Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Annapia Verri"'
Publikováno v:
Clinical Management Issues, Vol 6, Iss 3, Pp 97-103 (2012)
Specific forms of epilepsy may be found at various ages in Down Syndrome (DS) and a sharp increase in the incidence of epilepsy with age has been documented. A specific type of myoclonic epilepsy associated with cognitive decline has been reported as
Externí odkaz:
https://doaj.org/article/5608efe3df7d4ff183cea8491580921b
Autor:
Annapia Verri, Anna Cremante
Publikováno v:
Clinical Management Issues, Vol 3, Iss 3, Pp 123-132 (2009)
Sex chromosome anomalies have been associated with psychoses. We report a patient with XYY chromosome anomaly who developed a paranoid psychosis. The second case deal with a 51-year-old woman affected by Turner Syndrome and Psychotic Disorder, with a
Externí odkaz:
https://doaj.org/article/12bbaab3f3024791af5ec4b8e93008d3
Publikováno v:
Case Reports in Immunology, Vol 2013 (2013)
Ataxia-telangiectasia (AT) is the most frequent progressive cerebellar ataxia in infancy and childhood. Immunodeficiency which includes both cellular and humoral arms has variable severity. Since the clinical presentation is extremely variable, a hig
Externí odkaz:
https://doaj.org/article/32562bd3165448eebf37e6e6af4c7289
Autor:
Giuseppe Roberto Burgio, Luigi Nespoli, Rita Maccario, Annapia Verri, Patrizia Comoli, Marco Zecca
Publikováno v:
Haematologica, Vol 97, Iss 9 (2012)
Externí odkaz:
https://doaj.org/article/8dc77d73c693473a8ad2038b3b8a35d2
Autor:
Giuseppe Roberto Burgio, Luigi Nespoli, Rita Maccario, Annapia Verri, Patrizia Comoli, Marco Zecca
Publikováno v:
Haematologica, Vol 97, Iss 4 (2012)
Externí odkaz:
https://doaj.org/article/87cc10a22cc14e979071e3e2726cc525
Autor:
Giovanni Assenza, Stefano Meletti, Loretta Giuliano, Roberto Michelucci, Ettore Beghi, Mario Tombini, Vincenzo Di Lazzaro, Lorenzo Ricci, Francesca Bisulli, Amedeo Bianchi, Umberto Aguglia, Vincenzo Belcastro, Fabrizio A. de Falco, Angelo Labate, Pasquale Striano, Francesco Pisani, Paolo Tinuper, Annapia Verri, Anna Teresa Giallonardo, Sara Gasparini, Silvana Franceschetti, Sara Casciato, Barbara Mostacci, Giancarlo Di Gennaro, Edoardo Ferlazzo, Alessandra Morano, Vincenzo Pizza, Angela La Neve, Flavio Villani, Paolo Benna, Gaetano Zaccara, Carlo Di Bonaventura, Giuliano Avanzini, Jacopo Lanzone, Adriana Magaudda, Ferdinando Sartucci, Vittoria Cianci
Background: Vagal nerve stimulation (VNS) is an effective palliative therapy in drug-resistant epileptic patients and is also approved as a therapy for treatment-resistant depression. Depression is a frequent comorbidity in epilepsy and it affects th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee5ac57b36bc9a54ebf574812b814f00
http://hdl.handle.net/11585/781473
http://hdl.handle.net/11585/781473
Autor:
Isabella Mammi, Diana Postorivo, Aminta Varricchio, Maria Garzo, Elisa Nalesso, Teresa Mattina, Ilaria Catusi, Maria Paola Recalcati, Laura Cardarelli, Nicola Beltrami, Anna Sajeva, Maria Teresa Bonati, Daniela Giardino, Annapia Verri, Lidia Larizza, Asia Costa, Nicoletta Villa, Anna Maria Nardone
Publikováno v:
European Journal of Medical Genetics. 61:173-180
Only a few subjects carrying supernumerary marker chromosomes derived from 19 chromosome (sSMC(19)) have been described to date and for a small portion of them the genic content has been defined at the molecular level. We present seven new different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ee44c49bf4aa6e1d6440e91216290a5
https://doi.org/10.1016/j.ejmg.2017.11.007
https://doi.org/10.1016/j.ejmg.2017.11.007
Autor:
Clerici Federica, D’Angelo Carmen, Cremante Anna, Mauri Anna, Annapia Verri, Castelletti Chiara
Publikováno v:
Journal of Antimicrobial Agents.
Sex Chromosomal Aneuploidies (SCAs) are the most frequently occurring chromosomal abnormalities with an incidence of 1 in 450 births. Males with SCAs are known to have variability in their developmental profile. Aim of this paper is to illustrate cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f65cbc090d87fe68ea52c4d2d9df229
https://doi.org/10.4172/2167-0250.1000175
https://doi.org/10.4172/2167-0250.1000175
Autor:
Annapia Verri, Chris Oliver
Publikováno v:
Journal of Intellectual Disability Research. 54:877-880
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51a7d5866cc7dd8bc0543e5ff2653688
https://doi.org/10.1111/j.1365-2788.2010.01327.x
https://doi.org/10.1111/j.1365-2788.2010.01327.x
Autor:
Jacqueline Schoumans, Helena Malmgren, Anna Lindstrand, Ann Nordgren, Britt-Marie Anderlid, Elisa Benetti, Irina Golovleva, Elisabeth Blennow, Maud Eriksson, Annapia Verri
Publikováno v:
American Journal of Medical Genetics Part A. :1233-1243
Chromosome 10p terminal deletions have been associated with DiGeorge phenotype, and within the same genomic region haploinsufficiency of GATA3 causes the HDR syndrome (hypoparathyroidism, sensorineural deafness, renal dysplasia). We have performed de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4c10ae2052601ef3fe0fdc8008bceb0
https://doi.org/10.1002/ajmg.a.33366
https://doi.org/10.1002/ajmg.a.33366