CAO, MICHELANGELO

CAO, MICHELANGELO  

Università di Padova  

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Risultati 1 - 4 di 4 (tempo di esecuzione: 0.012 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
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 - -
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 - -