Zobrazeno 1 - 10 of 35 pro vyhledávání: '"L Lupica"'
2
Mycoplasma genitalium in males with nongonococcal urethritis: prevalence and clinical efficacy of eradication
Autor: Massimo Ghislanzoni, Irene Decleva, Marco Cusini, L. Lupica, Daniele Gambini, Elvio Alessi
Publikováno v: Sexually transmitted diseases. 27(4)
Mycoplasma genitalium is regarded as a potential pathogen of the human urogenital tract based on prevalence findings of several European studies.To determine the prevalence of M genitalium in urethral specimens of symptomatic patients with nongonococ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec0105df655b26f01b3eb6134a4b78d3
https://pubmed.ncbi.nlm.nih.gov/10782745
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3
Unilesional follicular mycosis fungoides
Autor: Emilio Berti, Elvio Alessi, L. Lupica, Angelo V. Marzano
Follicular mycosis fungoides (FMF) is an unusual clinical and histological variant of MF, characterized by selective involvement of hair follicles by atypical lymphocytes. We describe a female patient who had follicular papules located only on the me
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08fa24b85f3dcdf056c2b95ac1d035a5
http://hdl.handle.net/10281/49617
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4
Heterogeneity of hemochromatosis in Italy
Autor: Paolo Gasparini, Paolo Pasquero, Giuliana Montosi, Antonella Roetto, Mirella Fraquelli, Maurizio Sampietro, Silvia Fargion, Clara Camaschella, Antonello Pietrangelo, Cristina Arosio, Anna Vergani, Dario Conte, L. Lupica, Alberto Piperno, Domenico Girelli
Background & Aims: Patients with hemochromatosis show variable phenotype expression. We evaluated the frequency of hemochromatosis gene (HFE) mutations and the contribution of HFE genotype, ancestral haplotype, ethnic background, and additional facto
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08c356c465afe2073a6456c135deb57b
http://hdl.handle.net/10281/58231
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5
High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda
Autor: Alberto Piperno, Anna Ludovica Fracanzani, Cristina Arosio, L. Lupica, I. Malosio, Maurizio Sampietro, Michela Mattioli, Silvia Fargion, Gemino Fiorelli, Noemi Corbetta, Anna Vergani, Maria Domenica Cappellini
Sporadic porphyria cutanea tarda (PCT) is caused by a reduced activity of uroporphyrinogen decarboxylase (URO-D) in the liver. Mild to moderate iron overload is common in PCT, as iron is one of the factors which trigger the clinical manifestations of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc1b579448728fe6c7676823e30c2447
http://hdl.handle.net/10281/58229
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6
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency
Autor: Luca Perrero, Franco Martinez di Montemuros, A. Comino, Maurizio Sampietro, L. Lupica, Maria Domenica Cappellini, Gemino Fiorelli
Publikováno v: British journal of haematology. 99(2)
We evaluated the effect of Gilbert's syndrome, the most common defect of bilirubin conjugation, on the bilirubin levels of subjects with inherited haematological disorders which cause increased bilirubin production. 57 patients heterozygous for beta-
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c43ce6145664a2cf611e946f47a18868
https://pubmed.ncbi.nlm.nih.gov/9375769
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7
In Memoriam / Announcements
Autor: Yukitoshi Yamaguchi, W. Skarabis, R.J.A. Wanders, H.S. Zackheim, A.G. Knight, Z. Demetriou, Noriaki Shinomiya, K. Nakamura, Jean-Charles Piette, K. Peris, A. Carrassi, Sylvie Legrain, T. Murakami, B. Bjarnason, G. Orecchia, J. Rey, Felix Heitzmann, Masakazu Asahi, Ryuzo Saito, Kanako Kikuchi, P. Elsner, Osamu Yamamoto, B. Granel, S. Dhar, A. Sardella, Masahisa Watanabe, Margit Nindl, A. Katsambas, G. Sacerdoti, Marie-Sylvie Doutre, Caroline Roudier-Pujol, J. Economidou, Itsuro Matsuo, S. Yano, Masayuki Amagai, O. Avcı, Leila Jeskanen, G. Kaya, Arja-Leena Kariniemi, Anne Auperin, S. Chimenti, D. Degiannis, Marie Beylot Barry, Hiroko Gomi, Hiromi Kazama, François Laurent, G.K. Patel, F. Châtillon, Peter Itin, G. Lodi, M. Yoshida, C. Bez, T. Fischer, Stubb S, P.J. Weiller, Takaaki Kobayashi, Emilio Berti, C. Beylot, P.M. Steijlen, M.A. de Rie, Kayo Yamaguchi, Tamihiro Kawakami, J. Cilliers, Hachiro Tagami, E. Flosadóttir, S.E. Shephard, G. Avgerinou, R.G. Panizzon, Ikuo Murata, Tapio Rantanen, Xavier Roques, M.A.A.P. Willemsen, Yasushi Tomita, A. Rebora, Elvio Alessi, Thiem Nguyen, G. Kolde, W. Sterry, Nobuko Tabata, Yoshinori Miyamura, A.T. Güneş, H. Audring, Peter Schiller, J. Stock, L. Presenti, Misako Tanaka, C. de Beer, Tugutoshi Aoki, V. Marlière, Patrick Blanco, Muneo Tanita, Claire Beylot, C. Romano, E. Ellidokuz, Masahiro Hara, J. Serratrice, A. Oga, I. Şimşek, H. Ihn, A. Denizot, J.J. Rotteveel, Yoichi Nagata, Marie-Fançoise Avril, B. Büyükgebiz, Kentaro Yoshinaga, A. Köhler, C. Chizzolini, A. Vareltzidis, Angelo V. Marzano, Ellen Benhamou, A. Della Volpe, R.U. Peter, Eriko Nakamura, P. Berbis, Jun Matsunaga, Pierre Duvillard, M. Beylot-Barry, M. Muto, M. Fazio, Masutaka Furue, K. Tamaki, S.M. Clark, S.K. Todi, Gilles Raguin, M.-S. Doutre, Yoshinao Fujikawa, L. Muscardin, T. Shimizu, F. Drago, E. Ranieri, C. Hauser, K. Psarra, J. Barkis, L. Lupica, Ichiro Katayama, P. Disdier, M.M.U. Chowdhury, Akira Kawada, L. Massai, H. Okochi, Sandra Ly, H. Gall, Miwako Dakeishi-Hara, Hiroaki Aoyama, Fumihide Ogawa, Antti Lauerma, Hirotsugu Yamanouchi, M. Worm, Bernhard Stamm, L. Borradori
Publikováno v: Dermatology. 199:199-199
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::435576ff793add6d00402d3b9604baf0
https://doi.org/10.1159/000018248
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