Results 101 to 110 of about 944 (117)
Some of the next articles are maybe not open access.

A novel compound heterozygous EPM2A mutation in a Chinese boy with Lafora disease

Neurological Sciences, 2020
Yujiao Fu, Xiaosu Yang, Bo Xiao
exaly  

Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease

Epilepsia, 2010
Gaëtan Lesca   +2 more
exaly  

Mutational spectrum of the EPM2A gene in progressive myoclonus epilepsy of Lafora: high degree of allelic heterogeneity and prevalence of deletions

European Journal of Human Genetics, 2000
Pilar Gómez-Garre   +2 more
exaly  

A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood

Seizure: the Journal of the British Epilepsy Association, 2017
Gozde Yesil   +2 more
exaly  

Epm2a suppresses tumor growth in an immunocompromised host by inhibiting Wnt signaling

Cancer Cell, 2006
Xincheng Zheng   +2 more
exaly  

Lafora progressive myoclonus epilepsy mutation database-EPM2A and NHLRC1 (EMP2B) genes

Human Mutation, 2005
Leonarda Ianzano   +2 more
exaly  

Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters

Clinical Neurology and Neurosurgery, 2003
Pasquale Striano   +2 more
exaly  

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