Uibo O - Search Results

1

Parents' satisfaction with medical and social assistance provided to children with Down syndrome: experience in Estonia.

Reimand T, Uibo O, Zordania R, Palmiste V, Ounap K, Tqlvik T. Reimand T, et al. Among authors: uibo o. Community Genet. 2003;6(3):166-70. doi: 10.1159/000078164. Community Genet. 2003. PMID: 15243997

2

Descriptive epidemiology of Down's syndrome in Estonia.

Reimand T, Ounap K, Zordania R, Ilus T, Uibo O, Sitska M, Talvik T. Reimand T, et al. Among authors: uibo o. Paediatr Perinat Epidemiol. 2006 Nov;20(6):512-9. doi: 10.1111/j.1365-3016.2006.00758.x. Paediatr Perinat Epidemiol. 2006. PMID: 17052289

3

Girl with combined cellular immunodeficiency, pancytopenia, malformations, deletion 11q23.3 --> qter, and trisomy 8q24.3 --> qter.

Ounap K, Bartsch O, Uibo O, Laidre P. Ounap K, et al. Among authors: uibo o. Am J Med Genet. 2002 Apr 1;108(4):322-6. doi: 10.1002/ajmg.10284. Am J Med Genet. 2002. PMID: 11920839

4

De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis.

Pajusalu S, Reimand T, Uibo O, Vasar M, Talvik I, Zilina O, Tammur P, Õunap K. Pajusalu S, et al. Among authors: uibo o. Eur J Med Genet. 2015 Jun-Jul;58(6-7):336-40. doi: 10.1016/j.ejmg.2015.04.002. Epub 2015 Apr 20. Eur J Med Genet. 2015. PMID: 25907420

5

Incidence of Childhood Epilepsy in Estonia.

Veri K, Talvik I, Vaher U, Napa A, Ilves P, Uibo O, Õiglane-Shlik E, Laugesaar R, Rein R, Kolk A, Noormets K, Reimand T, Õunap K, Talvik T. Veri K, et al. Among authors: uibo o. J Child Neurol. 2018 Aug;33(9):587-592. doi: 10.1177/0883073818776760. Epub 2018 Jun 4. J Child Neurol. 2018. PMID: 29862897

6

Three patients with 9p deletions including DMRT1 and DMRT2: a girl with XY complement, bilateral ovotestes, and extreme growth retardation, and two XX females with normal pubertal development.

Ounap K, Uibo O, Zordania R, Kiho L, Ilus T, Oiglane-Shlik E, Bartsch O. Ounap K, et al. Among authors: uibo o. Am J Med Genet A. 2004 Nov 1;130A(4):415-23. doi: 10.1002/ajmg.a.30269. Am J Med Genet A. 2004. PMID: 15481033

7

A new case of 2q duplication supports either a locus for orofacial clefting between markers D2S1897 and D2S2023 or a locus for cleft palate only on chromosome 2q13-q21.

Ounap K, Ilus T, Laidre P, Uibo O, Tammur P, Bartsch O. Ounap K, et al. Among authors: uibo o. Am J Med Genet A. 2005 Sep 1;137A(3):323-7. doi: 10.1002/ajmg.a.30890. Am J Med Genet A. 2005. PMID: 16094674 Review.

8

Screening for celiac disease in Down's syndrome patients revealed cases of subtotal villous atrophy without typical for celiac disease HLA-DQ and tissue transglutaminase antibodies.

Uibo O, Teesalu K, Metskula K, Reimand T, Saat R, Sillat T, Reimand K, Talvik T, Uibo R. Uibo O, et al. Among authors: uibo r. World J Gastroenterol. 2006 Mar 7;12(9):1430-4. doi: 10.3748/wjg.v12.i9.1430. World J Gastroenterol. 2006. PMID: 16552815 Free PMC article.

9

Antibodies to neurofilaments.

Talja I, Reimand T, Uibo O, Reimand K, Aun S, Talvik T, Janmey PA, Uibo R. Talja I, et al. Among authors: uibo o, uibo r. Ann N Y Acad Sci. 2009 Sep;1173:130-6. doi: 10.1111/j.1749-6632.2009.04624.x. Ann N Y Acad Sci. 2009. PMID: 19758141

10

Patients with down syndrome have increased prevalence of rheumatoid factor but not autoantibodies to anti-cyclic citrullinated peptide.

Orro E, Alnek K, Reimand T, Reimand K, Uibo O, Talvik T, Haller-Kikkatalo K, Kisand K, Uibo R. Orro E, et al. Among authors: uibo o. Clin Chim Acta. 2019 Aug;495:40-42. doi: 10.1016/j.cca.2019.03.1614. Epub 2019 Mar 16. Clin Chim Acta. 2019. PMID: 30890397

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