1,721,111 research outputs found
studio clinico, istologico ed immunologico di un caso di morbo di Kaposi con successiva localizzazione in sede orofaringea
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amiloidosi cutanea organo-dipendente: studio istologico, ultrastrutturale, immunologico ed istochimico.
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Two rare diseases in the same patient: Neurofibromatosis type 1 and Madelung's disease
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Juvenile myelomonocytic leukemia in a patient with neurofibromatosis type 1 and xanthogranulomas
No full textMarie Unna hereditary hypotrichosis
No full textHereditary congenital :hypotrichosis is an autosomal dominant pilar dysplasia first described by Marie Unna in an extended German family. The diffuse hair defect typically occurs as an isolated phenomenon and the ultrastructural hair findings consist of-both torsion and longitudinal grooving of the hair shaft. A large pedigree comprising 6 generations with 20 members affected by Marie Unna hypotrichosis from Italy is reported
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