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E Vamos

Showing results (51-60 of 129) with videos related to

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Placenta|July 1, 1987
Placental electron microscopy and histochemistry in a case of sialic acid storage disorderE Jauniaux, E Vamos, J Libert, et al.
Lancet (London, England)|January 23, 1993
In-utero carbon monoxide poisoning and multiple fetal abnormalitiesY Hennequin, D Blum, E Vamos, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Assessment of an electron-impact GC-MS method for organic acids and glycine conjugates in amniotic fluidA Kumps, E Vamos, Y Mardens, et al.
The Journal of Pediatrics|January 1, 1992
Hyperphosphatasemia in GM1 gangliosidosisR Denis, J L Wayemberg, M Vermeulen, et al.
Acta Paediatrica Belgica|April 1, 1981
Major congenital malformations in 5448 newborns: comments on genetic counseling and prenatal diagnosisN Van Regemorter, J Dodion, C Druart, et al.
Bruxelles Medical|October 1, 1974
[Antenatal diagnosis of congenital diseases: indications, limitations, and technic]E Vamos-Hurwitz, P Petit, M Mathy, et al.
Acta Paediatrica Scandinavica|January 1, 1978
Farber's disease as a ceramidosis: clinical, radiological and biochemical aspectsM Toppet, E Vamos-Hurwitz, G Jonniaux, et al.
Cancer Genetics and Cytogenetics|July 1, 1993
Chromosomal findings in cultured melanocytes from a giant congenital nevusP Heimann, G Ogur, C De Busscher, et al.
Acta Paediatrica Belgica|April 1, 1976
Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie caseM Tondeur, E Vamos-Hurwitz, M Cantz, et al.
Acta Paediatrica Scandinavica|November 1, 1975
Mannosidosis: findings in cultured fibroblasts and urineE Vamos-Hurwitz, M Tondeur, R Humbel, et al.
Pageof 13

Showing results (51-60 of 129) with videos related to

Sort By:
Pageof 13
Placenta|July 1, 1987
Placental electron microscopy and histochemistry in a case of sialic acid storage disorderE Jauniaux, E Vamos, J Libert, et al.
Lancet (London, England)|January 23, 1993
In-utero carbon monoxide poisoning and multiple fetal abnormalitiesY Hennequin, D Blum, E Vamos, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Assessment of an electron-impact GC-MS method for organic acids and glycine conjugates in amniotic fluidA Kumps, E Vamos, Y Mardens, et al.
The Journal of Pediatrics|January 1, 1992
Hyperphosphatasemia in GM1 gangliosidosisR Denis, J L Wayemberg, M Vermeulen, et al.
Acta Paediatrica Belgica|April 1, 1981
Major congenital malformations in 5448 newborns: comments on genetic counseling and prenatal diagnosisN Van Regemorter, J Dodion, C Druart, et al.
Bruxelles Medical|October 1, 1974
[Antenatal diagnosis of congenital diseases: indications, limitations, and technic]E Vamos-Hurwitz, P Petit, M Mathy, et al.
Acta Paediatrica Scandinavica|January 1, 1978
Farber's disease as a ceramidosis: clinical, radiological and biochemical aspectsM Toppet, E Vamos-Hurwitz, G Jonniaux, et al.
Cancer Genetics and Cytogenetics|July 1, 1993
Chromosomal findings in cultured melanocytes from a giant congenital nevusP Heimann, G Ogur, C De Busscher, et al.
Acta Paediatrica Belgica|April 1, 1976
Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie caseM Tondeur, E Vamos-Hurwitz, M Cantz, et al.
Acta Paediatrica Scandinavica|November 1, 1975
Mannosidosis: findings in cultured fibroblasts and urineE Vamos-Hurwitz, M Tondeur, R Humbel, et al.
Pageof 13