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European Journal of Pediatrics
|
August 3, 2000
Cutaneous porphyria in a neonate with tyrosinaemia type 1
S Vanden Eijnden, D Blum, A Clercx, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis
S Seneca, M Abramowicz, W Lissens, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1986
[Echographic evaluation of non-immunologic feto-placental anasarca. A series of 24 cases]
N Elkhazen, E Jauniaux, J Dodion, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 1, 1996
[Leukemia lymphoma T-cell as first manifestation of ataxia-telangiectasia]
C de Laet, G Casimir, J Duchâteau, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1992
[Collection of fetal cord blood for karyotyping]
C Donner, F Avni, R Karoubi, et al.
Revue Medicale De Bruxelles
|
June 1, 1990
[The value of prenatal chromosomal diagnosis in cases of fetal abnormalities: results obtained in 468 pathological pregnancies]
E Vamos, C Elmer, S Lévi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1988
Cholesteryl ester storage disease with secondary lecithin cholesterol acyl transferase deficiency
S Van Erum, D Gnat, C Finne, et al.
The Journal of Pediatrics
|
September 1, 1971
Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture
M Tondeur, E Vamos-Hurwitz, S Mockel-Pohl, et al.
Acta Gastro-Enterologica Belgica
|
January 1, 1979
[Cold hemagglutinin disease revealing an intramucosal carcinoma of the stomach (author's transl)]
F Lustman, A Salhadin, P Andre, et al.
Pediatric Research
|
May 1, 1983
Alterations in cultured fibroblasts of sibs with an infantile form of a free (unbound) sialic acid storage disorder
G H Thomas, J Scocca, J Libert, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 129) with videos related to
Sort By:
Page
of 13
European Journal of Pediatrics
|
August 3, 2000
Cutaneous porphyria in a neonate with tyrosinaemia type 1
S Vanden Eijnden, D Blum, A Clercx, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis
S Seneca, M Abramowicz, W Lissens, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1986
[Echographic evaluation of non-immunologic feto-placental anasarca. A series of 24 cases]
N Elkhazen, E Jauniaux, J Dodion, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 1, 1996
[Leukemia lymphoma T-cell as first manifestation of ataxia-telangiectasia]
C de Laet, G Casimir, J Duchâteau, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1992
[Collection of fetal cord blood for karyotyping]
C Donner, F Avni, R Karoubi, et al.
Revue Medicale De Bruxelles
|
June 1, 1990
[The value of prenatal chromosomal diagnosis in cases of fetal abnormalities: results obtained in 468 pathological pregnancies]
E Vamos, C Elmer, S Lévi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1988
Cholesteryl ester storage disease with secondary lecithin cholesterol acyl transferase deficiency
S Van Erum, D Gnat, C Finne, et al.
The Journal of Pediatrics
|
September 1, 1971
Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture
M Tondeur, E Vamos-Hurwitz, S Mockel-Pohl, et al.
Acta Gastro-Enterologica Belgica
|
January 1, 1979
[Cold hemagglutinin disease revealing an intramucosal carcinoma of the stomach (author's transl)]
F Lustman, A Salhadin, P Andre, et al.
Pediatric Research
|
May 1, 1983
Alterations in cultured fibroblasts of sibs with an infantile form of a free (unbound) sialic acid storage disorder
G H Thomas, J Scocca, J Libert, et al.
Page
of 13