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F Dijoud

Showing results (21-30 of 46) with videos related to

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The European Journal of Medicine|October 1, 1992
Fatal haemolytic uraemic syndrome in an AIDS patientL Cotte, M P Preckel, R Cahen, et al.
Journal of Pediatric Surgery|May 1, 1997
Juvenile granulosa cell tumor of the ovary in infants: a clinicopathologic study of three cases and review of the literatureE Bouffet, T Basset, N Chetail, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 18, 2022
Severe neonatal hypercalcemia revealing congenital mesoblastic nephroma: A case report and management of neonatal hypercalcemia: Severe neonatal hypercalcemia revealing congenital mesoblastic nephromaC Tanné, J-P Pracros, F Dijoud, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 2009
[Granulocytic sarcoma, a diagnostic challenge: 3 pediatric cases]C Rénard, S Girard, J P Pracros, et al.
La Revue De Medecine Interne|February 1, 2011
[Rapidly progressive ANCA positive glomerulonephritis as the presenting feature of infectious endocarditis]W Hanf, J-E Serre, J-H Salmon, et al.
Gastroenterologie Clinique Et Biologique|June 1, 2010
[Pediatric gastrointestinal stromal tumors: report of three cases]B Samarji, T Walter, F Dijoud, et al.
Pediatric Radiology|November 1, 1995
Sclerosing hemangioma of the lung: radiological findings and pathological diagnosisL Guibaud, J P Pracros, V Rode, et al.
Hepatology (Baltimore, Md.)|December 1, 1992
Pulmonary hemorrhage and glomerulonephritis in primary biliary cirrhosisF Bissuel, T Bizollon, F Dijoud, et al.
Pediatric Nephrology (Berlin, Germany)|July 1, 1990
Familial infantile nephrotic syndrome with ocular abnormalitiesC Glastre, P Cochat, R Bouvier, et al.
Clinical Genetics|November 22, 2008
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney diseaseL Michel-Calemard, F Dijoud, M Till, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
The European Journal of Medicine|October 1, 1992
Fatal haemolytic uraemic syndrome in an AIDS patientL Cotte, M P Preckel, R Cahen, et al.
Journal of Pediatric Surgery|May 1, 1997
Juvenile granulosa cell tumor of the ovary in infants: a clinicopathologic study of three cases and review of the literatureE Bouffet, T Basset, N Chetail, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 18, 2022
Severe neonatal hypercalcemia revealing congenital mesoblastic nephroma: A case report and management of neonatal hypercalcemia: Severe neonatal hypercalcemia revealing congenital mesoblastic nephromaC Tanné, J-P Pracros, F Dijoud, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 2009
[Granulocytic sarcoma, a diagnostic challenge: 3 pediatric cases]C Rénard, S Girard, J P Pracros, et al.
La Revue De Medecine Interne|February 1, 2011
[Rapidly progressive ANCA positive glomerulonephritis as the presenting feature of infectious endocarditis]W Hanf, J-E Serre, J-H Salmon, et al.
Gastroenterologie Clinique Et Biologique|June 1, 2010
[Pediatric gastrointestinal stromal tumors: report of three cases]B Samarji, T Walter, F Dijoud, et al.
Pediatric Radiology|November 1, 1995
Sclerosing hemangioma of the lung: radiological findings and pathological diagnosisL Guibaud, J P Pracros, V Rode, et al.
Hepatology (Baltimore, Md.)|December 1, 1992
Pulmonary hemorrhage and glomerulonephritis in primary biliary cirrhosisF Bissuel, T Bizollon, F Dijoud, et al.
Pediatric Nephrology (Berlin, Germany)|July 1, 1990
Familial infantile nephrotic syndrome with ocular abnormalitiesC Glastre, P Cochat, R Bouvier, et al.
Clinical Genetics|November 22, 2008
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney diseaseL Michel-Calemard, F Dijoud, M Till, et al.
Pageof 5