Results 121 to 130 of about 11,120 (153)

[Andersen-Tawil Syndrome, a differential of bidirectional ventricular tachycardia: a case report]. [PDF]

Arch Peru Cardiol Cir Cardiovasc
Tejeda-Camargo MJ, Vanegas-Rincón PN, Villamil-Ramírez LE, Rojas-Rojas JC, Soto Becerra R.   +4 more
europepmc   +1 more source

Prenatal diagnosis of Freeman-Sheldon syndrome using ultrasound and genetic testing. Case report [PDF]

Rev Colomb Obstet Ginecol, 2023
Annicchiarico-López W, Peña-Pardo LX, Miranda-Quintero JE.   +2 more
europepmc   +1 more source

[Hepatic encephalopathy from cholangitis in a young patient with ornithine transcarbamylase mutation]. [PDF]

Rev Med Inst Mex Seguro Soc
Rojas-Salazar YL, Gómez-Montañez E, Rojas-Salazar JG.   +2 more
europepmc   +1 more source

[Key Measures in Epidemiology: Risk Difference, Relative Risk and Odds Ratio]. [PDF]

Rev Neurol
Carazo-Díaz C, Prieto-Valiente L.
europepmc   +1 more source

[Ziresovir: a potent, selective, and oral inhibitor of the respiratory syncytial virus fusion (F) protein]. [PDF]

Rev Esp Quimioter
Reina J, Bosch-Durán J.
europepmc   +1 more source

[Breast MRI: Kaiser score agreement with and without diffusion]. [PDF]

Rev Med Inst Mex Seguro Soc
López-Méndez JMI, Delgadillo-Cristerna R, Campiram-Gutiérrez J.   +2 more
europepmc   +1 more source

Genetic screening of FFPE breast cancer biopsies for the <i>BRCA1</i>-185delAG mutation in Trinidad and Tobago. [PDF]

Rev Panam Salud Publica
Abrahim SC, Bansraj D, Edwards R, Thompson R, Rambaran R, Roach A, Warner WA, Chalapathi Rao AV, Unakal C, Haraksingh RR.   +9 more
europepmc   +1 more source

Genomic diversity of uropathogenic Escherichia coli in clinical isolates from six latin american countries, 2018-2023. [PDF]

Rev Peru Med Exp Salud Publica
Caballero F, Martinez-Ventura A, Cuicapuza D, Fajardo-Loyola A, Gutierrez-Ajalcriña R, Soto-Pastrana J, Asmat-Marrufo P, Barco-Yaipen de Vera E, Meza-Fernandez H, Chambi-Quispe M, Pino-Dueñas J, Laura-Rivas N, Briones-Alejo A, Diaz-Rengifo P, Peralta-Siesquen C, Salvatierra G, Tsukayama P, Marcos-Carbajal P.   +17 more
europepmc   +1 more source

Identification of a variant in the USH1G gene in a family with Usher syndrome [PDF]

Biomedica
Gélvez N, López G, Tamayo ML.
europepmc   +1 more source

First report of PURA syndrome in a Colombian patient with de novo missense variant c.692T>C (p.Phe231Ser) [PDF]

Biomedica
Cerón SM, Pérez DA, Montaño JH, Acosta MA.   +3 more
europepmc   +1 more source