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Author Report for: Stevanin G

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    Title: Current Knowledge of Endolysosomal and Autophagy Defects in Hereditary Spastic Paraplegia
    Toupenet Marchesi L, Leblanc M, Stevanin G
    Ref: Cells, 10:, 2021 : PubMed

            

    Title: Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia
    Yahia A, Elsayed LEO, Valter R, Hamed AAA, Mohammed IN, Elseed MA, Salih MA, Esteves T, Auger N and Stevanin G <19 more author(s)>
    Ref: Front Neurol, 12:720201, 2021 : PubMed

            

    Title: Lipids in the Physiopathology of Hereditary Spastic Paraplegias
    Darios F, Mochel F, Stevanin G
    Ref: Front Neurosci, 14:74, 2020 : PubMed

            

    Title: Update on the Genetics of Spastic Paraplegias
    Boutry M, Morais S, Stevanin G
    Ref: Curr Neurol Neurosci Rep, 19:18, 2019 : PubMed

            

    Title: Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders
    Novarino G, Fenstermaker AG, Zaki MS, Hofree M, Silhavy JL, Heiberg AD, Abdellateef M, Rosti B, Scott E and Gleeson JG <42 more author(s)>
    Ref: Science, 343:506, 2014 : PubMed

            

    Title: Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance
    Finsterer J, Loscher W, Quasthoff S, Wanschitz J, Auer-Grumbach M, Stevanin G
    Ref: Journal of Neurology Sci, 318:1, 2012 : PubMed

            


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