Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Paola Drigo"'
Autor:
Paola Drigo
Tres mujeres en un camino de la Italia rural: una madre exhausta y enferma y sus dos hijas, niñas todavía. Maria Zef, la hija mayor, tira, como si fuera una bestia, de un carromato cargado de cacharros en venta al tiempo que vigila constantemente p
Autor:
Michele Gangemi, Paola Drigo, Valentina Sellaroli, Franca Benini, Marco Spizzichino, Roberta Vecchi, L Manfredini, Luciano Orsi, Pierina Lazzarin, Momcilo Jankovic, Marcello Orzalesi
Publikováno v:
Tumori. 103(1)
Purpose The death of a child is a devastating and tragic event for all those involved. This charter aims to help healthcare workers and people assisting terminally ill children to recognize some important rights of the child, with some related sugges
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b4017a3151227a6427edf564d3d547a
https://pubmed.ncbi.nlm.nih.gov/27741348
https://pubmed.ncbi.nlm.nih.gov/27741348
Autor:
Matteo Cassina, Chiara Rigon, Marilena Vecchi, Luca De Palma, Alberto Casarin, Paola Drigo, Maurizio Clementi
Publikováno v:
Seizure. 20:813-816
Epilepsies can be caused by specific genetic anomalies or by non-genetic factors, but in many cases the underlying cause is unknown.Mutations in the SCN1A and SCN2A genes are reported in childhood epilepsies; in particular SCN1A was found mutated in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e073c4fd0cb210cb8ce410cd4934ae0
https://doi.org/10.1016/j.seizure.2011.07.008
https://doi.org/10.1016/j.seizure.2011.07.008
Publikováno v:
Pediatric Radiology. 41:962-970
Congenital cytomegalovirus (CMV) infection can lead to severe neurological sequelae, but a defined brain magnetic resonance (MR) pattern and MR predictors of clinical outcome are still lacking. Clinical and MR findings of 14 children with symptomatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::767b2d1803c81cd5c699612b0e35da04
https://doi.org/10.1007/s00247-011-2120-5
https://doi.org/10.1007/s00247-011-2120-5
Autor:
Milena Calderone, Irene Toldo, Rodica Mardari, Paola Drigo, Pier Antonio Battistella, Anna Maria Laverda, Diego Cecchin, Stefano Sartori, Francesca Cattelan
Publikováno v:
Cephalalgia. 31:751-756
Background: Hemiplegic migraine (HM) is a rare variety of migraine with aura, characterized by motor deficits during the aura, often beginning in childhood. The hemiplegic attacks can be severe and prolonged but the prognosis is usually good. Data on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::503935bac0ee42b0d33040820153b7a8
https://doi.org/10.1177/0333102410392068
https://doi.org/10.1177/0333102410392068
Autor:
Isabella Mammi, Serena Redaelli, Leda Dalprà, Elisabetta Lenzini, Paola Drigo, Melissa Rosa-Rizzotto
Publikováno v:
Genetic Testing and Molecular Biomarkers. 14:695-701
The role of cryptic translocations in human syndromes is a matter of fact, though this phenomenon is apparently rare. Apart from episodic case reports due to the increasing application of new molecular cytogenetic techniques, no data on its frequency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0b7318b1ad3c06dacf7d0301f67fe3f
https://doi.org/10.1089/gtmb.2010.0079
https://doi.org/10.1089/gtmb.2010.0079
Autor:
Paola Drigo, Luigi Pentimalli, Maurizia Grazzini, Roberto Saetti, Domenico D'Avella, R. Faggin
Publikováno v:
Journal of Neurosurgery: Pediatrics. 4:262-265
The treatment of the transsphenoidal sphenopalatine encephalocele in infants has not been thoroughly described in the literature. Pterional and subfrontal transbasal approaches have been reported as the advised treatment for transethmoidal encephaloc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::457c099a0991c3b440c58863384f59ea
https://doi.org/10.3171/2009.4.peds0884
https://doi.org/10.3171/2009.4.peds0884
Autor:
Daniela Gambel-Benussi, Vanna Pecile, Paola Drigo, Lucia Ballarati, Daniela Giardino, Vincenzo Petix, Elisabetta Lenzini, Marco Carrozzi, Melissa Rosa Rizzotto
Publikováno v:
Genetic Testing and Molecular Biomarkers. 13:79-86
Subtelomeric rearrangements are one of the main causes of multiple congenital anomalies and mental retardation, and they are detected in 5% of patients. We report on a 6.5-year-old boy with mental retardation, dysmorphic features, and behavioral prob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93387e5b1d990a603721ea3face13e56
https://doi.org/10.1089/gtmb.2008.0075
https://doi.org/10.1089/gtmb.2008.0075
Autor:
Stefano Sartori, Alberto Casarin, Paola Drigo, Irene Toldo, Laura Anesi, Alessandra Murgia, Roberta Polli
Publikováno v:
Journal of Child Neurology. 23:912-915
Angelman syndrome is a neurodevelopmental disorder characterized by mental retardation, absence of speech, seizures, abnormal electroencephalography (EEG), and happy disposition. The syndrome results from lack of function of the maternal copy of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::056bf750e3efc77a2ba1b8f63b8d72bf
https://doi.org/10.1177/0883073808316367
https://doi.org/10.1177/0883073808316367
Autor:
Paola Drigo, I. Toldo
Publikováno v:
Rivista di Neuroradiologia. 18:292-295
Craniosynostosis, a skull growth disorder due to premature fusion of one or more sutures, is a common clinical problem requiring the attention of many specialists. In simple craniosynostosis (stenosis of a single suture) symptoms are usually mild: si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a1ef4d5658cf633cf650dc33796c99c
https://doi.org/10.1177/197140090501800304
https://doi.org/10.1177/197140090501800304