De Gregori Manuela
De Gregori Manuela
Fondazione IRCCS Policlinico San Matteo Pavia
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Cited by
Cited by
A recurrent 15q13. 3 microdeletion syndrome associated with mental retardation and seizures
AJ Sharp, HC Mefford, K Li, C Baker, C Skinner, RE Stevenson, ...
Nature genetics 40 (3), 322-328, 2008
Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients
M De Gregori, R Ciccone, P Magini, T Pramparo, S Gimelli, J Messa, ...
Journal of medical genetics 44 (12), 750-762, 2007
Research method: A tool for life
BC Beins
Cambridge University Press, 2017
Clinical and molecular delineation of the 17q21. 31 microdeletion syndrome
DA Koolen, AJ Sharp, JA Hurst, HV Firth, SJL Knight, A Goldenberg, ...
Journal of medical genetics 45 (11), 710-720, 2008
Morphine metabolism, transport and brain disposition
S De Gregori, M De Gregori, GN Ranzani, M Allegri, C Minella, M Regazzi
Metabolic brain disease 27 (1), 1-5, 2012
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis
BWM van Bon, DA Koolen, R Borgatti, A Magee, S Garcia-Minaur, ...
Journal of medical genetics 45 (6), 346-354, 2008
Genetic variability at COMT but not at OPRM1 and UGT2B7 loci modulates morphine analgesic response in acute postoperative pain
M De Gregori, G Garbin, S De Gregori, CE Minella, D Bugada, A Lisa, ...
European journal of clinical pharmacology 69 (9), 1651-1658, 2013
How and why to screen for CYP2D6 interindividual variability in patients under pharmacological treatments
M De Gregori, M Allegri, S De Gregori, G Garbin, C Tinelli, M Regazzi, ...
Current drug metabolism 11 (3), 276-282, 2010
Human genetic variability contributes to postoperative morphine consumption
M De Gregori, L Diatchenko, PM Ingelmo, V Napolioni, P Klepstad, ...
The Journal of Pain 17 (5), 628-636, 2016
Pain assessment in animal models: do we need further studies?
C Gigliuto, M De Gregori, V Malafoglia, W Raffaeli, C Compagnone, ...
Journal of pain research 7, 227, 2014
Pharmacogenetics and postoperative pain: a new approach to improve acute pain management
M Allegri, M De Gregori, T Niebel, C Minella, C Tinelli, S Govoni, ...
Minerva Anestesiologica 76 (11), 937, 2010
Contiguous gene syndrome due to an interstitial deletion in Xp22. 3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD
F Lonardo, G Parenti, DV Luquetti, I Annunziata, M Della Monica, ...
European journal of medical genetics 50 (4), 301-308, 2007
Inverted duplications: how many of them are mosaic?
T Pramparo, S Giglio, G Gregato, M De Gregori, MG Patricelli, R Ciccone, ...
European journal of human genetics 12 (9), 713-717, 2004
Combining pain therapy with lifestyle: the role of personalized nutrition and nutritional supplements according to the SIMPAR Feed Your Destiny approach
M De Gregori, C Muscoli, ME Schatman, T Stallone, F Intelligente, ...
Journal of pain research 9, 1179, 2016
Food pyramid for subjects with chronic pain: foods and dietary constituents as anti-inflammatory and antioxidant agents
M Rondanelli, MA Faliva, A Miccono, M Naso, M Nichetti, A Riva, ...
Nutrition research reviews 31 (1), 131, 2018
From micro-to nanostructured implantable device for local anesthetic delivery
L Zorzetto, P Brambilla, E Marcello, N Bloise, M De Gregori, L Cobianchi, ...
International journal of nanomedicine 11, 2695, 2016
A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation
T Pramparo, M De Gregori, S Gimelli, R Ciccone, D Frondizi, T Liehr, ...
American Journal of Medical Genetics Part A 146 (13), 1754-1760, 2008
Effect of postoperative analgesia on acute and persistent postherniotomy pain: a randomized study
D Bugada, P Lavand'Homme, AL Ambrosoli, C Klersy, A Braschi, ...
Journal of clinical anesthesia 27 (8), 658-664, 2015
Drug transporters and renal drug disposition in the newborn
S De Gregori, M De Gregori, GN Ranzani, A Borghesi, M Regazzi, ...
The Journal of Maternal-Fetal & Neonatal Medicine 22 (sup3), 31-37, 2009
A case of autism with an interstitial 1q deletion (1q23. 3‐24.2) and a de novo translocation of chromosomes 1q and 5q
M Della Monica, F Lonardo, F Faravelli, M Pierluigi, DV Luquetti, ...
American Journal of Medical Genetics Part A 143 (22), 2733-2737, 2007
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