Clinical and genetic study of a large SPG4 italian family with hereditary spastic paraplegia and early-onset familial Alzheimer’s disease

Autori: Lo Giudice T, Casella A, Mearini M, Montecchiani C, Miele M, Kawarai T, Orlacchio A.

Data: 2015

Ambito di interesse: Neurologia Alzheimer

Rivista: Alzheimer’s and dementia

Potrebbero interessarti anche:

Rivista 1.927

Human orf complicated with erythema multiforme. A neglected disease in Italian woman

Autori: Uccella I, Fabrizi P, Dell'uomo V, Casinelli K, Lunghi F

Data: 2019

Ambito di interesse: dermatologia infettivologica

Rivista: G Ital DermatolVenereol

Leggi dettagli

Rivista 14.03

Progressive Myoclonus Epilepsies: Diagnostic Yield With Next-Generation Sequencing in Previously Unsolved Cases

Autori: Canafoglia L, Franceschetti S, Gambardella A, Striano P, Giallonardo AT, Tinuper P, Di Bonaventura C, Michelucci R, Ferlazzo E, Granata T, Magaudda A, Licchetta L, Filla A, La Neve A, Riguzzi P, Cantisani TA, Fanella M, Castellotti B, Gellera C, Bahlo M, Zara F, Courage C, Lehesjoki AE, Oliver KL, Berkovic SF

Data: 2021

Ambito di interesse: Epilessia

Rivista: Neurol Genet. 2021 Nov 12;7(6):e641

Leggi dettagli

Rivista 9.473

Oral fingolimod rescues the functional deficits of synapses in experimental autoimmune encephalomyelitis.

Autori: Rossi S*, Lo Giudice T*, De Chiara V, Musella A, Studer V, Motta C, Bernardi G, Martino G, Furlan R, Martorana A, Centonze D.

Data: 2012

Ambito di interesse: Neurologia SM

Rivista: British Journal of Pharmacology

Leggi dettagli

Clinical and genetic study of a large SPG4 italian family with hereditary spastic paraplegia and early-onset familial Alzheimer’s disease

Potrebbero interessarti anche:

Human orf complicated with erythema multiforme. A neglected disease in Italian woman

Progressive Myoclonus Epilepsies: Diagnostic Yield With Next-Generation Sequencing in Previously Unsolved Cases

Oral fingolimod rescues the functional deficits of synapses in experimental autoimmune encephalomyelitis.

Cosa fare per