Zobrazeno 1 - 10
of 21
pro vyhledávání: '"César, Arjona"'
Autor:
César Arjona Sebastiá
Publikováno v:
Anuario de Filosofía del Derecho.
SANDEL, Michael: The Tyranny of Merit. What’s Become of the Common Good?
Autor:
Cristina Jou, Juan D. Ortigoza-Escobar, Maria M. O’Callaghan, Andres Nascimento, Alejandra Darling, Leticia Pias-Peleteiro, Belén Perez-Dueñas, Mercedes Pineda, Anna Codina, César Arjona, Judith Armstrong, Francesc Palau, Antonia Ribes, Laura Gort, Frederic Tort, Placido Navas, Eduardo Ruiz-Pesini, Sonia Emperador, Ester Lopez-Gallardo, Pilar Bayona-Bafaluy, Raquel Montero, Cecilia Jimenez-Mallebrera, Angels Garcia-Cazorla, Julio Montoya, Delia Yubero, Rafael Artuch
Publikováno v:
Journal of Clinical Medicine, Vol 8, Iss 1, p 68 (2019)
Mitochondrial diseases (MD) are a group of genetic and acquired disorders which present significant diagnostic challenges. Here we report the disease characteristics of a large cohort of pediatric MD patients (n = 95) with a definitive genetic diagno
Externí odkaz:
https://doaj.org/article/7a15245c5bf749658b694dba87179762
Autor:
Jordi Muchart, Dídac Casas-Alba, Alfredo García-Alix, Antonio Martinez-Monseny, Federico Ramos, César Arjona, Mercè Bolasell, Paula Casano, Loreto Martorell, Mercedes Serrano, Francesc Palau
Publikováno v:
American Journal of Medical Genetics Part A. 182:20-24
Okur-Chung neurodevelopmental syndrome (OCNS, MIM#617062) is a rare autosomal dominant syndrome related to CSNK2A1 mutations. It is characterized by intellectual disability, hypotonia, feeding and speech difficulties, dysmorphic features, and multisy
Autor:
César Arjona
Publikováno v:
Canadian Journal of Law & Jurisprudence. 32:259-283
This article maintains that the standard conception of legal ethics – the so-called ‘theory of amorality’ – is highly dependent on context and cannot be consistently applied to transnational legal practice. After defining in some detail the b
Autor:
Antonio, Martinez-Monseny, Daniel, Cuadras, Mercè, Bolasell, Jordi, Muchart, César, Arjona, Mar, Borregan, Adi, Algrabli, Raquel, Montero, Rafael, Artuch, Ramón, Velázquez-Fragua, Alfons, Macaya, Celia, Pérez-Cerdá, Belén, Pérez-Dueñas, Belén, Pérez, Mercedes, Serrano, Oscar, Garcia
Publikováno v:
Journal of Medical Genetics. 56:236-245
IntroductionPhosphomannomutase-2 deficiency (PMM2-CDG) is associated with a recognisable facial pattern. There are no early severity predictors for this disorder and no phenotype–genotype correlation. We performed a detailed dysmorphology evaluatio
Publikováno v:
Revista de Fomento Social, Iss 265 (2012)
Esta nota parte de las críticas que Amartya Sen realiza sobre las teorías de la justicia dominantes en la actualidad y los problemas detectados en el modelo de educación jurídica dominante. A partir de la relación existente entre ambos aspectos,
Externí odkaz:
https://doaj.org/article/53c24e6f29044bc4b2506efe9d588779
Autor:
Sira Abenoza, César Arjona
Publikováno v:
The Law Teacher. 51:453-468
Based on an educational experience that brought together law students and inmates in the same classroom, this paper reflects on the connections between emotions, justice and democracy. After a brie...
Autor:
Sira Abenoza, César Arjona
Publikováno v:
The Law Teacher. 51:327-348
This paper describes a particular educational experience: a course that took place in prison involving law students and inmates. One of the co-authors was the leading instructor in the course, whereas the other played an active role during its design
Autor:
Mahshid S. Azamian, Angeles Garcia-Cazorla, Qin Sun, Brian J. Shayota, Francesc Palau, Rafael Artuch, Daryl A. Scott, Nishitha R. Pillai, Delia Yubero, César Arjona, Nuria Brandi, Alfonso Oyarzabal, Rajarshi Ghosh, Seema R. Lalani
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 179(12)
Hartnup disease is an autosomal recessive condition characterized by neutral aminoaciduria and behavioral problems. It is caused by a loss of B0 AT1, a neutral amino acid transporter in the kidney and intestine. CLTRN encodes the protein collectrin t
Autor:
Gemma Valls, Kenny Wheeler, Elena Garcia-Guixé, César Arjona, Ester Vilamajó, Olga Martínez-Pasarell, Jonás Sarasa, Carles Giménez, Dagan Wells
Publikováno v:
Reproductive BioMedicine Online. 31:770-775
Preimplantation genetic diagnosis (PGD) was carried out for a couple carrying a de-novo deletion in the TSC2 gene, responsible for tuberous sclerosis. Karyomapping, a method employing genome-wide analysis of single nucleotide polymorphisms (SNP), was