Search research articles
Contact Us
Filters
Showing results (91-100 of 346) with videos related to
Page
of 35
Sort By:
Mitochondrion
|
August 27, 2005
Mitochondrial-DNA nucleotides G4298A and T10010C as pathogenic mutations: the confirmation in two new cases
Marco Crimi, Sara Galbiati, Monica Sciacco, et al.
Neuroscience Letters
|
June 1, 2005
The T-786C NOS3 polymorphism in Alzheimer's disease: association and influence on gene expression
Eliana Venturelli, Daniela Galimberti, Carlo Lovati, et al.
Frontiers in Neurology
|
August 30, 2017
Progressive Encephalomyelitis with Rigidity and Myoclonus Associated With Anti-GlyR Antibodies and Hodgkin's Lymphoma: A Case Report
Linda Borellini, Silvia Lanfranconi, Sara Bonato, et al.
Journal of Neurology
|
July 4, 2014
Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations
Rocco Liguori, Maria Pia Giannoccaro, Alessia Arnoldi, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society
|
December 24, 2019
Herpes Simplex virus type 2 myeloradiculitis with a pure motor presentation in a liver transplant recipient
Elena Abati, Delia Gagliardi, Daniele Velardo, et al.
Journal of Neurology
|
March 31, 2020
Mental health and coping strategies in families of children and young adults with muscular dystrophies
Alessandra Tesei, Maria Nobile, Paola Colombo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 11, 2017
Assessing mental health in boys with Duchenne muscular dystrophy: Emotional, behavioural and neurodevelopmental profile in an Italian clinical sample
Paola Colombo, Maria Nobile, Alessandra Tesei, et al.
European Neurology
|
July 5, 2012
Incontinence in late-onset Pompe disease: an underdiagnosed treatable condition
Gauthier Remiche, Anne-Geneviève Herbaut, Dario Ronchi, et al.
Molecular Neurobiology
|
August 29, 2020
Animal Models of CMT2A: State-of-art and Therapeutic Implications
Roberta De Gioia, Gaia Citterio, Elena Abati, et al.
Neurology
|
March 21, 2018
Clinical Reasoning: A 75-year-old man with parkinsonism, mood depression, and weight loss
Emanuele Frattini, Edoardo Monfrini, Giacomo Bitetto, et al.
Page
of 35
Search research articles
Search
Showing results (91-100 of 346) with videos related to
Sort By:
Page
of 35
Mitochondrion
|
August 27, 2005
Mitochondrial-DNA nucleotides G4298A and T10010C as pathogenic mutations: the confirmation in two new cases
Marco Crimi, Sara Galbiati, Monica Sciacco, et al.
Neuroscience Letters
|
June 1, 2005
The T-786C NOS3 polymorphism in Alzheimer's disease: association and influence on gene expression
Eliana Venturelli, Daniela Galimberti, Carlo Lovati, et al.
Frontiers in Neurology
|
August 30, 2017
Progressive Encephalomyelitis with Rigidity and Myoclonus Associated With Anti-GlyR Antibodies and Hodgkin's Lymphoma: A Case Report
Linda Borellini, Silvia Lanfranconi, Sara Bonato, et al.
Journal of Neurology
|
July 4, 2014
Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations
Rocco Liguori, Maria Pia Giannoccaro, Alessia Arnoldi, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society
|
December 24, 2019
Herpes Simplex virus type 2 myeloradiculitis with a pure motor presentation in a liver transplant recipient
Elena Abati, Delia Gagliardi, Daniele Velardo, et al.
Journal of Neurology
|
March 31, 2020
Mental health and coping strategies in families of children and young adults with muscular dystrophies
Alessandra Tesei, Maria Nobile, Paola Colombo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 11, 2017
Assessing mental health in boys with Duchenne muscular dystrophy: Emotional, behavioural and neurodevelopmental profile in an Italian clinical sample
Paola Colombo, Maria Nobile, Alessandra Tesei, et al.
European Neurology
|
July 5, 2012
Incontinence in late-onset Pompe disease: an underdiagnosed treatable condition
Gauthier Remiche, Anne-Geneviève Herbaut, Dario Ronchi, et al.
Molecular Neurobiology
|
August 29, 2020
Animal Models of CMT2A: State-of-art and Therapeutic Implications
Roberta De Gioia, Gaia Citterio, Elena Abati, et al.
Neurology
|
March 21, 2018
Clinical Reasoning: A 75-year-old man with parkinsonism, mood depression, and weight loss
Emanuele Frattini, Edoardo Monfrini, Giacomo Bitetto, et al.
Page
of 35