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Journal D'Urologie|January 1, 1988
[Renal tumors in children, excluding Wilms' tumor. Apropos of 29 cases]H Dodat, R B Galifer, P Montupet, et al.
Advances in Experimental Medicine and Biology|January 1, 1989
Cellular localization of erythropoietin gene transcriptionC Lacombe, J L Da Silva, P Bruneval, et al.
Orphanet Journal of Rare Diseases|April 2, 2026
Treatment-related benefit and satisfaction in patients with Fabry disease in France: insight into patients' expectations and preferences from the prospective, non-interventional SATIS-Fab studyOlivier Lidove, Agathe Masseau, Grégory Pugnet, et al.
International Journal of Public Health|January 2, 2023
Prevalence of Antimicrobial Resistance and Infectious Diseases in a Hospitalised Migrant Population in Paris, France, a Retrospective StudySarah Stabler, Olivier Paccoud, Léa Duchesne, et al.
European Journal of Biochemistry|December 16, 1985
Structural and functional studies of hemoglobin Poissy alpha 2 beta 2(56) (D7) Gly----Arg and 86 (F2) Ala----ProC Lacombe, C T Craescu, Y Blouquit, et al.
Annals of Surgery|May 22, 2012
Sleeve gastrectomy with transit bipartition: a potent intervention for metabolic syndrome and obesitySergio Santoro, Luis Carlos Castro, Manoel Carlos Prieto Velhote, et al.
Blood|January 29, 2005
Rescue of early-stage myelodysplastic syndrome-deriving erythroid precursors by the ectopic expression of a dominant-negative form of FADDYann-Erick Claessens, Sophie Park, Anne Dubart-Kupperschmitt, et al.
Journal of the National Cancer Institute|March 20, 1991
Radiotherapy alone versus combined chemotherapy and radiotherapy in nonresectable non-small-cell lung cancer: first analysis of a randomized trial in 353 patientsT Le Chevalier, R Arriagada, E Quoix, et al.
Journal of Vascular and Interventional Radiology : JVIR|December 24, 2005
Portal vein embolization with N-butyl cyanoacrylate before partial hepatectomy in patients with hepatocellular carcinoma and underlying cirrhosis or advanced fibrosisAlban Denys, Celine Lacombe, Frederic Schneider, et al.
European Journal of Human Genetics : EJHG|October 21, 2016
Complete loss of function of the ubiquitin ligase HERC2 causes a severe neurodevelopmental phenotypeFanny Morice-Picard, Giovanni Benard, Hamid R Rezvani, et al.
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