Results 131 to 140 of about 11,120 (153)

[Neurovascular pathology in a patient with neurofibromatosis type 1. Case report]. [PDF]

Rev Neurol
Simal-Antuña M, Fernández-Fernández C, Larrosa-Campo D.   +2 more
europepmc   +1 more source

Molecular identification of resistance to organophosphates and carbamates in Aedes aegypti of different physiological ages in a cemetery in Peru. [PDF]

Rev Peru Med Exp Salud Publica
Santillan-Valdivia RE, Yañez Cesti MM, Neyra-Palacios RN, Ruiz-Polo AA.   +3 more
europepmc   +1 more source

[The p-value of the test is not a 'mathematical index', it is simply a relative frequency]. [PDF]

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

[Terapias dirigidas en amiloidosis cardíaca por transtiretina: una revisión del contexto clínico contemporáneo]. [PDF]

Arch Cardiol Mex
Costabel JP, Suárez LL, Escalante-Seyffert MC, López-Ponce de León JD, Fernándes F, Berrios-Bárcenas EA.   +5 more
europepmc   +1 more source

Severe immunodeficiency spectrum associated with NHEJ1 gene mutation: Cernunnos/XLF deficiency [PDF]

Biomedica
Navarro AM, Mantilla G, Fernández JA, Unigarro MF, Suárez A, Ortega MC.   +5 more
europepmc   +1 more source

[Epilepsy in Angelman syndrome and the most common electroencephalographic findings]. [PDF]

Rev Neurol
Ebrat-Mancilla E, Sánchez-Aparicio A, Pérez de Vargas-Martínez A, Marín-Serrano ME, Vaquero-Martínez M, Iglesias-Escalera G, Cazorla MR, López-Pájaro LF.   +7 more
europepmc   +1 more source

[Childhood overweight and obesity: A biomedical challenge in Mexico]. [PDF]

Rev Med Inst Mex Seguro Soc
Vázquez-Moreno MA, Cruz-López M.
europepmc   +1 more source

Anomalía de Jordans en síndrome de Chanarin-Dorfman. [PDF]

Adv Lab Med
Sánchez-Cortés J, Gabaldó-Barrios X.
europepmc   +1 more source

Falso valor de HbA_1c debido a la variante inusual hemoglobina Petie Salpetriere coheredada con talasemia alfa. [PDF]

Adv Lab Med
Lepe Balsalobre E, Varo Sánchez GM, Rico Rodríguez M, Fuentes Cantero S.   +3 more
europepmc   +1 more source

[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