Kahre T - Search Results

1

Descriptive epidemiology of spinal muscular atrophy type I in Estonia.

Vaidla E, Talvik I, Kulla A, Kahre T, Hamarik M, Napa A, Metsvaht T, Piirsoo A, Talvik T. Vaidla E, et al. Among authors: kahre t. Neuroepidemiology. 2006;27(3):164-8. doi: 10.1159/000096128. Neuroepidemiology. 2006. PMID: 17035693

2

A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia.

Talkop UA, Kahre T, Napa A, Talvik I, Sööt A, Piirsoo A, Sander V, Talvik T. Talkop UA, et al. Among authors: kahre t. Eur J Paediatr Neurol. 2003;7(5):221-6. doi: 10.1016/s1090-3798(03)00077-1. Eur J Paediatr Neurol. 2003. PMID: 14511626

3

Prevalence of Angelman syndrome and Prader-Willi syndrome in Estonian children: sister syndromes not equally represented.

Oiglane-Shlik E, Talvik T, Zordania R, Põder H, Kahre T, Raukas E, Ilus T, Tasa G, Bartsch O, Väisänen ML, Ounap K. Oiglane-Shlik E, et al. Among authors: kahre t. Am J Med Genet A. 2006 Sep 15;140(18):1936-43. doi: 10.1002/ajmg.a.31423. Am J Med Genet A. 2006. PMID: 16906556

4

Aortic arch thrombosis in a neonate with heterozygous carrier status of factor V Leiden mutation.

Metsvaht T, Hermlin T, Kern H, Kahre T, Starkopf J. Metsvaht T, et al. Among authors: kahre t. Congenit Heart Dis. 2006 Jan;1(1-2):40-5. doi: 10.1111/j.1747-0803.2006.00007.x. Congenit Heart Dis. 2006. PMID: 18373789 Review.

5

Factor V Leiden and prothrombin 20210G>A [corrected] mutation and paediatric ischaemic stroke: a case-control study and two meta-analyses.

Laugesaar R, Kahre T, Kolk A, Uustalu U, Kool P, Talvik T. Laugesaar R, et al. Among authors: kahre t. Acta Paediatr. 2010 Aug;99(8):1168-74. doi: 10.1111/j.1651-2227.2010.01784.x. Epub 2010 Mar 2. Acta Paediatr. 2010. PMID: 20337781

6

Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome.

Zilina O, Kahre T, Talvik I, Oiglane-Shlik E, Tillmann V, Ounap K. Zilina O, et al. Among authors: kahre t. Eur J Med Genet. 2014 May-Jun;57(6):279-83. doi: 10.1016/j.ejmg.2014.03.007. Epub 2014 Apr 2. Eur J Med Genet. 2014. PMID: 24704109

7

Presumed Perinatal Stroke: Risk Factors, Clinical and Radiological Findings.

Ilves P, Laugesaar R, Loorits D, Kolk A, Tomberg T, Lõo S, Talvik I, Kahre T, Talvik T. Ilves P, et al. Among authors: kahre t. J Child Neurol. 2016 Apr;31(5):621-8. doi: 10.1177/0883073815609149. Epub 2015 Oct 7. J Child Neurol. 2016. PMID: 26446909

8

The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in Estonia.

Sarv S, Kahre T, Vaidla E, Pajusalu S, Muru K, Põder H, Gross-Paju K, Ütt S, Žordania R, Talvik I, Õiglane-Shlik E, Muhu K, Õunap K. Sarv S, et al. Among authors: kahre t. Front Genet. 2021 Dec 22;12:796862. doi: 10.3389/fgene.2021.796862. eCollection 2021. Front Genet. 2021. PMID: 35003227 Free PMC article.

9

Pharmacogenetics may explain part of the interindividual variability of dobutamine pharmacodynamics in neonates.

Hallik M, Soeorg H, Kahre T, Murumets Ü, Ilmoja ML, Kipper K, Metsvaht T. Hallik M, et al. Among authors: kahre t. Br J Clin Pharmacol. 2022 Sep;88(9):4155-4162. doi: 10.1111/bcp.15357. Epub 2022 Apr 29. Br J Clin Pharmacol. 2022. PMID: 35437830 Free article.

10

Prevalence of the fragile X syndrome among Estonian mentally retarded and the entire children's population.

Puusepp H, Kahre T, Sibul H, Soo V, Lind I, Raukas E, Ounap K. Puusepp H, et al. Among authors: kahre t. J Child Neurol. 2008 Dec;23(12):1400-5. doi: 10.1177/0883073808319071. J Child Neurol. 2008. PMID: 19073844

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