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E Vamos

Showing results (81-90 of 129) with videos related to

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Revue Medicale De Bruxelles|October 1, 1984
[Prenatal diagnosis of digestive system malformations using echography]N Elkhazen, J Dodion, E Vamos, et al.
Transplantation Proceedings|February 1, 1991
Differential inducibility of HLA class I and II antigens by r-IFN gamma in type III bare lymphocyte syndromeM Andrien, P Stordeur, E Vamos, et al.
Acta Endocrinologica. Supplementum|January 1, 1986
Generalized unresponsiveness to mineralocorticoid hormones: familial recessive pseudohypoaldosteronism due to aldosterone-receptor deficiencyD Bosson, U Kuhnle, N Mees, et al.
Cancer Research|December 1, 1992
Deletion of chromosome 11p13-11p15.5 sequences in invasive human ovarian cancer is a subclonal progression factorB Vandamme, W Lissens, K Amfo, et al.
European Journal of Pediatrics|October 1, 1983
Partial trisomy 3p in two siblings: clinical and pathological findingsN Van Regemorter, E Vamos, Y Gillerot, 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.
Journal of Inherited Metabolic Disease|January 1, 1990
Carnitine deficiency with cardiomyopathy presenting as neonatal hydrops: successful response to carnitine therapyP Steenhout, C Elmer, A Clercx, et al.
American Journal of Medical Genetics|April 1, 1990
Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblingsS Przedborski, A Ferster, S Goldman, 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.
Revue Medicale De Bruxelles|October 1, 1993
[Fetal cardiology: prenatal diagnosis of cardiac malformations]P Viart, G Rondia, H Dessy, et al.
Pageof 13

Showing results (81-90 of 129) with videos related to

Sort By:
Pageof 13
Revue Medicale De Bruxelles|October 1, 1984
[Prenatal diagnosis of digestive system malformations using echography]N Elkhazen, J Dodion, E Vamos, et al.
Transplantation Proceedings|February 1, 1991
Differential inducibility of HLA class I and II antigens by r-IFN gamma in type III bare lymphocyte syndromeM Andrien, P Stordeur, E Vamos, et al.
Acta Endocrinologica. Supplementum|January 1, 1986
Generalized unresponsiveness to mineralocorticoid hormones: familial recessive pseudohypoaldosteronism due to aldosterone-receptor deficiencyD Bosson, U Kuhnle, N Mees, et al.
Cancer Research|December 1, 1992
Deletion of chromosome 11p13-11p15.5 sequences in invasive human ovarian cancer is a subclonal progression factorB Vandamme, W Lissens, K Amfo, et al.
European Journal of Pediatrics|October 1, 1983
Partial trisomy 3p in two siblings: clinical and pathological findingsN Van Regemorter, E Vamos, Y Gillerot, 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.
Journal of Inherited Metabolic Disease|January 1, 1990
Carnitine deficiency with cardiomyopathy presenting as neonatal hydrops: successful response to carnitine therapyP Steenhout, C Elmer, A Clercx, et al.
American Journal of Medical Genetics|April 1, 1990
Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblingsS Przedborski, A Ferster, S Goldman, 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.
Revue Medicale De Bruxelles|October 1, 1993
[Fetal cardiology: prenatal diagnosis of cardiac malformations]P Viart, G Rondia, H Dessy, et al.
Pageof 13