Contents

Current Molecular Medicine, Volume 14 - Number 8

Editorial

Editorial (Thematic Issue: Neurology and Genetics: How Molecular Biology is Changing the Neurological Thoughts?)

, 14(8): 933

Michelangelo Mancuso


DOI: 10.2174/156652401408141013152207




Revised Genetic Classification of Limb Girdle Muscular Dystrophies

, 14(8): 934 - 943

F. Magri, S. Brajkovic, A. Govoni, R. Brusa and G.P. Comi


DOI: 10.2174/1566524014666141010130244




Adult-Onset Genetic Leukoencephalopathies. Focus on the More Recently Defined Forms

, 14(8): 944 - 958

I. Di Donato, S. Banchi, A. Federico and M.T. Dotti


DOI: 10.2174/1566524014666141010130545




Metabolic Ataxias in Adults

, 14(8): 959 - 970

A. Antenora, A. Filla, F.M. Santorelli, S. Peluso, F. Sacca and G. De Michele


DOI: 10.2174/1566524014666141010131213




Late-Onset Glycogen Storage Disease Type 2

, 14(8): 971 - 978

M. Filosto, M.S. Cotelli, V. Vielmi, A. Todeschini, F. Rinaldi, S. Rota, M. Scarpelli and A. Padovani


DOI: 10.2174/1566524014666141010131649




Common Genetic Conditions of Ischemic Stroke to Keep in Mind

, 14(8): 979 - 984

M. Mancuso, D. Orsucci, E. Caldarazzo Ienco, M. Brondi, C. Simoncini, A. Chiti, V. Montano, E. Terni, N. Giannini, G. Siciliano and U. Bonuccelli


DOI: 10.2174/1566524014666141010132258




Genetic Basis of Mitochondrial Optic Neuropathies

, 14(8): 985 - 992

A. Maresca, L. Caporali, D. Strobbe, C. Zanna, D. Malavolta, C. La Morgia, M.L. Valentino and V. Carelli


DOI: 10.2174/1566524014666141010132627




Genetics of Alzheimer's Disease and Frontotemporal Dementia

, 14(8): 993 - 1000

B. Nacmias, I. Piaceri, S. Bagnoli, A. Tedde, S. Piacentini and S. Sorbi


DOI: 10.2174/1566524014666141010152143




Mitochondrial Disorders in Adults

, 14(8): 1001 - 1008

A. Toscano and O. Musumeci


DOI: 10.2174/1566524014666141010152340




Charcot-Marie-Tooth Disease and Related Hereditary Neuropathies: From Gene Function to Associated Phenotypes

, 14(8): 1009 - 1033

D. Pareyson, P. Saveri and G. Piscosquito


DOI: 10.2174/1566524014666141010154205




Bridging Over the Troubled Heterogeneity of SPG-Related Pathologies: Mechanisms Unite What Genetics Divide

, 14(8): 1034 - 1042

A. Tessa, P.S. Denora, L. Racis, E. Storti, A. Orlacchio and F.M. Santorelli


DOI: 10.2174/1566524014666141010154526




Neuronal Ceroid Lipofuscinosis: The Increasing Spectrum of an Old Disease

, 14(8): 1043 - 1051

A. Simonati, F. Pezzini, F. Moro and F.M. Santorelli


DOI: 10.2174/1566524014666141010154913




Facioscapulohumeral Muscular Dystrophy: More Complex than it Appears

, 14(8): 1052 - 1068

G. Ricci, M. Zatz and R. Tupler


DOI: 10.2174/1566524014666141010155054




Mitochondrial Diseases in Childhood

, 14(8): 1069 - 1078

A. Ardissone, E. Lamantea, F. Invernizzi, M. Zeviani, S. Genitrini, I. Moroni and G. Uziel


DOI: 10.2174/1566524014666141010155317




Parkinson Disease Genetics: A "Continuum" from Mendelian to Multifactorial Inheritance

, 14(8): 1079 - 1088

S. Petrucci, F. Consoli and E.M. Valente


DOI: 10.2174/1566524014666141010155509




Amyotrophic Lateral Sclerosis: A Genetic Point of View

, 14(8): 1089 - 1101

C. Carlesi, E. Caldarazzo Ienco, M. Mancuso and G. Siciliano


DOI: 10.2174/1566524014666141010155822




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