Molecular Genetic Advances in Neurological DiseaseRANUM, Laura; LA SPADA, Al.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, 119 p., NSSerial Issue

Genetics of neurodegenerative diseases: insights from high-throughput resequencingTSUJI, Shoji.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R65-R70, NSArticle

A pivotal role for PINK1 and autophagy in mitochondrial quality control: implications for Parkinson diseaseCHU, Charleen T.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R28-R37, NSArticle

Molecular mechanisms of neurodegeneration in Alzheimer's diseaseCREWS, Leslie; MASLIAH, Eliezer.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R12-R20, NSArticle

Parkinson's disease: insights from pathwaysCOOKSON, Mark R; BANDMANN, Oliver.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R21-R27, NSArticle

Understanding the molecular mechanisms of Friedreich's ataxia to develop therapeutic approachesSCHMUCKER, Stéphane; PUCCIO, Hélène.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R103-R110, NSArticle

Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagyJU, Jeong-Sun; WEIHL, Conrad C.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R38-R45, NSArticle

Huntington's disease: progress toward effective disease-modifying treatments and a cureJOHNSON, Carl D; DAVIDSON, Beverly L.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R98-R102, NSArticle

Current status on Alzheimer disease molecular genetics: from past, to present, to futureBETTENS, Karolien; SLEEGERS, Kristel; VAN BROECKHOVEN, Christine et al.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R4-R11, NSArticle

Advances in understanding the molecular basis of FXTASGARCIA-AROCENA, Dolores; HAGERMAN, Paul J.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R83-R89, NSArticle

Partners in crime: bidirectional transcription in unstable microsatellite diseaseBATRA, Ranjan; CHARIZANIS, Konstantinos; SWANSON, Maurice S et al.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R77-R82, NSArticle

Pluripotent stem cells in neurodegenerative and neurodevelopmental diseasesMARCHETTO, Maria C. N; WINNER, Beate; GAGE, Fred H et al.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R71-R76, NSArticle

Spinal muscular atrophy: mechanisms and therapeutic strategiesLORSON, Christian L; RINDT, Hansjorg; SHABABI, Monir et al.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R111-R118, NSArticle

TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegenerationLAGIER-TOURENNE, Clotilde; POLYMENIDOU, Magdalini; CLEVELAND, Don W et al.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R46-R64, NSArticle

Molecular therapy in myotonic dystrophy: focus on RNA gain-of-functionMULDERS, Susan A. M; VAN ENGELEN, Baziel G. M; WIERINGA, Bé et al.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R90-R97, NSArticle