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Publikováno v:
Clinical Genetics; Jul2005, Vol. 68 Issue 1, p61-68, 8p
Autor:
Șorodoc, Victorița1,2 (AUTHOR), Indrei, Lucia3 (AUTHOR), Dobroghii, Catinca1 (AUTHOR), Asaftei, Andreea2 (AUTHOR) asafteiandreea96@gmail.com, Ceasovschih, Alexandr1,2 (AUTHOR) asafteiandreea96@gmail.com, Constantin, Mihai1,2 (AUTHOR), Lionte, Cătălina1,2 (AUTHOR), Morărașu, Bianca Codrina1,2 (AUTHOR), Diaconu, Alexandra-Diana1,2 (AUTHOR), Șorodoc, Laurențiu1,2 (AUTHOR)
Publikováno v:
Journal of Clinical Medicine. Oct2024, Vol. 13 Issue 20, p6094. 27p.
Autor:
Altakhaineh, Amjaad T.1 (AUTHOR) amjad123altakaineh@gmail.com, Alrawashdeh, Rula1 (AUTHOR) rular18@mutah.edu.jo, Zhou, Jiafeng2 (AUTHOR) rular18@mutah.edu.jo
Publikováno v:
Energies (19961073). Oct2024, Vol. 17 Issue 20, p5208. 27p.
Autor:
Choi, Woong1 (AUTHOR) choi_woong@naver.com, Cha, Seongkwang1,2 (AUTHOR) seong9211@korea.ac.kr, Kim, Kyoungmi1,3 (AUTHOR) seong9211@korea.ac.kr
Publikováno v:
Cells (2073-4409). Jul2024, Vol. 13 Issue 14, p1214. 32p.
Autor:
Berbel-García A, JESÚS PORTA-ETESSAM, Martínez-Salio A, Ballesta F, Ra, Sáiz-Díaz, Da, Pérez-Martínez, de Toledo M
Publikováno v:
ResearcherID
Europe PubMed Central
Europe PubMed Central
In the adult, hypoglycaemia is documented as a consequence of overdose of insulin or oral hypoglycaemic agents. Neonatal hypoglycaemia is common but rarely symptomatic due to protective mechanisms. Very few reports on hypoglycaemic injury are availab
Trisomy/tetrasomy 21 mosaicism was found in chorionic villi (semidirect preparation) obtained from a 40 year old pregnant woman. Since both cell lines were abnormal, the couple elected for pregnancy termination. Placenta and fetal tissue samples were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e36543407f2b8b1304d4cc6c9dc6d0e5
https://europepmc.org/articles/PMC1734340/
https://europepmc.org/articles/PMC1734340/
Publikováno v:
Europe PubMed Central
We reviewed retrospectively 12 patients with Wilson's disease diagnosed during a 16-year period (1974-1989). The prevalence rate was 0.6 per 100,000 individuals. Clinical onset was hepatic (50%) or neurologic (50%), but at diagnosis (6.4 years later)
Publikováno v:
Microwave Conference (EuMC), 2010 European; 2010, p930-933, 4p
Autor:
Milà, M., Kruyer, H., Glover, G., Sánchez, A., Carbonell, P., Castellví-Bel, S., Volpini, V., Rosell, J., Gabarrón, J., López, I., Villa, M., Ballesta, F., Estivill, X.
Publikováno v:
Human Genetics; 1994, Vol. 94 Issue 4, p395-400, 6p