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2.
Arch Ital Urol Nefrol Androl ; 64(4): 305-8, 1992 Dec.
Artigo em Italiano | MEDLINE | ID: mdl-1462153

RESUMO

The authors report their initial results in ESWL of urinary calculi with the Storz Modulith SL 20 lithotriptor, a multipurpose device for both urinary and biliary stone treatment. During 176 sessions, a total of 144 cases (81 renal and 63 ureteral) were treated and then, followed up. The over-all rate free of stones was 86.8% (90.1% for kidney and for ureteral stones). The treatment rate was 1.23 per patient. Auxiliary procedures before ESWL were performed in 7.9% of the sessions: insertion of "double-J" stent or nephrostomy tube; all ureteral stones received "in situ" treatment. Mean number of shock waves per session was 1836.1 (range 300-3020). The maximum voltage on the average reached was 17.1 kv. Sedo-analgesia by Diazepam and Ketoprofen was given in 75% of the cases. No serious complications were observed. The experience with this machine is discussed in regard to performance; the advantages of its fluoroscopy and ultrasound guided system of focusing are stressed.


Assuntos
Cálculos Renais/terapia , Litotripsia/instrumentação , Cálculos Ureterais/terapia , Adolescente , Adulto , Idoso , Criança , Estudos de Avaliação como Assunto , Seguimentos , Humanos , Cálculos Renais/diagnóstico por imagem , Pessoa de Meia-Idade , Recidiva , Ultrassonografia , Cálculos Ureterais/diagnóstico por imagem
3.
Acta Crystallogr D Biol Crystallogr ; 51(Pt 4): 496-503, 1995 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-15299836

RESUMO

Four novel antiviral WIN compounds, that contain a methyl tetrazole ring as well as isoxazole, pyridazine or acetylfuran rings, have had their structures determined in human rhinovirus serotype 14 at 2.9 A resolution. These compounds bind in the VP1 hydrophobic pocket, but are shifted significantly towards the pocket pore when compared to previously examined WIN compounds. A putative water network at the pocket pore is positioned to hydrogen bond with these four WIN compounds, and this network can account for potency differences seen in structurally similar WIN compounds.

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