Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marcela Fragoso-Benítez"'
Autor:
Fermín Guerrero-Del Ángel, Lilia Alejandra Dávila-Salazar, Hilda Issasi-Hernández, Enrique E Huitzil -Muñoz, Ariel Cabrera-Salazar, Rogelio Oliver-Parra, Marcela Fragoso- Benítez, José Martín Torres-Benítez
Publikováno v:
Revista de Odontopediatria Latinoamericana, Vol 2, Iss 1 (2021)
Objetivo: Identificar el estado de salud periodontal en pacientes con discapacidad en custodia versus pacientes independientes en su higiene oral. Material y métodos: Se examinaron pacientes con discapacidad, ambos sexos, 3 a 19 años que acuden al
Externí odkaz:
https://doaj.org/article/a26865cdf31e44fd87531a91fd18455d
Autor:
Marcela Fragoso-Benítez
Publikováno v:
The Journal of Reproduction. 2
Seven embryo biopsies from a 33 female and 39 male year-old couple were sent for PGD, all resulted in aneuploid embryos. When analysing the case, we notice that the male had a previous 15-year-old daughter and several semen analyses with fluctuating
Autor:
Fermín-Guerrero-Del Ángel, Lilia Alejandra-Dávila-Salazar, Hilda-Issasi-Hernández, Enrique E -Huitzil -Muñoz, Ariel-Cabrera-Salazar, Marcela-Fragoso- Benítez, Rogelio-Oliver-Parra, José Martín-Torres-Benítez
Publikováno v:
Revista de Odontopediatria Latinoamericana, Vol 2, Iss 1, Pp 21-35 (2012)
Objetivo: Identificar el estado de salud periodontal en pacientes con discapacidad en custodia versus pacientes independientes en su higiene oral. Material y métodos: Se examinaron pacientes con discapacidad, ambos sexos, 3 a 19 años que acuden al
Externí odkaz:
https://doaj.org/article/bc1532f8178840e3b89a1d7e990f00fd
Autor:
Petra Yescas, Marco Antonio Macías-Flores, Astrid Rasmussen, Tetsuo Ashizawa, Irene De Biase, Marcela Fragoso-Benítez, Adriana Ochoa, Sanjay I. Bidichandani, María Elisa Alonso
Publikováno v:
Annals of Neurology. 61:607-610
Spinocerebellar ataxia type 17 (SCA17) is caused by expansion of a CAG/CAA repeat in the TBP gene. Most pathogenic alleles are interrupted and are stably transmitted from parent to offspring without anticipation. We identified three SCA17 families wi
Autor:
Christopher Mader, Luis Ruano, Marcela Fragoso-Benítez, Adriana Ochoa, Leticia Martínez-Ruano, Petra Yescas, Misti C. White, Sanjay I. Bidichandani, Tetsuo Ashizawa, Roxana Gutiérrez, Astrid Rasmussen, Irene De Biase, Elisa Alonso
Publikováno v:
Movement Disorders. 22:1050-1053
Dominant ataxias show wide geographic variation. We analyzed 108 dominant families and 123 sporadic ataxia patients from Mexico for mutations causing SCA1-3, 6-8, 10, 12, 17 and DRPLA. Only 18.5% of dominant families remained undiagnosed; SCA2 accoun
Autor:
Astrid, Rasmussen, Irene, De Biase, Marcela, Fragoso-Benítez, Marco Antonio, Macías-Flores, Petra, Yescas, Adriana, Ochoa, Tetsuo, Ashizawa, María Elisa, Alonso, Sanjay I, Bidichandani
Publikováno v:
Annals of neurology. 61(6)
Spinocerebellar ataxia type 17 (SCA17) is caused by expansion of a CAG/CAA repeat in the TBP gene. Most pathogenic alleles are interrupted and are stably transmitted from parent to offspring without anticipation. We identified three SCA17 families wi