Micheli, Federico E
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Micheli, Federico E
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Micheli, Federico
Micheli, F E
Micheli, F E
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Results 1-4 of 4 (Search time: 0.002 seconds).
| Issue Date | Title | Author(s) | |
|---|---|---|---|
| 1 | Aug-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 |
| 2 | 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 |
| 3 | Sep-2011 | Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin America | Mata, Ignacio F ; Wilhoite, Greggory J ; Yearout, Dora ; Bacon, Justin A ; Cornejo-Olivas, Mario ; Mazzetti, Pilar ; Marca, Victoria ; Ortega, Olimpio ; Acosta, Oscar ; Cosentino, Carlos ; Torres, Luis ; Medina, Angel C ; Perez-Pastene, Carolina ; Díaz-Grez, Fernando ; Vilariño-Güell, Carles ; Venegas, Pablo ; Miranda, Marcelo ; Trujillo-Godoy, Osvaldo ; Layson, Luis ; Avello, Rodrigo ; Dieguez, Elena ; Raggio, Victor ; Micheli, Federico E ; Perandones, Claudia ; Alvarez, Victoria ; Segura-Aguilar, Juan ; Farrer, Matthew J ; Zabetian, Cyrus P ; Ross, Owen A |
| 4 | May-2014 | Mosaicism of alpha-synuclein gene rearrangements: report of two unrelated cases of early-onset parkinsonism | Perandones, Claudia ; Giugni, J C ; Calvo, D S ; Raina, G B ; De Jorge Lopez, L ; Volpini, V ; Zabetian, Cyrus P ; Mata, Ignacio F ; Caputo, Mariela ; Corach, Daniel ; Radrizzani, Martin ; Micheli, Federico E |