Results 251 to 260 of about 394,901 (310)

Juveniles and where to find them: a basin-scale habitat model for the lost years of loggerhead sea turtles in the North Atlantic. [PDF]

open access: yesMov Ecol
Bartolini M   +14 more
europepmc   +1 more source

Serological Evidence of Flavivirus Exposure and Limited Avian Influenza Exposure in Urban House Martins from Southwestern Spain. [PDF]

open access: yesAnimals (Basel)
Hernandez-Caballero I   +7 more
europepmc   +1 more source
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Juvenile Fibromyalgia

Rheumatic Disease Clinics of North America, 2021
Juvenile fibromyalgia is a common referral in pediatric rheumatology settings. Providing a clear diagnosis and explanation of altered pain processing offers reassurance that pain has a biologic basis and the symptoms are part of a recognized pain syndrome.
Jennifer E, Weiss   +1 more
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

Juvenile Xanthogranuloma

Journal of Pediatric Ophthalmology & Strabismus, 1982
Juvenile xanthogranuloma (JXG) is a disease of unknown etiology and pathogenesis which was first recognized by dermatologists. The ocular complications provide the primary concern and notably affect the iris, producing spontaneous hemorrhages in the anterior chamber.
R D, Harley, N, Romayananda, G H, Chan
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 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 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

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