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Refinado por: Base de dados/Biblioteca: BACON - Mir@bel - GLOBAL_LIBRESACCES remover Base de dados/Biblioteca: Springer journals remover MEDLINE Complete remover
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1
Attention control: The missing link between sensory discrimination and intelligence
Attention control: The missing link between sensory discrimination and intelligence
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Attention control: The missing link between sensory discrimination and intelligence

Tsukahara, Jason S. ; Harrison, Tyler L. ; Draheim, Christopher ; Martin, Jessie D. ; Engle, Randall W.

Attention, perception & psychophysics, 2020-10, Vol.82 (7), p.3445-3478 [Periódico revisado por pares]

New York: Springer US

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2
COVID-19 and the elaboration of personal plans in + 50: a Brazilian experience
COVID-19 and the elaboration of personal plans in + 50: a Brazilian experience
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COVID-19 and the elaboration of personal plans in + 50: a Brazilian experience

Garcia, Kerolyn Ramos ; Bento, Andrea Pecce ; de Oliveira, Aline Gomes ; da Silva, Rafaela Alves ; Chiarello, Marileusa Dosolina ; Chariglione, Isabelle Patriciá Freitas Soares ; Karnikowski, Margô Gomes de Oliveira

BMC public health, 2023-02, Vol.23 (1), p.221-221, Article 221 [Periódico revisado por pares]

England: BioMed Central Ltd

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3
Placental inflammatory cytokines mRNA expression and preschool children's cognitive performance: a birth cohort study in China
Placental inflammatory cytokines mRNA expression and preschool children's cognitive performance: a birth cohort study in China
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Placental inflammatory cytokines mRNA expression and preschool children's cognitive performance: a birth cohort study in China

Zhou, Jixing ; Tong, Juan ; Ru, Xue ; Teng, Yuzhu ; Geng, Menglong ; Yan, Shuangqin ; Tao, Fangbiao ; Huang, Kun

BMC medicine, 2023-11, Vol.21 (1), p.449-449, Article 449 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
A novel missense variant in the CASK gene causes intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia
A novel missense variant in the CASK gene causes intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia
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A novel missense variant in the CASK gene causes intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia

Wu, Sixian ; Jiang, Chuan ; Li, Jiaman ; Zhang, Guohui ; Shen, Ying ; Wang, Jing

BMC medical genomics, 2022-06, Vol.15 (1), p.127-127, Article 127 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Capitalising on the transformational opportunities of early clinical academic career training for nurses, midwives and allied health professionals
Capitalising on the transformational opportunities of early clinical academic career training for nurses, midwives and allied health professionals
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Capitalising on the transformational opportunities of early clinical academic career training for nurses, midwives and allied health professionals

Cowley, Alison ; Diver, Claire ; Edgley, Alison ; Cooper, Joanne

BMC medical education, 2020-11, Vol.20 (1), p.418-418, Article 418 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Neurodevelopmental outcome and respiratory management of congenital central hypoventilation syndrome: a retrospective study
Neurodevelopmental outcome and respiratory management of congenital central hypoventilation syndrome: a retrospective study
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Neurodevelopmental outcome and respiratory management of congenital central hypoventilation syndrome: a retrospective study

Ogata, Tomomi ; Muramatsu, Kazuhiro ; Miyana, Kaori ; Ozawa, Hiroshi ; Iwasaki, Motoki ; Arakawa, Hirokazu

BMC pediatrics, 2020-07, Vol.20 (1), p.342-342, Article 342 [Periódico revisado por pares]

England: BioMed Central Ltd

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7
Administrative data analysis of student attrition in hungarian medical training
Administrative data analysis of student attrition in hungarian medical training
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Administrative data analysis of student attrition in hungarian medical training

Pusztai, Gabriella ; Demeter-Karászi, Zsuzsanna ; Alter, Emese ; Marincsák, Rita ; Dabney-Fekete, Ilona Dóra

BMC medical education, 2022-04, Vol.22 (1), p.317-317, Article 317 [Periódico revisado por pares]

England: BioMed Central Ltd

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8
The most 5' truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: a case report
The most 5' truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: a case report
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The most 5' truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: a case report

Kuptanon, Chulaluck ; Srichomthong, Chalurmpon ; Sangsin, Apiruk ; Kovitvanitcha, Dool ; Suphapeetiporn, Kanya ; Shotelersuk, Vorasuk

BMC medical genetics, 2018-07, Vol.19 (1), p.117-117, Article 117 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
What does an enabling environment for infant and young child nutrition look like at implementation level? Perspectives from a multi-stakeholder process in the Breede Valley Sub-District, Western Cape, South Africa
What does an enabling environment for infant and young child nutrition look like at implementation level? Perspectives from a multi-stakeholder process in the Breede Valley Sub-District, Western Cape, South Africa
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What does an enabling environment for infant and young child nutrition look like at implementation level? Perspectives from a multi-stakeholder process in the Breede Valley Sub-District, Western Cape, South Africa

Du Plessis, L M ; McLachlan, M H ; Drimie, S E

BMC public health, 2018-02, Vol.18 (1), p.240-240, Article 240 [Periódico revisado por pares]

England: BioMed Central Ltd

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10
Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings
Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings
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Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings

Wang, Xiang ; Zhang, Zhu ; Zhang, Xueguang ; Shen, Ying ; Liu, Hongqian

Human genomics, 2020-06, Vol.14 (1), p.1-26, Article 26 [Periódico revisado por pares]

London: BioMed Central

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