Výsledky vyhledávání - "Carlos Viader"

Reactivity of C(sp2)-Pd and C(sp3)-Pd bonded palladacycles with diphosphines. Crystal and molecular structure of the novel A-frame complex [{Pd[2,5-Me2C6H2C(H) N(2,4,6-Me3C6H2)-C6]}2(μ-Ph2PCH2PPh2)2(μ-Cl)][PF6]

Autor: Antonio Rodríguez, Nina Gómez-Blanco, Jesús J. Fernández, José M. Vila, Digna Vázquez-García, Carlos Viader, Alberto Fernández, Margarita López-Torres

Publikováno v: Journal of Organometallic Chemistry. 696:764-771

Treatment of the halogen-bridged complexes [Pd{2,5-Me2C6H2C(H) N(2,4,6-Me3C6H2)-C6,N}(μ-X)]2 (1a, X = Cl; 2a, X = Br) with the tertiary diphosphine Ph2PCH2PPh2 (dppm), regardless of the molar ratio used, gave a mixture of two complexes: [Pd{2,5-Me2C

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b352bb5d0d26a4c783375e67a1fe6317
https://doi.org/10.1016/j.jorganchem.2010.09.071

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Versatile Behavior of the Schiff Base Ligand 2,5-Me2C6H3C(H)═N(2,4,6-Me3C6H2) toward Cyclometalation Reactions: C(sp2,phenyl)−H vs C(sp3,methyl)−H Activation

Autor: Carlos Viader, Nina Gómez-Blanco, José M. Vila, Antonio Rodríguez, Jesús J. Fernández, Digna Vázquez-García, Margarita López-Torres, Alberto Fernández

Publikováno v: Organometallics. 29:3303-3307

Treatment of the Schiff base ligand a with palladium(II) acetate in toluene gave 1a, with metalation of an aromatic phenyl carbon atom. Reaction at room temperature gave the trinuclear complex 4a. Treatment of a with palladium(II) acetate in refluxin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f7fa5ef39bcd64de57bb6b71e4d85216
https://doi.org/10.1021/om100238w

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Familial amyloid polyneuropathy associated with TTRSer50Arg mutation in two Iberian families presenting a novel single base change in the mutant gene

Autor: Miguel Munar-Qués, Teresa Coelho, Paul Moreira, Carlos Viader-Farré, Jaime Masjuan, Maria João Saraiva

Publikováno v: Amyloid. 14:147-152

We present two families, from Spain and Portugal, with familial amyloid polyneuropathy (FAP) associated with the mutation TTRSer50Arg. This mutation was first described in two Japanese patients from independent families and later in a French-Italian

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4279e95ef6f2b7b0862bffcd5518193
https://doi.org/10.1080/13506120701259580

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Genetic epidemiology of familial amyloid polyneuropathy in the Balearic Islands (Spain)

Autor: José María Zabay-Becerril, Juana María Mulet-Ferrer, Maria João Saraiva, Miguel Munar-Qués, Carlos Viader-Farré

Publikováno v: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis. 12(1)

Between 1976 and 2003, we diagnosed 144 patients with familial amyloid polyneuropathy (FAP) in the Balearic Islands (Spain). Analysis of genetic epidemiological data from 102 confirmed patients showed 62% were men. Parental transmission was paternal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e909bbef3fa952934aa33f5e0434e5c4
https://pubmed.ncbi.nlm.nih.gov/16076612

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Early diagnosis and management of patients with familial ATTR amyloidosis receiving livers from asymptomatic variant TTR carriers

Autor: José María Zabay-Becerril, Carlos Viader-Farré, Juana María Mulet-Ferrer, Miguel Munar-Qués

Publikováno v: Amyloid. 18:172-173

The possibility of a patient with familial ATTR amyloidosis receiving a liver from an asymptomatic variant TTR carrier is remote [corrected].However, in 2008, it was reported that this unlikely event occurred in a patient in Portugal. We report our p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bd11bb7dab1c115ef86fed93ed49bcc
https://doi.org/10.3109/13506129.2011.594822

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Two Spanish sibs with familial amyloidotic polyneuropathy homozygous for the V30M-TTR gene

Autor: Paul Moreira, Carlos Viader-Farré, Miguel Munar-Qués, J. M. López Domínguez, Maria João Saraiva

Publikováno v: CIÊNCIAVITAE
Scopus-Elsevier

Two Spanish sibs with familial amyloidotic polyneuropathy (FAP) homozygous for the V30M-TTR gene, were diagnosed by DNA and protein analyses. Their clinical picture was very similar to the Majorcan FAP heterozygous patients except for the sensorimoto

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ab33d77b29cff48d74318bdf36972c7
https://pubmed.ncbi.nlm.nih.gov/11409034

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Familial amyloidotic polyneuropathy. TTR Met 30 in Majorca (Spain)

Autor: Catalina Munar-Bernat, José Francisco Forteza-albertí, Carmen Cifuentes-Luna, Maria João Saraiva, Carlos Viader-Farré, Pedro P. Costa, Miguel Munar-Qués

Publikováno v: Scopus-Elsevier
CIÊNCIAVITAE

We analyzed data from 78 Majorcan patients with familial amyloidotic polyneuropathy (FAP): 57 confirmed and 21 non-confirmed. Diagnosis was established in the first group by histopathological study or detection of the biochemical marker in serum, and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::645a4a931cf111c5022250b384b69630
http://www.scopus.com/inward/record.url?eid=2-s2.0-0000859840&partnerID=MN8TOARS