Results 261 to 270 of about 393,493 (318)
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Juvenile Immunotoxicology

Toxicologic Pathology, 2012
Developmental immunotoxicity (DIT) testing is centered around the concern that exposure to immunotoxicants early in development may result in enhanced susceptibility of, or unique or more persistent effects on, the immune system, in comparison to adult exposure.
Michael P, Holsapple, Raegan, O'Lone
openaire   +2 more sources

Juvenile parkinsonism

Seminars in Pediatric Neurology, 2003
Juvenile parkinsonism (JP) is a clinically and etiologically heterogeneous entity. Unlike in the adult form, secondary causes, hereditary and metabolic conditions, are the predominant causes of JP. Idiopathic Parkinson's disease is very rare in this age group.
Ergun Y, Uc, Robert L, Rodnitzky
openaire   +2 more sources

Juvenile Firesetting

Child and Adolescent Psychiatric Clinics of North America, 2016
Juvenile firesetting is a significant cause of morbidity and mortality in the United States. Male gender, substance use, history of maltreatment, interest in fire, and psychiatric illness are commonly reported risk factors. Interventions that have been shown to be effective in juveniles who set fires include cognitive behavior therapy and educational ...
Brittany, Peters, Bradley, Freeman
openaire   +2 more sources

Juvenile Dermatomyositis

Rheumatic Disease Clinics of North America, 1991
Juvenile dermatomyositis is a relatively rare, multisystem disease characterized by a nonsuppurative myositis which causes symmetrical weakness, rash and vasculitis; this last can affect the gastrointestinal tract and the myocardium. Late development of calcinosis is seen in approximately two thirds of patients.
openaire   +3 more sources

Juvenile chronic arthritis and juvenile spondyloarthropathy

Current Opinion in Rheumatology, 1991
Clinically recognized subgroups of juvenile chronic arthritis and the juvenile spondyloarthropathies are gradually being shown to be immunogenetically distinct; greater subdivision may ultimately be required. Mechanisms by which the association of certain genes work await further elucidation. Meanwhile, therapy such as intravenous gamma globulin may be
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Juvenile nephronophthisis

Irish Journal of Medical Science, 1981
The clinical histories and laboratory investigations of 5 patients with juvenile nephronophthisis from 3 kindreds are described. Special emphasis is made on renal function replacement, especially transplantation, in which the original disease has not recurred.
J F, Walker   +4 more
openaire   +2 more sources

Juvenile Fibromatosis

Annals of Otology, Rhinology & Laryngology, 1979
Juvenile fibromatosis is a benign lesion with locally aggressive characteristics. Wide surgical excision is the treatment of choice. Radiation therapy can be used for inoperable cases or as adjunctive therapy. Steroid therapy has not been used extensively and deserves further evaluation.
W T, Morioka, V C, Heath, R W, Cantrell
openaire   +2 more sources

Juvenile spondyloarthropathies

Current Opinion in Rheumatology, 2000
This paper reviews the recent literature on the juvenile spondyloarthropathies. Several case reports emphasized clinical characteristics of the spondyloarthropathies including reactive arthritis. MR imaging seemed to enhance the detection of sacroiliitis in children with spondyloarthropathies.
P H, Pepmueller, T L, Moore
openaire   +2 more sources

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