Adult‐onset very‐long‐chain acyl‐CoA dehydrogenase deficiency (VLCADD) von Fatehi, F., Okhovat, A. A., Nilipour, Y., Mroczek, M., Straub, V., Töpf, A., Palibrk, A., Peric, S., Rakocevic Stojanovic, V., Najmabadi, H., Nafissi, S.

Volltext

Electrophysiological findings in patients with low density lipoprotein receptor related protein 4 positive myasthenia gravis von Nikolic, A. V., Bojic, S. D., Rakocevic Stojanovic, V. M., Basta, I. Z., Lavrnic, D. V.

Volltext

High frequency of DQB105 and absolute absence of DRB113 in muscle-specific tyrosine kinase positive myasthenia gravis von Nikolic, A. V., Andric, Z. P., Simonovic, R. B., Rakocevic Stojanovic, V. M., Basta, I. Z., Bojic, S. D., Lavrnic, D. V.

Volltext

Cerebrospinal fluid biomarkers of neurodegeneration in patients with juvenile and classic myotonic dystrophy type 1 von Peric, S., Mandic-Stojmenovic, G., Markovic, I., Stefanova, E., Ilic, V., Parojcic, A., Misirlic-Dencic, S., Ostojic, M., Rakocevic-Stojanovic, V., Kostic, V.

Volltext

Rupture of the middle cerebral artery aneurysm as a presenting symptom of late-onset Pompe disease in an adult with a novel GAA gene mutation von Peric, S., Fumic, K., Bilic, K., Reuser, A., Rakocevic Stojanovic, V.

Volltext

Epidemiology of Charcot-Marie-Tooth Disease in the Population of Belgrade, Serbia von Mladenovic, J., Milic Rasic, V., Keckarevic Markovic, M., Romac, S., Todorovic, S., Rakocevic Stojanovic, V., Kisic Tepavcevic, D., Hofman, A., Pekmezovic, T.

Volltext

Prospective analysis of gait characteristics in chronic inflammatory demyelinating polyradiculoneuropathy von Bozovic, I., Peric, S., Basta, I., Rakocevic-Stojanovic, V., Lavrnic, D., Stevic, Z., Radovanovic, S.

Volltext

Survival and mortality of myotonic dystrophy type 1 (Steinert's disease) in the population of Belgrade von Mladenovic, J., Pekmezovic, T., Todorovic, S., Rakocevic-Stojanovic, V., Savic, D., Romac, S., Apostolski, S.

Volltext

Significant impact of behavioral and cognitive impairment on quality of life in patients with myotonic dystrophy type 1 von Rakocevic-Stojanovic, V, Peric, S, Madzarevic, R, Dobricic, V, Ralic, V, Ilic, V, Basta, I, Nikolic, A, Stefanova, E

Volltext

Influence of multisystemic affection on health-related quality of life in patients with myotonic dystrophy type 1 von Peric, S, Stojanovic, V. Rakocevic, Basta, I, Peric, M, Milicev, M, Pavlovic, S, Lavrnic, D

Volltext

Extrathymic malignancies in a defined cohort of patients with myasthenia gravis von Basta, I, Pekmezovic, T, Peric, S, Nikolic, A, Rakocevic-Stojanovic, V, Stevic, Z, Marjanovic, I, Lavrnic, D

Volltext

Brain sonography insight into the midbrain and basal ganglia in myotonic dystrophy type 2 von Rakocevic-Stojanovic, V, Peric, S, Savic-Pavicevic, D, Pesovic, J, Lavrnic, D, Jovanovic, Z, Pavlovic, A

Volltext

Epidemiological Study of Adult-Onset Myasthenia Gravis in the Area of Belgrade (Serbia) in the Period 1979–2008 von Lavrnic, D., Basta, I., Rakocevic-Stojanovic, V., Stevic, Z., Peric, S., Nikolic, A., Marjanovic, I., Pekmezovic, T.

Volltext

Cardiac autonomic control in patients with myasthenia gravis and thymoma von Peric, S, Rakocevic-Stojanovic, V, Nisic, T, Pavlovic, S, Basta, I, Popovic, S, Damjanovic, S, Lavrnic, D

Volltext

Neuroanatomical patterns of central nervous system involvement in myotonic dystrophy type 1 and clinical correlates von Agosta, F, Peric, S, Rakocevic-Stojanovic, V, Sarro, L, Kostic, V.S, Filippi, M

Volltext

Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations von Johnson, K, Bertoli, M, Phillips, L, Töpf, A, Claeys, K, Rakocevic Stojanovic, V, Perić, S, Vissing, J, Hahn, A, Maddison, P, Akay, E, Bastian, A, Łusakowska, A, Lek, M, Xu, L, MacArthur, D, Straub, V

Volltext

20.Prognostic value of cardiovascular autonomic control impairment for onset of respiratory insufficiency in patients with amyotrophic lateral sclerosis von Pavlovic, S, Milovanovic, B, Stevic, Z, Milicic, B, Rakocevic-Stojanovic, V, Lavrnic, D

Volltext

The predictive value of the presence of different antibodies and thymus pathology to the clinical outcome in patients with generalized myasthenia gravis von Nikolic, A, Djukic, P, Basta, I, Hajdukovic, Lj, Stojanovic, V. Rakocevic, Stevic, Z, Nikolic, D, Bozic, V, Lavrnic, S, Lavrnic, D

Volltext

Syndroma Brown-Séquard as a rare manifestation of von Hippel–/INS;Lindau disease von Marjanovic, I, Jecmenica-Lukic, M, Milicev, M, Peric, S, Basta, I, Stevic, Z, Rakocevic-Stojanovic, V, Lavrnic, S, Lavrnic, D

Volltext

Shorter CTG repeats length in an oligodendroglioma from a myotonic dystrophy type 1 patient von Rakocevic-Stojanovic, V., Peric, S., Ralic, V., Milicevic, M., Dobricic, V.

Volltext