Professor of Pediatrics, University Wisc
Pediatrics
Dr. Norman C. Fost, MD
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Norman C. Fost is an expert in the field of Pediatrics. He researched medicine at Yale University School of Medicine. Yale University School of Medicine is a one of the best medicals schools. Yale University School of Medicine is ranked 7 in research and 57 in primary care medicine He received 1 awards: "Fellow (FAAP)". Norman Fost is a published physician. He published 97 publications, including: 'Ethical problems in pediatrics.'
Publications
- Genetic data and electronic health records: a discussion of ethical, logistical and technological considerations.
- Obesity and Neglect: It's about the Child.
- Study Newsletters, Community and Ethics Advisory Boards, and Focus Group Discussions Provide Ongoing Feedback for a Large Biobank.
- Research ethics in the MySpace era.
- Newborn screening technology: proceed with caution.
- Conception for donation.
- The dilemma of data-safety monitoring: provision of significant new data to research participants.
- A faculty-house staff retreat.
- Growth hormone therapy for short stature: panacea or Pandora's box?
- Ethics in cardiovascular medicine. Task Force III: Perspective on the allocation of limited resources in cardiovascular medicine.
- Current issues in neonatal screening for cystic fibrosis and implications of the CF gene discovery.
- Long-term mechanical ventilation in pediatric respiratory failure: medical and ethical considerations.
- Successful treatment of juvenile hemangiomas with prednisone.
- Ethical and regulatory challenges in a randomized control trial of adjuvant treatment for breast cancer in Vietnam.
- How would you handle these ethical dilemmas? Panel discussion.
- Monitoring a clinical trial conducted under the Food and Drug Administration regulations allowing a waiver of prospective informed consent: the diaspirin cross-linked ...
- Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor.
- An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility.
- MSJAMA: ethical issues in whistleblowing.
- Ethical issues in research and innovative therapy in children with mood disorders.
- Patient access to information on clinicians infected with blood-borne pathogens.
- Who should provide genetic education prior to gene testing? Computers and other methods for improving patient understanding.
- Can acutely ill patients consent to research? Resolving an ethical dilemma with facts.
- Access to IVF.
- Decisions regarding treatment of seriously ill newborns.
- Who is responsible for Baby Doe?
- Life and death decisions, Part 1.
- Ethical considerations surrounding first time procedures: a study and analysis of patient attitudes toward spinal taps by students.
- Waived consent for emergency research.
- Cystic fibrosis newborn screening: impact on reproductive behavior and implications for genetic counseling.
- Ethical dilemmas in medical innovation and research: distinguishing experimentation from practice.
- An interactive computer program for educating and counseling patients about genetic susceptibility to breast cancer.
- Seven reasons for Wisconsin physicians to oppose proposed legislation to legalize physician-assisted suicide.
- Commentary: ethics, ethics everywhere--ascertainment bias in new disorders.
- Genetic diagnosis and treatment. Ethical considerations.
- The baby in the body.
- Ten bad reasons for not treating Baby K.
- Doctors'' experience and traumatic lumbar punctures.
- Informed consent in emergency research. Consensus statement from the Coalition Conference of Acute Resuscitation and Critical Care Researchers.
- The limited moral significance of 'fetal viability'.
- Practicing procedures on dying children.
- Research on the brain dead.
- Ethical issues in the treatment of critically ill newborns.
- Counseling families who have a child with a severe congenital anomaly.
- The rights of emotionally abused children.
- The rights of infants with Down's syndrome.
- Passive euthanasia of patients with Down's syndrome.
- Putting hospitals on notice.
- Why do sickle screening in children?
- Our curious attitude toward the fetus.
- Hospital ethics committees. Administrative aspects.
- Banning drugs in sports: a skeptical view.
- Parents as decision makers for children.
- AIDS in context: ethical and social implications.
- Organs from anencephalic infants: an idea whose time has not yet come.
- Treatment of seriously ill and handicapped newborns.
- Informed consent, deception, and the use of disguised alcohol questionnaires.
- Maternal-fetal conflicts: ethical and legal considerations.
- Neonatal screening for cystic fibrosis in Wisconsin.
- Guiding principles for prenatal diagnosis.
- A prospective randomized trial of early diagnosis and treatment of cystic fibrosis: a unique ethical dilemma.
- Removing organs from anencephalic infants: ethical and legal considerations.
- Do the right thing: Samuel Linares and defensive law.
- The cystic fibrosis gene: medical and social implications for heterozygote detection.
- Ethical issues in genetics.
- Ethical considerations in testing victims of sexual abuse for HIV infection.
- Psychological impact of false-positive results when screening for cystic fibrosis.
- Ethical implications of screening asymptomatic individuals.
- Parents' knowledge of neonatal screening and response to false-positive cystic fibrosis testing.
- Ethical dilemmas in child and adolescent consultation psychiatry.
- Introduction: ethics, ethics everywhere.
- The introduction of cystic fibrosis carrier screening into clinical practice: policy considerations.
- Passive euthanasia of defective newborn infants: legal considerations.
- Ethical issues regarding case reports: to publish or perish the thought.
- Ethical problems in pediatrics.
- The goals of medical education.
- Sounding Board. Consent as a barrier to research.
- Children as renal donors.
- Prenatal diagnosis of Down''s syndrome.
- Doing right for children.
- The ambiguities of 'deferred consent'
- Deferring consent with incompetent patients in an intensive care unit.
- Food for thought: Dresser on anorexia.
- Perceived risks of participation in an epidemiologic study.
- "I was like -- whoa": a commentary on Shapiro's Performance enhancement and the control of attributes.
- A pilot seminar on ethical issues in clinical trials for cancer researchers in Vietnam.
- Ethical issues in clinical research on fracture prevention in patients with osteoporosis.
- Ethics and equipoise: rationale for a placebo-controlled study design of platelet glycoprotein IIb/IIIa inhibition in coronary intervention.
- Prenatal screening for cystic fibrosis: where are we now?
- Balancing benefits and risks for cystic fibrosis newborn screening: implications for policy decisions.
- Gather ye shibboleths while ye may.
- America's Gulag Archipelago.
- Reconsidering the dead donor rule: is it important that organ donors be dead?
- Health Insurance Portability Accountability Act (HIPAA) regulations: effect on medical record research.
- hGH for short stature: ethical issues raised by expanded access.
- Ashley revisited: a response to the critics.
Schools
Yale University
Harriet Lane Ser
Harriet Lane Opd
Johns Hopkins Hospital
Harvard School Pub Health
Doctors Specialties
- Pediatrics
Accepted Insurances
Awards
- Fellow (FAAP)
Education
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Johns Hopkins University -
Yale University School of Medicine
Hospital
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University of Wisconsin Hospital and Clinics
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