Results 101 to 110 of about 487 (144)

[20q11.2 microdeletion syndrome: a phenotypic spectrum expansion. Case report]. [PDF]

Rev Med Inst Mex Seguro Soc
Crisanto-López IE, García-González R, Saldaña-Guerrero MP, Hernández-Camacho RM, Castro-Coyotl DM.   +4 more
europepmc   +1 more source

Mapping the risk of Zika virus infections in pregnant persons and microcephaly in newborns in relation to socioeconomic indicators in Recife, Pernambuco, Brazil: A spatial analysis (2015 to 2021). [PDF]

PLoS Negl Trop Dis
Lucena Sá ACC, Oliveira ALS, Miranda-Filho DB, Martelli CMT, Araújo TVB, Brickley EB, Ximenes RAA, Montarroyos UR.   +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 outcomes of pediatric patients with congenital toxoplasmosis in a fourthlevel center Introduction. Congenital [PDF]

Biomedica
Posada-Bustos S, Mariño AC, Espinosa-García E.   +2 more
europepmc   +1 more source

[A descriptive overview of cases of congenital cytomegalovirus at a tertiary hospital between 2017 and 2023]. [PDF]

Rev Esp Quimioter
Medina García E, Berzosa A, Illán Ramos M, Cursach Pedrosa V, Aranda Cazón C, Herranz Carrillo G, Criado Vega E, Ramos Amador JT.   +7 more
europepmc   +1 more source

[Reporting of birth defects from the Zika outbreak in Colombia, 2015-2017Notificação de defeitos congênitos associados ao surto de vírus zika na Colômbia, 2015-2017]. [PDF]

Rev Panam Salud Publica, 2019
Mendivelso Duarte FO, Robayo García A, Rodríguez Bedoya M, Suárez Rángel G.   +3 more
europepmc   +1 more source

MICROCEFALIA E A ODONTOLOGIA BRASILEIRA

Journal Health NPEPS, 2016
Leite, Cristine Nobre, Varellis, Maria Lúcia Zarvos   +1 more
openaire   +1 more source

[Autosomal recessive limb-girdle muscular dystrophy-10. Case report]. [PDF]

Rev Med Inst Mex Seguro Soc
Pérez-Arzola AA, Juárez-Melchor D, Crisanto-López IE, Vera-Loaiza A, Hernández-Castañeda Y, Guzmán-Santiago TA, Jiménez-Pérez B, Rodríguez-Hurtado PO, Salazar-Bonilla W.   +8 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

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