Dr. Jamie Lynne Lohr M.D.
Cardiologist (Pediatric) | Pediatric Cardiology516 Delaware Street Se, Pwb Fourth Floor Room 4- Minneapolis MN, 55455
Dr. Jamie Lohr is a pediatric cardiologist practicing in Minneapolis, MN. Dr. Lohr specializes in caring for fetuses, infants, children and adolescents with cardiovascular or cardiac abnormalities. Practiced in both inpatient and outpatient settings, the scope of conditions cared for by pediatric cardiologists is large and includes congenital heart defects, heart muscle disorders, rhythm disturbances and hypertension.
Expert PublicationsData provided by the National Library of Medicine
- Expression of cardiac neural crest and heart genes isolated by modified differential display.
- Cardiac neural crest ablation alters Id2 gene expression in the developing heart.
- Molecular cloning and expression of Ena/Vasp-like (Evl) during Xenopus development.
- PINCH-1 expression during early avian embryogenesis: implications for neural crest and heart development.
- WNT5A mutations in patients with autosomal dominant Robinow syndrome.
- Implementation of critical congenital heart disease screening in Minnesota.
- A comparison of retesting rates using alternative testing algorithms in the pilot
- Compliance with Adult Congenital Heart Disease Guidelines: Are We Following the Recommendations?
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Patient Experience with Dr. Lohr
- Congenital Heart Defects
Surgical treatment is the most appropriate option for inborn heart defects, which is not something you can put off.What is a congenital heart defect (CHD)?It is combined damage of the heart muscle in which there are structural deformations and anomalies in the inner chamber partitions, as well as...
- Newborn Diagnosis: Tetralogy of Fallot
Tetralogy of FallotTetralogy of Fallot is a congenital heart defect, which affects the heart’s structure, causing blood with low levels of oxygen to circulate throughout the body. Babies born with tetralogy of Fallot tend to have a blue discoloration of the skin due to low oxygen levels in their...
- What Is Progeria?
Progeria or Hutchinson-Gilford progeria syndrome (HGPS), is a rare genetic condition characterized by a rapidly aging appearance in children. Newborns and infants born with this condition typically look healthy and normal, but may physically display characteristic facial features, such as prominent...
- What Is Neonatal Lupus?
Neonatal lupus is a not so common autoimmune disease. It is not true lupus as all the symptoms will completely disappear after 6 months of age. Neonatal lupus is also known by several other terms. The condition is also called as:...
- What is Kawasaki Disease?
Kawasaki disease is a rare childhood disease that causes inflammation of the arteries in the body. The characteristic symptoms of the disease, which is high fever and peeling skin, remains for almost a week. In most cases, it gets back to normal without any major issues. Children will be monitored...
- Different Types of Heart Doctors Explained
IntroductionDoctors who specialize in the diagnosis and treatment of conditions or diseases of the cardiovascular system (the heart and blood vessels) are called heart doctors or cardiologists. These specialists are trained to identify, treat, and help prevent heart issues. There are also different...
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