Results 171 to 180 of about 56,273 (232)

Radiographic findings in the mucocutaneous lymph node syndrome

American Journal of Roentgenology, 1979
The mucocutaneous lymph node syndrome was first described in English in 1974 by Kawasaki et al. [1]; before that time more than 6,000 cases had been reported in Japan. The syndrome has been clinically confused with the Dubin-Johnson syndrome and scarlet fever. Most patients are younger than 5 years and about half are younger than 2.
Albert J. Cook, Philippe Lheureux
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Mucocutaneous Lymph Node Syndrome in Denver

Archives of Pediatrics & Adolescent Medicine, 1976
Four children with acute febrile mucocutaneous lymph node syndrome (MLNS) were hospitalized in Denver over a two-year period. The children had most of the principle features of this recently described syndrome, including prolonged fever unresponsive to antibiotics, an erythematous rash, conjunctivitis, pharyngitis, and nonsuppurative cervical ...
Jim Todd, Frederic W. Bruhn, Brian A. Lauer, Warren A. Todd   +3 more
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Ultrasonography of mucocutaneous lymph node syndrome.

Radiology, 1981
Clinical findings associate mucocutaneous lymph node syndrome (MCLS) with diffuse arteritis leading to the formation of large aneurysms. Ultrasound assists in the diagnosis of the associated aneurysms, and aids the clinical management of the patients.
H Kangarloo, Josephine Isabel-Jones, M S Vangrov, H Heins, T G Di Sessa   +4 more
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Cardiac death in mucocutaneous lymph node syndrome

The American Journal of Cardiology, 1977
A 12 year old boy had 4 symptom-free years after hospitalization for acute febrile mucocutaneous lymph node syndrome before he died suddenly from extensive myocardial infarction. Current evidence suggests that many patients with this syndrome have coronary artery disease and that those with significant cardiac findings should be studied with coronary ...
Stanley M. Kegel, Thomas J. Dorsey, Marshall Rowen, William F. Taylor   +3 more
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Mucocutaneous lymph node syndrome with necrotic pharyngitis

European Journal of Pediatrics, 1980
We report a case of Kawasaki disease in which some unusual symptoms, including petechiae, an urticaria-like eruption, and necrotic pharyngitis, made the diagnosis difficult. No complications were detected during a follow-up period of 15 months.
Brion, Luc, Bachelart, D., Szliwowski, Henri, Dickstein, M, Tondeur, Marianne, Heenen, Michel, Courtoy, Michel   +6 more
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HLA Antigens in Mucocutaneous Lymph Node Syndrome

Archives of Pediatrics & Adolescent Medicine, 1977
Kawasaki disease or mucocutaneous lymph node syndrome (MLNS), first described by Kawasaki 1-2 in 1974, is an acute febrile disease of unknown etiology. Until recently, more than 6,000 cases of this disease have been listed in the survey of a special study group supported by the Japanese Ministry of Health and Welfare.
Shinzabro Hattori, Noriyuki Nagata, Akemi Wakisaka, Katsuki Itakura, Haruo Nambu, Ichiro Matsuda, Akio Fruse   +6 more
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Mucocutaneous Lymph Node Syndrome in a Young Adult

Archives of Internal Medicine, 1979
Mucocutaneous lymph node syndrome (MLNS) is an acute febrile illness of unknown cause first described in Japan but more recently reported in the United States. The mean age in confirmed cases was 3.8 years (range, 3 months to 13 years), and the mortality is 1% to 2% when associated with coronary artery thrombosis and aneurysm.
Terrence J. Lee, Daniel Vaughan
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Mucocutaneous Lymph Node Syndrome in the United States

Archives of Pediatrics & Adolescent Medicine, 1976
Sixteen patients with an unusual and distinct symptom complex were encountered during a four-year period. Principal features of this syndrome are (1) fever lasting more than seven days; (2) conjunctival injection; (3) changes in the mouth consisting of erythema of the oropharynx, "strawberry tongue", and erythema of the lips; (4) indurative edema of ...
Raquel Hicks, Eunice J. Larson, Marian E. Melish   +2 more
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Mucocutaneous lymph node syndrome with testicular involvement

Irish Journal of Medical Science, 1980
A case of mucocutaneous lymph-node syndrome (MLNS) occurring in a 6 year old boy is reported. This is the first case we are aware of in which epididymo-orchitis is described.
K. D. Connolly, Dolores Timmons
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Kawasaki Syndrome (The Mucocutaneous Lymph Node Syndrome)

Annual Review of Medicine, 1982
Kawasaki syndrome is a newly-recognized clinical entity characterized by multisystem involvement. It has an acute onset and triphasic clinical course. Although essentially a self-limiting disease, permanent vascular damage, especially involving the coronary arteries, may result.
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