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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 disease
M Toppet, A B Fall, A Ferster, et al.
Blood
|
February 15, 1993
Bone marrow transplantation corrects the splenic reticuloendothelial dysfunction in sickle cell anemia
A 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 findings
M 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 rickets
M Garabédian, M Vainsel, E Mallet, et al.
Blood
|
September 15, 1996
Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial
A 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 deficiency
L 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 disease
A Ferster, P Tahriri, C Vermylen, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 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 disease
M Toppet, A B Fall, A Ferster, et al.
Blood
|
February 15, 1993
Bone marrow transplantation corrects the splenic reticuloendothelial dysfunction in sickle cell anemia
A 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 findings
M 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 rickets
M Garabédian, M Vainsel, E Mallet, et al.
Blood
|
September 15, 1996
Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial
A 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 deficiency
L 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 disease
A Ferster, P Tahriri, C Vermylen, et al.
Page
of 5