IRIS

Sfoglia per Autore  

Opzioni
Mostrati risultati da 21 a 40 di 133
Titolo Data di pubblicazione Autore(i) File
Pediatric Hashimoto's encephalopathy with peripheral nervous system involvement 1-gen-2014 Salpietro, V.; Mankad, K.; Polizzi, A.; Sugawara, Y.; Granata, F.; David, E.; Ferrau, V.; Gallizzi, R.; Tortorella, G.; Ruggieri, M.
Adrenal disorders and the paediatric brain: Pathophysiological considerations and clinical implications 1-gen-2014 Salpietro, V.; Polizzi, A.; Di Rosa, G.; Romeo, A. C.; Dipasquale, V.; Morabito, P.; Chirico, V.; Arrigo, T.; Ruggieri, M.
High-mobility group box 1 (HMGB1) in childhood: From bench to bedside 1-gen-2014 Chirico, V.; Lacquaniti, A.; Salpietro, V.; Munafo, C.; Calabro, M. P.; Buemi, M.; Arrigo, T.; Salpietro, C.
Accessory oral cavity associated with duplication of the tongue and the mandible in a newborn: A rare case of Diprosopus. Multi-row detector computed tomography diagnostic role 1-gen-2014 Morabito, R.; Colonna, M. R.; Mormina, E.; Stagno D'Alcontres, F.; Salpietro, V.; Blandino, A.; Longo, M.; Granata, F.
Wide spectrum of congenital anomalies including choanal atresia, malformed extremities, and brain and spinal malformations in a girl with a de novo 5.6-Mb deletion of 13q12.11-13q12.13 1-gen-2014 Pavone, P.; Briuglia, S.; Falsaperla, R.; Warm, A.; Pavone, V.; Bernardini, L.; Novelli, A.; Pratico, A. D.; Salpietro, V.; Ruggieri, M.
Pediatric idiopathic intracranial hypertension and the underlying endocrine-metabolic dysfunction: A pilot study 1-gen-2014 Salpietro, V.; Mankad, K.; Kinali, M.; Adams, A.; Valenzise, M.; Tortorella, G.; Gitto, E.; Polizzi, A.; Chirico, V.; Nicita, F.; David, E.; Romeo, A. C.; Squeri, C. A.; Savasta, S.; Marseglia, G. L.; Arrigo, T.; Johanson, C. E.; Ruggieri, M.
LMNA gene mutation as a model of cardiometabolic dysfunction: From genetic analysis to treatment response 1-gen-2014 Chirico, V.; Ferrau, V.; Loddo, I.; Briuglia, S.; Amorini, M.; Salpietro, V.; Lacquaniti, A.; Salpietro, C.; Arrigo, T.
PRIMARY NOCTURNAL ENURESIS IN CHILDREN WITH ALLERGIC RHINITIS AND SEVERE ADENOTONSILLAR HYPERTROPHY: A SINGLE CENTER PILOT STUDY 1-gen-2015 Chimenz, R; Manti, S; Fede, C; Stroscio, G; Visalli, C; Nicotera, A; Di Rosa, G; Romeo, A C; Salpietro, V; Cuppari, C
The Role of Visfatin in Pregnancy, Complications and Procreation 1-gen-2015 Marseglia, L.; Manti, S.; D'Angelo, G.; Cuppari, C.; Salpietro, V.; Filippelli, M.; Chirico, V.; Gitto, E.; Salpietro, C.; Arrigo, T.
Sputum high mobility group box-1 in asthmatic children: A noninvasive sensitive biomarker reflecting disease status 1-gen-2015 Cuppari, C.; Manti, S.; Chirico, V.; Caruso, Rosangela; SALPIETRO DAMIANO, Vincenzo; Giacchi, V.; Laganà, Francesca; Arrigo, T.; Salpietro, C.; Leonardi, S.
Kenny Caffey syndrome with severe respiratory and gastrointestinal involvement: expanding the clinical phenotype 1-gen-2015 Christodoulou, L; Krishnaiah, A; Spyridou, C; Salpietro, V; Hannan, S; Saggar, A; Mankad, K; Deep, A; Kinali, M
Obesity and breastfeeding: The strength of association 1-gen-2015 Marseglia, L.; Manti, S.; D'Angelo, G.; Cuppari, C.; Salpietro, V.; Filippelli, M.; Trovato, A.; Gitto, E.; Salpietro, C.; Arrigo, T.
Molecular Modeling of Cerebrospinal Fluid Dynamics in Pediatric Pseudotumor Cerebri Syndrome: Altered Sodium Transport in Choroid Plexus by Lithium Treatment 1-gen-2015 Johanson, C. E.; Salpietro, V.
Recent Insights on Pediatric Pseudotumor Cerebri Syndrome Pathophysiology: From the Unifying Neuroendocrine Perspective to the Integrated Bioenergetic-Hormonal Mechanism" 1-gen-2015 Salpietro, V.; Ruggieri, M.; Concolino, D.; Johanson, C. E.; Weber, K. T.
The History of Pseudotumor Cerebri Syndrome among Courses and Recourses" 1-gen-2015 Ruggieri, M.; Salpietro, V.; Johanson, C. E.
The natural history of spinal neurofibromatosis: A critical review of clinical and genetic features 1-gen-2015 Ruggieri, M.; Polizzi, A.; Spalice, A.; Salpietro, V.; Caltabiano, R.; D'Orazi, V.; Pavone, P.; Pirrone, C.; Magro, G.; Platania, N.; Cavallaro, S.; Muglia, M.; Nicita, F.
Zellweger syndrome and secondary mitochondrial myopathy 1-gen-2015 Salpietro, V.; Phadke, R.; Saggar, A.; Hargreaves, I. P.; Yates, R.; Fokoloros, C.; Mankad, K.; Hertecant, J.; Ruggieri, M.; Mccormick, D.; Kinali, M.
Stickler syndrome associated with epilepsy: report of three cases 1-gen-2015 Savasta, S.; Salpietro, V.; Sparta, M. V.; Foiadelli, T.; Laino, D.; Lobefalo, L.; Marseglia, G. L.; Verrotti, A.
Pediatric Pseudotumor Cerebri Syndrome: Recent Insights and Future Directions 1-gen-2015 Salpietro, V.; Ruggieri, M.; Johanson, C. E.
Hyperhomocysteinemia and MTHFR polymorphisms as antenatal risk factors of white matter abnormalities in two cohorts of late preterm and full term newborns 1-gen-2015 Marseglia, L. M.; Nicotera, A.; Salpietro, V.; Giaimo, E.; Cardile, G.; Bonsignore, M.; Alibrandi, A.; Caccamo, D.; Manti, S.; D'Angelo, G.; Mami, C.; Di Rosa, G.
Mostrati risultati da 21 a 40 di 133
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile