Results 331 to 340 of about 1,138,095 (392)
Some of the next articles are maybe not open access.
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 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
Youth Violence and Juvenile Justice, 2020
Childhood maltreatment and inept parental disciplinary, attachment, and monitoring practices evidence a relationship with early and severe childhood and adolescent aggression and have figured prominently as causative factors in theoretical and empirical ...
Michael T. Baglivio +3 more
semanticscholar +1 more source
Childhood maltreatment and inept parental disciplinary, attachment, and monitoring practices evidence a relationship with early and severe childhood and adolescent aggression and have figured prominently as causative factors in theoretical and empirical ...
Michael T. Baglivio +3 more
semanticscholar +1 more source
Youth Violence and Juvenile Justice, 2020
A growing body of research has demonstrated the deleterious effects of adverse childhood experiences (ACEs). Less understood is the role of ACEs in gang involvement among juvenile offenders.
Kevin T. Wolff +5 more
semanticscholar +1 more source
A growing body of research has demonstrated the deleterious effects of adverse childhood experiences (ACEs). Less understood is the role of ACEs in gang involvement among juvenile offenders.
Kevin T. Wolff +5 more
semanticscholar +1 more source
Juvenile spondyloarthropathies
Current Opinion in Rheumatology, 2000This 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
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 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
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 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
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
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
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 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
Seminars in Hematology, 2002
Juvenile hemochromatosis or type 2 hemochromatosis is a rare inherited recessive disease, which leads to severe iron overload earlier in life than HFE-related hemochromatosis. Increased transferrin saturation and serum ferritin as well as parenchymal iron deposition and liver fibrosis may be observed in childhood.
C. Camaschella +2 more
openaire +3 more sources
Juvenile hemochromatosis or type 2 hemochromatosis is a rare inherited recessive disease, which leads to severe iron overload earlier in life than HFE-related hemochromatosis. Increased transferrin saturation and serum ferritin as well as parenchymal iron deposition and liver fibrosis may be observed in childhood.
C. Camaschella +2 more
openaire +3 more sources
Zeitschrift für Rheumatologie, 2006
Juvenile dermatomyositis (JDM) is an inflammatory multi-system disease of unknown etiology with classic involvement of the skin and striated muscles. Following a prodromal period, patients develop a progressive proximal muscle weakness. Typical skin involvement includes heliotrope rash, facial erythema, Gottron's sign and nailfold capillary ...
F, Dressler, H-I, Huppertz
openaire +2 more sources
Juvenile dermatomyositis (JDM) is an inflammatory multi-system disease of unknown etiology with classic involvement of the skin and striated muscles. Following a prodromal period, patients develop a progressive proximal muscle weakness. Typical skin involvement includes heliotrope rash, facial erythema, Gottron's sign and nailfold capillary ...
F, Dressler, H-I, Huppertz
openaire +2 more sources