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Novel genes and novel pathogenetic mechanisms in adult‐onset primary dystonia

Petrucci, Simona; Valente, Enza Maria

Movement disorders. Volume 28:Issue 4 (2013); pp 440-440 -- John Wiley & Sons

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LRP10: A novel disease gene bridging Parkinson's disease and dementia with Lewy body

Morgante, Francesca; Valente, Enza Maria

Movement disorders. Volume 34:Issue 1 (2019); pp 47-47 -- John Wiley & Sons

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KMT2B: A new twist in dystonia genetics

Balint, Bettina; Valente, Enza Maria

Movement disorders. Volume 32:Issue 4 (2017); pp 529-529 -- John Wiley & Sons

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Pink1 in the limelight: multiple functions of an eclectic protein in human health and disease

Arena, Giuseppe; Valente, Enza Maria

Journal of pathology. VOL 241; NUMBER 2, ; 2017, 251-263 -- John Wiley & Sons, Ltd

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LRP10: A novel disease gene bridging Parkinson's disease and dementia with Lewy body

Morgante, Francesca; Valente, Enza Maria

Movement disorders. Volume 34:Number 1 (2019, January); pp 47-47 -- John Wiley & Sons

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Phenotypic spectrum of alpha-synuclein mutations: New insights from patients and cellular models

Petrucci, Simona; Ginevrino, Monia; Valente, Enza Maria

Parkinsonism & related disorders. Volume 22 (2016) Supplement 1; pp S16-S20 -- Elsevier

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Solving Mendelian Mysteries: The Non-coding Genome May Hold the Key

Valente, Enza Maria; Bhatia, Kailash P.

Cell. Volume 172:Number 5 (2018, February 22nd); pp 889-891

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Joubert syndrome: congenital cerebellar ataxia with the molar tooth

Romani, Marta; Micalizzi, Alessia; Valente, Enza Maria

The Lancet neurology. Volume 12:Issue 9 (2013); pp 894-905 -- Elsevier

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Motile and non�motile cilia in human pathology: from function to phenotypes

Mitchison, Hannah M; Valente, Enza Maria

Journal of pathology. VOL 241; NUMBER 2, ; 2017, 294-309 -- John Wiley & Sons, Ltd

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PAEDIATRIC NEUROLOGICAL DISORDERS WITH CEREBELLAR INVOLVEMENT DIAGNOSIS AND MANGEMENT

D Arrigo, Stefano; Riva, Daria; Valente, Enza Maria

Scienza riabilitativa -- A.I.FI. -- Volume: 18 1; (pages 23-26) -- 2016

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