Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mariya M. Litvinova"'
Autor:
Ekaterina V. Pimkina, Mariya M. Litvinova, Andrei A. Ayginin, E.A. Dubtsova, Anna S. Speranskaya, Dmitry S. Bordin, Alina D. Matsvay, Kamil Khafizov, K.A. Nikolskaya, German A. Shipulin, L. Vinokurova
Publikováno v:
Pancreatology. 18:S33-S34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a33183943f072c1a71b0896bff79738e
https://doi.org/10.1016/j.pan.2018.05.090
https://doi.org/10.1016/j.pan.2018.05.090
Autor:
Gillian Lockitch, Mariya M. Litvinova
Publikováno v:
LaboratoriumsMedizin. 30:33-39
Hemochromatosis, once considered to be an autosomal recessive disorder of increased iron absorption, predominantly affecting men after the fourth decade of life, is now known to be a syndrome caused by mutations in at least five different genes, one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e702fe54864c230fc74ee4fcc3a33b6
https://doi.org/10.1515/jlm.2006.006
https://doi.org/10.1515/jlm.2006.006
Autor:
Gillian Lockitch, Andre Mattman, Diana Ralston, Daniel T. Holmes, Tara J. Morris, Mariya M. Litvinova
Publikováno v:
Blood cells, moleculesdiseases. 35(3)
We report a new mutation, Asn185Asp, in exon 6 of the ferroportin gene (FPN1) in 15 members of three successive generations of a Canadian family of Scandinavian origin with autosomal dominant hemochromatosis. Hyperferritinemia with low transferrin sa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31e7a5ada2e3b05f9db4d0912c4da164
https://pubmed.ncbi.nlm.nih.gov/16111902
https://pubmed.ncbi.nlm.nih.gov/16111902