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WILLIAM RHEAD, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1861445512Individual
Specialties, Licenses & Credentials
Pediatric Pathology Physician
Pathology — Pediatric Pathology
Code: 207ZP0213X
42007(WI)
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
42007(WI)
Research & Publications (20)
The call from the newborn screening laboratory: frustration in the afternoon.
PMID 15157599·Pediatr Clin North Am·2004
6-review
National academy of clinical biochemistry laboratory medicine practice guidelines: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summary.
PMID 19574465·Clin Chem·2009
6-review
Creating genetics-based infusion centers: a case study of two models.
PMID 18641514·Genet Med·2008
5-case
Rescue from neonatal death in the murine model of hereditary tyrosinemia by glutathione monoethylester and vitamin C treatment.
PMID 18023223·Mol Genet Metab·2008
7-preclinical
Survival after treatment with phenylacetate and benzoate for urea-cycle disorders.
PMID 17538087·N Engl J Med·2007
3-trial
2-methylbutyryl-CoA dehydrogenase deficiency in Hmong infants identified by expanded newborn screen.
PMID 17393751·WMJ·2007
8-other
Urea cycle disorders: clinical presentation outside the newborn period.
PMID 16227115·Crit Care Clin·2005
5-case
Considerations in the difficult-to-manage urea cycle disorder patient.
PMID 16227112·Crit Care Clin·2005
5-case
Unmasked adult-onset urea cycle disorders in the critical care setting.
PMID 16227111·Crit Care Clin·2005
5-case
Ascorbate decreases Fabry cerebral hyperperfusion suggesting a reactive oxygen species abnormality: an arterial spin tagging study.
PMID 15390234·J Magn Reson Imaging·2004
3-trial
Evaluation of liver fatty acid oxidation in the leptin-deficient obese mouse.
PMID 11914033·Mol Genet Metab·2002
7-preclinical
Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse.
PMID 11590124·Hum Mol Genet·2001
4-observational
Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency.
PMID 11134486·Pediatr Res·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
Via practice · 2 locations total
- Address
- 1500 HIGHLAND AVE
MADISON, WI 53705 - Phone
- (608) 262-2507
Quick Facts
- NPI
- 1861445512
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 2
- Publications
- 20
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