Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Eliana Cabascango"'
Autor:
Andrés López-Cortés, Ana Karina Zambrano, Patricia Guevara-Ramírez, Byron Albuja Echeverría, Santiago Guerrero, Eliana Cabascango, Andy Pérez-Villa, Isaac Armendáriz-Castillo, Jennyfer M. García-Cárdenas, Verónica Yumiceba, Gabriela Pérez-M, Paola E. Leone, César Paz-y-Miño
Publikováno v:
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-9 (2020)
Abstract Background Congenital insensitivity to pain with anhidrosis (CIPA) is an extremely rare autosomal recessive disorder characterized by insensitivity to pain, inability to sweat and intellectual disability. CIPA is caused by mutations in the n
Externí odkaz:
https://doaj.org/article/44654014f34642bfb39137e3cbfaf637
Autor:
Santiago Guerrero, Patricia Guevara-Ramírez, Verónica Yumiceba, Andy Pérez-Villa, Eliana Cabascango, Andrés López-Cortés, Paola E. Leone, Ana Karina Zambrano, B. Albuja Echeverría, Jennyfer M. García-Cárdenas, Isaac Armendáriz-Castillo, César Paz-y-Miño, Gabriela Pérez-M
Publikováno v:
Forensic Science International: Genetics Supplement Series. 7:126-128
Congenital insensitivity to pain with anhidrosis (CIPA) is an extremely rare autosomal recessive disorder characterized by self-mutilating behavior, unexplained fever, inability to sweat and intellectual disability. CIPA pathogenesis is associated wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d021b4e1cf0bf5e72943749805beca9c
https://doi.org/10.1016/j.fsigss.2019.09.049
https://doi.org/10.1016/j.fsigss.2019.09.049
Autor:
Ana Karina Zambrano, Andy Pérez-Villa, Andrés López-Cortés, Jennyfer M. García-Cárdenas, Gabriela Pérez-M, Patricia Guevara-Ramírez, Eliana Cabascango, Byron Albuja Echeverría, Verónica Yumiceba, Santiago Guerrero, Isaac Armendáriz-Castillo, César Paz-y-Miño, Paola E. Leone
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-9 (2020)
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-9 (2020)
Background Congenital insensitivity to pain with anhidrosis (CIPA) is an extremely rare autosomal recessive disorder characterized by insensitivity to pain, inability to sweat and intellectual disability. CIPA is caused by mutations in the neurotroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea4f64a5a05a7a64ac7d33812dfa19b2
http://europepmc.org/articles/PMC7437939
http://europepmc.org/articles/PMC7437939
Autor:
Patricia Guevara-Ramírez, Ana Karina Zambrano, Andy Pérez-Villa, Eliana Cabascango, Byron Albuja Echeverría, Jennyfer M. García-Cárdenas, Santiago Guerrero, Paola E. Leone, Verónica Yumiceba, Andrés López-Cortés, Gabriela Pérez-M, Isaac Armendáriz-Castillo, César Paz-y-Miño
Congenital insensitivity to pain with anhidrosis (CIPA) is an extremely rare autosomal recessive disorder characterized by insensitivity to pain, inability to sweat and intellectual disability. CIPA is caused by mutations in the neurotrophic tyrosine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8388e12c404dada2781b85b7d314092d
