Results 171 to 180 of about 6,050 (216)
Some of the next articles are maybe not open access.

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.
Nancy L. Kuntz   +5 more
openaire   +3 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 ...
Hugh Y. Elder   +2 more
openaire   +3 more sources

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

Adhesive Tape Anhidrosis

Archives of Dermatology, 1969
Eccrine anhidrosis was produced using occlusive techniques with porous and nonporous tapes. The degree of sweat inhibition was measured and the more occlusive tapes produced the most marked anhidrosis. Plastic occlusive film (Saran Wrap) produced nearly as much anhidrosis as the most adherent and occlusive tape.
Bernard I. Gordon, Howard I. Maibach
openaire   +3 more sources

Congenital insensitivity of pain with anhidrosis [PDF]

open access: possibleThe Indian Journal of Pediatrics, 2003
Congenital insensitivity to pain with anhidrosis is an autosomal recessive disorder included in a group of rare diseases termed as hereditary sensory-motor neuropathies. The diagnosis is made usually in early childhood period as most of the children present with recurrent unexplained hyperpyrexia.
openaire   +2 more sources

Acquired Generalized Anhidrosis

Archives of Dermatology, 1966
A case of subtotal generalized anhidrosis is reported. The clinical findings and history suggested a neurogenic origin or relationship.
Mark Allen Everett, Dennis A. Weigand
openaire   +3 more sources

Acquired Generalized Anhidrosis

Archives of Dermatology, 1976
A patient developed generalized anhidrosis, probably following sunstroke. Light microscopy showed an atrophic, deeply lobulated or elongated configuration of the eccrine sweat glands, most of them containing many vacuoles that possessed strong acid phosphatase activity.
Tetsuo Yamamoto, Takuo Tsuji
openaire   +3 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.
Mohsen Mahloudji, Kenneth E. Livingston
openaire   +3 more sources

Anhidrosis (hypohidrosis) in Sjögren's syndrome

Journal of the American Academy of Dermatology, 1987
There has been a relative lack of literature on the association of hypohidrosis in Sjögren's syndrome with any lesion having specific histologic findings. We looked at a recent case presentation of a 55-year-old man with complaints of dry mouth and dry eyes, becoming easily overheated in direct sunlight, and having difficulty in perspiring.
Jerry Mitchell   +4 more
openaire   +2 more sources

Hereditary insensitivity to pain with anhidrosis

Pediatric Neurology, 1998
Hereditary sensory neuropathy type IV is an autosomal-recessive disorder characterized by congenital insensitivity to pain and anhidrosis and resulting in recurrent hyperpyrexia, self-mutilation, recurrent infections, chronic osteomyelitis, bone and joint deformities, and limb amputations.
Tsivia Tauber   +4 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy