Õunap K - Search Results

1

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: ounap k. J Child Neurol. 2018 Aug;33(9):587-592. doi: 10.1177/0883073818776760. Epub 2018 Jun 4. J Child Neurol. 2018. PMID: 29862897

2

The incidence and characterization of phenylketonuric patients in Estonia.

Ounap K, Lilleväli H, Klaassen T, Metspalu A, Sitska M. Ounap K, et al. J Inherit Metab Dis. 1996;19(3):381-2. doi: 10.1007/BF01799278. J Inherit Metab Dis. 1996. PMID: 8803791 No abstract available.

3

Development of the phenylketonuria screening programme in Estonia.

Ounap K, Lilleväli H, Metspalu A, Lipping-Sitska M. Ounap K, et al. J Med Screen. 1998;5(1):22-3. doi: 10.1136/jms.5.1.22. J Med Screen. 1998. PMID: 9575455

4

Familial Williams-Beuren syndrome.

Ounap K, Laidre P, Bartsch O, Rein R, Lipping-Sitska M. Ounap K, et al. Am J Med Genet. 1998 Dec 28;80(5):491-3. doi: 10.1002/(sici)1096-8628(19981228)80:5<491::aid-ajmg10>3.0.co;2-j. Am J Med Genet. 1998. PMID: 9880214

5

Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32-->qter.

Talvik I, Ounap K, Bartsch O, Ilus T, Uibo O, Talvik T. Talvik I, et al. Among authors: ounap k. Am J Med Genet. 2000 Aug 28;93(5):399-402. Am J Med Genet. 2000. PMID: 10951464

6

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. Am J Med Genet. 2002 Apr 1;108(4):322-6. doi: 10.1002/ajmg.10284. Am J Med Genet. 2002. PMID: 11920839

7

Sudden death of a girl with Prader-Willi syndrome.

Oiglane E, Ounap K, Bartsch O, Rein R, Talvik T. Oiglane E, et al. Among authors: ounap k. Genet Couns. 2002;13(4):459-64. Genet Couns. 2002. PMID: 12558118

8

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: ounap k. Community Genet. 2003;6(3):166-70. doi: 10.1159/000078164. Community Genet. 2003. PMID: 15243997

9

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. 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

10

Two sisters with Silver-Russell phenotype.

Ounap K, Reimand T, Mägi ML, Bartsch O. Ounap K, et al. Am J Med Genet A. 2004 Dec 15;131(3):301-6. doi: 10.1002/ajmg.a.30379. Am J Med Genet A. 2004. PMID: 15523618

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