Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Maya El‐Hachem"'
Autor:
Hélène Aubert, Kathrin Thormann, Sebastien Barbarot, Pavel Chernyshov, Meete Deleuran, Maya El‐Hachem, Jette deGroot, Danielle Marcoux, Dagmar Simon, Florine Raymakers, Jean‐François Stalder
Publikováno v:
JEADV Clinical Practice, Vol 1, Iss 2, Pp 144-149 (2022)
Abstract Background Atopic dermatitis (AD) is a chronic inflammatory skin condition that has a major impact on the quality of life of patients and their families. Therapeutic patient education (TPE) is recommended for all patients with this condition
Externí odkaz:
https://doaj.org/article/7f9d962c5fa24d26a65e8d5d556617b1
Autor:
Mariangela Irrera, Elena Bozzola, Antonello Cardoni, Rita DeVito, Andrea Diociaiuti, Maya El Hachem, Katia Girardi, Alessandra Marchesi, Alberto Villani
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-13 (2023)
Abstract Background In literature, a few reports described an association between paraneoplastic pemphigus (PNP) and Castelman’s disease (CD), but no consensus have been proposed for the diagnostic-therapeutical approach. Aim of this study is to pr
Externí odkaz:
https://doaj.org/article/559eea6ec3ec4d36b6e64ba576ffd9e1
Autor:
Maria Chiriaco, Giorgiana Madalina Ursu, Donato Amodio, Nicola Cotugno, Stefano Volpi, Francesco Berardinelli, Simone Pizzi, Cristina Cifaldi, Matteo Zoccolillo, Ignazia Prigione, Silvia Di Cesare, Carmela Giancotta, Elisa Anastasio, Beatrice Rivalta, Lucia Pacillo, Paola Zangari, Alessandro G. Fiocchi, Andrea Diociaiuti, Alessandro Bruselles, Francesca Pantaleoni, Andrea Ciolfi, Valentina D’Oria, Giuseppe Palumbo, Marco Gattorno, Maya El Hachem, Jean-Pierre de Villartay, Andrea Finocchi, Paolo Palma, Paolo Rossi, Marco Tartaglia, Alessandro Aiuti, Antonio Antoccia, Gigliola Di Matteo, Caterina Cancrini
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Actin-related protein 2/3 complex subunit 1B (ARPC1B) deficiency is a recently described inborn error of immunity (IEI) presenting with combined immunodeficiency and characterized by recurrent infections and thrombocytopenia. Manifestations of immune
Externí odkaz:
https://doaj.org/article/89e21088048d4dbf915918df0ba93f6a
Autor:
Alessandra Marchesi, Donato Rigante, Rolando Cimaz, Angelo Ravelli, Isabella Tarissi de Jacobis, Alessandro Rimini, Fabio Cardinale, Marco Cattalini, Andrea De Zorzi, Rosa Maria Dellepiane, Patrizia Salice, Aurelio Secinaro, Andrea Taddio, Paolo Palma, Maya El Hachem, Elisabetta Cortis, Maria Cristina Maggio, Giovanni Corsello, Alberto Villani
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-12 (2021)
Abstract Aim of these revised recommendations for the general management of Kawasaki disease is to encourage its prompter recognition and warrant the most appropriate therapy, based on ascertained scientific data, raising awareness of the complicatio
Externí odkaz:
https://doaj.org/article/b8afe6f0e94d4a6eacda87e5ecd06888
Autor:
Jemima E. Mellerio, Maya El Hachem, Nathalia Bellon, Giovanna Zambruno, Hana Buckova, Rudolf Autrata, Carmen Salavastru, Tamara Caldaro, Celine Greco, Cristina Has, Christine Bodemer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Epidermolysis bullosa (EB) comprises a group of genetic disorders with the hallmark of fragility of the skin and mucosal surfaces. The severity of different types of EB varies markedly as does the occurrence of extra-cutaneous involvement an
Externí odkaz:
https://doaj.org/article/07f519bcf443446581d2b8e646e4026e
Autor:
