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Neurogenetics
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March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
C Ben Hamida, L Cavalier, S Belal, et al.
Journal of the Neurological Sciences
|
January 15, 2009
Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients
M Tazir, L Ali-Pacha, A M'Zahem, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish population
E Monrós, J Cañizares, M D Moltó, et al.
Journal of Neurology
|
July 19, 2024
Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxia
C Marelli, F Ramond, C Vignal, et al.
BMC Genomics
|
August 19, 2016
The beagle dog MicroRNA tissue atlas: identifying translatable biomarkers of organ toxicity
Erik M Koenig, Craig Fisher, Hugues Bernard, et al.
Journal of Neurology
|
February 17, 2015
A novel autosomal dominant leukodystrophy with specific MRI pattern
A Corlobé, F Taithe, P Clavelou, et al.
European Radiology
|
May 6, 2026
Prenatal alcohol exposure affects placental degradation-a retrospective fetal MRI study
Marlene Stuempflen, Michael Weber, Patric Kienast, et al.
Experimental Neurology
|
June 7, 2016
Cutaneous tissue damage induces long-lasting nociceptive sensitization and regulation of cellular stress- and nerve injury-associated genes in sensory neurons
Kristofer K Rau, Caitlin E Hill, Benjamin J Harrison, et al.
Physical Review Letters
|
July 5, 2002
Fast electron transport in ultraintense laser pulse interaction with solid targets by rear-side self-radiation diagnostics
J J Santos, F Amiranoff, S D Baton, et al.
Physical Review Letters
|
October 13, 2007
Direct observation of strong ion coupling in laser-driven shock-compressed targets
A Ravasio, G Gregori, A Benuzzi-Mounaix, et al.
Page
of 59
Search research articles
Search
Showing results (461-470 of 586) with videos related to
Sort By:
Page
of 59
Neurogenetics
|
March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
C Ben Hamida, L Cavalier, S Belal, et al.
Journal of the Neurological Sciences
|
January 15, 2009
Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients
M Tazir, L Ali-Pacha, A M'Zahem, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish population
E Monrós, J Cañizares, M D Moltó, et al.
Journal of Neurology
|
July 19, 2024
Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxia
C Marelli, F Ramond, C Vignal, et al.
BMC Genomics
|
August 19, 2016
The beagle dog MicroRNA tissue atlas: identifying translatable biomarkers of organ toxicity
Erik M Koenig, Craig Fisher, Hugues Bernard, et al.
Journal of Neurology
|
February 17, 2015
A novel autosomal dominant leukodystrophy with specific MRI pattern
A Corlobé, F Taithe, P Clavelou, et al.
European Radiology
|
May 6, 2026
Prenatal alcohol exposure affects placental degradation-a retrospective fetal MRI study
Marlene Stuempflen, Michael Weber, Patric Kienast, et al.
Experimental Neurology
|
June 7, 2016
Cutaneous tissue damage induces long-lasting nociceptive sensitization and regulation of cellular stress- and nerve injury-associated genes in sensory neurons
Kristofer K Rau, Caitlin E Hill, Benjamin J Harrison, et al.
Physical Review Letters
|
July 5, 2002
Fast electron transport in ultraintense laser pulse interaction with solid targets by rear-side self-radiation diagnostics
J J Santos, F Amiranoff, S D Baton, et al.
Physical Review Letters
|
October 13, 2007
Direct observation of strong ion coupling in laser-driven shock-compressed targets
A Ravasio, G Gregori, A Benuzzi-Mounaix, et al.
Page
of 59