Search Results - "Griso, D"

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    Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: Report of four novel mutations by di Montemuros, Franco Martinez, Di Pierro, Elena, Fargion, Silvia, Biolcati, Gianfranco, Griso, Daniela, Macrì, Annelisa, Fiorelli, Gemino, Cappellini, Maria Domenica

    Published in Human mutation (01-05-2000)
    “…Acute intermittent porphyria (AIP) is an autosomal disorder caused by molecular abnormalities in the hydroxymethylbilane synthase (HMBS) gene coding for the…”
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    Hepatitis C virus in patients with porphyria cutanea tarda: relationship to HCV-genotypes by Rivanera, D, Lilli, D, Griso, D, Macrì, A, Mancini, C

    Published in The New microbiologica (01-10-1998)
    “…Porphyria cutanea tarda (PCT) is a rare metabolic disorder characterized by an abnormal porphyrin metabolism and typical cutaneous lesions. Recently a strong…”
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    Iron and porphyria cutanea tarda by D'Alessandro Gandolfo, L, Griso, D, Macrì, A, Biolcati, G, Barlattani, A, Topi, G C

    “…In order to evaluate the pathogenetic role of iron in Porphyria cutanea tarda (PCT), the metabolism of iron was studied in 440 patient with PCT and associated…”
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    Incidence of hereditary porphyria cutanea tarda (PCT) in a sample of the Italian population by D'Alessandro, L, Griso, D, Biolcati, G, Macrì, A, Topi, G C

    Published in Archives of Dermatological Research (01-08-1992)
    “…The determination of the enzymatic activity of URO-D in erythrocytes is the screening method used for differentiation between hereditary and non-hereditary…”
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    Recovery from porphyria cutanea tarda with no specific therapy other than avoidance of hepatic toxins by Topi, G C, Amantea, A, Griso, D

    Published in British journal of dermatology (1951) (01-07-1984)
    “…Little is known of the natural progression of untreated porphyria cutanea tarda. We report sixteen cases (fourteen sporadic and two familial) in which the…”
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    Familial porphyria cutanea tarda with normal erythrocytic urodecarboxylase: an exception to the rule? by D'Alessandro Gandolfo, L, Griso, D, Macri, A, Biolcati, G, Topi, G C

    Published in Dermatologica (01-01-1989)
    “…The possibility that the differentiation between sporadic and familial porphyria cutanea tarda cannot always be made on the basis of the measurement of the…”
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    Porphyria cutanea tarda in a haemodialysed patient by Topi, G C, Alessandro, G L, Cancarini, G C, De Costanza, F, Griso, D, Ravelli, M

    Published in British journal of dermatology (1951) (01-05-1981)
    “…A bullous dermatosis, that arose about 2 years after the beginning of haemodialysis treatment, was due to a geniune hereditary porphyria cutanea tarda (PCT)…”
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    Acquired cutaneous toxoplasmosis by Topi, G, D'Alessandro Gandolfo, L, Giacalone, B, Griso, D, Zardi, O, Argiroffo, A

    Published in Dermatologica (1983)
    “…We examined more than 1,400 dermatologic patients with clinically defined (but having unknown or presumably multiple etiology) affections. The investigation…”
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    Hereditary coproporphyria: unusual nervous system involvement in two cases by CASALI, C, MONACO, M. L, D'ALESSANDRO, L, GRISO, D, AMANTEA, A, TOPI, G. C, TONALI, P

    Published in Journal of neurology (01-04-1984)
    “…Two cases of hereditary coproporphyria showed unusual nervous system involvement, one epilepsy with onset in childhood, and the other chronic central and…”
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    Porphyrins in Rotor's syndrome: a study on an Italian family by Rapaccini, G L, Topi, G C, Anti, M, D'Alessandro Gandolfo, L, Griso, D, Amantea, A, de Vitis, I, Fedeli, G

    Published in Hepato-gastroenterology (01-02-1986)
    “…Porphyrins in urine, plasma, erythrocytes and feces have been tested in two brothers affected by Rotor's syndrome and in three of their phenotypically normal…”
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    Non-alcoholic steatohepatitis induced by carbamazepine and variegate porphyria by GRIECO, Antonio, ALFEI, Barbara, DI ROCCO, Paola, MIELE, Luca, BIOLCATI, Gianfranco, GRISO, Daniela, VECCHIO, Fabio Maria, BIANCO, Alessandro, GASBARRINI, Giovanni

    “…A 42-year-old woman presented with acute bullous skin lesions and angio-oedema that had developed 3 months after initiation of treatment with carbamazepine for…”
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