WilliamBRizzoMD
Pediatrics • Omaha, NEMedical Genetics
Professor, Pediatrics, University of Nebraska Medical Center College of Medicine
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Office
988102 Nebraska Medical Ctr
Omaha, NE 68198Phone+1 402-559-6402Fax+1 402-559-5731
Education & Training
Johns Hopkins UniversityResidency, Pediatrics, 1977 - 1979
University of Illinois College of MedicineClass of 1977
Certifications & Licensure
NE State Medical License 2002 - 2026
VA State Medical License 1983 - 2002
MD State Medical License 1980 - 1983- American Board of Medical Genetics and Genomics Clinical Biochemical Genetics
- American Board of Medical Genetics and Genomics Clinical Genetics
- American Board of Pediatrics Pediatrics
Clinical Trials
- Sterol and Isoprenoid Disease Research Consortium: Smith-Lemli-Opitz Syndrome Start of enrollment: 2011 Jan 01
- B7 Coreceptor Molecules in Hyper IgD Syndrome Form of Mevalonate Kinase Deficiency Start of enrollment: 2012 Mar 01
- An Open-Label Phase 3 Study of BMN 165 for Adults With PKU Not Previously Treated w/ BMN 165 Start of enrollment: 2013 May 01
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Publications & Presentations
PubMed
- 1550 citationsNonalcoholic Steatohepatitis: Association of Insulin Resistance and Mitochondrial AbnormalitiesArun J. Sanyal, Carol Campbell-Sargent, Faridoddin Mirshahi, William B. Rizzo, Melissa J. Contos
Gastroenterology. 2001-04-01 - 32 citationsIsolation of a Chinese hamster fibroblast variant defective in dihydroxyacetonephosphate acyltransferase activity and plasmalogen biosynthesis: use of a novel two-step...Narasimhan Nagan, Amiya K. Hajra, Leslie K. Larkins, Paul B. Lazarow, P. Edward Purdue
The Biochemical Journal. 1998-05-15 - 73 citationsPlasma and muscle free carnitine deficiency due to renal Fanconi syndrome.Isa Bernardini, William B. Rizzo, Marinos C. Dalakas, J Bernar, William A. Gahl
The Journal of Clinical Investigation. 1985-04-01
Press Mentions
‘Health Care Works Are Exhausted,’ UNMC Letter Receives 2k+ SignaturesNovember 18th, 2020
Aldeyra Therapeutics Launches the Aldeyra Registry for Patients with Sjögren-Larsson SyndromeFebruary 22nd, 2017
Woman's Rare Condition Causes Unbearably Itchy Skin, Stiffened LimbsSeptember 19th, 2016
Grant Support
- Frontiers In Ichthyosis ResearchNational Institute Of Arthritis And Musculoskeletal And Skin Diseases2010
- Ichthyosis In Sjogren-Larsson SyndromeNational Institute Of Arthritis And Musculoskeletal And Skin Diseases2002–2010
- Ichthyosis In Sjogren-Larsson SyndromeNational Institute Of Arthritis And Musculoskeletal And Skin Diseases2001–2002
- Phenotypic Variation In Sjogren LarssonNational Center For Research Resources1999–2001
- Molecular Genetics Of Sjogren Larsson SyndromeNational Center For Research Resources1999–2001
- Ichthyosis In Sjogren/Larsson SyndromeNational Institute Of Arthritis And Musculoskeletal And Skin Diseases1997–2000
- Phenotype Variation In Sjogren LarssonNational Center For Research Resources1997
- Molecular Genetics Of Sjogren Larrson SyndromeNational Center For Research Resources1996–1997
- Metabolic Investigations Of L 2 Hydroxyglutaric AciduriaNational Center For Research Resources1996
- Dietary Therapy For Sjogren Larsson SyndromeNational Center For Research Resources1996
- Fatty Alcohol Metabolism In Sjogren-Larsson SyndromeNational Institute Of Diabetes And Digestive And Kidney Diseases1989–1991
- Fatty Acid Metabolism In AdrenoleukodystrophyNational Institute Of Diabetes And Digestive And Kidney Diseases1986–1990
- Fatty Acid Metabolism In AdrenoleukodystrophyNat Inst Of Arthritis, Diabetes, Digestive &Kidney Diseases1985
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