Search Results - "Pellene, Luis A."

A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2 by Perandones, Claudia, Micheli, Federico E., Pellene, Luis A., Bayly, Marta A., Berkovic, Samuel F., Dibbens, Leanne M.

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Holmes tremor: Clinical description, lesion localization, and treatment in a series of 29 cases by Raina, Gabriela B, Cersosimo, Maria G, Folgar, Silvia S, Giugni, Juan C, Calandra, Cristian, Paviolo, Juan P, Tkachuk, Veronica A, Zuñiga Ramirez, Carlos, Tschopp, Andrea L, Calvo, Daniela S, Pellene, Luis A, Uribe Roca, Marcela C, Velez, Miriam, Giannaula, Rolando J, Fernandez Pardal, Manuel M, Micheli, Federico E

“…OBJECTIVE:To describe the clinical features, etiology, findings from neuroimaging, and treatment results in a series of 29 patients with Holmes tremor (HT)…”
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Weight Loss in Parkinson’s Disease: The Relationship with Motor Symptoms and Disease Progression by Calandra, Cristian R., Micheli, Federico E., Pellene, Luis A., Raina, Gabriela B., Cersosimo, Maria Graciela, Maiola, Ricardo

“…Objectives. To determine the prevalence of weight loss (WL) in PD patients, its relationship to the severity of motor manifestations and appetite changes…”
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Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2 by Boot, Erik, Butcher, Nancy J, Udow, Sean, Marras, Connie, Mok, Kin Y, Kaneko, Satoshi, Barrett, Matthew J, Prontera, Paolo, Berman, Brian D, Masellis, Mario, Dufournet, Boris, Nguyen, Karine, Charles, Perrine, Mutez, Eugénie, Danaila, Teodor, Jacquette, Aurélia, Colin, Olivier, Drapier, Sophie, Borg, Michel, Fiksinski, Ania M, Vergaelen, Elfi, Swillen, Ann, Vogels, Annick, Plate, Annika, Perandones, Claudia, Gasser, Thomas, Clerinx, Kristien, Bourdain, Frédéric, Mills, Kelly, Williams, Nigel M, Wood, Nicholas W, Booij, Jan, Lang, Anthony E, Bassett, Anne S

“…OBJECTIVETo delineate the natural history, diagnosis, and treatment response of Parkinson disease (PD) in individuals with 22q11.2 deletion syndrome…”
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A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2 by Perandones, Claudia, Micheli, Federico E, Pellene, Luis A, Bayly, Marta A, Berkovic, Samuel F, Dibbens, Leanne M

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