D De Mattia
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Explore the profile of D De Mattia including associated specialties, affiliations and a list of published articles.
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90
Citations
318
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Recent Articles
1.
Giordano P, Cecinati V, Grassi M, Del Vecchio G, Dicuonzo F, Palma M, et al.
Neuropediatrics
. 2011 May;
42(2):55-9.
PMID: 21611938
Background: Thromboembolism is a complication of acute lymphoblastic leukemia therapy in children. The majority of thromboembolic events are cerebral thromboses and deep venous thromboses; many asymptomatic deep venous thromboses are...
2.
Delvecchio M, Cecinati V, Brescia L, Faienza M, De Mattia D, Cavallo L, et al.
J Endocrinol Invest
. 2009 Jul;
33(3):135-9.
PMID: 19636215
Objective: Scanty data are available about the thyroid function in childhood acute lymphoblastic leukemia (ALL) off-therapy patients treated only with chemotherapy. We aimed to assess the prevalence of thyroid autoimmunity...
3.
Delvecchio M, De Bellis A, De Mattia D, Cavallo L, Martire B
J Endocrinol Invest
. 2009 Jun;
32(8):637-40.
PMID: 19509479
Common variable immunodeficiency (CVID) is characterized by hypogammaglobulinemia and T-lymphocytes dysfunction. Autoimmune diseases are frequent. A 10.7-yr-old female, diagnosed with CVID when 7 yr old, was referred because of short...
4.
Giordano P, Nigro A, Lenato G, Guanti G, Suppressa P, Lastella P, et al.
J Thromb Haemost
. 2006 May;
4(6):1237-45.
PMID: 16706966
Background: Rendu-Osler-Weber syndrome, or hereditary hemorrhagic telangiectasia (HHT), is an autosomal dominant vascular disorder. The syndrome is characterized by telangiectases and arteriovenous malformations (AVMs) affecting skin, mucosae and internal organs....
5.
Giordano P, Nigro A, Del Vecchio G, Sabba C, De Mattia D
Curr Pharm Des
. 2006 Apr;
12(10):1221-5.
PMID: 16611104
Hereditary hemorrhagic telangiectasia (HHT) or the Rendu-Osler-Weber disease is a systemic fibrovascular autosomal dominant dysplasia, recognised when three of the following four clinical manifestations are present, according to the proposal...
6.
Del Vecchio G, Nigro A, Giordano P, De Mattia D
Curr Drug Targets Immune Endocr Metabol Disord
. 2005 Dec;
5(4):373-8.
PMID: 16375691
Liver disease is the second cause of mortality in thalassemia major. We present a review on the hepatic damage in thalassemic patients aimed at a knowledge of current preventive, diagnostic...
7.
Schettini Jr F, Miragliotta G, Carucci A, Mosca A, Del Vecchio G, Laforgia N, et al.
Minerva Pediatr
. 2003 Nov;
55(5):439-45.
PMID: 14608266
Aim: The nasopharyngeal carriage of Streptococcus pneumoniae is an important risk factor for pneumococcal diseases. Data regarding prevalence and serotype distribution of this pathogen are lacking in our population. Methods:...
8.
Mosca A, Carucci A, Santacroce L, Schettini F, De Mattia D, Miragliotta G
New Microbiol
. 2003 May;
26(2):187-92.
PMID: 12737202
The nasopharyngeal colonization rate of Streptococcus pneumoniae and its antibiotic susceptibility was determined in a given population of 317 young children (ages 1-7 years) in the area of Bari, Italy....
9.
Martire B, Burattini M, DE Santis A, Schettini Jr F, De Mattia D
Acta Paediatr
. 2001 Aug;
90(7):821-3.
PMID: 11519990
No abstract available.
10.
Di Bartolomeo P, Papalinetti G, Olioso P, Di Girolamo G, Bavaro P, De Mattia D, et al.
Hematology
. 2001 Jun;
4(4):313-318.
PMID: 11399572
Chronic granulomatous disease is caused by a genetic defect in the oxidase of phagocytic cells which results in increased susceptibility to recurrent infections. Conventional treatment includes the use of antimicrobials...