Suomalainen, J Kaukonen, P Amati, et al.
Revue Neurologique
|
November 9, 2010
[Hereditary optic atrophies]
C Scherer, V Procaccio, M Ferre, et al.
American Journal of Medical Genetics
|
September 24, 1999
Splenogonadal fusion limb defect syndrome: report of five new cases and review
D Bonneau, J Roume, M Gonzalez, et al.
Molecular and Cellular Probes
|
September 4, 1998
Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome gene
L Bisceglia, L d'Ambrosio, M R Piemontese, et al.
Oncogene
|
May 18, 1999
Medullary thyroid carcinomas in transgenic mice expressing a Polyoma carboxyl-terminal truncated middle-T and wild type small-T antigens
A Felici, M Giorgio, N Krauzewicz, et al.
Rivista Di Neurologia
|
July 1, 1991
[Expression of a defect in the respiratory chain in cultured human cells]
G Meola, G Rotondo, M Velicogna, et al.
American Journal of Human Genetics
|
December 1, 1990
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease
M Zeviani, N Bresolin, C Gellera, et al.
American Journal of Human Genetics
|
December 5, 1998
A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2
F Canzian, P Amati, H R Harach, et al.
Revue Neurologique
|
May 6, 2014
Perspectives of drug-based neuroprotection targeting mitochondria
V Procaccio, C Bris, J M Chao de la Barca, et al.
Page
of 8