Zobrazeno 1 - 10 of 211 pro vyhledávání: '"V, Biarese"'
1
[Systemic mastocytosis: a case with diffuse bone involvement]
Autor: V, Biarese, P, Raviolo, F, Cesarani, L, Lobetti
Publikováno v: Minerva medica. 87(1-2)
The authors report the case of a 54-year-old woman with systemic mastocytosis with cutaneous, gastroenteric and skeletal involvement. The patient, who had presented wine-coloured skin lesions for years diagnosed as urticaria pigmentosa on the basis o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6ede5d184c9ce40d8b2301ec9ad43553
https://pubmed.ncbi.nlm.nih.gov/8610023
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2
Benign recurrent intrahepatic cholestasis. Some reflections on a case followed for 20 years
Autor: P, Lovisetto, P, Raviolo, L, Marchi, V, Biarese, G, Monga, S, Quaranta
Publikováno v: Recenti progressi in medicina. 86(11)
Benign recurrent intrahepatic cholestasis (BRIC) is a form of cholestasis of obscure aetiology characterized by recurrent episodes of jaundice and itching associated with a morphological picture of pure intrahepatic cholestasis. No effective treatmen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1e5db5ce0b3999079d15e9a359c532e4
https://pubmed.ncbi.nlm.nih.gov/8539477
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6
[Osteopetrosis (Albers-Schönberg disease). I. Clinico-radiological and pathogenetic aspects]
Autor: P, Lovisetto, L, Donetto, V, Biarese, L, Marchi, S, Bianchi
Publikováno v: Minerva medica. 68(13)
An account is given of recent clinical and radiological findings with respect to Albers-Schönberg disease. Reference is made to its hereditary transmission modality and clinical picture (skeletal lesions and haematological distress), and to its radi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f9bf7dcb621fe3938a0e0d189b50a51a
https://pubmed.ncbi.nlm.nih.gov/850548
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8
[Fibrodysplasia ossificans progressiva or Münchmeyer's disease. Personal observation]
Autor: G, Galvagno, L, Marchi, D, Manachino, V, Biarese, P, Lovisetto
Publikováno v: Recenti progressi in medicina. 80(4)
We report here a case of fibrodysplasia ossificans progressiva in a 14-year-old boy, affected from birth by microdactyly of the big toes. This skeletal abnormality also existed in his paternal great-grandfather. When he was 7, some ectopic ossificati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1f9be75817c072cd375d3c8ae80e9c52
https://pubmed.ncbi.nlm.nih.gov/2762656
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10
[Angiitis caused by hypersensitivity or microscopic polyarteritis nodosa. Recent findings. I. Nosographic aspects]
Autor: P, Lovisetto, G, Galvagno, D, Manachino, V, Biarese, P, Andrione, L, Marchi
Publikováno v: Minerva medica. 78(12)
Hypersensitivity angiitis or microscopic polyarteritis nodosa is one of the necrotising angiitis and was not distinguished from classic polyarteritis nodosa until the Fifties. The present study examines the nosographic aspects of necrotising angiitid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d20353fab4dfb27355ac155b54fe40e8
https://pubmed.ncbi.nlm.nih.gov/2885785
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Plný text Recenzováno Digitální knihovna AV ČR
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