Edward E. Velayos, M.D.; Harry Robinson, SC.D.; Mary Betty Stevens, M.D., F.A.C.P.; Alfonse T. Masi, M.D., F.A.C.P.
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In order to better define the clinical and laboratory manifestations of Raynaud's phenomenon data abstracted from records of 137 patients diagnosed from 1952 to 1963 in a university hospital were analyzed. The cases were subdivided into three groups: I. Raynaud's phenomenon with no other diagnoses; II. Raynaud's phenomenon with other diseases but not connective tissue disorders; and III. Raynaud's phenomenon with connective tissue disorders. Some demographic data on the case series are shown in the table.
Group II had 16% unilateral disease with approximately equal numbers of males and females with similar onset ages. In contrast, the other groups had
Velayos EE, Robinson H, Stevens MB, et al. Clinical-Laboratory Correlation Analysis Among 137 Patients With Raynaud's Phenomenon.. Ann Intern Med. 1970;72:782–783. doi: 10.7326/0003-4819-72-5-782_4
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Published: Ann Intern Med. 1970;72(5):782-783.
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