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2004 (v1)PublicationUploaded on: April 14, 2023
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2000 (v1)Publication
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Uploaded on: April 14, 2023 -
2002 (v1)Publication
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Uploaded on: April 14, 2023 -
1988 (v1)Publication
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Uploaded on: March 31, 2023 -
2002 (v1)Publication
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Uploaded on: October 11, 2023 -
2001 (v1)Publication
To determine in a prospective analysis whether baseline demographic, clinical, and laboratory variables predict the outcome of intraarticular corticosteroid (IAC) injection of the knees in children with juvenile idiopathic arthritis (JIA).We studied consecutive patients who met the criteria for the diagnosis of JIA and received their initial...
Uploaded on: March 31, 2023 -
2001 (v1)Publication
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Uploaded on: March 31, 2023 -
1987 (v1)Publication
We describe a girl who presented at age 5 with objective signs of arthritis and was initially diagnosed as having juvenile rheumatoid arthritis. Over the following years, she developed slowly progressive joint deformities indicative of Jaccoud's arthropathy. When she was 11 years old, symptoms typical of systemic lupus erythematosus appeared,...
Uploaded on: April 14, 2023 -
1996 (v1)Publication
A macrophage activation syndrome, possibly related to methotrexate toxicity, developed in a boy with systemic juvenile rheumatoid arthritis. Corticosteroid administration was ineffective, whereas a prompt response to cyclosporine was observed. Two months later, Pneumocystis carinii pneumonia developed.
Uploaded on: March 27, 2023 -
1991 (v1)Publication
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Uploaded on: April 14, 2023 -
1986 (v1)Publication
A 10-month-old female presented with anuria due to bilateral cystine urolithiasis. Although bilateral obstruction of the ureters by calculi is very rare in children, it may be the presenting feature of cystinuria even in the first year of life.
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1987 (v1)Publication
We describe a 14-month-old child with dermatomyositis in whom calcinosis was the first sign of the disease. This case shows that calcinosis, usually a late complication of dermatomyositis, may be the presenting sign of the disease even in young children and when Gottron's sign is still absent and muscular weakness not prominent.
Uploaded on: March 31, 2023 -
1988 (v1)Publication
Hypergammaglobulinemic purpura is a rare syndrome characterized by long-standing recurrent purpura of the lower limbs, polyclonal hypergammaglobulinemia, increased erythrocyte sedimentation rate and high titer rheumatoid factor positivity. The syndrome can occur isolated or in association with a systemic disease. Few cases have been described...
Uploaded on: March 27, 2023 -
1999 (v1)Publication
To investigate the efficacy of folinic acid in reducing the side effects associated with methotrexate (MTX) therapy in children with juvenile idiopathic arthritis (JIA) and to determine whether folate supplementation may reduce the benefit of MTX administration.This was a retrospective, non-controlled study. Inclusion criteria were: 1)...
Uploaded on: March 27, 2023 -
1990 (v1)Publication
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Uploaded on: March 31, 2023