PMID: 13712535Oct 15, 1960Paper

Chromosomal trisomy associated with the Sturge-Weber syndrome

Lancet
M D HAYWARD, B D BOWER

Abstract

No abstract listed.

References

Jun 7, 1958·Nature·C E FORDL G LAJTHA
Apr 9, 1960·Lancet·J H EDWARDSO H WOLFF
Apr 2, 1960·Lancet·M FRACCAROJ LINDSTEN
Jun 4, 1960·Lancet·P A JACOBSJ A STRONG

Citations

May 25, 1963·Canadian Medical Association Journal·K L Moore, J C Hay
Jan 1, 1969·Zeitschrift Für Kinderheilkunde·J Keutel, I Dauner
Jan 1, 1976·Seminars in Roentgenology·C M CoulamD F Reese
Sep 7, 1963·Lancet·T DENTJ D DELHANTY
Aug 17, 1961·The New England Journal of Medicine·L ATKINS, M K ROSENTHAL
Oct 12, 1967·The New England Journal of Medicine·M S Al-AishJ C Robinson
May 1, 1996·International Journal of Dermatology·C Schepis, C Romano
Jul 1, 1962·Annals of Human Genetics·J R ELLISL S PENROSE
Nov 1, 1965·Annals of Human Genetics·M D Crawfurd, K P Lele
Jul 1, 1983·Pediatric Dermatology·J C Alper, L B Holmes
Jun 1, 1963·The British Journal of Ophthalmology·J F CULLEN, H G BUTLER
Jun 1, 1965·Journal of Medical Genetics·J ISHMAEL, K M LAURENCE
Jun 1, 1967·Journal of Medical Genetics·C B LozzioM A Gambin
Sep 1, 1968·Journal of Medical Genetics·M J ThorburnR Bell
Dec 1, 1968·Journal of Medical Genetics·W M Brown
May 1, 1961·Postgraduate Medical Journal·M D HAYWARDO H WOLFF
Mar 1, 1961·Eugenics Quarterly·O J MILLERK HIRSCHHORN
Apr 1, 1964·The American Journal of Medicine·K L MELMON, S W ROSEN
Jun 1, 1982·Acta Neurologica Scandinavica·I Granberg-OhmanJ Mark
Aug 1, 1981·Clinical Pediatrics·S R Patil, H Zellweger
Jul 1, 1976·Clinical Pediatrics·H ZellwegerL Burmeister
Jul 1, 1976·Journal of Neurosurgery·K Shapiro, K Shulman
Sep 13, 2006·Acta Ophthalmologica Scandinavica·François AudrenJean-Louis Dufier
Jul 1, 1969·The American Journal of Orthopsychiatry·K K Minde, J S Werry
Dec 1, 1966·Acta Medica Scandinavica·J NielsenA Froland
Jan 1, 1974·Clinical Genetics·L O SulicaS A Shah
Jan 1, 1965·Acta neurochirurgica·J M SCHROEDER, C V BRUNNGRABER
Jun 1, 1973·Clinical Genetics·S MuldalR Harris
Dec 1, 1964·Journal of Mental Deficiency Research·P M LORDF J ESHER
Jan 1, 1963·Acta Paediatrica. Supplement·B HALL
May 1, 1964·Australasian Annals of Medicine·D PITTA G BAIKIE
Nov 18, 1961·The Medical Journal of Australia·A N JENNINGS, B TURNER

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.

Spatio-Temporal Regulation of DNA Repair

DNA repair is a complex process regulated by several different classes of enzymes, including ligases, endonucleases, and polymerases. This feed focuses on the spatial and temporal regulation that accompanies DNA damage signaling and repair enzymes and processes.

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.

Separation Anxiety

Separation anxiety is a type of anxiety disorder that involves excessive distress and anxiety with separation. This may include separation from places or people to which they have a strong emotional connection with. It often affects children more than adults. Here is the latest research on separation anxiety.

KIF1A Associated Neurological Disorder

KIF1A associated neurological disorder (KAND) is a rare neurodegenerative condition caused by mutations in the KIF1A gene. KAND may present with a wide range and severity of symptoms including stiff or weak leg muscles, low muscle tone, a lack of muscle coordination and balance, and intellectual disability. Find the latest research on KAND here.

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.