Results 71 to 80 of about 1,066 (125)

[RYR1 myopathies in childhood: phenotype-genotype correlation and incidence]. [PDF]

Rev Neurol
Del Arco-Guzmán N, Lobato-López S, Calvo-Medina R, Vera-Medialdea R, Ruiz-Pérez C, Ramos-Fernández JM.   +5 more
europepmc   +1 more source

Airway management in the obstetric patient: management strategy [PDF]

Rev Colomb Obstet Ginecol
Laverde-Sabogal CE, Aguilar Schotborgh MÁ.   +1 more
europepmc   +1 more source

[Landau-Kleffner Syndrome and Continuous Spike-and-Wave During Sleep Syndrome: Comparison of Clinical, Neurophysiological, and Neuropsychological Characteristics]. [PDF]

Rev Neurol
Benítez-Provedo C, González-Alguacil E, García-Fernández M, Orduña BE, Casanova NL, Peñas JJG, Rodríguez AD, Soto-Insuga V.   +7 more
europepmc   +1 more source

[Neurodevelopmental and Movement Disorder Due to a Mutation in the GNAO1 Gene: A Case Report]. [PDF]

Rev Neurol
Hernández Yeneris SM, González-Solano MA, Lince-Rivera I, Rojas-Martínez JA, Ramón-Gómez JL.   +4 more
europepmc   +1 more source

[Clinical and genetic characterisation of hereditary distal myopathies in a series of Colombian patients]. [PDF]

Rev Neurol
Oliveros-Acuña N, Tafur-Gómez N, Ortiz-Corredor F, Castellar-Leones S, Rojas-García W, Correa-Arrieta C.   +5 more
europepmc   +1 more source

Aspectos fundamentales en la solicitud y determinación de la lipoproteína(a) en el laboratorio clínico. [PDF]

Adv Lab Med
Arrobas Velilla T, Fernández Prendes C, Amigó Grau N, Calmarza P, Camós Anguila S, Candas Estébanez B, Castro Castro MJ, Ceacero D, González Martínez I, Martín Palencia M, Puzo Foncillas J, Romero Román C, en nombre de la Comisión de Lipoproteínas y Enfermedades Cardiovasculares de la SEQCML.   +12 more
europepmc   +1 more source

Spatial population genetic structure of Caquetaia kraussii (Steindachner, 1878) evidenced by species-specific microsatellite loci in the middle and low basin of the Cauca River, Colombia. [PDF]

PLoS One
Cataño Tenorio I, Joya CD, Márquez EJ.
europepmc   +1 more source

Septo-optic dysplasia plus: A case report for reviewing and recognizing this condition [PDF]

Biomedica
Reyes A, Galvis J, Estupiñán Y.
europepmc   +1 more source

[Partial trisomy 9p syndrome: Expanding the phenotype]. [PDF]

Rev Med Inst Mex Seguro Soc
Pérez-Castillo JA, Reyes-Rosales M, Cardoso-Enciso HR, Rodríguez-Cuevas JL.   +3 more
europepmc   +1 more source

[Selection of pharmacogenomic variants and methodology for their use in community pharmacy]. [PDF]

Farm Comunitarios
Montero-Gómez A, Sánchez Pozo A.
europepmc   +1 more source