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Neuroscience
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June 10, 2008
Modulation of SIRT1 expression in different neurodegenerative models and human pathologies
M Pallàs, J G Pizarro, J Gutierrez-Cuesta, et al.
Redox Biology
|
August 17, 2025
Nuclear pore complex dysfunction drives TDP-43 pathology in ALS
O Ramírez-Núñez, S Rico-Ríos, P Torres, et al.
Human Molecular Genetics
|
April 23, 2013
Impaired mitochondrial oxidative phosphorylation in the peroxisomal disease X-linked adrenoleukodystrophy
J López-Erauskin, J Galino, M Ruiz, et al.
Human Molecular Genetics
|
April 20, 2001
Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment
N López-Bigas, M Olivé, R Rabionet, et al.
Journal of Neurology
|
June 14, 2019
Globular glial tauopathy caused by MAPT P301T mutation: clinical and neuropathological findings
M E Erro, M V Zelaya, M Mendioroz, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
September 10, 2014
Can total IgE/specific IgE ratio predict tolerance in cow's milk allergic children?
A Machinena-Spera, M T Giner-Muñoz, M Alvaro-Lozano, et al.
Cell Death and Differentiation
|
March 31, 2015
Activation of sirtuin 1 as therapy for the peroxisomal disease adrenoleukodystrophy
L Morató, M Ruiz, J Boada, et al.
Neuropathology and Applied Neurobiology
|
June 20, 2019
Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseases
F Llorens, A Villar-Piqué, M Schmitz, et al.
NMR in Biomedicine
|
August 27, 1998
Towards a method for automated classification of 1H MRS spectra from brain tumours
A R Tate, J R Griffiths, I Martínez-Pérez, et al.
Scientific Reports
|
November 17, 2017
Differential overexpression of SERPINA3 in human prion diseases
S Vanni, F Moda, M Zattoni, et al.
Page
of 65
Search research articles
Search
Showing results (601-610 of 642) with videos related to
Sort By:
Page
of 65
Neuroscience
|
June 10, 2008
Modulation of SIRT1 expression in different neurodegenerative models and human pathologies
M Pallàs, J G Pizarro, J Gutierrez-Cuesta, et al.
Redox Biology
|
August 17, 2025
Nuclear pore complex dysfunction drives TDP-43 pathology in ALS
O Ramírez-Núñez, S Rico-Ríos, P Torres, et al.
Human Molecular Genetics
|
April 23, 2013
Impaired mitochondrial oxidative phosphorylation in the peroxisomal disease X-linked adrenoleukodystrophy
J López-Erauskin, J Galino, M Ruiz, et al.
Human Molecular Genetics
|
April 20, 2001
Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment
N López-Bigas, M Olivé, R Rabionet, et al.
Journal of Neurology
|
June 14, 2019
Globular glial tauopathy caused by MAPT P301T mutation: clinical and neuropathological findings
M E Erro, M V Zelaya, M Mendioroz, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
September 10, 2014
Can total IgE/specific IgE ratio predict tolerance in cow's milk allergic children?
A Machinena-Spera, M T Giner-Muñoz, M Alvaro-Lozano, et al.
Cell Death and Differentiation
|
March 31, 2015
Activation of sirtuin 1 as therapy for the peroxisomal disease adrenoleukodystrophy
L Morató, M Ruiz, J Boada, et al.
Neuropathology and Applied Neurobiology
|
June 20, 2019
Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseases
F Llorens, A Villar-Piqué, M Schmitz, et al.
NMR in Biomedicine
|
August 27, 1998
Towards a method for automated classification of 1H MRS spectra from brain tumours
A R Tate, J R Griffiths, I Martínez-Pérez, et al.
Scientific Reports
|
November 17, 2017
Differential overexpression of SERPINA3 in human prion diseases
S Vanni, F Moda, M Zattoni, et al.
Page
of 65