Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Massimo Guarna"'
Publikováno v:
European Journal of Medical Research, Vol 28, Iss 1, Pp 1-8 (2023)
Abstract Background The hypoglossal canal is a dual bone canal at the cranial base near the occipital condyles. The filaments of the hypoglossal nerve pass through the canal. It also transmits the meningeal branch of the ascending pharyngeal artery,
Externí odkaz:
https://doaj.org/article/974653a8cbf141409982c194b13ac7b1
Publikováno v:
Italian Journal of Anatomy & Embryology / Archivio Italiano di Anatomia Ed Embriologia. 2021, Vol. 125 Issue 1, p11-17. 7p.
Neuroblastoma (NB) is the most common extracranial solid cancer in childhood and the most common cancer in infancy. Our purpose was to investigate in vitro how cancer cell survival occurs in presence of morphine in undifferentiated and differentiated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0ab48edbe270570f47a73e9205b59f9
http://hdl.handle.net/11365/974456
http://hdl.handle.net/11365/974456
Autor:
Ranuccio Nuti, Nila Volpi, Nicola Giordano, Roberto Leoncini, Antonella Fioravanti, A Montella, Claudio Corallo, Emilio Battisti, Massimo Guarna, Daniela Vannoni, A. Albanese, G. Landi, Daniela Franci
Publikováno v:
Rheumatology international. 33(6)
Osteoarthritis (OA) is the most common joint disease, characterized by matrix degradation and changes in chondrocyte morphology and metabolism. Literature reported that electromagnetic fields (EMFs) can produce benefits in OA patients, even if EMFs m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a74a4b9f45cb48e3d3e2cf7ff4441c7
https://pubmed.ncbi.nlm.nih.gov/23263545
https://pubmed.ncbi.nlm.nih.gov/23263545
Autor:
George B. Stefano, Wei Zhu, Monica Norcini, Massimo Guarna, Nicoletta Galeotti, E. Vivoli, Carla Ghelardini, Enrica Bianchi
Previous evidence demonstrates that low dose morphine systemic administration induces acute thermal hyperalgesia in normal mice through microOR stimulation of the inositol signaling pathway. We investigated the site of action of morphine and the mech
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16971eb8a5270dab921994146177b918
http://hdl.handle.net/11365/26485
http://hdl.handle.net/11365/26485
Publikováno v:
PainReferences. 123(3)
Systemic administration of morphine induced a hyperalgesic response in the hot plate test, at an extremely low dose (1-10 microg/kg). We have examined in vivo whether morphine, at an extremely low dose, induces acute central hypernociception followin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::942c9d18bdf4550ec17754d5bca2e351
https://pubmed.ncbi.nlm.nih.gov/16650582
https://pubmed.ncbi.nlm.nih.gov/16650582
Publikováno v:
Medical science monitor : international medical journal of experimental and clinical research. 11(6)
Endogenous morphine is present in the mammalian brain as determined by gas chromatography/mass spectrometry. The criteria essential for satisfying the definition of morphine as a neurotransmitter are examined. The detection of endogenous morphine-lik
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b4d56347ea3f6d99bfe7854830bfce4e
https://pubmed.ncbi.nlm.nih.gov/15917730
https://pubmed.ncbi.nlm.nih.gov/15917730
Nitric oxide (NO) signalling is at the forefront of intense research interest because its many effects remain controversial and seemingly contradictory. This paper examines its role as a potential mediator of pain and tolerance. Within this context d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be93565074597f5e8f83f2c94d931e0c
http://hdl.handle.net/11365/470217
http://hdl.handle.net/11365/470217
Autor:
Wei, Zhu, Yuliang, Ma, Achim, Bell, Tobias, Esch, Massimo, Guarna, Thomas V, Bilfinger, Enrica, Bianchi, George B, Stefano
Publikováno v:
Medical science monitor : international medical journal of experimental and clinical research. 10(12)
We have identified a novel mu opiate receptor, p3, which is expressed in several human tissues, is selective for opiate alkaloids, insensitive to opioid peptides, and also is coupled to constitutive nitric oxide release. We, and others, have also dem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::99b7bcd8de72303a42c6d69a462aeab8
https://pubmed.ncbi.nlm.nih.gov/15567973
https://pubmed.ncbi.nlm.nih.gov/15567973