PMID: 13715441Sep 1, 1961Paper

Atherosclerosis--a pediatric nutrition problem?

The American Journal of Clinical Nutrition
R L HOLMAN

Abstract

No abstract listed.

Citations

Jan 1, 1975·Clinical Pediatrics·S G Bergman
Mar 1, 1986·Arteriosclerosis : an Official Journal of the American Heart Association, Inc·S Ylă-HerttualaH K Akerblom
Jun 5, 2003·Journal of Cardiopulmonary Rehabilitation·Paul Poirier, Jean-Pierre Després
Mar 12, 2005·Annual Review of Public Health·John Lynch, George Davey Smith
Nov 8, 2012·Experimental Diabetes Research·Laura J MarcoAnne-Louise Ponsonby
Jan 1, 1990·Pediatric Pathology·M D Haust
Jan 1, 1991·Annals of the New York Academy of Sciences·J P Strong
Jun 1, 1992·Journal of the American College of Nutrition·J P StrongM C Oalmann
Jun 1, 1993·Arteriosclerosis and Thrombosis : a Journal of Vascular Biology·M S WolfeL L Rudel
Jan 1, 1984·Journal of the American College of Nutrition·W B Kannel
Oct 4, 2002·Current Atherosclerosis Reports·Paul Poirier, Robert H Eckel
Jan 1, 1985·Acta Paediatrica Scandinavica. Supplement·H K AkerblomK Kouvalainen
Jun 3, 2018·Irish Journal of Medical Science·Karen KingClodagh S O'Gorman
Dec 29, 2019·American Journal of Human Biology : the Official Journal of the Human Biology Council·Suziane Ungari Cayres-SantosRomulo Araújo Fernandes
Jan 1, 1991·Annals of the New York Academy of Sciences·S Ylă-Herttuala
Dec 11, 1999·Current Opinion in Pediatrics·M R MascarenhasN Stettler
Feb 1, 2007·Annals of Saudi Medicine·M A El-Hazmi, A S Warsy
Nov 1, 1967·Journal of the American Oil Chemists' Society·K K Carroll
Jun 21, 1975·The Medical Journal of Australia·J C Quoyle

Related Concepts

Trending Feeds

COVID-19

Coronaviruses encompass a large family of viruses that cause the common cold as well as more serious diseases, such as the ongoing outbreak of coronavirus disease 2019 (COVID-19; formally known as 2019-nCoV). Coronaviruses can spread from animals to humans; symptoms include fever, cough, shortness of breath, and breathing difficulties; in more severe cases, infection can lead to death. This feed covers recent research on COVID-19.

STING Receptor Agonists

Stimulator of IFN genes (STING) are a group of transmembrane proteins that are involved in the induction of type I interferon that is important in the innate immune response. The stimulation of STING has been an active area of research in the treatment of cancer and infectious diseases. Here is the latest research on STING receptor agonists.

Chronic Fatigue Syndrome

Chronic fatigue syndrome is a disease characterized by unexplained disabling fatigue; the pathology of which is incompletely understood. Discover the latest research on chronic fatigue syndrome here.

Hereditary Sensory Autonomic Neuropathy

Hereditary Sensory Autonomic Neuropathies are a group of inherited neurodegenerative disorders characterized clinically by loss of sensation and autonomic dysfunction. Here is the latest research on these neuropathies.

Glut1 Deficiency

Glut1 deficiency, an autosomal dominant, genetic metabolic disorder associated with a deficiency of GLUT1, the protein that transports glucose across the blood brain barrier, is characterized by mental and motor developmental delays and infantile seizures. Follow the latest research on Glut1 deficiency with this feed.

Regulation of Vocal-Motor Plasticity

Dopaminergic projections to the basal ganglia and nucleus accumbens shape the learning and plasticity of motivated behaviors across species including the regulation of vocal-motor plasticity and performance in songbirds. Discover the latest research on the regulation of vocal-motor plasticity here.

Neural Activity: Imaging

Imaging of neural activity in vivo has developed rapidly recently with the advancement of fluorescence microscopy, including new applications using miniaturized microscopes (miniscopes). This feed follows the progress in this growing field.

Nodding Syndrome

Nodding Syndrome is a neurological and epileptiform disorder characterized by psychomotor, mental, and growth retardation. Discover the latest research on Nodding Syndrome here.

LRRK2 & Microtubules

Mutations in the LRRK2 gene are risk-factors for developing Parkinson’s disease (PD). LRRK2 mutations in PD have been shown to enhance its association with microtubules. Here is the latest research.