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35篇 您的检索式：作者名="Frishberg"

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	题名	作者	年代	出处	被引量
1	Mutations in NPHS2 encoding podocin are a prevalent cause of steroid- resistant nephrotic syndrome among Israeli-Arab children 显示文摘	Frishberg Y Rinat C Megged O	2002	J Am Soc Nephrol2002，13，2：	1
2	Mutated podocin manifesting as CMV - associated congenital nephrotic syndrome 显示文摘	Frishberg Y Rinat C Feinstein S	2003	Pediatr Nephrol2003，18，3：	1
3	Genetic polymorphisms of the rennin-angiotensin system and the outcome of focal segmental glomerulosclerosis in children显示文摘	FRISHBERG Y BECKER-COHEN R HALLE D	1998	Kidney Int Dec1998，54，6：	1
4	Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders显示文摘	Frishberg Y Topaz O Bergman R	2005	J Mol Med2005，83，1：	1
5	Effect of ultrafine powders in lubricants on performance of friction pairs显示文摘	Frishberg I V Kishkoperov N V Zolotukhina L V	2003	Wear2003，254，：	1
6	Familial inheritance of crossed fused renal ectopia显示文摘	Rinat C Farkas A Frishberg Y	2001	Pediatr Nephrol2001，16，3：	1
7	Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children显示文摘	Frishberg Y Rinat C Megged O	2002	J Am Soc Nephrol2002，13，2：	1
8	TGF-beta and regulation of interstitial pulmonary显示文摘	Frishberg Y Kelly CJ		0，，05：	1
9	Severe reversible renal failure due to naproxen-associated acute interstitial nephritis 显示文摘	Becker-Cohen R Frishberg Y	2001	Eur J Pediatr2001，160，5：	1
10	Transverse scalp sec- tions: a proposed method for laboratory processing显示文摘	Frishberg DP Sperling I C Guthrie VM	1996	J Am A-cad Dermatol1996，35，21：	1
11	Genetic polymorphism in paraoxonase is a risk factor for childhood focal segmental glomerulosclerosis显示文摘	FRISHBERG Y TOLEDANO H BECKER-COHEN R	2000	Am J Kidney Dis2000，36，6：	1
12	TGF-bete and regulation of inter-stitial nephritis显示文摘	Frishberg Y Kelly CJ	1998	Miner Electrolyte Metab1998，24，23：	1
13	Effect of ultrafine powders in lubricants on performance of friction pairs显示文摘	FRISHBERG I V KISHKOPAROV N V ZOLOTUKHINA L V	2003	Wear2003，254，：	1
14	Primary hyperoxaluria type III - a model for studying perturbations in glyoxylate metabolism 显示文摘	Belostotsky R Pitt JJ Frishberg Y	2012	J Mol Med(Berl)2012，90，：	1
15	Signers of Tales:The Case for the Literary Status of an Unwritten Language显示文摘	Frishberg Nancy	1988	Sign Language Studies1988，，59：	1
16	Dent's disease manifesting as focal glomerulosclerosis:is it the tip of the iceberg?显示文摘	Frishberg Y Dinour D Belostotsky R	2009	Pediatr Nephrol2009，24，12：	1
17	Dent' s disease manifesting as focal glomerulosclerosis : is it the tip of the ice- berg? 显示文摘	Frishberg Y Dinour D Belostotsky R el al	2009	Pediatr Nephrol2009，24，12：	1
18	Mutations in NPHS2 en- coding podoein are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children 显示文摘	Frishberg Y Rinat C Megged O	2002	J Am Soc Nephrol2002，13，6：	1
19	Dent’s diseasemanifesting as focal glomerulosclerosis: Is it the tip of theiceberg- 显示文摘	Frishberg Y Dinour D Belostotsky R	2009	Pediatr Nephrol2009，24，12：	1
20	Mutated podocin manifesting as CMV-associated congenital nephrotic syndrome 显示文摘	Frishberg Y Rinat C Feinstein S	2003	Pediatr Nephrol2003，18，：	1

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