Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nicolas Abreu"'
Publikováno v:
Case Reports in Radiology, Vol 2013 (2013)
Externí odkaz:
https://doaj.org/article/2da603aed0784743841c02247d365fad
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Thiago Jose Masseran Antunes Parreiras, Sergio Gomes, Tiago Santana do Amaral, Marcelo Rosado da Costa, Nicolas Abreu Rocha Leite Netto
Publikováno v:
IEEE Transactions on Power Systems. :1-10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::273d7000a350f60acf1bdfa9ed4f8b58
https://doi.org/10.1109/tpwrs.2023.3249477
https://doi.org/10.1109/tpwrs.2023.3249477
Publikováno v:
Wednesday, April 26.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0084f9360621bb8a2bc65f2594c9a40
https://doi.org/10.1212/wnl.0000000000202137
https://doi.org/10.1212/wnl.0000000000202137
Autor:
Emily de los Reyes, Nicolas Abreu
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 35
Batten disease, also known as neuronal ceroid lipofuscinosis, refers to a diverse group of 13 hereditary inborn errors of metabolism resulting in the abnormal accumulation of autofluorescent storage material in lysosomes leading to neurodegeneration,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c838349d2021f09f243584ed9253306
https://pubmed.ncbi.nlm.nih.gov/34844861
https://pubmed.ncbi.nlm.nih.gov/34844861
Autor:
Anne M. Comi, Mustafa Sahin, Adrienne Hammill, Emma H. Kaplan, Csaba Juhász, Paula North, Karen L. Ball, Alex V. Levin, Bernard Cohen, Jill Morris, Warren Lo, E. Steve Roach, Nicolas Abreu, Maria Acosta, Audina Berrocal, Joyce Bischoff, James Brodie, Craig Burkhart, Gosia Dymerska, David Eckstein, Mabel Enriquez-Algeciras, Joshua Ewen, Brian Fisher, Sharon Freedman, Emily Germain-Lee, Roy Geronemus, Michael Gold, Rashmi Gopal-Srivastava, Adelaide Hebert, Lan Huang, Henry Jampel, Matsanga Kaseka, Yasmine Kirkorian, Eric Kossoff, Doris Lin, Jeffrey Loeb, Kalyani Marathe, Doug Marchuk, Alice Mead, Scott Mellis, Timothy Murray, Thuy Phung, Anna Pinto, Kate Puttgen, Nancy Ratner, Jennifer Reeve, Steve Roach, Charles Swindell, Hung Tseng, Miriya Tune, Sarah Wetzel-Strong, Monica White, Vicky Whittemore
Publikováno v:
Pediatric Neurology. 58:12-24
Sturge-Weber syndrome (SWS) is a vascular neurocutaneous disorder that results from a somatic mosaic mutation in GNAQ, which is also responsible for isolated port-wine birthmarks. Infants with SWS are born with a cutaneous capillary malformation (por
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b90717af1fbd35c3ab3bfdfcf30cf073
https://doi.org/10.1016/j.pediatrneurol.2015.11.009
https://doi.org/10.1016/j.pediatrneurol.2015.11.009
Autor:
Nicolas Abreu, Mikhail Kazachkov, Nataliya Tkachenko, Sanjeev V. Kothare, Kanwaljit Singh, Kathyrn Fitzgerald, Christy Day, Anne Marie Morse
Publikováno v:
Pediatric Neurology. 57:39-45.e1
Background Children with medical complexity have a high prevalence of sleep disorders. However, outpatient polysomnography to evaluate for these conditions may be difficult to perform because of lack of skilled nursing care. The aim of this study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a13611dfd48e329a5d5045cc3526671
https://doi.org/10.1016/j.pediatrneurol.2015.12.020
https://doi.org/10.1016/j.pediatrneurol.2015.12.020