Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Simona, Santucci"'
Autor:
Simona Santucci, Chiara Cuzzupè, Elda Pitrolo, Francesco Monaco, Carmelo Romeo, Concetta Sferlazzas, Mariella Valenzise, Filippo De Luca
Publikováno v:
Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche, Vol 105, Iss 2 (2017)
Pleural empyema represents a severe complication of community acquired pneumonia with an incidence of 0.6% among hospitalized children. Clinical manifestations of picture may be different in infants and young children and it should always be suspecte
Externí odkaz:
https://doaj.org/article/9cfbfd7508e54d6aa54f2ef9087e2dc2
Autor:
Chiara Cuzzupè, Simona Santucci, Elda Pitrolo, Celeste Casto, Irene Viola, Claudio Romano, Mariella Valenzise, Filippo De Luca
Publikováno v:
Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche, Vol 105, Iss 2 (2017)
Chronic granulomatous disease is a rare, inherited immunodeficiency caused by deletions or mutations in genes that encode subunits of the NADPH oxidase complex. The pattern of chronic granulomatous disease inheritance can be X-linked (about 70% of ca
Externí odkaz:
https://doaj.org/article/71dbed3b2a0746ce82ccf858d41ad4ff
Publikováno v:
Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche, Vol 105, Iss 1 (2017)
The occurrence of dysphagia in a child may be a sign of various pathological conditions and mainly gastrointestinal disorders; neurological causes are not very frequent, but they should be taken in to considerations. Etiological diagnosis is importan
Externí odkaz:
https://doaj.org/article/2f3f182ec2f24dbdac87691b5f0afe3e
Publikováno v:
Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche, Vol 105, Iss 1 (2017)
Congenital Adrenal hypoplasia (CAH) is a rare genetic disorder which can present two distinct modalities of transmission: recessive X-linked or recessive autosomal modality. That linked to the X chromosome is generally associated with hypogonadotropi
Externí odkaz:
https://doaj.org/article/a099dcbea8b3426191b65ce8565c1bbc
Autor:
Domenico Corica, Simona Santucci, Giuseppina Salzano, Filippo De Luca, Tommaso Aversa, Giuseppina Zirilli, Mariella Valenzise
Publikováno v:
Italian Journal of Pediatrics
Aim of this commentary is to report the most recent views about natural history of subclinical hypothyroidism (SH) according to the different etiologies. In children with idiopathic SH the natural evolution is often favourable, with a high percentage
Autor:
Giuseppina, Zirilli, Simona, Santucci, Chiara, Cuzzupè, Domenico, Corica, Elda, Pitrolo, Giuseppina, Salzano
Publikováno v:
Acta bio-medica : Atenei Parmensis
Background: No reviews have specifically addressed, to now, whether autoimmune polyglandular syndromes (APSs) may have a peculiar epidemiology and phenotypical expression in pediatric age. Objectives: To review the most recent literature data about t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8a3aa90b941995d050ad582508f5fc31
http://hdl.handle.net/11570/3134920
http://hdl.handle.net/11570/3134920
Autor:
Domenico Corica, Mariaausilia Catena, Maria Rosa Velletri, Simona Santucci, Malgorzata Wasniewska, F. De Luca, Stefania Arasi, Vincenzo Ramistella
Publikováno v:
La Pediatria Medica e Chirurgica, Vol 36, Iss 5-6 (2014)
Background: Numerous studies have shown that GH, in addition to promoting linear growth, exerts a key role in many metabolic processes. However, there are only few studies aiming at evaluating the metabolic panel of children with GH deficiency (GHD).
Autor:
M. Romeo, E. Pitrolo, Simona Santucci, Mariella Valenzise, F. Chiera, Gilberto Candela, S. Nigro, Giuseppina Zirilli, Domenico Corica, Federica Porcaro
Publikováno v:
La Pediatria Medica e Chirurgica, Vol 36, Iss 4 (2014)
We describe a case of a 14-years old caucasian female affected by autoimmune hemolytic anemia and thrombocytopenia successfully treated with intravenous immunoglobulin and steroids. Nevertheless, neutropenia occurred during follow-up period. Positivi
Autor:
Stefania Arasi, Malgorzata Wasniewska, M. Romeo, E. Pitrolo, Domenico Corica, R. Crisafulli, M.R. Velletri, Mariella Valenzise, Simona Santucci, A. Santisi, Giuseppina Zirilli
Publikováno v:
La Pediatria Medica e Chirurgica, Vol 35, Iss 5 (2013)
A prepubescent 11 year-old girl came to our attention for short stature. Auxological evaluation showed peculiar phenotype. In order to exclude Turner syndrome standard karyotype was performed with normal result. Because of anemia and selective defici
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 39, Iss 1, p 8 (2013)
Italian Journal of Pediatrics, Vol 39, Iss 1, p 8 (2013)
Aim of this survey is to report the most recent views about Hashimoto’s thyroiditis (HT) natural history according to the different presentations. In children presenting with either euthyroidism or subclinical hypothyroidism HT spontaneous course i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::934f4512044f845c5c745a0950dc34dc
http://hdl.handle.net/11570/2671219
http://hdl.handle.net/11570/2671219