R. Dumas

发表

[Corticosensitive nephrotic syndrome (or nephrosis) in children. Therapeutic guideline proposed by the Pediatric Society of Nephrology].

M. Fischbach, E. Bérard, C. Loirat, 2005, Nephrologie & therapeutique.

Comparison of ultrasound and dimercaptosuccinic acid scintigraphy changes in acute pyelonephritis

P. Kotzki, J. Astruc, D. Morin, 1999, Pediatric Nephrology.

The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor

M. Fellous, C. Sultan, P. Niaudet, 1999, Human mutation.

Lupus nephritis. Collaborative study by the French Society of Paediatric Nephrology.

R. Dumas, 1985, Archives of disease in childhood.

Les rachitismes vitaminorésistants

R. Dumas, 1999 .

Type II hyperprolinaemia with renal involvement

H. Daudet, D. Morin, R. Dumas, 1991, Journal of Inherited Metabolic Disease.

[Familial cases of intracranial aneurysms. Review of the literature and case report].

R. Dumas, D. Binnert, A. Nivelon, 1972, Neuro-Chirurgie.

Congenital Adrenal Hyperplasia Associated with Hyperphosphatemic Rickets

C. Sultan, M. Garabédian, P. Garandeau, 1988, Clinical pediatrics.

[Association of severe bronchial disease (bronchial casts, bronchiectasis) and partial abnormal pulmonary venous drainage in 2 children with Turner's syndrome].

S. Guillaumont, M. Voisin, L. Ichay, 1999, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Dialysis Bone Disease in Childhood: Treatment with 25-Hydroxycholecalciferol

P. Meunier, R. Dumas, J. Luciani, 1979, Pediatric Research.

Distinct molecular origins for Denys-Drash and Frasier syndromes

M. Gessler, J. Giltay, C. Sultan, 1993, Human Genetics.

[Urinary lithiasis in children].

R. Dumas, 1990, Archives francaises de pediatrie.

Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndrome.

J. Weill, J. Lobaccaro, C. Sultan, 1993, The Journal of clinical endocrinology and metabolism.

Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndrome

J. Weill, J. Lobaccaro, C. Sultan, 1992 .

PCR analysis and sequencing of the SRY sex determining gene in four patients with bilateral congenital anorchia

P. Czernichow, J. Guthmann, J. Lobaccaro, 1993, Clinical endocrinology.

Hypertension and segmental renal hypoplasia causing a syndrome of haemolysis and uraemia.

P. Baldet, B. Rolin, R. Dumas, 1981, Archives of disease in childhood.

Molecular analysis of the sex-determining region from the Y chromosome in two patients with Frasier syndrome.

S. Taviaux, J. Lobaccaro, C. Sultan, 1992, Hormone research.

Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12.

G. Chazot, J. Pouget, P. Latour, 1996, Clinical chemistry.

[Neurological manifestations in monoclonal gammapathies. Pure neurological manifestations. Immunofluorescence study].

G. Chazot, C. Barbaret, R. Creyssel, 1976, Revue neurologique.

Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French population

G. Chazot, J. Pouget, N. Lévy, 1997, Neurogenetics.

[Hereditary nephrogenic diabetes insipidus].

D. Morin, R. Dumas, Y. Ala, 1995, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[An unusual cause of digestive hemorrhage: gastric botryomycosis].

B. Taillan, G. Garnier, P. Dujardin, 1993, La Revue de medecine interne.

Hematuria revealing primary hyperparathyroidism

D. Morin, L. Ichay, R. Dumas, 1999 .