Chemotherapy induced peripheral neuropathy. Case reports

Autor: Pedro Miguel Parreira da Silva, Vanessa Capelo Feijão, Maria Teresa Gonzalez Fontinhas

Publikováno v: BrJP, Vol 7 (2024)

BACKGROUND AND OBJECTIVES: Chemotherapy-induced peripheral neuropathy (CIPN) is a common side effect reported by patients receiving cancer treatment, and it can affect treatment success, patient outcomes, and quality of life. CIPN typically begins wi

Externí odkaz: https://doaj.org/article/9f603c9e63ee4ad0aa05c083efe08f3e

Health-related quality of life in children with congenital adrenal hyperplasia

Autor: Alyssa Halper, Mary C. Hooke, Maria Teresa Gonzalez-Bolanos, Nancy Vanderburg, Thang N. Tran, Jane Torkelson, Kyriakie Sarafoglou

Publikováno v: Health and Quality of Life Outcomes, Vol 15, Iss 1, Pp 1-7 (2017)

Abstract Background Children with congenital adrenal hyperplasia (CAH) require life-long glucocorticoid replacement and have daily intermittent hyper/hypocortisolemia and hyperandrogenemia. Health-related quality of life (HRQL) is important for under

Externí odkaz: https://doaj.org/article/51fb71ad48f9449eb3fadd5268edeef1

Wisdom of the Ensemble: Improving Consistency of Deep Learning Models

Autor: Wang, Lijing, Ghosh, Dipanjan, Diaz, Maria Teresa Gonzalez, Farahat, Ahmed, Alam, Mahbubul, Gupta, Chetan, Chen, Jiangzhuo, Marathe, Madhav

Deep learning classifiers are assisting humans in making decisions and hence the user's trust in these models is of paramount importance. Trust is often a function of constant behavior. From an AI model perspective it means given the same input the u

Externí odkaz: http://arxiv.org/abs/2011.06796

Barite Precipitation on Suspended Organic Matter in the Ocean Water Column

Autor: Francisca Martinez-Ruiz, Adina Paytan, Maria Teresa Gonzalez-Muñoz, Fadwa Jroundi, Maria del Mar Abad, Phoebe J. Lam, Tristan J. Horner, Miriam Kastner

Despite decades of research, barite formation in the ocean water column has been widely discussed since most of the world´s ocean mesopelagic zone, in which barite forms, is generally undersaturated with respect to this mineral. Recent evidence from

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ed9cb7855e7f0c894ad9926045c43ba0
https://doi.org/10.5194/egusphere-egu22-12842

International Consensus on the Use of Genetics in the Management of Hereditary Angioedema

Autor: Jose Fabiani, Emel Aygören-Pürsün, Sladjana Andrejevic, Christian Drouet, Nóra Veszeli, Matija Rijavec, Georg Dewald, Markus Magerl, Michael Kirschfink, Marco Cicardi, Camila Lopes Veronez, Imola Beatrix Nagy, Massimo Triggiani, Maria Zamanakou, Henrik Halle Boysen, Matthaios Speletas, Maria Bova, Maria Staevska, Maurizio Margaglione, Sandra C. Christiansen, Teresa Caballero, Milos Jesenak, Vesna Grivcheva-Panovska, Allen P. Kaplan, Kinga Viktoria Köhalmi, Anthony J. Castaldo, Roman Hakl, Gaëlle Hardy, Walter A. Wuillemin, Inmaculada Martinez Saguer, Margarita López Trascasa, João Bosco Pesquero, Sven Cichon, Jonathan A. Bernstein, Grzegorz Porebski, Patrik Nordenfelt, C. Katelaris, Anette Bygum, Maria Teresa Gonzalez-Quevedo, Stephen Jolles, Henriette Farkas, Sandra A. Nieto, William R. Lumry, Hilary Longhurst, Spath Peter, Iris Leibovich, Nihal M. Gökmen, Christina Weber, Noemi-Anna Bara, Konrad Bork, Alberto López Lera, Dorottya Csuka, Fotis Psarros, Laurence Bouillet, Marc A. Riedl, Bruce L. Zuraw, Anete Sevciovic Grumach, Farrukh R. Sheikh, Marcin Stobiecki, Anastasios E. Germenis, Ágnes Szilágyi, Avner Reshef, Susan Waserman, J. Gooi

Publikováno v: Germenis, A E, Margaglione, M, Pesquero, J B, Farkas, H, Cichon, S, Csuka, D, Lera, A L, Rijavec, M, Jolles, S, Szilagyi, A, Trascasa, M L, Veronez, C L, Drouet, C, Zamanakou, M & Hereditary Angioedema International Working Group 2020, ' International Consensus on the Use of Genetics in the Management of Hereditary Angioedema ', The Journal of Allergy and Clinical Immunology: In Practice, vol. 8, no. 3, pp. 901-911 . https://doi.org/10.1016/j.jaip.2019.10.004

Hereditary angioedema (HAE) is becoming much more genetically complex than was initially considered. Thus, the role of HAE genetics is expanding beyond research laboratories, and the genotyping of subjects suffering from HAE has become diagnostically

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dea94416edd37dfc324e3c33be73422
https://doi.org/10.1016/j.jaip.2019.10.004