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Neurogastroenterology and Motility|October 1, 2010
Normal oxidative phosphorylation in intestinal smooth muscle of childhood chronic intestinal pseudo-obstructionL Galmiche, F Jaubert, F Sauvat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2005
[Congenital hyperinsulinism in newborn and infant]I Giurgea, M-J Ribeiro, N Boddaert, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|May 26, 1999
Chronic intestinal pseudo-obstruction syndrome in pediatric patientsO Goulet, A Jobert-Giraud, J L Michel, et al.
The Journal of Clinical Endocrinology and Metabolism|September 18, 2008
Chromosome 11p15 paternal isodisomy in focal forms of neonatal hyperinsulinismL Damaj, M le Lorch, V Verkarre, et al.
Pediatric Pulmonology|July 27, 2010
Surfactant protein C gene (SFTPC) mutation-associated lung disease: high-resolution computed tomography (HRCT) findings and its relation to histological analysisM Mechri, R Epaud, S Emond, et al.
Biomedical Materials (Bristol, England)|February 23, 2019
Optimising the biocompatibility of 3D printed photopolymer constructs in vitro and in vivoC G Y Ngan, C D O'Connell, R Blanchard, et al.
Journal of Inherited Metabolic Disease|May 4, 2005
Dominantly inherited hyperinsulinaemic hypoglycaemiaP de Lonlay, I Giurgea, C Sempoux, et al.
Human Mutation|March 27, 1999
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumorA S Barbosa, C G Hadjiathanasiou, C Theodoridis, et al.
Human Pathology|February 17, 2007
Neonatal hyperinsulinism: clinicopathologic correlationP Delonlay, A Simon, L Galmiche-Rolland, et al.
The Journal of Pathology|March 19, 2008
FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD)R Hersmus, N Kalfa, B de Leeuw, et al.
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