Results 91 to 100 of about 832 (131)

Predisposition to atherosclerosis in children and adults with trisomy 21: biochemical and metabolomic studies. [PDF]

Pediatr Endocrinol Diabetes Metab, 2023
Hetman M, Mielko K, Placzkowska S, Bodetko A, Młynarz P, Barg E.   +5 more
europepmc   +1 more source

Polymorphism in interferon alpha/beta receptor contributes to glucocorticoid response and outcome of ARDS and COVID-19. [PDF]

Crit Care, 2023
Jalkanen J, Khan S, Elima K, Huttunen T, Wang N, Hollmén M, Elo LL, Jalkanen S.   +7 more
europepmc   +1 more source

Does Chorionic Villus Sampling Increase the Risk of Preeclampsia or Gestational Hypertension? [PDF]

Int J Prev Med, 2019
Shirazi M, Rabiei M, Rahimi F, Niroomanesh S, Golshahi F, Eftekhar Yazdi M.   +5 more
europepmc   +1 more source

[The adult with tetralogy of fallot: what the clinical cardiologist needs to know]. [PDF]

Arch Peru Cardiol Cir Cardiovasc, 2021
Chávez-Saldívar S, Mego JC, Tauma-Arrué A, Coronado J, Luis-Ybáñez O, Bravo-Jaimes K.   +5 more
europepmc   +1 more source

Tamizaje prenatal de trisomía 21 en el Perú por medio del test combinado ampliado contingente en el primer trimestre

, 2018
Introduction. The combined first-trimester screening test is the international recommendation for prenatal screening of trisomy 21. The combined plus screening test adds one or more ultrasound markers (ductus venosus, tricuspid flow, nasal bone).
Bazán Lossio de Diez, Magdalena Gladys, Diez Chang, Guillermo   +1 more
core  

[Autoimmune Regulatory Gene (AIRE) and Development of Autoimmune Thyroiditis in Down Syndrome]. [PDF]

Rev Med Inst Mex Seguro Soc
Moran-Espinosa MC, Granados-Riverón JT, Benítez-Arvizu G, Sosa-Delgado SM, Gómez-Mejía MA, Diaz-Garcia H.   +5 more
europepmc   +1 more source

Presentación de un caso clínico de Trisomía 13 (Síndrome de Patau) con sobrevivencia excepcional de más de un año, en Ciego de Ávila

, 2014
Trisomy 13 or Patau syndrome described, apparently by Bartholin in 1657, as a general rule it was not recognized the  etiology of this trisomy until Patau and collaborators described it in 1960. The incidence is approximately 1:5000 live births.
Betancourt Castellanos, Liset, Carrasco Fontes, Dania L., Espinosa Lazo, Dania, Avello Benedico, Iranaka, Martínez Martínez, Mercedes, Lozano Lezcano, Livania   +5 more
core  

Síndrome de la arteria mesentérica superior asociado a Trisomía 21, a propósito de un caso

Gaceta Médica Estudiantil
El síndrome de Down es una anomalía genética congénita que puede asociarse a otras alteraciones, como el síndrome de la arteria mesentérica superior (síndrome de Wilkie), una causa infrecuente de obstrucción intestinal proximal.
Denis Fernández-Sánchez, Juan Leonardo Pacios-Dorado, Wilmarys Estrada-Gamboa, Gabriela María Martínez-Perez   +3 more
doaj  

Implementación del ADN libre circulante para la detección de aneuploidías fetales. [PDF]

Adv Lab Med
Madrigal Bajo I, Jodar Bifet M, Badenas Orquin C.   +2 more
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