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M Toppet

Showing results (41-50 of 50) with videos related to

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Revue Medicale De Bruxelles|June 1, 1992
[Indications for bone marrow graft in severe hemoglobinopathies]A Ferster, N Azzi, W Bujan, et al.
Journal De Genetique Humaine|December 1, 1989
[Nanism with short limbs, dysmorphism, renal dysplasia, growth hormone deficiency with pituitary hypoplasia and psychomotor delay: a new syndrome?]C Elmer, G Van Vliet, C Heinrichs, et al.
Lancet (London, England)|November 9, 2000
Antisickling activity of sodium cromoglicate in sickle-cell diseaseM Toppet, A B Fall, A Ferster, et al.
Blood|February 15, 1993
Bone marrow transplantation corrects the splenic reticuloendothelial dysfunction in sickle cell anemiaA Ferster, W Bujan, F Corazza, et al.
Scandinavian Journal of Haematology|May 1, 1982
Fanconi's anaemia. Simultaneous onset in 2 siblings and unusual cytological findingsM de Vroede, W Feremans, E de Maertelaere-Laurent, et al.
The Journal of Pediatrics|September 1, 1983
Circulating vitamin D metabolite concentrations in children with nutritional ricketsM Garabédian, M Vainsel, E Mallet, et al.
Blood|September 15, 1996
Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trialA Ferster, C Vermylen, G Cornu, et al.
Revue Medicale De Bruxelles|August 8, 2001
[Prevention of hemoglobinopathies in Brussels: a necessity?]B Gulbis, F Cotton, V Hansen, et al.
European Journal of Pediatrics|February 7, 1998
Growth failure, encephalopathy, and endocrine dysfunctions in two siblings, one with 5-oxoprolinase deficiencyL H Cohen, E Vamos, C Heinrichs, et al.
Blood|May 23, 2001
Five years of experience with hydroxyurea in children and young adults with sickle cell diseaseA Ferster, P Tahriri, C Vermylen, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Revue Medicale De Bruxelles|June 1, 1992
[Indications for bone marrow graft in severe hemoglobinopathies]A Ferster, N Azzi, W Bujan, et al.
Journal De Genetique Humaine|December 1, 1989
[Nanism with short limbs, dysmorphism, renal dysplasia, growth hormone deficiency with pituitary hypoplasia and psychomotor delay: a new syndrome?]C Elmer, G Van Vliet, C Heinrichs, et al.
Lancet (London, England)|November 9, 2000
Antisickling activity of sodium cromoglicate in sickle-cell diseaseM Toppet, A B Fall, A Ferster, et al.
Blood|February 15, 1993
Bone marrow transplantation corrects the splenic reticuloendothelial dysfunction in sickle cell anemiaA Ferster, W Bujan, F Corazza, et al.
Scandinavian Journal of Haematology|May 1, 1982
Fanconi's anaemia. Simultaneous onset in 2 siblings and unusual cytological findingsM de Vroede, W Feremans, E de Maertelaere-Laurent, et al.
The Journal of Pediatrics|September 1, 1983
Circulating vitamin D metabolite concentrations in children with nutritional ricketsM Garabédian, M Vainsel, E Mallet, et al.
Blood|September 15, 1996
Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trialA Ferster, C Vermylen, G Cornu, et al.
Revue Medicale De Bruxelles|August 8, 2001
[Prevention of hemoglobinopathies in Brussels: a necessity?]B Gulbis, F Cotton, V Hansen, et al.
European Journal of Pediatrics|February 7, 1998
Growth failure, encephalopathy, and endocrine dysfunctions in two siblings, one with 5-oxoprolinase deficiencyL H Cohen, E Vamos, C Heinrichs, et al.
Blood|May 23, 2001
Five years of experience with hydroxyurea in children and young adults with sickle cell diseaseA Ferster, P Tahriri, C Vermylen, et al.
Pageof 5