Sneddon syndrome revealing dysfibrinogenemia.

Khosrotehrani, Kiarash; Leroy-Matheron, Catherine; Mourier, Claude; Revuz, Jean; Bagot, Martine

Khosrotehrani, Kiarash; Leroy-Matheron, Catherine; Mourier, Claude; Revuz, Jean; Bagot, Martine.

Affiliation

Khosrotehrani K; Department of Dermatology, Hôpital Henri Mondor, Créteil Cedex, France.

Int J Dermatol ; 42(7): 561-2, 2003 Jul.

Article in En | MEDLINE | ID: mdl-12839611

Subject(s)

Blood Coagulation Disorders, Inherited/complications; Fibrinogens, Abnormal/biosynthesis; Sneddon Syndrome/complications; Adult; Aspirin/therapeutic use; Blood Coagulation Disorders, Inherited/drug therapy; Blood Coagulation Disorders, Inherited/metabolism; Fibrinolytic Agents/therapeutic use; Humans; Sneddon Syndrome/drug therapy

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Collection: 01-internacional Database: MEDLINE Main subject: Fibrinogens, Abnormal / Sneddon Syndrome / Blood Coagulation Disorders, Inherited Limits: Adult / Humans Language: En Journal: Int J Dermatol Year: 2003 Document type: Article Affiliation country: France Country of publication: United kingdom

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