Výsledky vyhledávání - "Tiina Klaassen"

Duchenne and Becker muscular dystrophies: an Estonian experience

Autor: Valentin Sander, Ene Essenson, Ulvi Astra Talkop, Tiina Klaassen, Jaana Tammur, Andres Piirsoo, Aita Napa, Tiina Talvik

Publikováno v: Brain and Development. 21:244-247

The clinical and molecular features of 25 Duchenne (DMD), two intermediate (D/BMD) and three Becker (BMD) muscular dystrophy patients from 26 unrelated families were evaluated. Early psychomotor development was normal in patients with D/BMD and BMD.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa5f95c36e0ee6e3cd99750a6d5fca34
https://doi.org/10.1016/s0387-7604(99)00016-9

Zobrazit plný text záznamu

Distribution of CFTR gene mutations in cystic fibrosis patients from Estonia

Autor: Maris Teder, Eneli Oitmaa, Krista Kaasik, Andres Metspalu, Tiina Klaassen

Publikováno v: Journal of Medical Genetics. 37:16e-16

Editor—Cystic fibrosis (CF) is the most common recessive genetic disorder affecting about 1 in 2500 white live births with a carrier frequency of 1 in 25.1 The incidence of this disease has been found to be somewhat lower in Nordic countries,2 espe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29fb14bb5fddbfaaf3b6df6227ec8946
https://doi.org/10.1136/jmg.37.8.e16

Zobrazit plný text záznamu

Akademický článek

Distribution of CFTR gene mutations in cystic fibrosis patients from Estonia.

Autor: TEDER, MARIS, KLAASSEN, TIINA, OITMAA, ENELI, KAASIK, KRISTA, METSPALU, ANDRES

Publikováno v: Journal of Medical Genetics; Aug2000, p1-4, 4p, 2 Charts, 1 Graph

Zobrazit plný text záznamu

Akademický článek

Neonatal screening for the cystic fibrosis main mutation ΔF508 in Estonia.

Autor: Klaassen, Tiina, Teder, Maris, Viikmaa, Mart, Metspalu, Andres

Publikováno v: Journal of Medical Screening; Mar1998, Vol. 5 Issue 1, p16-19, 4p, 2 Diagrams, 1 Map

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání