Results 111 to 120 of about 1,774,169 (170)

Germline TP53 p.R337H and XAF1 p.E134* Variants: Prevalence in Paraguay and Comparison with Rates in Brazilian State of Paraná and Previous Findings at the Paraguayan-Brazilian Border. [PDF]

Curr Oncol
Falcon-de Legal E, Ascurra M, Vega-Paredes R, Sade E, Monteiro M, Paraízo M, Colman M, Florentin AG, Ojeda C, Legal-Ayala H, Ries A.   +10 more
europepmc   +1 more source

Strengthening Undergraduate Medical Education for Inclusive Health Care for People With Down Syndrome and Intellectual and Developmental Disabilities in Medical Schools: Protocol for a Scoping Review. [PDF]

JMIR Res Protoc
Amaral de Almeida Bistafa I, Antonio Ribeiro Filho M, Dos Santos Costa AC, Pimenta Saad AF, Ferreira Franco R, Aparecida de Sales Floriano J, Roberto Dos Santos E, de Souza Menezes JD, Querino da Silva M, Nunes Longhi Aleixo D, Fazuoli Chubaci E, Karina Stefani A, Donegá Martinez W, Belchior da Silveira Junior P, Mirtes Zecchin A, Gonçalves Cristóvão NB, Bertolazzo Quitério A, Mendonça Ribeiro R, Cristina Móz Vaz Oliani D, Hélio Oliani A, Alahmar Bianchin M, Cesar Fava Spessoto L, Helú Mendonça Ribeiro RC, César André J.   +23 more
europepmc   +1 more source

Sociodemographic and clinical characteristics of gestational syphilis in Cali, 2018 [PDF]

Biomedica, 2021
Benítez J, Yépez MA, Hernández-Carrillo M, Martínez DM, Cubides-Munevar Á, Holguín-Ruiz JA, Muñoz MA.   +6 more
europepmc   +1 more source

Hospital mortality among psychiatric inpatients: a cross-sectional study, Brazil, 2023. [PDF]

Epidemiol Serv Saude
Souza MLP.
europepmc   +1 more source

[Birth conditions and attention deficit/hyperactivity disorders (ADHD) in adults in the Pelotas (Brazil) birth cohorts of 1982 and 1993]. [PDF]

Cad Saude Publica, 2023
Farias CP, Soares PSM, Barros FC, Menezes AMB, Gonçalves H, Wehrmeister FC, Pinheiro RT, Quevedo LA, Horta BL.   +8 more
europepmc   +1 more source

Síndrome de Rett: microcefalia con retardo mental y autismo. Reporte de un caso

, 2007
Resumen El síndrome de Rett es un grave proceso del desarrollo neurológico que afecta exclusivamente mujeres, se considera una enfermedad monogénica dominante ligada al cromosoma X debida a mutaciones en el gen MECP2 codificador de la proteína 2 de unión a metil-CpG.
Aviña Fierro, Jorge Arturo, Hernández Aviña, Daniel Alejandro   +1 more
openaire   +1 more source

Temporal associations between cultural identity conflict and psychological symptoms among Syrian young adults with refugee backgrounds: a four-wave longitudinal study. [PDF]

Eur J Psychotraumatol
Rahim HF, Mooren TTM, Knipscheer JW, Chung JM, Laceulle OM, Boelen PA.   +5 more
europepmc   +1 more source

[Retirement and depression: perspective for enlarged clinicJubilación y depresión: perspectiva para la clínica ampliada]. [PDF]

Rev Salud Publica (Bogota), 2023
Barretto Costa M, Rosa RS, Pereira Guedes T, Silva de Oliveira Boery RN, Santana Cardoso Santos I, Zambrano Contreras JC, Dos Santos Souza A, Meira Pires J, Teixeira Pinto LL, Tavares Reis T, Souza Santos T, de Bessa J.   +11 more
europepmc   +1 more source

Búsqueda Fenotípica del Retardo Mental Ligado al Sexo: Síndrome del Xq-Frágil [PDF]

Revista chilena de pediatría, 1982
Lacassie S, Ives, Zavala B, Alejandro, Curotto L, Bianca, Alliende R, M. Angélica, De Andraca O, Isidora   +4 more
openaire   +2 more sources

Delayed infant development: content analysis of a nursing diagnosis proposal. [PDF]

Rev Esc Enferm USP
Aquino MDST, Mariano SPS, Monteiro FPM, Morais HCC, Freire VECS, Lima MNQ, Sousa QL.   +6 more
europepmc   +1 more source