about
Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2.Intellectual ability in the duchenne muscular dystrophy and dystrophin gene mutation location.Quality of life in patients with myotonic dystrophy type 2.Genetic testing of individuals with pre-senile cataract identifies patients with myotonic dystrophy type 2.Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions.Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2.Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walking.Brain sonography insight into the midbrain in myotonic dystrophy type 2.Neuromyelitis Optica in a Patient from Family with both Myotonic Dystrophy Type 1 and 2.Repeat Interruptions Modify Age at Onset in Myotonic Dystrophy Type 1 by Stabilizing Expansions in Somatic CellsJoint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patientsMagnetic resonance imaging of leg muscles in patients with myotonic dystrophiesMyotonic Dystrophy Type 2 - Data from the Serbian Registry
P50
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P50
description
researcher ORCID ID = 0000-0002-8304-2067
@en
name
Jovan Pešović
@ast
Jovan Pešović
@en
Jovan Pešović
@es
Jovan Pešović
@nl
type
label
Jovan Pešović
@ast
Jovan Pešović
@en
Jovan Pešović
@es
Jovan Pešović
@nl
prefLabel
Jovan Pešović
@ast
Jovan Pešović
@en
Jovan Pešović
@es
Jovan Pešović
@nl
P1153
15725996300
P31
P496
0000-0002-8304-2067