Zobrazeno 1 - 10
of 144
pro vyhledávání: '"M, Eltze"'
Publikováno v:
Clinical Neurophysiology. 131:609-615
Objective To determine the relationship between seizure onset, sleep stage and focal cortical dysplasia type 2 (FCD2) location in sleep related epilepsy (SRE). Methods We reviewed scalp video-EEG data of 77 patients with SRE among 130 surgically trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d6bfaca128ad213ee3a6400af53d57d
https://doi.org/10.1016/j.clinph.2019.11.055
https://doi.org/10.1016/j.clinph.2019.11.055
Autor:
Christin M, Eltze, Wui K, Chong, Tim, Cox, Andrea, Whitney, Mario, Cortina-Borja, Richard F M, Chin, Rod C, Scott, J Helen, Cross
Publikováno v:
Epilepsia. 54(3)
Most published data on infants presenting with epilepsy originate from hospital/specialist clinic settings and may therefore not be representative of the general population. We carried out a population-based study to estimate the incidence of epileps
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc90ad396cf87728428d42bfc108cc13
https://pubmed.ncbi.nlm.nih.gov/23252366
https://pubmed.ncbi.nlm.nih.gov/23252366
Publikováno v:
Pulmonary Pharmacology. 7:109-120
The inhibition of preganglionic and postganglionic contractions of the rabbit isolated bronchus/trachea by antagonists with selectivity for different muscarinic receptor subtypes was compared with their affinities at M1, M2, M3 and M4 receptors. Neit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20894101e07d5839f4963421098c251a
https://doi.org/10.1006/pulp.1994.1013
https://doi.org/10.1006/pulp.1994.1013
Publikováno v:
Journal of Autonomic Pharmacology. 11:337-342
1. Highly controversial claims have been put forward in the literature as to the involvement of either M1 or non-M1 muscarinic receptors in the field (vagal) stimulation of gastric acid secretion. This mini-review considers three available sets of da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e15b54bd47f4ac42b7fe37d3cfef5e3e
https://doi.org/10.1111/j.1474-8673.1991.tb00257.x
https://doi.org/10.1111/j.1474-8673.1991.tb00257.x
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 297(1)
We have investigated the bronchodilator and anti-inflammatory properties of roflumilast (3-cyclopropylmethoxy-4-difluoromethoxy-N-[3,5-dichloropyrid-4-yl]-benzamide), a novel, highly potent, and selective phosphodiesterase 4 (PDE4) inhibitor. Additio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::49280c8844a538b1ae80aafd46b22717
https://pubmed.ncbi.nlm.nih.gov/11259555
https://pubmed.ncbi.nlm.nih.gov/11259555
Autor:
M, Eltze
Publikováno v:
Journal of neural transmission. Supplementum. 56
Four major components of the mechanism of action have been identified for the antiparkinsonian drug budipine up to now. 1) The primary action of budipine is an indirect dopaminergic effect as shown by facilitation of dopamine (DA) release, inhibition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::25c5d6534d0e4fe51a29b3ec76ba24de
https://pubmed.ncbi.nlm.nih.gov/10370904
https://pubmed.ncbi.nlm.nih.gov/10370904
Autor:
M. Eltze
Publikováno v:
Journal of Neural Transmission. Supplementa ISBN: 9783211832752
Four major components of the mechanism of action have been identified for the antiparkinsonian drug budipine up to now. 1) The primary action of budipine is an indirect dopaminergic effect as shown by facilitation of dopamine (DA) release, inhibition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dfe53510a8c86409678d0f4380878ab
https://doi.org/10.1007/978-3-7091-6360-3_4
https://doi.org/10.1007/978-3-7091-6360-3_4
Autor:
M. Eltze
Publikováno v:
Methods in Pulmonary Research ISBN: 9783034898034
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3aefaafc3ea1930f88c95742ca2886f
https://doi.org/10.1007/978-3-0348-8855-4_4
https://doi.org/10.1007/978-3-0348-8855-4_4
Publikováno v:
Agents and actions. Supplements. 34
Zardaverine is shown to inhibit selectively two out of five isoenzyme classes of phosphodiesterases, namely PDE III from human platelets and PDE IV from human polymorphonuclear leucocytes (PMN) with IC50 values of 0.58 and 0.17 microM, respectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4d2d0a900dba79a0b8ae7aebdf2a4001
https://pubmed.ncbi.nlm.nih.gov/1665311
https://pubmed.ncbi.nlm.nih.gov/1665311
The muscarinic activities of the heterocyclic acetylcholine analogues, N-ethyl-nor-arecaidine propargyl ester (NEN-APE), (R)- and (S)-nipecotic acid ethyl ester (NAEE) and guvacine propargyl ester (GPE), were determined at presynaptic M1- and postsyn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02e7ddaa08381a1968beca4c0e291365
https://doi.org/10.1016/b978-0-08-041165-1.50015-6
https://doi.org/10.1016/b978-0-08-041165-1.50015-6