Pretraga
Rezultati
Genotype-phenotype correlation in Friedreich's ataxia
[2017]
Kovačević, G.; Todorović, S.; Novaković, Ivana 
; Pavićević-Savić, D.; Milić-Rašić, Vedrana ; Svetel, Marina ; Dobričić, Valerija
Episodic ataxia associated with a de novo SCN2A mutation [2016]
Leach, Emma L.; van, Karnebeek Clara D.M.; Townsend, Katelin N.; Tarailo Graovac, Maja; Hukin, Juliette; Gibson, William T.
A family with paroxysmal nonkinesigenic dyskinesias (PNKD): Evidence of mitochondrial dysfunction [2015]
Ghezzi, Daniele; Canavese, Carlotta; Kovacevic, Gordana S ; Zamurovic, Dragan R; Barzaghi, Chiara; Giorgi, Carlotta; Zorzi, Giovanna; Zeviani, Massimo; Pinton, Paolo; Garavaglia, Barbara;
Nardocci, Nardo;
Electroencephalogram in unilateral multilobar polymicrogyria with nonconvulsive status epilepticus [2008]
Martinović, Žarko; Jović, Nebojša J.The usefulness of visual evoked potentials in the assessment of the pediatric multiple sclerosis
[2022]
Nikolić, Blažo ; Zaletel, Ivan ; Ivančević, Nikola ; Rovčanin, Branislav; Pepić, Ana; Samardžić, Janko ; Jančić, Jasna
Epileptic encephalopathy with bilateral continuous spike-waves during slow sleep in a child with vacuolating megalencephalic leukoencephalopathy [2007]
Jocić-Jakubi, Bosanka; Martinović, Žarko; Kozić, Duško
Provoked seizures at the onset of progressive disease contribute to diagnosis delay - A tertiary center experience in a cohort of 22 children with CLN2
[2022]
Kravljanac, Ružica ; Vučetić-Tadić, Biljana
A clinical diagnostic algorithm for early onset cerebellar ataxia [2019]
Brandsma, R; ...; Brankovic-Sreckovic, Vesna; ...; (broj, koautora 34)EFFECT OF BOTULINUM TOXIN TREATMENT IN CHILDREN WITH CEREBRAL PALSY, Eur J Ped Neurol
[2010]
Čolović, Hristina ; Dimitrijević Lidija; Lazić Lj; Marinković Olga
Leber hereditary optic neuropathy in the population of Serbia
[2014]
Jančić, Jasna ; Dejanović, Ivana; Samardžić, Janko ; Radovanović, Saša M. ; Pepić, Ana; Kosanović-Jaković, Natalija ; Ćetković, Mila ; Kostić, Vladimir S.
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