Results 151 to 160 of about 4,940 (188)
Some of the next articles are maybe not open access.

Mucocutaneous Lymph Node Syndrome

Journal of Computer Assisted Tomography, 1984
A 3-year-old child presented with a short clinical history of fever and diffuse cervical lymphadenopathy, and the diagnosis of mucocutaneous lymph node syndrome was reached. We include a discussion of the case history and a brief review of this disorder.
M, Puczynski   +3 more
openaire   +2 more sources

Acute Febrile Mucocutaneous Lymph Node Syndrome

open access: yesClinical Pediatrics, 1977
G, Hicsönmez   +3 more
openaire   +3 more sources

Mucocutaneous lymph node syndrome.

IMJ. Illinois medical journal, 1978
Mucocutaneous lymph node syndrome (MLNS) is a recently described disease entity of unknown etiology that mainly affects children. The disease is characterized by fever, oral mucosal changes, cervical lymphadenopathy and a peripheral skin rash with induration of hands and feet and subsequent desquamation.
M, Miriovsky, J S, Downing
openaire   +3 more sources

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, D, Timmons
openaire   +2 more sources

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.
A, Cook, P, L'Heureux
openaire   +2 more sources

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 ...
M E, Melish, R M, Hicks, E J, Larson
openaire   +2 more sources

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   +6 more
openaire   +3 more sources

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.
I, Matsuda   +4 more
openaire   +2 more sources

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 ...
S M, Kegel   +3 more
openaire   +2 more sources

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