Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Annalisa Pedrolli"'
Publikováno v:
Clinical and Experimental Dermatology. 48:545-547
Purely cutaneous Rosai–Dorfman disease is a self-limiting and benign histiocytosis; however, some patients may be concerned about the aesthetic appearance, with a negative effect on quality of life. Even though many treatments have been proposed, n
Autor:
Riccardo Balestri, Laura Rizzoli, Annalisa Pedrolli, Silvana Anna Maria Urru, Giulia Rech, Iria Neri, Carlo R. Girardelli, Michela Magnano
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADVREFERENCES.
Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous syndrome causing hamartomatous growths in multiple organs. Facial angiofibromas occur in up to 80% of patients and can be highly disfiguring. Treatment for these lesions is chal
Publikováno v:
Skeletal radiology. 51(12)
Autor:
Pierpaola Tannorella, Luciano Calzari, Cecilia Daolio, Ester Mainini, Alessandro Vimercati, Davide Gentilini, Fiorenza Soli, Annalisa Pedrolli, Maria Teresa Bonati, Lidia Larizza, Silvia Russo
Publikováno v:
Clinical Epigenetics. 14
Beckwith–Wiedemann syndrome (BWS, OMIM # 130650) is an imprinting disorder, associated with overgrowth and increased risk of embryonal tumors. Patients carrying hypomethylation in the KCNQ1OT1:TSS DMR (11p15.5) show MLID (Multilocus Imprinting Dist
Publikováno v:
Skeletal Radiology. 51:2321-2322
Autor:
L Rizzoli, Carlo Renè Girardelli, Giulia Rech, Luigi Speziali, Annalisa Pedrolli, Maria Grazia Zorzi, Riccardo Balestri
Publikováno v:
Pediatric Dermatology. 35:e147-e150
Papular epidermal nevus with "skyline" basal cell layer is a newly described keratinocytic nevus. Recently, papular epidermal nevus with "skyline" basal cell layer has been reported in association with extracutaneous involvement, and the term papular
Autor:
Riccardo Troncone, Ausilia Elce, Giuseppe Castaldo, Peter Heinz-Erian, Antonio Calignano, Roberto Berni Canani, Chiara Centenari, Vincenza Pezzella, Felice Amato, Rossella Tomaiuolo, Gianluca Terrin, Annalisa Pedrolli
Publikováno v:
Orphanet Journal of Rare Diseases
Background: Congenital chloride diarrhea (CLD) is an autosomal recessive disorder characterized by life-long, severe diarrhea with intestinal Cl - malabsorption. It results from a reduced activity of the down regulated in adenoma exchanger (DRA), due
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e56e101f3d2a765a81998bf5b7f8269