Alessandra Marchesi, Isabella Tarissi de Jacobis, Donato Rigante, Alessandro Rimini, Walter Malorni, Giovanni Corsello, Grazia Bossi, Sabrina Buonuomo, Fabio Cardinale, Elisabetta Cortis, Fabrizio De Benedetti, Andrea De Zorzi, Marzia Duse, Domenico Del Principe, Rosa Maria Dellepiane, Livio D’Isanto, Maya El Hachem, Susanna Esposito, Fernanda Falcini, Ugo Giordano, Maria Cristina Maggio, Savina Mannarino, Gianluigi Marseglia, Silvana Martino, Giulia Marucci, Rossella Massaro, Christian Pescosolido, Donatella Pietraforte, Maria Cristina Pietrogrande, Patrizia Salice, Aurelio Secinaro, Elisabetta Straface, Alberto Villani
Publikováno v:
Italian Journal of Pediatrics, Vol 44, Iss 1, Pp 1-18 (2018)
Abstract The primary purpose of these practical guidelines related to Kawasaki disease (KD) is to contribute to prompt diagnosis and appropriate treatment on the basis of different specialists’ contributions in the field. A set of 40 recommendation
Externí odkaz:
https://doaj.org/article/de5f0fb3fb314a1aaa1706939d68220e
Autor:
Alessandra Marchesi, Isabella Tarissi de Jacobis, Donato Rigante, Alessandro Rimini, Walter Malorni, Giovanni Corsello, Grazia Bossi, Sabrina Buonuomo, Fabio Cardinale, Elisabetta Cortis, Fabrizio De Benedetti, Andrea De Zorzi, Marzia Duse, Domenico Del Principe, Rosa Maria Dellepiane, Livio D’Isanto, Maya El Hachem, Susanna Esposito, Fernanda Falcini, Ugo Giordano, Maria Cristina Maggio, Savina Mannarino, Gianluigi Marseglia, Silvana Martino, Giulia Marucci, Rossella Massaro, Christian Pescosolido, Donatella Pietraforte, Maria Cristina Pietrogrande, Patrizia Salice, Aurelio Secinaro, Elisabetta Straface, Alberto Villani
Publikováno v:
Italian Journal of Pediatrics, Vol 44, Iss 1, Pp 1-18 (2018)
Abstract This second part of practical Guidelines related to Kawasaki disease (KD) has the goal of contributing to prompt diagnosis and most appropriate treatment of KD resistant forms and cardiovascular complications, including non-pharmacologic tre
Externí odkaz:
https://doaj.org/article/97b6695be6e94eb6a751868558b56ebd
Autor:
Maya El Hachem, Francesco Gesualdo, Andrea Diociaiuti, Irene Berti, Nadia Vercellino, Valeria Boccaletti, Iria Neri, Giulio Porcedda, Antonella Greco, Claudia Carnevale, Teresa Oranges, Mario Cutrone, Pietro Dalmonte
Publikováno v:
Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-6 (2017)
Abstract Background Despite not being licensed for the treatment of infantile hemangiomas (IH) in infants younger than 5 weeks or older than 5 months, propranolol is often used in these age groups to prevent or to treat potentially severe complicatio
Externí odkaz:
https://doaj.org/article/e985ebfe224b4be28d90611b2ae0eb92
Autor:
Marina Macchiaiolo, Filippo M. Panfili, Davide Vecchio, Fabiana Cortellessa, Michaela V. Gonfiantini, Paola S. Buonuomo, Andrea Pietrobattista, Paola Francalanci, Lorena Travaglini, Enrico S. Bertini, Maya El Hachem, Andrea Bartuli
Publikováno v:
American Journal of Medical Genetics Part A. 188:2920-2931
POIKiloderma, tendon contractures, myopathy, pulmonary fibrosis is a congenital multisystem disorder due to FAM111B dominant variants. We present a literature review focusing on the frequency and the impact of hepatic involvement and a case report of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba7e6c26da04d9d1b469918c6b560154
https://doi.org/10.1002/ajmg.a.62906
https://doi.org/10.1002/ajmg.a.62906
Autor:
Claudia Carnevale, Daniele Castiglia, Andrea Diociaiuti, Vittoria Proto, Simona Giancristoforo, Renata Boldrini, Giovanna Zambruno, Maya El Hachem
Publikováno v:
Acta Dermato-Venereologica, Vol 97, Iss 10, Pp 1249-1251 (2017)
Externí odkaz:
https://doaj.org/article/e8335c5b678e471bafbc8113e34c5f00