WilliamNAdkinsJr.MD
Pediatrics • Madison, WINeurodevelopmental Disabilities, Medical Genetics
Asst Medical Director Central WI Center or the Developmentally Disabled
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Office
317 Knutson Dr
Madison, WI 53704Phone+1 608-301-1958Fax+1 608-301-1811- Is this information wrong?
Summary
- I am board certified in pediatrics and board eligible in clinical genetics. I spent 37 years as primary physician and genetics consultant in a 600 bed institution for the developmentally disabled. I retired in 2014 but wish to remain active in a outpatient clinical pediatrics setting. I enjoy the opportunity to teach students, residents, and nurses.
Education & Training
University of Wisconsin Hospitals and ClinicsResidency, Pediatrics, 1976 - 1979
Nationwide Children's Hospital/Ohio State UniversityResidency, Pediatrics, 1971 - 1973- Nationwide Childrens HospitalInternship, Transitional Year, 1970 - 1971
Ohio State University College of MedicineClass of 1970
Earlham CollegeA.B., 1966
Certifications & Licensure
WI State Medical License 1977 - 2023- American Board of Pediatrics Pediatrics
Awards, Honors, & Recognition
- Landacre Society for Medical Student Research Ohio State University, 1969
Publications & Presentations
PubMed
- 1 citationsThe influence of nutrition on IGF-1 in tube-fed profoundly retarded adults.Norris R. Glick, Milton H. Fischer, William N. Adkins> ;Journal of the American College of Nutrition. 2001 Feb 1
- 10 citationsDecreased maternal age with hydranencephaly.Mark S. Lubinsky, William N. Adkins, E. G. Kaveggia> ;American Journal of Medical Genetics. 1997 Mar 31
- 8 citationsImproved selenium, carnitine and taurine status in an enterally fed population.Milton H. Fischer, William N. Adkins, Pat Scaman, Judith A. Marlett> ;JPEN. Journal of Parenteral and Enteral Nutrition. 1990 May 1
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Journal Articles
- Remembered: Elisabeth G KaveggiaGastroenterol. Nutr, Am J Med Genet Part A, 1/1/2015
- Decreased Maternal Age With HydranencephalyLubinsky MS, Adkins W, Kaveggia EG, Am J Med Genet, 1/1/1997
- Osteoporosis-Pseudoglioma Syndrome, a Disorder Affecting Skeletal Strength and Vision, Is Assigned to Chromosome Region 11q12-13Gong Y, Vikkula M, Boon L, Liu J, Beighton P, Ramesar R, Peltonen L, Somer H, Hirose T, Dallapiccola B, De Paepe A, Swoboda W, Zabel B, Superti-Furga A, Steinmann B, B..., Am J Hum Genet, 1/1/1996
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Lectures
- Hereditary Multiple System Degeneration: Clinicopathologic Features and Detection1/1/1983
- A Prospective, Randomized, Double-blind Study of Gastroesophageal Reflux Surgery: Nissen Fundoplication vs. Angelchik Prosthesis1/1/1983
- The Use of a Computer-assisted Diagnostic Program by Clerical Personnel1/1/1973
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