Buscar por Autor Pellene, Luis A
Mostrando resultados 1 a 3 de 3
| Fecha de publicación | Título | Autor(es) |
|---|---|---|
| ago-2012 | A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2 | Perandones, Claudia ; Micheli, Federico E ; Pellene, Luis A ; Bayly, Marta A ; Berkovic, Samuel F ; Dibbens, Leanne M |
| jun-2013 | Analysis of D216H polymorphism in Argentinean patients with primary dystonia | Caputo, Mariela ; Irisarri, Maximiliano ; Perandones, Claudia ; Alechine, Evguenia ; Pellene, Luis A ; Roca, Claudia Uribe ; Micheli, Federico E ; Corach, Daniel |
| 30-jun-2015 | Letter to the Editor: Hypothesis: Somatic Mosaicism and Parkinson Disease | Perandones, Claudia ; Pellene, Luis A ; Giugni, J C ; Calvo, D S ; Raina, G B ; Cuevas, S M ; Mata, Ignacio F ; Zabetian, Cyrus P ; Caputo, Mariela ; Corach, Daniel ; Micheli, Federico E ; Radrizzani, Martin |