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S N Wickramasinghe

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European Journal of Haematology|April 1, 1993
Observations on two members of the Swedish family with congenital dyserythropoietic anaemia, type IIIS N Wickramasinghe, A Wahlin, D Anstee, et al.
Haematologica|May 9, 2000
Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?A Iolascon, V Servedio, R Carbone, et al.
Ultrastructural Pathology|November 10, 2009
Invasion of erythroblasts by Pasmodium vivax: A new mechanism contributing to malarial anemiaYong-Xin Ru, Bing-Yu Mao, Feng-kui Zhang, et al.
Blood|February 1, 1994
A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]S F Parsons, J Jones, D J Anstee, et al.
The Journal of Clinical Investigation|June 1, 1984
Hematologic and biosynthetic studies in homozygous hemoglobin Constant SpringS Derry, W G Wood, M Pippard, et al.
British Journal of Haematology|October 16, 1999
Role of FcgammaRI (CD64) in erythrocyte elimination and its up-regulation in thalassaemiaE Wiener, D Allen, R J Porter, et al.
European Journal of Haematology|December 18, 2007
Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous Arg1042Trp mutation in codanin-1)H Tamary, H Offret, O Dgany, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damageB C Blount, M M Mack, C M Wehr, et al.
British Journal of Haematology|September 6, 2000
Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha-interferon therapyN Parez, M Dommergues, V Zupan, et al.
British Journal of Haematology|October 16, 1999
Suppression of CDA II expression in a homozygoteA Beauchamp-Nicoud, P O Schischmanoff, N Alloisio, et al.
Pageof 20

Showing results (191-200 of 200) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 200 results.
European Journal of Haematology|April 1, 1993
Observations on two members of the Swedish family with congenital dyserythropoietic anaemia, type IIIS N Wickramasinghe, A Wahlin, D Anstee, et al.
Haematologica|May 9, 2000
Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?A Iolascon, V Servedio, R Carbone, et al.
Ultrastructural Pathology|November 10, 2009
Invasion of erythroblasts by Pasmodium vivax: A new mechanism contributing to malarial anemiaYong-Xin Ru, Bing-Yu Mao, Feng-kui Zhang, et al.
Blood|February 1, 1994
A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]S F Parsons, J Jones, D J Anstee, et al.
The Journal of Clinical Investigation|June 1, 1984
Hematologic and biosynthetic studies in homozygous hemoglobin Constant SpringS Derry, W G Wood, M Pippard, et al.
British Journal of Haematology|October 16, 1999
Role of FcgammaRI (CD64) in erythrocyte elimination and its up-regulation in thalassaemiaE Wiener, D Allen, R J Porter, et al.
European Journal of Haematology|December 18, 2007
Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous Arg1042Trp mutation in codanin-1)H Tamary, H Offret, O Dgany, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damageB C Blount, M M Mack, C M Wehr, et al.
British Journal of Haematology|September 6, 2000
Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha-interferon therapyN Parez, M Dommergues, V Zupan, et al.
British Journal of Haematology|October 16, 1999
Suppression of CDA II expression in a homozygoteA Beauchamp-Nicoud, P O Schischmanoff, N Alloisio, et al.
Pageof 20