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26篇 您的检索式：作者名="Pollak MR"

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	题名	作者	年代	出处	被引量
1	Focal segmental glomerulosclerosis : recent advances 显示文摘	Pollak MR	2008	Curr Opin Nephrol Hypertens2008，17，2：	1
2	Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint显示文摘	Pollak MR	2002	J Am Soc Nephrol2002，13，12：	1
3	Inherited podocytopathies:FSGS and nephrotic syndrome from a genetic viewpoint显示文摘	Pollak MR	2002	J Am Soc Nephrol2002，13，：	1
4	The genetic basis of FSGS and steroid-resistant nephrosis显示文摘	Pollak MR	2003	Semin Nephrol2003，23，2：	1
5	Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism显示文摘	Pollak MR Brown EM Chou YH	1993	Cell1993，75，：	1
6	A suPAR circulating factor causes kidney disease显示文摘	Shankland SJ Pollak MR	2011	Nat Med2011，17，8：	1
7	Genetic testing for nephrotic syndrome and FSGS in the era of next-generation sequencing显示文摘	Brown EJ Pollak MR Barua M	2014	Kidney Int2014，85，5：	1
8	Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint显示文摘	Pollak MR	2002	J Am Soc Nephrol2002，13，12：	1
9	Metabolite profiling identifies markers of uremia显示文摘	Rhee EP Souza A Farrell L Pollak MR Lewis GD Steele DJ	2010	J Am Soc Nephrol2010，21，6：	1
10	APOLI and kidney disease 显示文摘	Pollak MR Genovese G Friedman OJ	2012	CUIT Opin Nephrol Hypertens2012，21，2：	1
11	The genetic basis of FSGS and steroid - resistant nephrosis显示文摘	Pollak MR	2003	Senin Nephrol2003，23，2：	1
12	Inherited podocytopathies:FSGS and nephrotic syndrome from a genetic viewpoint显示文摘	Pollak MR	2002	JAm SocNephrol2002，13，：	1
13	Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint显示文摘	Pollak MR	2002	J Am Soc Nephrol2002，13，12：	1
14	The genetic basis of FSGS and steroid-resistant nephrosis显示文摘	Pollak MR	2003	Semin Nephrol2003，23，：	1
15	Renin-angiotensin axis blockade reduces proteinuria in presymptomatic patients with familial FSGS 显示文摘	Copelovitch L Guttenberg M Pollak MR	2007	Pediatr Nephrol2007，22，10：	1
16	Mutations in the human Ca2+-sensing gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism显示文摘	Pollak MR Brown EM Chou YH	1993	Cell1993，75，7：	1
17	Autosomal dominant hypocalcemia caused by a Ca2+-sensing receptor gene mutation 显示文摘	Pollak MR Brown EM Estep HL	1994	Nat Genet1994，8，3：	1
18	A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31显示文摘	Martin R Patricia F Pollak MR	2000	J Am Soc Nephrol2000，11，9：	1
19	A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31显示文摘	Martin R Patricia F Pollak MR	2000	J Am Soc Nephrol2000，11，9：	1
20	A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25 -31 显示文摘	Martin R Patricia F Pollak MR	2000	J Am Soc Nephrol2000，11，9：	1

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