Propranolol for familial cerebral cavernous malformation (Treat_CCM): study protocol for a randomized controlled pilot trial

Autor: Lanfranconi, S., Scola, E., Bertani, G. A., Zarino, B., Pallini, Roberto, D'Alessandris, Quintino Giorgio, Mazzon, E., Marino, S., Carriero, M. R., Scelzo, E., Farago, G., Castori, M., Fusco, C., Petracca, A., D'Agruma, L., Tassi, L., D'Orio, P., Lampugnani, M. G., Nicolis, E. B., Vasami, A., Novelli, D., Torri, V., Meessen, J. M. T. A., Salman, R. A. -S., Dejana, E., Latini, R., Pignotti, Fabrizio, Sturiale, Carmelo Lucio, Albanese, Alessio, Valcamonica, G., Ronchi, D., Pogliani, S., De Grazia, U., Bossi, C., Ciurleo, R., Raggi, P., Simeone, A., Balconi, G., Foresta, A., Buratti, M. G., Carrara, M., Ojeda-Fernandez, M. L., Treglia, R., Maggioni, A. P., Beghi, E., Tettamanti, M., Regna-Gladin, C., Prelle, A., Mangiavacchi, M., Poloni, M., Lazzaroni, F., Malinverno, M., Ungaro, C., Raucci, F.

Publikováno v: 2020, ' Propranolol for familial cerebral cavernous malformation (Treat_CCM): study protocol for a randomized controlled pilot trial ', Trials, vol. 21, no. 1 . https://doi.org/10.1186/s13063-020-4202-x
Trials, Vol 21, Iss 1, Pp 1-10 (2020)
Trials

Background Cerebral cavernous malformations (CCMs) are vascular malformations characterized by clusters of enlarged leaky capillaries in the central nervous system. They may result in intracranial haemorrhage, epileptic seizure(s), or focal neurologi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5126fec22dd3210a8fb315bfc51e90d
https://hdl.handle.net/20.500.11820/e02c57ba-c0be-4f5c-9b2e-862e8f8e0968

Search for heavy particles decaying into top-quark pairs using lepton-plus-jets events in proton-proton collisions at root s=13 TeV with the ATLAS detector

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L, Collaboration, ATLAS

A search for new heavy particles that decay into top-quark pairs is performed using data collected from proton–proton collisions at a centre-of-mass energy of 13 TeV by the ATLAS detector at the Large Hadron Collider. The integrated luminosity of t

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https://eprints.whiterose.ac.uk/138005/7/Aaboud2018_Article_SearchForHeavyParticlesDecayin.pdf

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Functional and structural characterization of novel mutations and genotype-phenotype correlation in 51 phenylalanine hydroxylase deficient families from Southern Italy

Autor: Daniele A., Cardillo G., Pennino C., Ungaro C., Sibilio M., Esposito L, SCALA, IRIS, PARENTI, GIANCARLO, ZAGARI, ADRIANA, ANDRIA, GENEROSO, SALVATORE, FRANCESCO

Publikováno v: The FEBS journal. 276(7)

Hyperphenylalaninemia (Online Mendelian Inheritance in Man database: 261600) is an autosomal recessive disorder mainly due to mutations in the gene for phenylalanine hydroxylase; the most severe form of hyperphenylalaninemia is classic phenylketonuri

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::42c004e961054c5ecd485bc1d4947b29
https://pubmed.ncbi.nlm.nih.gov/19292873

Search for Scalar Diphoton Resonances in the Mass Range 65-600 GeV with the ATLAS Detector in pp Collision Data at root s=8 TeV

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Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::466607729dbefcbdddfc176f2e8b70a8
http://hdl.handle.net/11573/804194