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6篇 您的检索式：作者名="Michell IR"

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		题名	作者	年代	出处	被引量
	1	Deep fascia of the foot: anatomical and clinical consideration显示文摘	Michell IR MeyerC		JAPMA0，199，7：	1
	2	Mitochondrial DNA cytochrome oxidase Ⅰ gene: potential for distinction between immature stages of some forensically important fly species (Diptera) in western Australia 显示文摘	Michelle L Harvey IR Dadour SG	2003	Forensic Sci Int2003，131，：	1
	3	Robot‐assisted radical prostatectomy compared with open and laparoscopic approaches: A systematic review and meta‐analysis显示文摘	Patrick S Moran Michelle O’Neill Conor Teljeur Martin Flattery Linda A Murphy Gordon Smyth Máirín Ryan	2013	Int J Urol2013，，3：	1
	4	Deep fascia of the foot: anatomicaland clini-cal consideration显示文摘	Michell IR Meyer C	1991	JAPMA1991，81，7：	1
	5	Deep fascia of the foot:anatomical and clinical consideration显示文摘	Michell IR Meyer C	1991	JAPMA1991，81，7：	1
	6	Adenine phosphoribosyltransferase deficiency: Leave no stone unturned显示文摘Adenine phosphoribosyltransferase(APRT)deficiency is a rare autosomal recessive disease leading to generation of large amounts of 2,8-dihydroxyadenine(DHA).DHA is excreted in urine,where it precipitates into crystals due to its low solubility.DHA crystals can aggregate into stones or cause injury to the renal parenchyma(DHA nephropathy).Recurrent urolithiasis and DHA nephropathy are the two clinical manifestations of APRT deficiency.Diagnosis of APRT deficiency can be made during childhood as well as adulthood.Diagnosis mainly relies on the recognition of DHA in stones or urine crystals.Measurement of APRT activity and genetic testing are useful for confirmation of diagnosis,for family screening and should be considered in difficult cases of urolithiasis or crystalline nephropathy.Allopurinol therapy is the cornerstone of treatment and is highly effective in preventing recurrence of stones and kidney disease.High fluid intake and dietary modifications are also recommended.Early diagnosis and treatment are of paramount importance to prevent renal damage.Unfortunately,diagnosis of APRT deficiency is often overlooked and irreversible renal failure still occurs in a substantial proportion of patients.Clinicians must be alert to the possibility of APRT deficiency and consider the appropriate diagnostic tests in certain cases.This review discusses the genetic and biochemical mechanisms of APRT deficiency,and the issues of diagnosis and management.	Guillaume Bollée Michel Daudon Irène Ceballos-Picot	2014	World Journal of Clinical Urology2014，3，3：	0

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