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MITZI WASSERSTEIN, M.D.
M.D.
Psychiatry Physician
NPI: 1679517916Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
276364-1205(UT)
Research & Publications (20)
Newborn screening for Krabbe disease: the New York State model.
PMID 19302934·Pediatr Neurol·2009
8-other
Safety and efficacy of 22 weeks of treatment with sapropterin dihydrochloride in patients with phenylketonuria.
PMID 18932221·Am J Med Genet A·2008
4-observational
A prospective, cross-sectional survey study of the natural history of Niemann-Pick disease type B.
PMID 18625664·Pediatrics·2008
8-other
Combined liver-kidney transplant for the management of methylmalonic aciduria: a case report and review of the literature.
PMID 17964841·Mol Genet Metab·2008
5-case
Clinical, enzymatic and molecular characterization of nine new patients with malonyl-coenzyme A decarboxylase deficiency.
PMID 17186413·J Inherit Metab Dis·2007
5-case
Acid sphingomyelinase deficiency: prevalence and characterization of an intermediate phenotype of Niemann-Pick disease.
PMID 17011332·J Pediatr·2006
5-case
Natural history of Type A Niemann-Pick disease: possible endpoints for therapeutic trials.
PMID 16434659·Neurology·2006
8-other
Cerebral glucose metabolism in adults with early treated classic phenylketonuria.
PMID 16343970·Mol Genet Metab·2006
8-other
Type B Niemann-Pick disease: findings at chest radiography, thin-section CT, and pulmonary function testing.
PMID 16304086·Radiology·2006
8-other
The natural history of type B Niemann-Pick disease: results from a 10-year longitudinal study.
PMID 15545621·Pediatrics·2004
8-other
Lipid abnormalities in children with types A and B Niemann Pick disease.
PMID 15238911·J Pediatr·2004
8-other
Biochemical effect of intravenous arginine butyrate in X-linked adrenoleukodystrophy.
PMID 12838202·J Pediatr·2003
5-case
The demographics and distribution of type B Niemann-Pick disease: novel mutations lead to new genotype/phenotype correlations.
PMID 12369017·Am J Hum Genet·2002
8-other
Enzyme replacement therapy for Fabry disease, an inherited nephropathy.
PMID 11837797·Clin Nephrol·2002
6-review
Fabry disease: clinical features and recent advances in enzyme replacement therapy.
PMID 11692469·Adv Nephrol Necker Hosp·2001
6-review
Fabry disease (alpha-galactosidase A deficiency): renal involvement and enzyme replacement therapy.
PMID 11688379·Contrib Nephrol·2001
6-review
Maple syrup urine disease: identification and carrier-frequency determination of a novel founder mutation in the Ashkenazi Jewish population.
PMID 11509994·Am J Hum Genet·2001
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
- 500 FOOTHILL BLVD, 116OP
SALT LAKE CITY, UT 84148 - Phone
- (801) 584-1217
Quick Facts
- NPI
- 1679517916
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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