Ultrasonographic renal volume measurements in early autosomal dominant polycystic disease: Comparison with CT-scan renal volume calculations
Hammoud, S, Tissier, A.-M, Elie, C, Pousset, M, Knebelman, B, Joly, D, Hélénon, O, Correas, J.-M
Published in Diagnostic and interventional imaging (01.01.2015)
Published in Diagnostic and interventional imaging (01.01.2015)
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860 Uric acid is the main component of kidney stones in patients with autosomal dominant polycystic kidney disease (ADPKD) – a study based on stone composition, morphology and infrared spectophotometry analysis
Nikolov, I, Ivanovski, O, Daudon, M, Sikole, A, Knebelman, B
Published in European urology supplements : official journal of the European Association of Urology (01.02.2012)
Published in European urology supplements : official journal of the European Association of Urology (01.02.2012)
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S55 MORPHOLOGY AND COMPOSITION OF KIDNEY STONES IN PATIENTS WITH AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE (ADPKD)
Nikolov, I.G, Ivanovski, O, Daudon, M, Sikole, A, Knebelman, B
Published in European urology supplements : official journal of the European Association of Urology (2011)
Published in European urology supplements : official journal of the European Association of Urology (2011)
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Peritoneal dialysis in polycystic kidney disease patients. Report from the French peritoneal dialysis registry (RDPLF)
Lobbedez, Thierry, Touam, Malick, Evans, David, Ryckelynck, Jean-Philippe, Knebelman, Bertrand, Verger, Christian
Published in Nephrology, dialysis, transplantation (01.07.2011)
Published in Nephrology, dialysis, transplantation (01.07.2011)
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L’amylose inflammatoire (AA) de causes multiples existe-t-elle ? À propos de 61 cas issus de la cohorte française de 290 patients avec amylose AA
Delplanque, M., Bourguiba, R., Lea, S., Audard, V., Knebelman, B., Karras, A., Boffa, J.J., Grateau, G., Buob, D., Georgin-Lavialle, S.
Published in La revue de medecine interne (01.12.2023)
Published in La revue de medecine interne (01.12.2023)
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Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome
KNEBELMAN, B, BREILLAT, C, GUBLER, M.-C, ANTIGNAC, C, FORESTIER, L, ARRONDEL, C, JACASSIER, D, GIATRAS, I, DROUOT, L, DESCHENES, G, GRÜNFELD, J.-P, BROYER, M
Published in American journal of human genetics (01.12.1996)
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Published in American journal of human genetics (01.12.1996)
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SFP PC-73 – Données clinico-biologiques des patients homozygotes et hétérozygotes mutés pour CYP24A1
Figueres, M., Allain-Launay, E., Roussey-Kesler, G., Bienaimé, F., Linglart, A., Isidor, B., Knebelman, B., Kury, S., Lambert, A., Nathanson, S., Prier, D., Ryckwaert, A., Souberbielle, J., Kottler, M., Hourmant, M.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.05.2014)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.05.2014)
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