Search Results - "Garaix, Florentine"

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    Quality of life of transplanted children and their parents: a cross-sectional study by Duvant, Pauline, Fillat, Magali, Garaix, Florentine, Roquelaure, Bertrand, Ovaert, Caroline, Fouilloux, Virginie, Tsimaratos, Michel, Auquier, Pascal, Fabre, Alexandre, Baumstarck, Karine

    Published in Orphanet journal of rare diseases (17-08-2021)
    “…Abstract Background Transplantation is a saving therapeutic that has heavy consequences. The quality of life (QoL) of transplanted children and their parents…”
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    Journal Article
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    Technical feasibility and correlations between shear-wave elastography and histology in kidney fibrosis in children by Desvignes, Catherine, Dabadie, Alexia, Aschero, Audrey, Ruocco, Alix, Garaix, Florentine, Daniel, Laurent, Ferlicot, Sophie, Villes, Virginie, Loundou, Anderson D., Gorincour, Guillaume, Petit, Philippe

    Published in Pediatric radiology (01-09-2021)
    “…Background Ultrasound elastography has been suggested for assessing organ fibrosis. Objective To study the feasibility of shear-wave elastography in children…”
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    Journal Article
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    Dilatation of the aorta in children with advanced chronic kidney disease by Quennelle, Sophie, Ovaert✉, Caroline, Cailliez, Mathilde, Garaix, Florentine, Tsimaratos, Michel, El Louali, Fedoua

    Published in Pediatric nephrology (Berlin, West) (01-07-2021)
    “…Background The peculiarity of the cardiovascular risk profile with increased arterial vulnerability is well known in adults with chronic kidney disease (CKD)…”
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    COQ6 mutation in patients with nephrotic syndrome, sensorineural deafness, and optic atrophy by Justine Perrin, R., Rousset‐Rouvière, Caroline, Garaix, Florentine, Cano, Aline, Conrath, John, Boyer, Olivia, Tsimaratos, Michel

    Published in JIMD reports (01-07-2020)
    “…Introduction Primary coenzyme Q10 (CoQ10) deficiencies are a group of mitochondrial disorders that has proven responsiveness to replacement therapy. Mutations…”
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    Journal Article
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    Rituximab fails where eculizumab restores renal function in C3nef-related DDD by Rousset-Rouvière, Caroline, Cailliez, Mathilde, Garaix, Florentine, Bruno, Daniele, Laurent, Daniel, Tsimaratos, Michel

    Published in Pediatric nephrology (Berlin, West) (01-06-2014)
    “…Background Dense deposit disease (DDD), a C3 glomerulopathy (C3G), is a rare disease with unfavorable progression towards end-stage kidney disease. The…”
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    Journal Article
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    Bernard-Soulier syndrome: first human case due to a homozygous deletion of GP9 gene by Ghalloussi, Dorsaf, Rousset‐rouvière, Caroline, Popovici, Cornel, Garaix, Florentine, Saut, Noémie, Saultier, Paul, Tsimaratos, Michel, Chambost, Hervé, Alessi, Marie-Christine, Baccini, Véronique

    Published in British journal of haematology (19-02-2020)
    “…Bernard–Soulier Syndrome (BSS) is a rare (1:1 million) hereditary bleeding disorder caused by defects in the platelet glycoprotein (GP)‐Ib/IX/V complex, a…”
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    Journal Article
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    Human papillomavirus type 7‐associated anal condyloma after renal transplantation in a child by Garaix, Florentine, Hery, Geraldine, Tsimaratos, Michel, Colson, Philippe, Tamalet, Catherine

    Published in Pediatric transplantation (01-08-2019)
    “…The prevalence, clinical significance, and spectrum of many HPV genotypes are currently largely untapped. We report a case of anal condyloma associated with a…”
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    Characteristics of the pediatric patient before transplantation by Garaix, Florentine

    Published in Néphrologie & thérapeutique (01-12-2011)
    “…Renal transplantation is the treatment of choice for end-stage renal disease during childhood. In France, access to transplantation is good and even better for…”
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    Journal Article
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