Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Magdalena SANDU"'
Publikováno v:
Romanian Journal of Neurology, Vol 15, Iss 4, Pp 178-182 (2016)
Fetal stroke is a rare disease that occurs between 14 weeks of gestation and the onset of labor and can be caused by ischemic, thrombotic or hemorrhagic injury produced during pregnancy. One of the maternal conditions associated with fetal stroke is
Externí odkaz:
https://doaj.org/article/1fbf209b98d84140955ca245c8bb83ec
Publikováno v:
Romanian Journal of Neurology, Vol 13, Iss 4, Pp 220-222 (2014)
Multiple sclerosis (MS) is an autoimmune inflammatory disease of the central nervous system which is often diagnosed in young adults. We present a case of tumefactive multiple sclerosis in a child, an unusual form of presentation of MS, especially at
Externí odkaz:
https://doaj.org/article/14e4e4f5e1054543b17acf4b8f350954
Publikováno v:
Romanian Journal of Neurology, Vol 12, Iss 3, Pp 152-155 (2013)
This article aims to present the cases of two pediatric patients with Subcortical Band Heterotopia, monitored in our clinic over a period of one year with respect to seizure frequency and cognitive as well as behavioral evolution. While one of the p
Externí odkaz:
https://doaj.org/article/5104041eba404c709a9750091e96cbfb
Autor:
Cătălin TECUCIANU, Crucița-Loredana BACIU, Elena-Steluţa DINU, Teodora DOBRE, Emilia - Elena CLUCERESCU (TĂNASE), Filip NALASKOWSKI, Andreea Emilia DUŢĂ, Ion PANAIT, Paul DUŢĂ, Flavius-Cristian MĂRCĂU, Silvian-Emanuel MAN, Răzvan MUNTEANU, Crina SOROIU, Diana Catalina CAZANGIU, Natalia FURTUNA, Nicolae (MĂNESCU) RALUCA, Nedelcu ANIŞOR, Traian Eugen BOLFA, Iulia BOGHIRNEA, Ion Cristinel RUJAN, Dana VULPAȘU, Dagna DEJNA, Elena BRAN, Nicolaie MĂNESCU, Marin AURELIA CAMELIA, Voicu TATIANA, Răzvan BRAN, Raul Constantin TĂNASE, Cosmin CIORA, Mircea DICULESCU, Raluca Ioana TELEANU, Magdalena SANDU, Daniel Mihai TELEANU, Smaranda NIȚĂ, Dan Vasile POP, Marius TEODORESCU, Daniela RADU, Iulia SAVU
Publikováno v:
Research and Science Today (2014)
RESEARCH AND SCIENCE TODAY is a biannual science journal established in 2011. The journal is an informational platform that publishes assessment articles and the results of various scientific research carried out by academics. We provide the authors
Externí odkaz:
https://doaj.org/article/ac9dcfbb35b64aacb881b72c494f8fed
Publikováno v:
Romanian Journal of Neurology, Vol 12, Iss 4, Pp 183-184 (2013)
Stroke remains a leading cause of disability and mortality all over the world despite the efforts made towards improving treatment. Most of the clinical studies have not shown significant beneficial effects in the evaluation of various molecules for
Externí odkaz:
https://doaj.org/article/fae6db64cf8e419793c8f960ec871359
Autor:
Cristina Rusu, Selma Dounia Bensemmane, Mingyan Fang, Magdalena Sandu, Lyudmilla Angelova, Marcella Neri, Veneta Bojinova, Jadranka Sekelj Fureš, Fernanda Fortunato, Ivan Litvinenko, Maria Judith Molnar, Anna Potulska-Chromik, Oussama Dendane, C. Burloiu, Samira Makri-Mokrane, Daniela Vasile, Monica Panzaru, Zhiyuan Lu, Yamina Sifi, Niculina Butoianu, Oana Alexandra Iuhas, Birute Burnyte, Butnariu Lacramioara, Rachele Rossi, Djawed Bouchenak Khelladi, Ivan Lehman, Cecilia Trabanelli, Velina Guergueltcheva, Mariela Militaru, Léna Szabó, Anna Lusakowska, Mihaela Vintan, Sanja Delin, Monica Mager, Anna Kostera-Pruszczyk, Gabriela Visa, Agnes Herczegfalvi, Yurtsever Vildan, Andriy V. Shatillo, Dmitry Vlodavets, Balint Fekete, Adela Chirita Emandi, Rita Selvatici, Ivan S. Ivanov, Francesca Gualandi, Alessandra Ferlini, Alice Margutti, Diana Epure, Theodore Kyriakides
Publikováno v:
Neurology Genetics
Neurology genetics, Philadelphia : Lippincot Williams & Wilkins, 2021, vol. 7, iss. 1, art. no. e536, p. [1-12]
Neurology: Genetics
article-version (Version of Record) 3
Neurology genetics, Philadelphia : Lippincot Williams & Wilkins, 2021, vol. 7, iss. 1, art. no. e536, p. [1-12]
Neurology: Genetics
article-version (Version of Record) 3
ObjectiveGenetic diagnosis and mutation identification are now compulsory for Duchenne (DMD) and Becker muscular dystrophies (BMD), which are due to dystrophin (DMD) gene mutations, either for disease prevention or personalized therapies. To evaluate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26d68b8b9b14e4902793ab448668394d
https://www.bib.irb.hr/1113042
https://www.bib.irb.hr/1113042
Autor:
Raluca Ioana Teleanu, Magdalena Sandu, Catalin Carstoveanu, Ileana Barascu, Bucharest Pharmacy
Publikováno v:
Romanian Journal of Neurology, Vol 15, Iss 4, Pp 178-182 (2016)
Scopus-Elsevier
Scopus-Elsevier
Fetal stroke is a rare disease that occurs between 14 weeks of gestation and the onset of labor and can be caused by ischemic, thrombotic or hemorrhagic injury produced during pregnancy. One of the maternal conditions associated with fetal stroke is
Publikováno v:
Journal for Neurology & Psychiatry of Child & Adolescent in Romania. 2016, Vol. 19 Issue 4, p5-10. 6p.
Publikováno v:
ORL.ro. 4:56-59
Melatonin is a hormone produced by the pineal gland during the night, as a response to the light-darkness variation. The endogenous melatonin levels have a cyclic evolution throughout the entire life. Various roles have been cited such as the in uter
Autor:
E Moţa, Mihaela Bîcu, Mihaela Vladu, Magdalena Sandu, Diana Clenciu, Daniel Bîcu, Sigina Gârgavu, Maria Moţa
Publikováno v:
Romanian Journal of Diabetes Nutrition and Metabolic Diseases, Vol 23, Iss 2, Pp 177-182 (2016)
Background and Aims: Studies have shown an increased incidence of chronic complications in people with type 1 diabetes mellitus (T1DM) with insulin resistance (IR) compared to people with T1DM without IR. Estimated glucose disposal rate (eGDR) is an