Lalic T - Search Results

1

White SJ, Aartsma-Rus A, Flanigan KM, Weiss RB, Kneppers AL, Lalic T, Janson AA, Ginjaar HB, Breuning MH, den Dunnen JT. White SJ, et al. Among authors: lalic t. Hum Mutat. 2006 Sep;27(9):938-45. doi: 10.1002/humu.20367. Hum Mutat. 2006. PMID: 16917894

2

Deletion and duplication screening in the DMD gene using MLPA.

Lalic T, Vossen RH, Coffa J, Schouten JP, Guc-Scekic M, Radivojevic D, Djurisic M, Breuning MH, White SJ, den Dunnen JT. Lalic T, et al. Eur J Hum Genet. 2005 Nov;13(11):1231-4. doi: 10.1038/sj.ejhg.5201465. Eur J Hum Genet. 2005. PMID: 16030524

3

[Deletions in the dystrophin gene and its phenotype expression].

Lalić T, Guć-Sćekić M, Djurisić M, Radivojević D, Zamurović D, Todorović S. Lalić T, et al. Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:3-5. Srp Arh Celok Lek. 2001. PMID: 15637982 Serbian.

4

Lower incidence of deletions in the survival of motor neuron gene and the neuronal apoptosis inhibitory protein gene in children with spinal muscular atrophy from Serbia.

Miskovic M, Lalic T, Radivojevic D, Cirkovic S, Vlahovic G, Zamurovic D, Guc-Scekic M. Miskovic M, et al. Among authors: lalic t. Tohoku J Exp Med. 2011 Nov;225(3):153-9. doi: 10.1620/tjem.225.153. Tohoku J Exp Med. 2011. PMID: 21971302 Free article.

5

Spectrum of cystic fibrosis mutations in Serbia and Montenegro and strategy for prenatal diagnosis.

Radivojevic D, Djurisic M, Lalic T, Guc-Scekic M, Savic J, Minic P, Antoniadi T, Tzetis M, Kanavakis E. Radivojevic D, et al. Among authors: lalic t. Genet Test. 2004 Fall;8(3):276-80. doi: 10.1089/gte.2004.8.276. Genet Test. 2004. PMID: 15727251

6

Newborn screening for cystic fibrosis in Serbia: a pilot study.

Radivojevic D, Sovtic A, Minic P, Grkovic S, Guc-Scekic M, Lalic T, Miskovic M. Radivojevic D, et al. Among authors: lalic t. Pediatr Int. 2013 Apr;55(2):181-4. doi: 10.1111/ped.12009. Epub 2013 Feb 27. Pediatr Int. 2013. PMID: 23163630

7

Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from Serbia.

Miskovic M, Lalic T, Radivojevic D, Cirkovic S, Ostojic S, Guc-Scekic M. Miskovic M, et al. Among authors: lalic t. Int J Gynaecol Obstet. 2014 Jan;124(1):55-8. doi: 10.1016/j.ijgo.2013.07.025. Epub 2013 Oct 5. Int J Gynaecol Obstet. 2014. PMID: 24144239

8

[Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].

Radivojević D, Guć-Sćekić M, Djurisić M, Lalić T, Minić P, Kanavakis E. Radivojević D, et al. Among authors: lalic t. Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:6-9. Srp Arh Celok Lek. 2001. PMID: 15637983 Serbian.

9

Complex small supernumerary marker chromosomes - an update.

Liehr T, Cirkovic S, Lalic T, Guc-Scekic M, de Almeida C, Weimer J, Iourov I, Melaragno MI, Guilherme RS, Stefanou EG, Aktas D, Kreskowski K, Klein E, Ziegler M, Kosyakova N, Volleth M, Hamid AB. Liehr T, et al. Among authors: lalic t. Mol Cytogenet. 2013 Oct 31;6:46. doi: 10.1186/1755-8166-6-46. eCollection 2013. Mol Cytogenet. 2013. PMID: 24171835 Free PMC article.

10

The improvement in diagnosis and epilepsy managing in children with progressive myoclonus epilepsy during the last decade - A tertiary center experience in cohort of 51 patients.

Kravljanac R, Vucetic Tadic B, Djordjevic M, Lalic T, Kravljanac D, Cerovic I. Kravljanac R, et al. Among authors: lalic t. Epilepsy Behav. 2020 Dec;113:107456. doi: 10.1016/j.yebeh.2020.107456. Epub 2020 Nov 2. Epilepsy Behav. 2020. PMID: 33142201

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