C. Fékété

发表

Pancreatic venous samplings in infants and children with primary hyperinsulinism

P. Czernichow, F. Brunelle, J. Saudubray, 2006, Pediatric Radiology.

Factitious Hyperinsulinism Leading to Pancreatectomy: Severe Forms of Munchausen Syndrome by Proxy

C. Sempoux, F. Brunelle, F. Mochel, 2005, Pediatrics.

PERSISTENCE OF MÜLLERIAN DUCTS IN MALE PSEUDOHERMAPHRODITISM, AND ITS RELATIONSHIP TO CRYPTORCHIDISM

R. Rappaport, C. Nezelof, N. Josso, 1983, Clinical endocrinology.

The surgical management of congenital hyperinsulinemic hypoglycemia in infancy.

F. Brunelle, J. Saudubray, P. de Lonlay, 2004, Journal of pediatric surgery.

Preservation of ovarian function by ovarian transposition performed before pelvic irradiation during childhood.

J. Zucker, R. Brauner, R. Rappaport, 1992, The Journal of pediatrics.

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

Marc Fellous, Ken McElreavey, M. Gubler, 1997, Nature Genetics.

Management of 46, XY partial gonadal dysgenesis--revisited.

G. Amann, V. Kirchlechner, J. Crone, 2002, Wiener klinische Wochenschrift.

Biofeedback re-education of faecal continence in children

P. Arhan, C. Faverdin, G. Devroede, 1994, International Journal of Colorectal Disease.

Solitary intestinal fibromatosis: a rare cause of neonatal obstruction.

D. Canioni, C. Nezelof, C. Fékété, 1989, Pediatric pathology.

Radiological aspects of the small bowel after extensive resection in children

J. Sauvegrain, C. Ricour, P. Devred, 1979, Pediatric Radiology.

Early pregnancy diagnosis with a battery-operated ultrasonic scanner in sows.

O. Szenci, I. Merics, C. Fékété, 1992, The Canadian veterinary journal = La revue veterinaire canadienne.

[Neonatal primary hyperparathyroidism caused by clear cell hyperplasia].

G. Lenoir, G. Chomette, G. Chéron, 1985, Pediatrie.

[Munchausen's syndrome by proxy and chronic intestinal pseudo-obstruction].

O. Goulet, C. Ricour, J. Limal, 1989, Archives francaises de pediatrie.

Enterocutaneous fistulas of the small bowel in children (25 cases).

C. Ricour, J. Duhamel, C. Lecoultre, 1978, Journal of pediatric surgery.

Morphological mosaicism of the pancreatic islets: a novel anatomopathological form of persistent hyperinsulinemic hypoglycemia of infancy.

C. Sempoux, C. Bellanné-Chantelot, Y. Aigrain, 2011, The Journal of clinical endocrinology and metabolism.

Proposal for a Standardized Protocol for 18F-DOPA-PET (PET/CT) in Congenital Hyperinsulinism

O. Blankenstein, H. Minn, H. Minn, 2006, Hormone Research in Paediatrics.

[Intestinal obstruction in the new born].

M. Cloup, C. Fékété, D. Pellerin, 1977, Annales de pediatrie.

Urological manifestations associated with chronic intestinal pseudo-obstructions in children.

O. Goulet, S. Lapointe, C. Rivet, 2002, The Journal of urology.

Primary intestinal myopathy, a cause of chronic idiopathic intestinal pseudoobstruction syndrome (CIPS): clinicopathological studies of seven cases in children.

O. Goulet, C. Ricour, M. Nonaka, 1989, Pediatric pathology.

Partial elective pancreatectomy is curative in focal form of permanent hyperinsulinemic hypoglycaemia in infancy: A report of 45 cases from 1983 to 2000.

F. Brunelle, J. Saudubray, J. Rahier, 2002, Journal of pediatric surgery.

[Nesidioblastosis and persistent neonatal hyperinsulinism].

C. Sempoux, F. Brunelle, J. Saudubray, 1995, Journees annuelles de diabetologie de l'Hotel-Dieu.

Results of renal transplantation for Wilms’ tumour

Y. Révillon, J. Zucker, C. Loirat, 1996 .

around and after transition

M. Polak, P. Czernichow, G. Pinto, 2013 .

[Infantile phrenic dehiscence. Study of 36 cases between 1951 and 1980 (author's transl)].

Y. Révillon, C. Fékété, 1982, Annales de Chirurgie.