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30篇 您的检索式：作者名="BOckenhauer D"

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	题名	作者	年代	出处	被引量
1	Potassium leak channels and the KCNK family of two-P- domain subunits显示文摘	Goldstein SA Bockenhauer D O'Kelly I	2001	Nat Rev Neurosci2001，2，3：	1
2	The enzyme 4- hydroxy- 2- oxoglutarate aldolase is deficient in primary hyperoxaluria type 3显示文摘	Williams EL Bockenhauer D van't Hoff WG	2012	Nephrol Dial Transplant2012，27，：	1
3	KCNK2: reversible conversion of a hippocampal potassium into a voltagedependent channel显示文摘	Bockenhauer D Zilberberg N Goldstein SA	2001	Nat Neurosci2001，4，5：	1
4	Dent-2 dis-ease: a miid variant of Lowe syndrome显示文摘	Bokenkamp A Bockenhauer D Cheong HI	2009	J Pediatr2009，155，1：	1
5	Bartter syndromes and other salt-losing tu- bulopathies 显示文摘	Kleta R Bockenhauer D	2006	Nephron Physiol2006，104，2：	1
6	Renal malformations associated with mutations of developmental genes: messages from the clinic显示文摘	Adalat S Bockenhauer D Ledermarm SE	2010	Pediatr Nephrol2010，25，11：	1
7	KCNK2:reversible conversion of a hippocampal potassium leak into a voltage-dependent channel显示文摘	BOCKENHAUER D ZILBERBERG N COLDSTEIN S A	2001	Nat Neurosci2001，4，5：	1
8	Potassium Leak Channels and the KCNK Family of Two-P-domain Subunits显示文摘	Goldstein SA Bockenhauer D O'Kelly I	2001	Nat Rev Neurosei(S1471-003X)2001，2，3：	1
9	Clinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty years 显示文摘	Kari JA Montini G Bockenhauer D	2014	Pediatr Nephrol2014，29，11：	1
10	The enzyme 4 - hydroxy - 2 - oxoglutarate aldolase is deficient in primary hyperoxaluria type 3显示文摘	Williams EL Bockenhauer D van' t Hoff WG	2012	Nephrol Dial Transplant2012，27，8：	1
11	Potassium leak channels and the KCNK family of two-P-domain sub- units显示文摘	Goldstein SA Bockenhauer D O' Kelly I	2001	Nat Rev Neurosci2001，2，3：	1
12	Dent 2 disease=a mild variant of Lowe syndrome显示文摘	Bokenkamp A BOckenhauer D Cheong HI	2009	J Pediatr2009，155，：	1
13	Epilepsy, ataxia,sensorineural deafness, tubulopathy, and KCNJ10 mutations显示文摘	Bockenhauer D Feather S Stanescu HC	2009	NEngl J Med2009，360，19：	1
14	A premature termination mutation in a patient with lowe syndrome without congenital cataracts: Dropping the' 0' in ocrl显示文摘	Pasternack SM Bockenhauer D Refke M	2013	Klin Padiatr2013，225，1：	1
15	The salt-wastingphenotype of EAST syndrome, a disease with multifaceted symptomslinked to the KCNJ10 K+ channel显示文摘	Bandulik S Schmidt K Bockenhauer D	2011	Pflugers Arch2011，461，4：	1
16	Cystic fibrosis,aminoglycoside treatment and acute renal failure:the not so gentle micin显示文摘	BOCKENHAUER D HUG M J KLETA R	2009	Pediatric Nephrology2009，24，5：	1
17	The enzyme 4 -hydroxy- 2 -oxoglutarate aldolase is deficient in primary hy- peroxaluria type 3 显示文摘	Williams EL Bockenhauer D vant Hoff WG	2012	Nephrol Dial Transplant2012，27，：	1
18	KCNK2:Reversible conversion of a hippocampal potassium leak into a voltage-dependent channel显示文摘	Bockenhauer D Zilberberg N Goldstein S A	2001	Nat Neurosci2001，4，5：	1
19	KCNK2: reversible conversion of a hippocampal potassium leak into a voltage-dependent channel 显示文摘	BOCKENHAUER D ZILBERBERG N GOLDSTEINS A	2001	Nat Neurosei2001，4，5：	1
20	Dent-2 disease:a mild variant of Lowe syndrome显示文摘	Bokenkamp A Bockenhauer D Cheong HI	2009	J Pediatr2009，155，1：	1

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