Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ireri Jm"'
Publikováno v:
East African Medical Journal; Vol 85, No 8 (2008); 412-416
Hereditary haemorrhagic telangiectasia, (HHT) or Rendu-Osler-Weber disease is a genetic autosomal dominant disorder that is characterised by telangiectasias, (small vascular malformations), in mucocutaneous tissues and arterial venous malformations,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b86e3c81377638557a3a9680f8d0192e
https://www.ajol.info/index.php/eamj/article/view/9659
https://www.ajol.info/index.php/eamj/article/view/9659
Autor:
Galiatsatos, Panagis1,2,3,4 (AUTHOR) panagis@jhmi.edu, Wilson, Cheri3 (AUTHOR), O'Brien, Jaime5 (AUTHOR), Gong, Anna J.2 (AUTHOR), Angiolillo, Dylan4 (AUTHOR), Johnson, James4 (AUTHOR), Myers, Carlie6 (AUTHOR), Strout, Sara7 (AUTHOR), Mathai, Stephen1 (AUTHOR), Robinson, Gina2 (AUTHOR), Rowan, Nicholas R.2 (AUTHOR), Weiss, Clifford R.2 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 6/13/2022, Vol. 17 Issue 1, p1-6. 6p.
Autor:
Mutize, Tendaishe T., Seedat, Riaz Y., Ploos van Amstel, Johannes K., Mager, Johannes J., Brown, Stephen C., Gebremariam, Fekade, Coetzee, Marius J.
Publikováno v:
Molecular Biology Reports; 2020, Vol. 47 Issue 12, p9967-9972, 6p
Autor:
Garisch, Dawn
Publikováno v:
SAMJ: South African Medical Journal; Apr2014, Vol. 104 Issue 4, p257-258, 2p
Autor:
Canzonieri, Cecilia, Ornati, Federica, Matti, Elina, Chu, Francesco, Manfredi, Guido, Olivieri, Carla, Buscarini, Elisabetta, Pagella, Fabio
Publikováno v:
SAMJ: South African Medical Journal; Apr2014, Vol. 104 Issue 4, p256-257, 2p