Pavlović S - Search Results

1

N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome.

Rakocević-Stojanović V, Milić-Rasić V, Perić S, Baets J, Timmerman V, Dierick I, Pavlović S, De Jonghe P. Rakocević-Stojanović V, et al. Among authors: pavlovic s. J Neurol Sci. 2010 Sep 15;296(1-2):107-9. doi: 10.1016/j.jns.2010.06.015. Epub 2010 Jul 3. J Neurol Sci. 2010. PMID: 20598714

2

[Antiphospholipid antibodies in a female patient with the Sneddon syndrome].

Rakocević-Stojanović V, Lavrnić D, Pavlović S, Apostolski S. Rakocević-Stojanović V, et al. Among authors: pavlovic s. Vojnosanit Pregl. 1998 Jul-Aug;55(4):435-8. Vojnosanit Pregl. 1998. PMID: 9769746 Serbian.

3

Pathohistological changes in endomyocardial biopsy specimens in patients with myotonic dystrophy.

Rakocević-Stojanović V, Pavlović S, Seferović P, Vasiljević J, Lavrnić D, Marinković Z, Apostolski S. Rakocević-Stojanović V, et al. Among authors: pavlovic s. Panminerva Med. 1999 Mar;41(1):27-30. Panminerva Med. 1999. PMID: 10230253 Clinical Trial.

4

Epidemiological and clinical characteristics of myasthenia gravis in Belgrade, Yugoslavia (1983-1992).

Lavrnić D, Jarebinski M, Rakocević-Stojanović V, Stević Z, Lavrnić S, Pavlović S, Trikić R, Tripković I, Nesković V, Apostolski S. Lavrnić D, et al. Among authors: pavlovic s. Acta Neurol Scand. 1999 Sep;100(3):168-74. doi: 10.1111/j.1600-0404.1999.tb00733.x. Acta Neurol Scand. 1999. PMID: 10478580

5

[Diagnostic problems in patients with myasthenia gravis].

Lavrnić D, Rakocević-Stojanović V, Tripković I, Pavlović S, Stević Z, Trikić R, Nesković V, Apostolski S. Lavrnić D, et al. Among authors: pavlovic s. Srp Arh Celok Lek. 2000 Jul-Aug;128(7-8):247-52. Srp Arh Celok Lek. 2000. PMID: 11089431 Serbian.

6

Myotonic dystrophy and cardiac disorders.

Rakocević-Stojanović V, Grujić M, Seferović P, Lavrnić D, Pavlovic S, Nesković V, Romac S, Apostolski S. Rakocević-Stojanović V, et al. Among authors: pavlovic s. Panminerva Med. 2000 Dec;42(4):257-61. Panminerva Med. 2000. PMID: 11294088

7

Hereditary neuropathy with liability to pressure palsies associated with central nervous system myelin lesions.

Dacković J, Rakocević-Stojanović V, Pavlović S, Zamurović N, Dragasević N, Romac S, Apostolski S. Dacković J, et al. Among authors: pavlovic s. Eur J Neurol. 2001 Nov;8(6):689-92. doi: 10.1046/j.1468-1331.2001.00306.x. Eur J Neurol. 2001. PMID: 11784354

8

Cyclosporine in the treatment of myasthenia gravis.

Lavrnic D, Vujic A, Rakocevic-Stojanovic V, Stevic Z, Basta I, Pavlovic S, Trikic R, Apostolski S. Lavrnic D, et al. Among authors: pavlovic s. Acta Neurol Scand. 2005 Apr;111(4):247-52. doi: 10.1111/j.1600-0404.2005.00378.x. Acta Neurol Scand. 2005. PMID: 15740576 Clinical Trial.

9

Arterial ischemic stroke in a child with beta-thalassemia trait and methylentetrahydrofolate reductase mutation.

Brankovic-Sreckovic V, Milic Rasic V, Djordjevic V, Kuzmanovic M, Pavlovic S. Brankovic-Sreckovic V, et al. Among authors: pavlovic s. J Child Neurol. 2007 Feb;22(2):208-10. doi: 10.1177/0883073807300306. J Child Neurol. 2007. PMID: 17621484

10

Cardiac autonomic nervous system in patients with myotonic dystrophy type 1.

Rakocević-Stojanović V, Milovanović B, Ivić N, Ille T, Marjanović I, Stević Z, Pavlović S, Lavrnić D. Rakocević-Stojanović V, et al. Among authors: pavlovic s. Acta Myol. 2007 Oct;26(2):112-4. Acta Myol. 2007. PMID: 18421899 Free PMC article.

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