Výsledky vyhledávání - "Maria Scalzone"

Mycophenolate mofetil and Sirolimus as second or further line treatment in children with chronic refractory Primitive or Secondary Autoimmune Cytopenias: a single centre experience

Autor: Michaela Calvillo, Concetta Micalizzi, Johanna Svahn, Laura Banov, Tiziana Lanza, Elena Palmisani, Maria Scalzone, Francesca Fioredda, Maurizio Miano, Paola Terranova, Ilaria Caviglia, Carlo Dufour, Katia Perri

Publikováno v: British Journal of Haematology. 171:247-253

Summary The management of refractory autoimmune cytopenias in childhood is challenging due to the lack of established evidence on escalating treatments. The long-term efficacy of immunosuppressive drugs was evaluated in children with refractory autoi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7456f7f0afff1be350df5347c2ef6e9
https://doi.org/10.1111/bjh.13533

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Platinum compounds in children with cancer

Autor: Silvia Triarico, Maria Scalzone, Roberta Arena, Riccardo Riccardi, Giovanna Trombatore, Antonio Ruggiero, Pietro Ferrara, Filomena Pierri

Publikováno v: Anti-Cancer Drugs. 24:1007-1019

Platinum compounds are widely used in the treatment of pediatric tumors such as neuroblastoma, germ-cell tumors, osteosarcoma, retinoblastoma, hepatoblastoma, brain tumors (low-grade gliomas and medulloblastoma/PNET), and relapsed and refractory lymp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dd51ff0bf71e4b8db656f6418780f5d
https://doi.org/10.1097/cad.0b013e3283650bda

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Chronic Idiopathic Thrombocytopenic Purpura in children: predictive factors and outcome

Autor: Maria Scalzone, Giorgio Attinà, Nadia Puma, Andrea Battista, Riccardo Riccardi, Antonio Ruggiero, Vita Ridola, Paola Coccia, Giuseppe Cerchiara, Roberta Arena

Publikováno v: Open Medicine, Vol 7, Iss 4, Pp 525-528 (2012)

Idiopathic thrombocytopenic purpura (ITP) is the most common cause of acquired thrombocytopenia in children. In 20% of cases, this condition is classified as chronic when the thrombocytopenia is persistent 6 months after diagnosis. The aim of the pre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d60e07f92d432d71af35b16e1b2aa1a7
https://doaj.org/article/311708127a0041168a7dd9b605001009

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Management of children with Thrombocytopenia-absent radius syndrome: An institutional experience

Autor: Giorgio Attinà, Mauro Pittiruti, Paola Coccia, Palma Maurizi, Riccardo Riccardi, Maria Scalzone, Stefano Mastrangelo, Antonio Ruggiero, Giuseppe Zampino

Publikováno v: Journal of Paediatrics and Child Health. 48:166-169

Aim: Thrombocytopenia-absent radius (TAR) syndrome is characterised by bilateral absence of the radii in the presence of both thumbs and hypomegakaryocytic thrombocytopenia. We report our experience of three patients affected by TAR syndrome presenti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4ca90bcb0ea95f268ed66511ed914e18
https://doi.org/10.1111/j.1440-1754.2011.02069.x

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Aplastic anaemia in childhood. Description of two cases and review of the literature

Autor: Antonio Ruggiero, Maria Scalzone, Palma Maurizi, Maria Giuseppina Cefalo, Riccardo Riccardi, Paola Coccia, Lucia Liotti, Giorgio Attinà

Publikováno v: Open Medicine, Vol 4, Iss 3, Pp 363-368 (2009)

Childhood aplastic anaemia (AA) is an uncommon but potentially fatal haematological disorder. Patients with AA receive supportive care based on transfusions and timely treatment of opportunistic infections, along with specific therapies, which may be

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba8e0895d712ce453f22d96991b94c4b
https://doi.org/10.2478/s11536-009-0024-7

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The Neurofibromatosis type 1:A dominantly inherited tumors-predisposing disorder

Autor: Ilaria Lazzareschi, Antonio Ruggiero, Stefano Mastrangelo, Maria Scalzone, Riccardo Riccardi, Paola Coccia

Publikováno v: Open Medicine, Vol 4, Iss 1, Pp 11-16 (2009)

Neurofibromatosis type I (NF1) is a hereditary multisystem disease involving the skin and nervous system. It is the most common form of autosomal dominant phakomatoses with 100% penetrance but wide phenotypic variability. The NF1 gene is located on c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::146cb21c2e311e42047d37f45164b7ee
https://doaj.org/article/88218a76bd8c4d6184b19a2666c8dbae

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Hemophagocytic lymphohistiocytosis and visceral leishmaniasis in children: case report and systematic review of literature

Autor: Vita Ridola, Stefano Mastrangelo, Riccardo Riccardi, Antonio Ruggiero, Maria Scalzone, Palma Maurizi, Giovanna Trombatore

Publikováno v: Journal of infection in developing countries. 10(1)

Hemophagocytic lymphohistiocytosis is a potentially fatal disorder resulting from excessive activation and non-malignant proliferation of T lymphocytes and macrophages. Neoplasms, autoimmune disorders and systemic infections can cause secondary hemop

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c85ec45c86d146943c40345f39ffe6b
https://pubmed.ncbi.nlm.nih.gov/26829545

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Temozolomide in the treatment of newly diagnosed diffuse brainstem glioma in children: a broken promise?

Autor: Palma Maurizi, Cesare Colosimo, Vita Ridola, Riccardo Riccardi, Daniela Rizzo, Maria Scalzone, Antonio Ruggiero, Stefano Mastrangelo, Giorgio Attinà, Massimo Caldarelli, Ilaria Lazzareschi, Mario Balducci

Publikováno v: Journal of chemotherapy (Florence, Italy). 27(2)

Background: The purpose of this study was to assess the efficacy and toxicity of radiotherapy (RT) with concurrent temozolomide (TMZ) chemotherapy followed by adjuvant TMZ in children with diffuse intrinsic pontine glioma (DIPG). Methods: Patients yo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7c5ace575e011397e827e6b1eb39c0e
https://pubmed.ncbi.nlm.nih.gov/25466729

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