Y0000744
Dextranomer
European Pharmacopoeia (EP) Reference Standard
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About This Item
Empfohlene Produkte
Qualität
pharmaceutical primary standard
API-Familie
dextranomer
Hersteller/Markenname
EDQM
Anwendung(en)
pharmaceutical (small molecule)
Format
neat
Lagertemp.
2-8°C
Allgemeine Beschreibung
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.
Anwendung
Dextranomer EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.
Verpackung
The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.
Sonstige Hinweise
Sales restrictions may apply.
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Intermediate to long-term follow-up indicates low risk of recurrence after double HIT endoscopic treatment for primary vesico-ureteral reflux.
Journal of pediatric urology, 8(4), 449-449 (2011-11-08)
Urologia internationalis, 87(2), 192-198 (2011-08-26)
We evaluated whether real-time 3D ultrasound (4D-US) together with clinical evaluation is an alternative to voiding cystourethrography (VCUG) after endoscopic treatment of vesicoureteral reflux (VUR) in children at postoperative follow-up. We reviewed 178 children who underwent endoscopic therapy with dextranomer/hyaluronic
The Cochrane database of systematic reviews, (5)(5), CD006214-CD006214 (2011-05-13)
Surgical wounds that become infected are often debrided because clinicians believe that removal of this necrotic or infected tissue will expedite wound healing. There are numerous methods available but no consensus on which one is most effective for surgical wounds.
Journal of pediatric urology, 8(1), 40-46 (2011-02-01)
To evaluate outcome of further continence procedures after failure of endoscopic injections of dextranomer-based bulking agent. From 1997, 89 children (3-18 years) and one young adult were treated for incontinence with 145 endoscopic injections of dextranomer. On evaluation, each patient
Nihon Hinyokika Gakkai zasshi. The japanese journal of urology, 101(5), 676-682 (2010-08-19)
To investigate the efficacy and safety of endoscopic treatment with the injectable gel of dextranomer beads in stabilized non-animal sodium hyaluronate (NASHA/Dx gel) administered submucosally close to the proximity of ureteral orifice, we performed the multi-center open study of Japanese
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