Претрага
Резултати
A retrospective clinical study of the treatment of slow-channel congenital myasthenic syndrome [2012]
Chaouch, A; ...; Rakocevic-Stojanovic, Vidosava M; ...; (broj, koautora 16)The predictive value of anti-titin antibodies in patients with myasthenia gravis
[2006]
Lavrnić, Dragana Intravenous immunoglobulins therapy in two patients with myasthenia gravis and pemphigus vulgaris [2006]
Stojanović-Rakočević, Vidosava; Lavrnić, DraganaImpact of discontinuation and reintroduction of alglucoidase alpha in patients with late-onset Pompe disease
[2024]
Andrejić, Nikola; Virić, Vanja Novel mutations in the CHRNB1 gene in three patients affected by a congenital myasthenic syndrome [2006]
Mueller, Juliane S.; Hoellen, Friederike; Schara, Ulrike; Johannsen, J.; Bentele, K.; Rakočević-Stojanović, Vidosava; Milić-Rašić, Vedrana; Todorović, Slobodanka; Abicht, Angela; Lochmueller, HannsEosinophilic myositis as presenting symptom in gamma-sarcoglycanopathy [2009]
Baumeister, Sarah K.; Todorović, Slobodanka; Milić-Rašić, Vedrana; Dekomien, Gabriele; Lochmueller, Hanns; Walter, Maggie C.Amifampridine safety and efficacy in spinal muscular atrophy ambulatory patients: a randomized placebo-controlled, crossover, phase 2 trial
[2022]
Bonanno, Silvia; Giossi, Riccardo; Zanin, Riccardo; Porcelli, Valentina; Iannacone, Claudio; Baranello, Giovanni; Ingenito, Gary; Iyadurai, Stanley; Stević, Zorica D.
Maggi, Lorenzo;
156P Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma in clinically silent and childhood-onset SMA individuals from Serbia
[2024]
Brkušanin, M. Genetic heterogeneity of desmin-related myopathy with Mallory body-like inclusions [2005]
Parain, K.; Milić-Rašić, Vedrana; Cabello, A.; Chinchon, I.; Illa, I.; Guicheney, P.; Richard, P.; Bertini, E.; Ferreiro, A.Glucose and lipid metabolism disorders in children and adolescents with spinal muscular atrophy types 2 and 3
[2021]
Đorđević, Stefan A.; Milić-Rašić, Vedrana M. Филтери
По типу
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