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Gastroenterological disorders in inborn errors of immunity. Part 1. Epidemiology, classification, symptoms, diagnosis, and treatment. [PDF]

open access: yesPrz Gastroenterol
Napiórkowska-Baran K   +7 more
europepmc   +1 more source

Prenatal Identification of an EDA Variant in Dichorionic Male Twins: CfDNA Signal with Invasive Confirmation. [PDF]

open access: yesGenes (Basel)
Marcella S   +14 more
europepmc   +1 more source
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Equine anhidrosis

Veterinary Clinics of North America: Equine Practice, 2002
The molecular basis of the pathophysiology of anhidrosis is still not well understood. Therefore, treatments are more often based on clinical impressions than on scientific fact. Treatment options for this condition will improve only when more is known about the molecular events that cause anhidrosis, especially as they relate to beta2-receptor ...
Jeremy D, Hubert   +2 more
openaire   +2 more sources

Chronic idiopathic anhidrosis

Annals of Neurology, 1985
AbstractWe describe the cases of eight patients with chronic idiopathic anhidrosis. These patients were heat intolerant and became hot, flushed, dizzy, dyspneic, and weak but did not sweat when the ambient temperature was high or when they exercised.
P A, Low   +5 more
openaire   +2 more sources

Equine sweating and anhidrosis
Part 2: anhidrosis

Veterinary Dermatology, 2007
AbstractThe condition of anhidrosis is described in this review, and the latest theories on the causal factors are explored. The evidence supports the hypothesis that anhidrosis is an inappropriate response to prolonged climatic stress (generally combined heat and high humidity), which can be evoked in a small (∼10 ± 5%) proportion of the equine ...
David McEwan, Jenkinson   +2 more
openaire   +2 more sources

Progressive Isolated Segmental Anhidrosis

Archives of Neurology, 1982
A patient had progressive segmental anhidrosis, which proved after extensive neurologic and autonomic workup to be an isolated abnormality. Intradermal acetylcholine produced localized sweating in areas of thermoregulatory anhidrosis five months after the onset of symptoms but failed to do so at two years.
A I, Faden, P, Chan, E, Mendoza
openaire   +2 more sources

Familial and Congenital Simple Anhidrosis

Archives of Pediatrics & Adolescent Medicine, 1967
THE TERM anhidrotic ectodermal dysplasia originally suggested by Weech in 1929,1is now generally accepted for a syndrome characterized by anhidrosis, hypodontia, and hypotrichosis. This is a congenital disorder of world-wide distribution and although it is rare, the literature that has accumulated on the subject is considerable.
M, Mahloudji, K E, Livingston
openaire   +2 more sources

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