Zobrazeno 1 - 9
of 9
pro vyhledávání: '"F. S. Camporeale"'
Publikováno v:
The Italian Journal of Neurological Sciences. 12:407-413
A 42 year old woman with foot process disease, was treated with corticosteroids for 6 years. She had been suffering, for about 3 years from progressive muscle weakness of the limbs, accompanied by general paresthesia, cramps of the calves and burning
Autor:
M. Cioffi, A. V. M. Orsini, G. De Mattia, M. Ricci, M. Marolda, F. S. Camporeale, G. A. Buscaino
Publikováno v:
Italian journal of neurological sciences. 13(1)
We report the case of a 49 year old woman with clinical, electrophysiological and histochemical signs of facio-scapulohumeroperoneal dystrophy characterized by highly inflammatory changes. Lymphocyte typing by immunofluorescence and immunoperoxidase
Publikováno v:
Italian journal of neurological sciences. 12(4)
A 42 year old woman with foot process disease, was treated with corticosteroids for 6 years. She had been suffering, for about 3 years from progressive muscle weakness of the limbs, accompanied by general paresthesia, cramps of the calves and burning
Autor:
F S Camporeale, R Santagelo, M Marolda, F Barbieri, V Vecchione, Salvatore Striano, Michele Ragno, A Catalano, C. Crisci, G Orefice
Publikováno v:
The Italian Journal of Neurological Sciences. 10:79-84
A case of idiopathic hypereosinophilic syndrome (HES) is reported. The disease started at the age of 31, with polyneuropathic-like symptoms and disorders of the gastrointestinal tract. Hypereosinophilia and leukocytosis were observed. Instrumental in
Publikováno v:
Rivista di neurologia. 53(3)
The authors describe the case of a 36 years old woman suffering from muscular weakness with proximo-distal distribution to legs, and proximal to arms. The disease, appeared during the third decade of life, is slowly becoming more serious. Hematochemi
Autor:
M, Marolda, F S, Camporeale
Publikováno v:
Acta neurologica. 9(5-6)
Publikováno v:
Rivista di neurologia. 56(3)
A clinical, histologic and ultrastructural study of a woman suffering for a slight form of spinal muscular atrophy and his heterozygotic husband is reported. The woman is daughter of kindred and her brothers have variable clinical manifestation of th
Autor:
F. S. Camporeale, M. Cauli, M. Cioffi, S. Noce, A. V. M. Orsini, M. Marolda, A. Bassi, M. Carandente, R. De Mercato
Publikováno v:
Italian journal of neurological sciences. 10(4)
We report 3 cases of AIDS complicated by muscular disease: 2 with acute polymyositis and 1 with severe noninflammatory myopathy. Tests for an alternative infectious etiology were negative. HIV may well have a tropism for muscle tissue.