Navegar por autor "Dacruz Álvarez, David"

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16p11.2 microdeletion associated to early onset benign childhood seizures

2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Perez Gay, Laura; Dacruz Álvarez, David [et al.]
Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene

2015- Beiras Iglesias, Andrés; Castro Gago, Manuel; Pintos Martínez, Elena; Dacruz Álvarez, David
Enfermedad de alpers juvenil

2013- Rodríguez Núñez, Antonio; Castro Gago, Manuel; Gómez Lado, María del Carmen; Perez Gay, Laura; Eiris Puñal, Jesús; [et al.]
Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletion

2014- Beiras Iglesias, Andrés; Castro Gago, Manuel; Pintos Martínez, Elena; Dacruz Álvarez, David
Microdeleción 16p11.2 asociada a convulsiones benignas de la primera infancia

2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Perez Gay, Laura; Dacruz Álvarez, David [et al.]
Microdeleción 2q23.1 y hallazgos sindrómicos

2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Eiris Puñal, Jesús; Dacruz Álvarez, David; [et al.]
Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Castro Gago, Manuel; Perez Gay, Laura; Eiris Puñal, Jesús; [et al.]
Second-line rescue therapy with moxifloxacin after failure of treatment to eradicate helicobacter pylori infection: A prospective multicenter study

2015- Dacruz Álvarez, David