Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Claudio, Fonda"'
Autor:
Elena Sieni, Carmen Barba, Marzia Mortilla, Sara Savelli, Laura Grisotto, Gianpiero Di Giacomo, Katiuscia Romano, Claudio Fonda, Annibale Biggeri, Renzo Guerrini, Maurizio Aricò
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0131635 (2015)
Neurodegenerative Langerhans Cell Histiocytosis (ND-LCH) is a rare, unpredictable consequence that may devastate the quality of life of patients cured from LCH. We prospectively applied a multidisciplinary diagnostic work-up to early identify and fol
Externí odkaz:
https://doaj.org/article/1695e223c0e747769191ff1282da0a3a
Autor:
Gabriele Simonini, Rolando Cimaz, Sara Savelli, Marco Matucci-Cerinic, Ilaria Pagnini, Claudio Fonda
Publikováno v:
The Journal of Rheumatology. 37:2395-2401
Objective.To identify early predictors of sacroiliac (SI) involvement in a cohort of patients with enthesitis-related arthritis (ERA).Methods.During a 7-year followup period, all consecutive patients fulfilling the ILAR classification criteria for ER
Autor:
Erica Del Giudice, Norma Decaminada, M. Mortilla, Désirée Caselli, Maria Cappellini, Claudio Fonda, Maurizio Aricò, Elena Sieni
Publikováno v:
Child's Nervous System. 26:121-127
Familial hemophagocytic lymphohistiocytosis (FHL) is a rare multisystem congenital disorder characterized by uncontrolled proliferation and infiltration of activated lymphocytes and histiocytes, secreting high amounts of inflammatory cytokines; this
Publikováno v:
Acta Paediatrica. 94:968-971
Aim The problem of kernicterus in infants with bronze baby syndrome (BBS) has been reviewed on the basis of cases reported in the literature. In addition, a new case concerning an infant with severe Rh haemolytic disease, who presented with BBS and w
Autor:
Renzo Guerrini, Maurizio Aricò, Elena Sieni, Carmen Barba, Gianpiero Di Giacomo, Laura Grisotto, Katiuscia Romano, M. Mortilla, Sara Savelli, Claudio Fonda, Annibale Biggeri
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 7, p e0131635 (2015)
PLoS ONE, Vol 10, Iss 7, p e0131635 (2015)
Background Neurodegenerative Langerhans Cell Histiocytosis (ND-LCH) is a rare, unpredictable consequence that may devastate the quality of life of patients cured from LCH. We prospectively applied a multidisciplinary diagnostic work-up to early ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7002746b638fbd16329d0fb9a1ad992
http://hdl.handle.net/11577/3409190
http://hdl.handle.net/11577/3409190
Publikováno v:
European Journal of Radiology. 58:252-259
Mermaid or sirens have been part of the cultural tradition of the sailors during the first expeditions in the western world. The Siren's Myth appeared for a first time with Homer, who described in the Odyssey some singing creatures that lured the enc
Publikováno v:
Rivista di Neuroradiologia. 19:57-60
We studied a case of middle interhemispheric variant of holoprosencephaly by magnetic resonance. A five-year-old child presented a mild language delay and relational disorders. The etiopathogenesis of the disorder remains controversial, the two main
Autor:
Sergio Mugnai, Marco Moretti, Laura Bracco, Giovanna Carlucci, Carolina Piccini, Claudio Fonda, Giovanni Pracucci, M Prieto, Domenico Inzitari, A. Di Carlo
Publikováno v:
Neurological Sciences. 26:61-66
Cognitive impairment and gait disturbances are the most frequent clinical findings in patients with leukoaraiosis (LA). Corpus callosum (CC) atrophy has been associated with dementia in patients with LA, as well as with gait disturbances in patients
Publikováno v:
Università degli studi di Firenze-IRIS
Herpes simplex encephalitis classically involves the periventricular white matter in infants and the mesial temporal lobes, inferior frontal lobes, and insula in older children and adults. However, the increasing use of polymerase chain reaction to d
Lo studio delle malformazioni fetali rappresenta uno degli argomenti più complessi nell'ambito della medicina fetale.Negli ultimi anni il ruolo della risonanza magnetica (RM) nell'inquadramento diagnostico delle malformazioni fetali isolate e comple