Keckarević D - Search Results

1

Lafora disease: severe phenotype associated with homozygous deletion of the NHLRC1 gene.

Kecmanović M, Jović N, Cukić M, Keckarević-Marković M, Keckarević D, Stevanović G, Romac S. Kecmanović M, et al. Among authors: keckarevic markovic m, keckarevic d. J Neurol Sci. 2013 Feb 15;325(1-2):170-3. doi: 10.1016/j.jns.2012.12.006. Epub 2013 Jan 11. J Neurol Sci. 2013. PMID: 23317923 Review.

2

The status of SCA1, MJD/SCA3, FRDA, DRPLA and MD triplet containing genes in patients with Huntington disease and healthy controls.

Keckarevic D, Culjkovic B, Savic D, Stojkovic O, Kostic V, Vukosavic S, Romac S. Keckarevic D, et al. J Neurogenet. 2000 Dec;14(4):257-63. doi: 10.3109/01677060009084502. J Neurogenet. 2000. PMID: 11342385

3

250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1.

Savić D, Rakocvic-Stojanovic V, Keckarevic D, Culjkovic B, Stojkovic O, Mladenovic J, Todorovic S, Apostolski S, Romac S. Savić D, et al. Among authors: keckarevic d. Hum Mutat. 2002 Feb;19(2):131-9. doi: 10.1002/humu.10027. Hum Mutat. 2002. PMID: 11793472

4

Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?

Savić D, Topisirović I, Keckarević M, Keckarević D, Major T, Culjković B, Stojković O, Rakocević-Stojanović V, Mladenović J, Todorović S, Apostolski S, Romac S. Savić D, et al. Among authors: keckarevic m, keckarevic d. Psychiatr Genet. 2001 Dec;11(4):201-5. doi: 10.1097/00041444-200112000-00004. Psychiatr Genet. 2001. PMID: 11807410

5

Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia.

Topisirovic I, Dragasevic N, Savic D, Ristic A, Keckarevic M, Keckarevic D, Culjkovic B, Petrovic I, Romac S, Kostic VS. Topisirovic I, et al. Among authors: keckarevic m, keckarevic d. Clin Genet. 2002 Oct;62(4):321-4. doi: 10.1034/j.1399-0004.2002.620412.x. Clin Genet. 2002. PMID: 12372061

6

[Duchenne's and Becker's muscular dystrophy: analysis of phenotype-genotype correlation in 28 patients] ].

Keckarević M, Savić D, Culjković B, Zamurović N, Major T, Keckarević D, Todorović S, Romac S. Keckarević M, et al. Among authors: keckarevic d. Srp Arh Celok Lek. 2002 May-Jun;130(5-6):154-8. doi: 10.2298/sarh0206154k. Srp Arh Celok Lek. 2002. PMID: 12395434 Free article. Serbian.

7

Population data on 14 STR loci from population of Serbia and Montenegro (new and renewed data).

Keckarević D, Savić D, Keckarević M, Stevanović M, Tarasjev A, Culjković B, Darmati A, Vukosavić S, Romac S. Keckarević D, et al. Among authors: keckarevic m. Forensic Sci Int. 2005 Jul 16;151(2-3):315-6. doi: 10.1016/j.forsciint.2005.01.009. Forensic Sci Int. 2005. PMID: 15939169

8

Human Y-specific STR haplotypes in population of Serbia and Montenegro.

Stevanović M, Dobricić V, Keckarević D, Perović A, Savić-Pavićević D, Keckarević-Marković M, Jovanović A, Romac S. Stevanović M, et al. Among authors: keckarevic markovic m, keckarevic d. Forensic Sci Int. 2007 Sep 13;171(2-3):216-21. doi: 10.1016/j.forsciint.2006.05.038. Epub 2006 Jun 30. Forensic Sci Int. 2007. PMID: 16806776

9

Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro.

Sarić M, Zamurović Lj, Keckarević-Marković M, Keckarević D, Stevanović M, Savić-Pavićević D, Jović J, Romac S. Sarić M, et al. Among authors: keckarevic markovic m, keckarevic d. Clin Genet. 2006 Aug;70(2):170-2. doi: 10.1111/j.1399-0004.2006.00655.x. Clin Genet. 2006. PMID: 16879202 No abstract available.

10

Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history.

Savić D, Keckarević D, Branković-Srećković V, Apostolski S, Todorović S, Romac S. Savić D, et al. Among authors: keckarevic d. Int J Neurosci. 2006 Dec;116(12):1509-18. doi: 10.1080/00207450600553182. Int J Neurosci. 2006. PMID: 17145685

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