Dr. George Porter is a pediatric cardiologist practicing in New Haven, CT. Dr. Porter 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.
- The medical consequences of nuclear war: introduction.
- Sinus node dysfunction associated with lithium therapy in a child.
- Non-contrast-enhanced computerized tomography and analgesic-related kidney disease: report of the national analgesic nephropathy study.
- Novel sorbents for removal of gadolinium-based contrast agents in sorbent dialysis and hemoperfusion: preventive approaches to nephrogenic systemic fibrosis.
- Bioenergetics, mitochondria, and cardiac myocyte differentiation.
- The permeability transition pore controls cardiac mitochondrial maturation and myocyte differentiation.
- Mitochondria as a drug target in ischemic heart disease and cardiomyopathy.
- SIRT3 deficiency exacerbates ischemia-reperfusion injury: implication for aged hearts.
- Bcl-xL in neuroprotection and plasticity.
- Initiation of electron transport chain activity in the embryonic heart coincides with the activation of mitochondrial complex 1 and the formation of supercomplexes.
- Cell death disguised: The mitochondrial permeability transition pore as the c-subunit of the F(1)F(O) ATP synthase.
- Extraembryonic but not embryonic SUMO-specific protease 2 is required for heart development.
- The Mitochondrial Permeability Transition Pore and ATP Synthase.
- Erratum to: The Mitochondrial Permeability Transition Pore and ATP Synthase.
- Preventing permeability transition pore opening increases mitochondrial maturation, myocyte differentiation and cardiac function in the neonatal mouse heart.
- Analyzing Supercomplexes of the Mitochondrial Electron Transport Chain with Native Electrophoresis, In-gel Assays, and Electroelution.
- Cyclophilin D regulates the dynamic assembly of mitochondrial ATP synthase into synthasomes.
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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 Duchenne Muscular Dystrophy? Causes, Symptoms, and Treatment
Muscular dystrophies are a group of diseases that make the muscles of the body weaker over a period of time. The muscles become less flexible in this condition. Out of the nine types of muscular dystrophy, Duchenne muscular dystrophy is one of the most common.The main characteristics of this medical...
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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...
- Muscular Dystrophy: Telling a Child the Truth About His/Her Condition
Muscular dystrophy is a category of muscle diseases that cause progressive weakness and loss of muscle mass. Muscular dystrophy (MD) is either inherited or can be due to a genetic mutation. Kids with MD usually follow a normal pattern of growth development in the first few years of their lives,...
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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...
- 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...
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