Results 251 to 260 of about 36,453 (301)
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Acute Intermittent Porphyria

Australian and New Zealand Journal of Surgery, 1973
This rare inherited disease presents with abdominal pain, psychiatric symptoms and neuropathies. Because it may mimic an acute surgical (or less frequently, psychiatric) emergency, it is important in clinical practice. The complication of respiratory paralysis, with a mortality of over 90%, is almost solely due to aggravation of an attack by drugs ...
openaire   +2 more sources

Acute intermittent porphyria presenting with posterior reversible encephalopathy syndrome (PRES) and abdominal pain

Practical Neurology, 2020
Acute intermittent porphyria is a rare genetic condition in which disrupted haem synthesis causes overproduction of porphyrin precursors. Occasionally, it is associated with posterior reversible encephalopathy syndrome (PRES), presenting with headache ...
G. Swart, Su San Lim, M. Jude
semanticscholar   +1 more source

Intermittent Acute Porphyria

Archives of Internal Medicine, 1982
PAULA Davis, MD, Senior Assistant Resident in Medicine, the Jewish Hospital of St Louis: A 26-year-old woman was admitted for the first time at the Jewish Hospital for evaluation of a seizure disorder, weakness, hypertension, and possible tularemia. In August 1981, the patient was hospitalized because of fatigue and aching pain in the lower part of the
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Recurrence of Acute Intermittent Porphyria After Liver Transplantation

Annals of Internal Medicine, 2019
Background: Acute intermittent porphyria (AIP) is a rare indication for liver transplantation, but published cases describe resolution of disease after transplantation, with clinical remission and normalization of biochemical parameters within 72 hours ...
H. Al-Samkari   +3 more
semanticscholar   +1 more source

Molecular genetic study of acute intermittent porphyria in Russia: HMBS gene mutation spectrum and problem of penetrance

Clinical Genetics, 2019
Acute intermittent porphyria (AIP) is the most common and severe form of porphyrias. This is a dominant inherited disorder with low penetrance, caused by mutations in gene coding hydroxymethylbilane synthase (HMBS).
M. Goncharova   +5 more
semanticscholar   +1 more source

Acute Intermittent Porphyria

Annals of Internal Medicine, 1981
K E, Anderson, S, Sassa, A, Kappas
openaire   +4 more sources

Acute Intermittent Porphyria

Psychosomatics, 1999
L, Regan, L, Gonsalves, G, Tesar
openaire   +2 more sources

Acute Intermittent Porphyria

Psychosomatic Medicine, 1954
J S, VISHER, C K, ALDRICH
openaire   +2 more sources

Acute Intermittent Porphyria

JAMA: The Journal of the American Medical Association, 1990
openaire   +2 more sources

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