Eva Roomets

https://www.etis.ee/CV/Eva_Roomets/est
3.10.1978
eva.roomets@itk.ee

Teenistuskäik

Töökohad ja ametid
01.01.2008–...   
Ida Tallinna Keskkhaigla, oftalmoloogia resident
01.01.2005–...   
Helsingi Ülikool, doktorant
01.01.2003–31.12.2005   
Tartu Ülikool, meditsiinigeneetika resident
01.01.2002–31.12.2003   
Pärnu Haigla,intern
 
 
Haridustee
2008–...   
Tartu Ülikool, residentuur
2005–...   
Helsingi Ülikool, doktorantuur
2002–2003   
Tartu Ülikool, internatuur
1996–2002   
Tartu Ülikool, Arstiteaduskond

Publikatsioonid

Klass
Aasta
Publikatsioon
 
1.1.
2012
Roomets, E.; Polinati, P.P.; Euro, L.; Eskelin, P.M.; Paganus, A.; Tyni, T. (2012). Carrier frequency of a common mutation of Carnitine palmitoyltransferase 1A deficiency and long-term follow-up in Finland. The Journal of Pediatrics, 160 (3), 473−479.
1.3.
2009
Roomets, Eva (2009). Silma eesmise osa infektsioonid: konjunktiviit, keratiit, iridotsükliit. Lege Artis, 19−23.
1.1.
2008
E. Roomets, T. Kivelä, T. Tyni (2008). Carnitine palmitoyltransferase I and acyl-CoA dehydrogenase 9 in retina: insights of chorioretinopathy in mitochondrial trifunctional protein defectsl. Investigative Ophtalmology & Visual Science, 49 (4), 1660−1664.
5.1.
2007
Roomets, Eva; Tyni, Tiina (2007). A common mutation in Carnitine palmitoyltransferase I deficiency in Finland: a report of 5 cases. Journal of Inherited Metabolic Disease: SSIEM Annual Symposium 2007. 52−52. (30 Suppl. 1).
1.1.
2006
E. Roomets, N. Lundbom, H. Pihko, S. Heikkinen, T. Tyni (2006). Lipids detected by brain MRS during coma caused by carnitine palmitoyltransferase deficiency. Neurology, 67 (8), 1516−1517 .
5.1.
2005
Õunap, K.; Kahre, T.; Roomets, E.; Zordania, R.; Laht, T.-M.; Wanders, R. J. A. (2005). Screening for the common LCAD mutation G1528C in Estonian population. In: .SSIEM, 42 Annual Symposium, Paris. Kluwer Scientific Publishers.
5.1.
2004
Mikelsaar, Ruth; Roomets, Eva; Pihlau, Helju (2004). New syndrome - chromosome 19q distal deletion syndrome. European Journal of Human Genetics, 12, 136.
5.2.
2004
Mikelsaar, R.; Roomets, E.; Pihlau, E. (2004). Uus kromosoomihaigus - 19q distaalne deletsioon. Eesti Arst, 83. 619.
12.04.2019

Eva Roomets

https://www.etis.ee/CV/Eva_Roomets/eng
3.10.1978
eva.roomets@itk.ee

Career

Institution(s) and position(s)
01.01.2008–...   
East Tallinn Central Hospital, ophthamology resident
01.01.2005–...   
University of Helsinki, Ph.D student
01.01.2003–31.12.2005   
University of Tartu, resident of medical genetics
01.01.2002–31.12.2003   
Pärnu Hospital, intern
 
 
Education
2008–...   
University of Tartu, residency
2005–...   
Univeristy of Helsinki, postgraduate studies
2002–2003   
University of Tartu, Faculty of Medicine, intern
1996–2002   
University of Tartu, Faculty of Medicine

Publications

Category
Year
Publication
 
1.1.
2012
Roomets, E.; Polinati, P.P.; Euro, L.; Eskelin, P.M.; Paganus, A.; Tyni, T. (2012). Carrier frequency of a common mutation of Carnitine palmitoyltransferase 1A deficiency and long-term follow-up in Finland. The Journal of Pediatrics, 160 (3), 473−479.
1.3.
2009
Roomets, Eva (2009). Silma eesmise osa infektsioonid: konjunktiviit, keratiit, iridotsükliit. Lege Artis, 19−23.
1.1.
2008
E. Roomets, T. Kivelä, T. Tyni (2008). Carnitine palmitoyltransferase I and acyl-CoA dehydrogenase 9 in retina: insights of chorioretinopathy in mitochondrial trifunctional protein defectsl. Investigative Ophtalmology & Visual Science, 49 (4), 1660−1664.
5.1.
2007
Roomets, Eva; Tyni, Tiina (2007). A common mutation in Carnitine palmitoyltransferase I deficiency in Finland: a report of 5 cases. Journal of Inherited Metabolic Disease: SSIEM Annual Symposium 2007. 52−52. (30 Suppl. 1).
1.1.
2006
E. Roomets, N. Lundbom, H. Pihko, S. Heikkinen, T. Tyni (2006). Lipids detected by brain MRS during coma caused by carnitine palmitoyltransferase deficiency. Neurology, 67 (8), 1516−1517 .
5.1.
2005
Õunap, K.; Kahre, T.; Roomets, E.; Zordania, R.; Laht, T.-M.; Wanders, R. J. A. (2005). Screening for the common LCAD mutation G1528C in Estonian population. In: .SSIEM, 42 Annual Symposium, Paris. Kluwer Scientific Publishers.
5.1.
2004
Mikelsaar, Ruth; Roomets, Eva; Pihlau, Helju (2004). New syndrome - chromosome 19q distal deletion syndrome. European Journal of Human Genetics, 12, 136.
5.2.
2004
Mikelsaar, R.; Roomets, E.; Pihlau, E. (2004). Uus kromosoomihaigus - 19q distaalne deletsioon. Eesti Arst, 83. 619.
12.04.2019
Detailne otsing
  • Leitud 1 kirjet
ProgrammLiikNumberNimiProjekti algusProjekti lõppVastutav täitjaAsutusFinantseerijapoolne rahastamine
ETFETF5486Vaimse alaarengu ja teiste patoloogiliste seisundite tekkepõhjuste uurimine molekulaarsete ja tsütogeneetiliste meetoditega01.01.200331.12.2006Ruth MikelsaarTartu Ülikool, Arstiteaduskond18 090,45 EUR