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E Vamos

Showing results (21-30 of 129) with videos related to

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Revue Medicale De Bruxelles|May 1, 1988
[Endocrine abnormalities in alcoholic cirrhosis]M Struelens, S Jamsin, E Vamos, et al.
Human Genetics|March 1, 1992
Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunitL De Meirleir, W Lissens, E Vamos, et al.
American Journal of Medical Genetics|August 5, 2000
Further evidence for autosomal dominant inheritance and ectodermal abnormalities in Kabuki syndromeW Courtens, A Rassart, J J Stene, et al.
Bruxelles Medical|February 1, 1972
[Storage diseases. Some clinical and ultrastructural aspects and study of cell cultures]M Tondeur, E Vamos-Hurwitz, A Resibois, et al.
Acta Paediatrica Scandinavica|January 1, 1971
Mucopolysaccharidosis in a three months old infant. Clinical and ultrastructural studiesM Tondeur, E Vamos-Hurwitz, N Cremer, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|May 1, 1977
The cellular lesions of Farber's disease and their experimental reproduction in tissue cultureJ Rutsaert, M Tondeur, E Vamos-Hurwitz, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunitL J de Meirleir, W Lissens, E Vamos, et al.
Neurofibromatosis|January 1, 1988
Hereditary intestinal neurofibromatosis. II. Translocation between chromosomes 12 and 14A Verhest, R Heimann, J Verschraegen, et al.
Genes, Chromosomes & Cancer|September 17, 1998
Alveolar soft-part sarcoma: further evidence by FISH for the involvement of chromosome band 17q25P Heimann, C Devalck, C Debusscher, et al.
The Journal of Pediatrics|February 28, 2002
Hypergonadotropic hypogonadism in a boy with Fanconi anemia with growth hormone deficiency and pituitary stalk interruptionGuy G Massa, C Heinrichs, E Vamos, et al.
Pageof 13

Showing results (21-30 of 129) with videos related to

Sort By:
Pageof 13
Revue Medicale De Bruxelles|May 1, 1988
[Endocrine abnormalities in alcoholic cirrhosis]M Struelens, S Jamsin, E Vamos, et al.
Human Genetics|March 1, 1992
Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunitL De Meirleir, W Lissens, E Vamos, et al.
American Journal of Medical Genetics|August 5, 2000
Further evidence for autosomal dominant inheritance and ectodermal abnormalities in Kabuki syndromeW Courtens, A Rassart, J J Stene, et al.
Bruxelles Medical|February 1, 1972
[Storage diseases. Some clinical and ultrastructural aspects and study of cell cultures]M Tondeur, E Vamos-Hurwitz, A Resibois, et al.
Acta Paediatrica Scandinavica|January 1, 1971
Mucopolysaccharidosis in a three months old infant. Clinical and ultrastructural studiesM Tondeur, E Vamos-Hurwitz, N Cremer, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|May 1, 1977
The cellular lesions of Farber's disease and their experimental reproduction in tissue cultureJ Rutsaert, M Tondeur, E Vamos-Hurwitz, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunitL J de Meirleir, W Lissens, E Vamos, et al.
Neurofibromatosis|January 1, 1988
Hereditary intestinal neurofibromatosis. II. Translocation between chromosomes 12 and 14A Verhest, R Heimann, J Verschraegen, et al.
Genes, Chromosomes & Cancer|September 17, 1998
Alveolar soft-part sarcoma: further evidence by FISH for the involvement of chromosome band 17q25P Heimann, C Devalck, C Debusscher, et al.
The Journal of Pediatrics|February 28, 2002
Hypergonadotropic hypogonadism in a boy with Fanconi anemia with growth hormone deficiency and pituitary stalk interruptionGuy G Massa, C Heinrichs, E Vamos, et al.
Pageof 13