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Kaur Liivak

https://www.etis.ee/CV/Kaur_Liivak/eng
23.08.1975
5161697
kaurliivak@gmail.com

Career

Institutions and positions
2008–...   
East Tallinn Central Hospital, Surgical resident (0,80)
01.01.2003–31.12.2008   
Prison of Tartu General Practitioner
 
 
Education
1982–2009   
1982 – 1990 Käru Primary School, 1990 – 1993 Rapla´s I Secondary School, 1994 – 2003 Tartu Unverity´s medical faculty, 2004 – 2009 Tartu University doctoral studies

Qualifications

Academic degrees
Kaur Liivak, Doctor's Degree, 2009, (sup) Vallo Tillmann, Classical Form of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency in Estonia: Incidence, Genotype and Ghenotype with Special Attention to Short-term Growth and 24-hour Blood pressure, University of Tartu, Faculty of Medicine.
 
 
Fields of research
ETIS CLASSIFICATION: 3. Health; 3.7. Clinical Medicine
 
 

Completed projects

Publications

Category
Year
Publication
 
1.1.
2009
Liivak, K.; Foster, P.J.; Thalange, N.; Tillmann, V. (2009). Short-term growth in children with congenital adrenal hyperplasia. Hormone Research, 71 (3), 142−147.
1.1.
2009
Liivak, K.; Tillmann, V. (2009). 24-hour blood pressure profiles in children with congenital adrenal hyperplasia on two different hydrocortisone treatment regimens. Journal of Pediatric Endocrinology and Metabolism, 22 (6), 511−517.
1.3.
2009
Ormisson, Anne; Toome, Liis; Mägi, Marja-Liis; Neupokojeva, Ilona; Rjabova, Tatjana; Areda, Merle; Liivak, Kaur; Antson, Anne; Kaasik, Birgit (2009). Eesti väga väikese sünnikaaluga enneaegsete laste tervisetulem 3 aasta vanuselt. Eesti Arst, 88, 6−11.
2.3.
2009
Liivak, K. (2009). Classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Estonia: incidence, genotype and phenotype with special attention to short-term growth and 24-hour blood pressure. (Tartu likool.; Arstiteaduskond.; Tartu likool.; Lastekliinik.; ). Tartu: Tartu University Press.
1.1.
2008
Liivak, K.; Tobi, S.; Schlecht, H.; Tillmann, V. (2008). Incidence of classical 21-hydroxylase deficiency and distribution of CYP21A2 mutations in Estonia. Hormone Research, 69, 227−232.
5.2.
2004
Liivak, K.; Tillmann, V. (2004). Kaasasündinud adrenogenitaalse sündroomi levimus ja kliiniline pilt Eestis. Eesti Arst, 83 (5), 352.
5.04.2018

Kaur Liivak

https://www.etis.ee/CV/Kaur_Liivak/est
23.08.1975
5161697
kaurliivak@gmail.com

Teenistuskäik

Töökohad ja ametid
2008–...   
AS Ida-Tallinna Keskhaigla, Kirurgia resident (0,80)
01.01.2003–31.12.2008   
Tartu Vangla Üldarst
 
 
Haridustee
1982–2009   
1982 - 1990 Käru Põhikool, 1990-1993 Rapla I Keskkool, 1994-2003 Tartu Ülikooli arstiteaduskond,2004-2009 Tartu Ülikooli doktorantuur

Kvalifikatsioon

Teaduskraadid
Kaur Liivak, Doctor's Degree, 2009, (sup) Vallo Tillmann, Classical Form of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency in Estonia: Incidence, Genotype and Ghenotype with Special Attention to Short-term Growth and 24-hour Blood pressure, University of Tartu, Faculty of Medicine.
 
 
Teadustöö põhisuunad
ETIS KLASSIFIKAATOR: 3. Terviseuuringud; 3.7. Kliiniline meditsiin

Lõppenud projektid

Publikatsioonid

Klass
Aasta
Publikatsioon
 
1.1.
2009
Liivak, K.; Foster, P.J.; Thalange, N.; Tillmann, V. (2009). Short-term growth in children with congenital adrenal hyperplasia. Hormone Research, 71 (3), 142−147.
1.1.
2009
Liivak, K.; Tillmann, V. (2009). 24-hour blood pressure profiles in children with congenital adrenal hyperplasia on two different hydrocortisone treatment regimens. Journal of Pediatric Endocrinology and Metabolism, 22 (6), 511−517.
1.3.
2009
Ormisson, Anne; Toome, Liis; Mägi, Marja-Liis; Neupokojeva, Ilona; Rjabova, Tatjana; Areda, Merle; Liivak, Kaur; Antson, Anne; Kaasik, Birgit (2009). Eesti väga väikese sünnikaaluga enneaegsete laste tervisetulem 3 aasta vanuselt. Eesti Arst, 88, 6−11.
2.3.
2009
Liivak, K. (2009). Classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Estonia: incidence, genotype and phenotype with special attention to short-term growth and 24-hour blood pressure. (Tartu likool.; Arstiteaduskond.; Tartu likool.; Lastekliinik.; ). Tartu: Tartu University Press.
1.1.
2008
Liivak, K.; Tobi, S.; Schlecht, H.; Tillmann, V. (2008). Incidence of classical 21-hydroxylase deficiency and distribution of CYP21A2 mutations in Estonia. Hormone Research, 69, 227−232.
5.2.
2004
Liivak, K.; Tillmann, V. (2004). Kaasasündinud adrenogenitaalse sündroomi levimus ja kliiniline pilt Eestis. Eesti Arst, 83 (5), 352.
5.04.2018

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ProgramTypeNumberNameProject startProject endPrincipal investigatorInstitutionFinancing
ETFETF5835Congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Estonia: prevalence, relationship between genotype and clinical picture with particularly interest on blood pressure and short-term growth01.01.200431.12.2007Vallo TillmannUniversity of Tartu, Faculty of Medicine43 785,95 EUR
SFSF0182695s05Early riskfactors that influence child’s development and pathogenesis of chronic disorders in children: further opportunities for their improvement and treatment.01.01.200531.12.2010Vallo TillmannUniversity of Tartu, Faculty of Medicine577 556,01 EUR
SFSF0180004s11Factors that influence child’s development, pathogenesis and diagnosis of childhood chronic illnesses and their long-term outcome: further opportunities for their improvement and treatment. 01.01.201131.12.2016Vallo TillmannUniversity of Tartu; University of Tartu, Faculty of Medicine, Institute of Clinical Medicine830 340,00 EUR