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SUSAN FEATHER, M.D.
M.D.
Anesthesiology Physician
NPI: 1942298526Individual
Specialties, Licenses & Credentials
Anesthesiology PhysicianPrimary
Anesthesiology
Code: 207L00000X
34260(AZ)
Research & Publications (17)
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations.
PMID 19420365·N Engl J Med·2009
7-preclinical
Successful outcome of paediatric en bloc kidney transplantation from the youngest donation-after-cardiac-death donor in the United Kingdom.
PMID 19309478·Transpl Int·2009
5-case
Expression and localisation of aquaporin water channels in human urothelium in situ and in vitro.
PMID 18718702·Eur Urol·2009
8-other
The long-term outcome of prenatally detected posterior urethral valves: a 10 to 23-year follow-up study.
PMID 18485035·BJU Int·2008
8-other
Mineral metabolism and vascular damage in children on dialysis.
PMID 17942964·J Am Soc Nephrol·2007
8-other
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations.
PMID 17476318·J Pediatr Urol·2007
8-other
Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux.
PMID 17357069·Am J Hum Genet·2007
4-observational
Mutation analyses of Uroplakin II in children with renal tract malformations.
PMID 17012268·Nephrol Dial Transplant·2006
5-case
De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure.
PMID 15888565·J Am Soc Nephrol·2005
8-other
OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis.
PMID 15466260·J Am Soc Nephrol·2004
4-observational
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity.
PMID 15200408·Kidney Int·2004
7-preclinical
Oral-facial-digital syndrome VII is oral-facial-digital syndrome I: a clarification.
PMID 14598343·Am J Med Genet A·2003
5-case
OFD1, the gene mutated in oral-facial-digital syndrome type 1, is expressed in the metanephros and in human embryonic renal mesenchymal cells.
PMID 12595504·J Am Soc Nephrol·2003
8-other
Recent insights into kidney diseases associated with glomerular cysts.
PMID 11956871·Pediatr Nephrol·2002
6-review
PALML, a novel paralemmin-related gene mapping on human chromosome 1p21.
PMID 11707320·Gene·2001
7-preclinical
Identification of the gene for oral-facial-digital type I syndrome.
PMID 11179005·Am J Hum Genet·2001
8-other
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.
PMID 10739767·Am J Hum Genet·2000
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3390 N CAMPBELL AVE, STE 110
TUCSON, AZ 85719 - Phone
- (520) 795-7650
Quick Facts
- NPI
- 1942298526
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 17
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