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STEPHEN SCHEINMAN, M.D.
M.D.
Internal Medicine Physician
NPI: 1821119975Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
49433(MA)
Research & Publications (17)
OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variability.
PMID 19390221·Nephron Physiol·2009
4-observational
A novel renal carbonic anhydrase type III plays a role in proximal tubule dysfunction.
PMID 18322545·Kidney Int·2008
7-preclinical
Isolation and confirmation of a calcium excretion quantitative trait locus on chromosome 1 in genetic hypercalciuric stone-forming congenic rats.
PMID 16611718·J Am Soc Nephrol·2006
7-preclinical
A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.
PMID 15498972·Science·2004
8-other
Inherited hypercalciuric syndromes: Dent's disease (CLC-5) and familial hypomagnesemia with hypercalciuria (paracellin-1).
PMID 14730510·Semin Nephrol·2004
6-review
Quantitative trait loci for hypercalciuria in a rat model of kidney stone disease.
PMID 12819244·J Am Soc Nephrol·2003
7-preclinical
Altered polarity and expression of H+-ATPase without ultrastructural changes in kidneys of Dent's disease patients.
PMID 12631345·Kidney Int·2003
8-other
Nephrolithiasis, osteoporosis, and mutations in the type 2a sodium-phosphate cotransporter.
PMID 12529474·N Engl J Med·2003
7-preclinical
Responsiveness of hypercalciuria to thiazide in Dent's disease.
PMID 12444212·J Am Soc Nephrol·2002
3-trial
Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.
PMID 12081599·Kidney Int·2002
8-other
Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.
PMID 11752029·J Am Soc Nephrol·2002
8-other
Glomerular protein sieving and implications for renal failure in Fanconi syndrome.
PMID 11703607·Kidney Int·2001
7-preclinical
New insights into causes and treatments of kidney stones.
PMID 10737240·Hosp Pract (1995)·2000
6-review
Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
PMID 10620205·Kidney Int·2000
8-other
Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria.
PMID 10620204·Kidney Int·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 234 BAL CROSS DR
BAL HARBOUR, FL 33154 - Phone
- (305) 308-0400
Quick Facts
- NPI
- 1821119975
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 17
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