Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Laura Blanzuoli"'
Publikováno v:
Springer Seminars in Immunopathology. 19:459-478
This study has provided information on the spectrum of changes which can occur in different PID. Using a pattern-based approach for the analysis of the lymph node parenchyma, it is obvious that there are no morphological features specifically associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::908e6309f4dceb333ac99454196271ba
https://doi.org/10.1007/bf00792602
https://doi.org/10.1007/bf00792602
Autor:
Laura Blanzuoli, Roberto Cattaneo, Fabio Facchetti, Luigi D. Notarangelo, Alberto G. Ugazio, Duilio Brugnoni, Paolo Airò
Publikováno v:
European Journal of Immunology. 27:2765-2773
Omenn's syndrome (OS) is characterized by erythrodermia, hepatosplenomegaly, lymphadenopathy, hypereosinophilia and elevated IgE levels associated with increased susceptibility to severe infections. Peripheral blood T cells, though usually present in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad2463693a1d7010860609297c066cab
https://doi.org/10.1002/eji.1830271104
https://doi.org/10.1002/eji.1830271104
Publikováno v:
Updates in surgery. 63(2)
A 54-year-old male presented with a painless, hard, irregular lump in his right breast, with fixation to the pectoralis muscle. Mammography and ultrasound showed a 2.5-cm mass suspicious of malignancy. The patient underwent a wide local excision. A 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bdb844838c782c9b684cc2ce65264ca
https://pubmed.ncbi.nlm.nih.gov/21318418
https://pubmed.ncbi.nlm.nih.gov/21318418
Autor:
Pierangelo, Spedini, Laura, Blanzuoli
Publikováno v:
Haematologica. 87(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9caeeeac4cd851c06998eafba3fe9773
https://pubmed.ncbi.nlm.nih.gov/12368176
https://pubmed.ncbi.nlm.nih.gov/12368176
Publikováno v:
Haematologica. 87(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::211a3b7273549bcb964657d6274d68da
https://pubmed.ncbi.nlm.nih.gov/12091142
https://pubmed.ncbi.nlm.nih.gov/12091142
Publikováno v:
Haematologica. 87(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::90b8e2e3b26985c2fd2d1ebbd51cc5bf
https://pubmed.ncbi.nlm.nih.gov/12031935
https://pubmed.ncbi.nlm.nih.gov/12031935
Publikováno v:
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery. 257(7)
Schwannomas are neurogenic neoplasms rarely found in the sinonasal tract, where localization to the nasal septum is exceedingly rare (only 11 cases have been described in the western literature). We report the case of a 29-year-old white male with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f17822d93b30a0f7c1d320790c54afac
https://pubmed.ncbi.nlm.nih.gov/11052256
https://pubmed.ncbi.nlm.nih.gov/11052256
Autor:
Piergiovanni Grigolato, Francesco Donato, Laura Blanzuoli, William Vermi, Carla E. Marino, Giuseppe Loffredo, Fabio Facchetti, Daniele Alberti, Luigi D. Notarangelo, Madeleine D. Kraus
The Wiskott-Aldrich syndrome (WAS) is a X-linked hematologic disorder characterized by thrombocytopenia, eczema, and immunodeficiency of variable severity. Reported here are the results of a morphologic, morphometric, and immunophenotypic analysis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f4a4243007f668edf42b0eb0066e111
http://hdl.handle.net/11379/27297
http://hdl.handle.net/11379/27297
Autor:
Donn M. Stewart, R M Blaese, Laura Blanzuoli, Fabio Facchetti, David L. Nelson, Fabio Candotti
Boys affected with Wiskott-Aldrich syndrome (WAS) present with variable association of thrombocytopenia, eczema and immune deficiency. If untreated, WAS patients may succumb to intracerebral hemorrhages, severe infections or malignancies. Allogeneic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb0f43c94b5e51c95dc7bec9fcc5f9fa
http://hdl.handle.net/11379/501135
http://hdl.handle.net/11379/501135
Autor:
Anders Fasth, Fabio Facchetti, Silvia Giliani, William Vermi, Luigi D. Notarangelo, David L. Nelson, Maurilia Fiorini, Laura Blanzuoli, Donn M. Stewart
The Wiskott-Aldrich syndrome (WAS) is a rare X-linked recessive disorder characterized by eczema, thrombocytopenia, and immunodeficiency. An allelic variant of the disease is characterized by isolated thrombocytopenia (XLT). The gene responsible for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fca929f821fdb4adf62d7e3807841776
http://hdl.handle.net/11379/27264
http://hdl.handle.net/11379/27264