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La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
June 2, 1983
[Congenital atrophoderma in multiple plaques. A new clinical form of mastocytosis?]
A L Claudy, D Schmitt, C Hermier, et al.
Journal of Autism and Developmental Disorders
|
June 13, 2002
A case of N-acetyl galactosaminidase deficiency (Schindler disease) associated with autism
Y C Blanchon, C Gay, G Gibert, et al.
Archives Francaises De Pediatrie
|
March 1, 1983
[Prenatal diagnosis of Xeroderma pigmentosum]
H Barthelemy, A L Claudy, B Lauras, et al.
Pediatrie
|
July 1, 1974
[Congenital esophageal stenosis in a 1-year-old infant]
Y Chavrier, B Lauras, J B Gérard, et al.
Annales De Genetique
|
January 1, 1986
Six cases of partial duplication-deficiency 21 syndrome: 21(dupq22delp23) due to maternal pericentric inversion: inv(21)(p12;q22). A family study
J Fraisse, T Philip, M F Bertheas, et al.
Annales De Pediatrie
|
January 1, 1983
[Congenital cutaneous atrophy in multiple plaques. A new clinical form of mastocytosis?]
A L Claudy, D Schmitt, C Hermier, et al.
Pediatrie
|
January 1, 1975
[Congenital hemolytic anemia due to triosephosphate isomerase deficiency]
F Freycon, B Lauras, F Bovier-Lapierre, et al.
Archives Francaises De Pediatrie
|
November 1, 1971
[Clinical and anatomical case of an aortic aneurysm in the course of Bourneville's tuberous sclerosis]
F Larbre, R Loire, P Guibaud, et al.
Pediatrie
|
January 1, 1980
[Intralobar sequestration revealed by neonatal cardio-respiratory failure. Surgical correction]
G Teyssier, Y Chavrier, M André, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 7, 2002
[Radiological case of the month. Acquired idiopathic Brown's syndrome in a 10-year-old boy]
A Depras, S Chabrier, D Allard, et al.
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of 8
Search research articles
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Showing results (21-30 of 79) with videos related to
Sort By:
Page
of 8
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
June 2, 1983
[Congenital atrophoderma in multiple plaques. A new clinical form of mastocytosis?]
A L Claudy, D Schmitt, C Hermier, et al.
Journal of Autism and Developmental Disorders
|
June 13, 2002
A case of N-acetyl galactosaminidase deficiency (Schindler disease) associated with autism
Y C Blanchon, C Gay, G Gibert, et al.
Archives Francaises De Pediatrie
|
March 1, 1983
[Prenatal diagnosis of Xeroderma pigmentosum]
H Barthelemy, A L Claudy, B Lauras, et al.
Pediatrie
|
July 1, 1974
[Congenital esophageal stenosis in a 1-year-old infant]
Y Chavrier, B Lauras, J B Gérard, et al.
Annales De Genetique
|
January 1, 1986
Six cases of partial duplication-deficiency 21 syndrome: 21(dupq22delp23) due to maternal pericentric inversion: inv(21)(p12;q22). A family study
J Fraisse, T Philip, M F Bertheas, et al.
Annales De Pediatrie
|
January 1, 1983
[Congenital cutaneous atrophy in multiple plaques. A new clinical form of mastocytosis?]
A L Claudy, D Schmitt, C Hermier, et al.
Pediatrie
|
January 1, 1975
[Congenital hemolytic anemia due to triosephosphate isomerase deficiency]
F Freycon, B Lauras, F Bovier-Lapierre, et al.
Archives Francaises De Pediatrie
|
November 1, 1971
[Clinical and anatomical case of an aortic aneurysm in the course of Bourneville's tuberous sclerosis]
F Larbre, R Loire, P Guibaud, et al.
Pediatrie
|
January 1, 1980
[Intralobar sequestration revealed by neonatal cardio-respiratory failure. Surgical correction]
G Teyssier, Y Chavrier, M André, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 7, 2002
[Radiological case of the month. Acquired idiopathic Brown's syndrome in a 10-year-old boy]
A Depras, S Chabrier, D Allard, et al.
Page
of 8