José Leal Loureiro
Instituto de Ciências Biomédicas Abel Salazar
20 papers found
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Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia
Download from www.ncbi.nlm.nih.govPLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease
Download from academic.oup.comHereditary Ataxia and Spastic Paraplegia in Portugal
Download from archneur.jamanetwork.comAutosomal Dominant Spastic Paraplegias
Download from jamanetwork.comAlu elements mediate large SPG11 gene rearrangements: further spatacsin mutations.
Download from www.nature.comSPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
Download from www.researchgate.netAsian Origin for the Worldwide-Spread Mutational Event in Machado-Joseph Disease
Download from archneur.jamanetwork.comClinical Heterogeneity of Autosomal Recessive Spastic Paraplegias
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