Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: results of a single-center case-control study

By El-Karaksy Hanaa  

Annals of Hematology, Vol. 83, Iss. 11, 2004-11 ,pp. : 712-715

Springer Publishing Company

Access to resources Recommend Favorite

Tau gene mutations: dissecting the pathogenesis of FTDP-17

By Ingram E.M.   Spillantini M.G.  

Trends in Molecular Medicine, Vol. 8, Iss. 12, 2002-12 ,pp. : 555-562

Elsevier

Access to resources Recommend Favorite

Frequency of the HFE Gene Mutations in Five Italian Populations

By Candore G.   Mantovani V.   Balistreri C.R.   Lio D.   Colonna-Romano G.   Cerreta V.   Carru C.   Deiana L.   Pes G.   Menardi G.   Perotti L.   Miotti V.   Bevilacqua E.   Amoroso A.   Caruso C.  

Blood Cells, Molecules, and Diseases, Vol. 29, Iss. 3, 2002-01 ,pp. : 267-273

Academic Press

Access to resources Recommend Favorite

Ankyrin gene mutations in japanese patients with hereditary spherocytosis

By Nakanishi Hidekazu   Kanzaki Akio   Yawata Ayumi   Yamada Osamu   Yawata Yoshihito  

International Journal of Hematology, Vol. 73, Iss. 1, 2001-01 ,pp. : 54-63

Springer Publishing Company

Access to resources Recommend Favorite

CEBPA gene mutations in Egyptian acute myeloid leukemia patients: impact on prognosis

By Awad Mohamed M.   Aladle Doaa A.   Abousamra Nashwa K.   Elghannam Doaa M.   Fawzy Iman M.  

Hematology, Vol. 18, Iss. 2, 2013-03 ,pp. : 61-68

Maney Publishing

Access to resources Recommend Favorite