CAO, MICHELANGELO

CAO, MICHELANGELO  

Università di Padova  

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Risultati 1 - 4 di 4 (tempo di esecuzione: 0.008 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype 2016 BERTOLIN, CINZIAQUERIN, GIORGIABELLO, LUCACAO, MICHELANGELOERMANI, MARIOPEGORARO, ELENASORARU', GIANNIPENNUTO, MARIA + EUROPEAN JOURNAL OF NEUROLOGY - -
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations 2016 CAO, MICHELANGELODONA', MARTASEMPLICINI, CLAUDIOCASSINA, MATTEOSORARU', GIANNISTRAMARE, ROBERTOSALVIATI, LEONARDOPEGORARO, ELENA + NEUROGENETICS - -
Facio-scapulo-humeral dystrophy: clinical follow-up and role of chromosome X inactivation in female patients - SHP2: a novel therapeutic target in MuSK-myasthenia 2018 Cao, Michelangelo - - -
FSHD1 and FSHD2 form a disease continuum 2019 Cao, MichelangeloPegoraro, ElenaSalviati, Leonardo + NEUROLOGY - -