Search Result "Hereditary Spastic Paraparesis"
Combined Treatment Fkt-Botulinum Toxin Type A (Btx-A) in Patients with Strumpell-Lorrain Disease
Journal: Current Pharmaceutical Design
Volume: 22 Issue: 6 Year: 2016 Page: 758-763
Author(s): Marvulli Riccardo,Lopopolo Angela,Dantone Angela,Palmisano Vita,Lancioni Giulio,Fiore Pietroq,Ianieri Giancarlo,Megna Marisa
Bridging Over the Troubled Heterogeneity of SPG-Related Pathologies: Mechanisms Unite What Genetics Divide
Journal: Current Molecular Medicine
Volume: 14 Issue: 8 Year: 2014 Page: 1034-1042
Author(s): A. Tessa,P.S. Denora,L. Racis,E. Storti,A. Orlacchio,F.M. Santorelli
Charcot-Marie-Tooth Disease and Related Hereditary Neuropathies: From Gene Function to Associated Phenotypes
Journal: Current Molecular Medicine
Volume: 14 Issue: 8 Year: 2014 Page: 1009-1033
Author(s): D. Pareyson,P. Saveri,G. Piscosquito
Models of Hereditary Neurodegenerative, Neurological, and Psychiatric Diseases Based on Induced Pluripotent Stem Cell-Derived Neurons
Ebook: Frontiers in Stem Cell and Regenerative Medicine Research
Volume: 3 Year: 2017
Author(s): Sergey P. Medvedev,Suren M. Zakian
Doi: 10.2174/9781681082578117030005
Transforming Growth Factor-β Signaling in Motor Neuron Diseases
Journal: Current Molecular Medicine
Volume: 11 Issue: 1 Year: 2011 Page: 48-56
Author(s): M. Katsuno, H. Adachi, H. Banno, K. Suzuki, F. Tanaka, G. Sobue
Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA)
Journal: Current Neuropharmacology
Volume: 11 Issue: 1 Year: 2013 Page: 59-79
Author(s): Susanne A. Schneider,Petr Dusek,John Hardy,Ana Westenberger,Joseph Jankovic,Kailash P. Bhatia
Genetic Basis of Mitochondrial Optic Neuropathies
Journal: Current Molecular Medicine
Volume: 14 Issue: 8 Year: 2014 Page: 985-992
Author(s): A. Maresca,L. Caporali,D. Strobbe,C. Zanna,D. Malavolta,C. La Morgia,M.L. Valentino,V. Carelli
Metabolic Ataxias in Adults
Journal: Current Molecular Medicine
Volume: 14 Issue: 8 Year: 2014 Page: 959-970
Author(s): A. Antenora,A. Filla,F.M. Santorelli,S. Peluso,F. Sacca,G. De Michele
Molecular Chaperone Disorders: Defective Hsp60 in Neurodegeneration
Journal: Current Topics in Medicinal Chemistry
Volume: 12 Issue: 2 Year: 2012 Page: 2491-2503
Author(s): Peter Bross, Raffaella Magnoni, Anne Sigaard Bie
Updates on Pediatric Demyelinating Disorders
Ebook: Common Pediatric Diseases: an Updated Review
Volume: 1 Year: 2022
Author(s):
Doi: 10.2174/9789815039658122010011