Zobrazeno 1 - 6 of 6 pro vyhledávání: '"Sheila Pinto García"'
1
Complete functional characterization of disease-associated genetic variants in the complement factor H gene
Autor: Emilia Arjona, Jesús García-Fernández, Héctor Martín Merinero, Agustín Tortajada, Santiago Rodríguez de Córdoba, Sheila Pinto García
Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
instname
30 p.-7 fig.
Genetic analyses in atypical hemolytic uremic syndrome (aHUS) and C3-glomerulopathy (C3G) patients have provided an excellent understanding of the genetic component of the disease and informed genotype-phenotype correlations support
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1706959899a627965bf25fb38fd09e6
https://doi.org/10.1016/j.kint.2017.07.015
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2
Extravascular hemolysis and complement consumption in Paroxysmal Nocturnal Hemoglobinuria patients undergoing eculizumab treatment
Autor: Héctor Martín Merinero, Fernando A. González-Fernández, Santiago Rodríguez de Córdoba, Rafael Fores, Ana Villegas, Emilio Ojeda, A. López, Jaouad Anter, Margarita López-Trascasa, Marta Subías Hidalgo, Sheila Pinto García
Publikováno v: Biblos-e Archivo. Repositorio Institucional de la UAM
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Digital.CSIC. Repositorio Institucional del CSIC
35 p.-3 fig.-4 tab. Subías, Marta et al.
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired hemolytic anemia characterized by complement-mediated intravascular hemolysis that is effectively treated with eculizumab. However, treatment resp
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bed3affd0a72f3203bfdd2ba03f1a13f
https://doi.org/10.1016/j.imbio.2016.09.002
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3
Factor H Competitor Generated by Gene Conversion Events Associates with Atypical Hemolytic Uremic Syndrome
Autor: Giuseppe Remuzzi, Santiago Rodríguez de Córdoba, Marina Noris, Sheila Pinto García, Héctor Martín Merinero, Jesús García-Fernández, Sara Gastoldi, Agustín Tortajada, Emilia Arjona, Elena Goicoechea de Jorge, Mercedes Cao
Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
instname
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
10 p.-6 fig.-1 tab.
Atypical hemolytic uremic syndrome (aHUS), a rare form of thrombotic microangiopathy caused by complement pathogenic variants, mainly affects the kidney microvasculature. A retrospective genetic analysis in our aHUS cohort (n
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a44fab3937950417e055dfedf5069a3c
https://pubmed.ncbi.nlm.nih.gov/28993505
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Plný text Recenzováno Digitální knihovna AV ČR
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