Zobrazeno 1 - 10
of 65
pro vyhledávání: '"S. Sinicropi"'
Autor:
Giuseppina Tommonaro, Maria S. Sinicropi, Ada Popolo, Aldo Pinto, Chiara Palladino, Barbara Nicolaus, Stefania Marzocco, Anna Caruso, Giuseppina Autore, Carmela Saturnino
Publikováno v:
Molecules, Vol 15, Iss 3, Pp 2028-2038 (2010)
This study reports the synthesis and antioxidant activity of some new acetamide derivatives. The compounds’ structures were elucidated by NMR analysis and their melting points were measured. The in vitro antioxidant activity of these compounds was
Externí odkaz:
https://doaj.org/article/b139e2d5e2b04a8e9b7238958d6c260e
Autor:
D, Dhanyalayam, G, Palma, A R, Cappello, A, Mariconda, M S, Sinicropi, F, Giordano, V, Del Vecchio, A, Ramunno, C, Arra, P, Longo, C, Saturnino
Publikováno v:
Anti-cancer agents in medicinal chemistry. 18(5)
Due to an oversight one of the author’s name was published wrong in the article entitled “Phosphonium Salt Displays Cytotoxic Effects Against Human Cancer Cell Lines” in “Anti-Cancer Agents in Medicinal Chemistry, 2015, Vol. 17, No. 13. pp. 1
Publikováno v:
Trends in General Practice. 1
Autor:
Simona Portaro, Teresa Brizzi, Demetrio Milardi, Alessia Bramanti, Carmelo Rodolico, S. Sinicropi, Antonino Lupica, Placido Bramanti, Alberto Cacciola, Antonio Toscano, Maria Cristina De Cola
Publikováno v:
Medicine
Rationale: To report our experience on 7 patients (4 males and 3 females), affected by nonparaneoplastic Lambert–Eaton myasthenic syndrome, treated with 3,4-diaminopyridine phosphate (3,4-DAPP) either alone or in combination with other immunosuppre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff06ad58dceedf9754b2f237fdccbed0
http://hdl.handle.net/11570/3121995
http://hdl.handle.net/11570/3121995
Autor:
S. Sinicropi, Paolo Girlanda, Olimpia Musumeci, Carmelo Rodolico, Giuseppe Vita, Daniela Parisi, Antonio Toscano, Sonia Messina, Simona Portaro, Fiammetta Biasini, A. Ciranni
BACKGROUND Myasthenia gravis (MG) is an autoimmune disorder presenting with fluctuating, fatigable muscle weakness. Initial symptoms classically involve ocular and proximal limb muscles. Rarely, MG may onset with unusual features, so it can be misdia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30276dd947321383b2b15611861f6890
http://hdl.handle.net/11570/3097363
http://hdl.handle.net/11570/3097363
Autor:
Simona Portaro, Olimpia Musumeci, Antonio Toscano, Carmelo Rodolico, S. Sinicropi, Mariella Valenzise
Sodium channel myotonias are inherited muscle diseases linked to mutations in the voltage-gated sodium channel. These diseases may also affect newborns with variable symptoms. More recently, severe neonatal episodic laryngospasm (SNEL) has been descr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::153ae5c68c01d7c79493076f4f52caf7
http://hdl.handle.net/11570/3096868
http://hdl.handle.net/11570/3096868
Autor:
Maria Concetta Granieri, Paola Ungaro, S. Sinicropi, Luigi Albano, Paolo Emidio Macchia, Carmine Rocca, Daniela Amelio, T. Angelone, Immacolata Cristina Nettore
Publikováno v:
Vascular Pharmacology. :58
Objective: Obesity is often accompanied by an increased morbidity and mortality due to an increase of the cardiovascular disease risk factors, diabetes mellitus and dyslipidemia. Research is constantly working on protective molecules against obesity.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
C. Pastura, Giuseppe Vita, Corrado Messina, S. Sinicropi, A. Toscano, Paolo Girlanda, Carmelo Rodolico
Limb-girdle myasthenia is a rare disorder which includes familial and autoimmune forms. Myasthenia gravis is an uncommon disease in children and its diagnosis may be difficult. We report here five cases of autoimmune juvenile LGM starting before the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49d1d7463a0846600fce778fa584f84d
http://hdl.handle.net/11570/1432205
http://hdl.handle.net/11570/1432205
Autor:
Denise Cassandrini, Carla Gliubizzi, Gabriella Silvestri, Aldobrando Broccolini, Serenella Servidei, Claudio Bruno, Mario Pescatori, Carmelo Rodolico, Pietro Attilio Tonali, Carlo Minetti, Massimiliano Mirabella, S. Sinicropi, Emmanuel Tonoli, Federico Zara, Enzo Ricci
Publikováno v:
Human mutation. 23(6)
The most common form of autosomal recessive (AR) hereditary inclusion-body myopathy (HIBM), originally described in Persian-Jewish families, is characterized by onset in early adult life with weakness and atrophy of distal lower limb muscles, which p