Piussan C - Search Results

1

[Renal osteodystrophy in children. Pathogenic role and modalities of control of phosphate retention].

Boudailliez B, Bony-Trifunovic H, Berquin P, Piussan C, Fournier A. Boudailliez B, et al. Among authors: piussan c. Arch Fr Pediatr. 1991 Apr;48(4):279-86. Arch Fr Pediatr. 1991. PMID: 2069483 Review. French. No abstract available.

2

[Role of ultrasound in studying the first urinary infection in children].

Boudailliez B, McMahon Y, Grumbach Y, Baratte B, Caraco MH, Piussan C. Boudailliez B, et al. Among authors: piussan c. Arch Fr Pediatr. 1989 Feb;46(2):113-5. Arch Fr Pediatr. 1989. PMID: 2660762 Review. French.

3

[Evaluation of maximal filtration capacity and renal functional reserve by an oral protein-loading test in adults and children].

Colome MF, Boudailliez B, Renaud H, Makdassi R, el Esper N, Grégoire I, Piussan C, Fournier A. Colome MF, et al. Among authors: piussan c. Nephrologie. 1987;8(4):197-204. Nephrologie. 1987. PMID: 3696369 French.

4

[Dubowitz syndrome. A diagnosis not to be missed].

Mathieu M, Berquin P, Epelbaum S, Lenaerts C, Piussan C. Mathieu M, et al. Among authors: piussan c. Arch Fr Pediatr. 1991 Dec;48(10):715-8. Arch Fr Pediatr. 1991. PMID: 1793348 French.

5

[Adrenoleukodystrophy: significance for genetic counseling of the determination of very long-chain fatty acids and of molecular biology].

Mathieu M, Aubourg P, Guidoux S, Epelbaum S, Benhamou P, Berquin P, Boudailliez B, Piussan C. Mathieu M, et al. Among authors: piussan c. Ann Pediatr (Paris). 1990 Mar;37(3):157-61. Ann Pediatr (Paris). 1990. PMID: 2350140 French.

6

Possible person-to-person transmission of Escherichia coli O111--associated hemolytic uremic syndrome.

Boudailliez B, Berquin P, Mariani-Kurkdjian P, Ilef D, Cuvelier B, Capek I, Tribout B, Bingen E, Piussan C. Boudailliez B, et al. Among authors: piussan c. Pediatr Nephrol. 1997 Feb;11(1):36-9. doi: 10.1007/s004670050229. Pediatr Nephrol. 1997. PMID: 9035170 Clinical Trial.

7

Trichomegaly, pigmentary degeneration of the retina and growth disturbances. A probable autosomal recessive disorder.

Mathieu M, Goldfarb A, Berquin P, Boudailliez B, Labeille B, Piussan C. Mathieu M, et al. Among authors: piussan c. Genet Couns. 1991;2(2):115-8. Genet Couns. 1991. PMID: 1781955

8

Leukaemia-associated hypercalcaemia in a 10-year-old boy: effectiveness of aminohydroxypropylidene biphosphonate.

Boudailliez BR, Pautard BJ, Sebert JL, Kremp O, Piussan CX. Boudailliez BR, et al. Among authors: piussan cx. Pediatr Nephrol. 1990 Sep;4(5):510-1. doi: 10.1007/BF00869834. Pediatr Nephrol. 1990. PMID: 2242318

9

Fragile X mutation and FG syndrome-like phenotype.

Piussan C, Mathieu M, Berquin P, Fryns JP. Piussan C, et al. Am J Med Genet. 1996 Aug 9;64(2):395-8. doi: 10.1002/(SICI)1096-8628(19960809)64:2<395::AID-AJMG32>3.0.CO;2-8. Am J Med Genet. 1996. PMID: 8844090

10

[The importance of continuous ambulatory peritoneal dialysis technics in relation to intermittent peritoneal dialysis in acute renal insufficiency in children. Apropos of 7 cases].

Boudailliez B, Kremp O, Canarelli JP, Risbourg B, Piussan C. Boudailliez B, et al. Among authors: piussan c. Ann Pediatr (Paris). 1989 Sep;36(7):457-60. Ann Pediatr (Paris). 1989. PMID: 2683945 Review. French.

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