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Refinado por: Base de dados/Biblioteca: Journals@Ovid Complete remover nível superior: Revistas revisadas por pares remover Wiley-Blackwell Full Collection 2013 remover xxx: xxx remover
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1
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review
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Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review

LEGGETT, VICTORIA ; JACOBS, PATRICIA ; NATION, KATE ; SCERIF, GAIA ; BISHOP, DOROTHY V M

Developmental medicine and child neurology, 2010-02, Vol.52 (2), p.119-129 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX
Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX
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Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX

van Rijn, S. ; Swaab, H.

Genes, brain and behavior, 2015-02, Vol.14 (2), p.200-208 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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3
A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome
A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome
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A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome

Lenroot, R. K. ; Blumenthal, J. D. ; Wallace, G. L. ; Clasen, L. S. ; Lee, N. R. ; Giedd, J. N.

Genes, brain and behavior, 2014-11, Vol.13 (8), p.841-849 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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4
X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization
X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization
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X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization

Kushima, Itaru ; Aleksic, Branko ; Kimura, Hiroki ; Nakatochi, Masahiro ; Lo, Tzuyao ; Ikeda, Masashi ; Arai, Makoto ; Hashimoto, Ryota ; Numata, Shusuke ; Okamura, Yasunobu ; Obara, Taku ; Inada, Toshiya ; Ozaki, Norio

Psychiatry and clinical neurosciences, 2022-12, Vol.76 (12), p.667-673 [Periódico revisado por pares]

Melbourne: John Wiley & Sons Australia, Ltd

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5
Sex chromosome trisomies are not associated with atypical lateralization for language
Sex chromosome trisomies are not associated with atypical lateralization for language
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Sex chromosome trisomies are not associated with atypical lateralization for language

Wilson, Alexander C ; Bishop, Dorothy V M

Developmental medicine and child neurology, 2018-11, Vol.60 (11), p.1132-1139 [Periódico revisado por pares]

England: John Wiley and Sons Inc

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6
PRKRA‐Related Disorders: Bilateral Striatal Degeneration in Addition to DYT16 Spectrum
PRKRA‐Related Disorders: Bilateral Striatal Degeneration in Addition to DYT16 Spectrum
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PRKRA‐Related Disorders: Bilateral Striatal Degeneration in Addition to DYT16 Spectrum

Masnada, Silvia ; Martinelli, Diego ; Correa‐Vela, Marta ; Agolini, Emanuele ; Baide‐Mairena, Heidy ; Marcé‐Grau, Anna ; Parazzini, Cecilia ; Veggiotti, Pierangelo ; Perez‐Duenas, Belen ; Tonduti, Davide

Movement disorders, 2021-04, Vol.36 (4), p.1038-1040 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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7
Polygenic risk scores in schizophrenia with clinically significant copy number variants
Polygenic risk scores in schizophrenia with clinically significant copy number variants
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Polygenic risk scores in schizophrenia with clinically significant copy number variants

Taniguchi, Satoru ; Ninomiya, Kohei ; Kushima, Itaru ; Saito, Takeo ; Shimasaki, Ayu ; Sakusabe, Takaya ; Momozawa, Yukihide ; Kubo, Michiaki ; Kamatani, Yoichiro ; Ozaki, Norio ; Ikeda, Masashi ; Iwata, Nakao

Psychiatry and clinical neurosciences, 2020-01, Vol.74 (1), p.35-39 [Periódico revisado por pares]

Melbourne: John Wiley & Sons Australia, Ltd

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8
Losing sleep over mitochondria: a new player in the pathophysiology of fatal familial insomnia
Losing sleep over mitochondria: a new player in the pathophysiology of fatal familial insomnia
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Losing sleep over mitochondria: a new player in the pathophysiology of fatal familial insomnia

Glatzel, Markus ; Sepulveda‐Falla, Diego

Brain pathology (Zurich, Switzerland), 2017-01, Vol.27 (1), p.107-108 [Periódico revisado por pares]

Switzerland: John Wiley & Sons, Inc

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9
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

Simpson, Nuala H ; Addis, Laura ; Brandler, William M ; Slonims, Vicky ; Clark, Ann ; Watson, Jocelynne ; Scerri, Thomas S ; Hennessy, Elizabeth R ; Bolton, Patrick F ; Conti‐Ramsden, Gina ; Fairfax, Benjamin P ; Knight, Julian C ; Stein, John ; Talcott, Joel B ; O'Hare, Anne ; Baird, Gillian ; Paracchini, Silvia ; Fisher, Simon E ; Newbury, Dianne F ; Consortium, SLI

Developmental medicine and child neurology, 2014-04, Vol.56 (4), p.346-353 [Periódico revisado por pares]

England: BlackWell Publishing Ltd

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10
Neuroarchitecture of the Drosophila central complex: A catalog of nodulus and asymmetrical body neurons and a revision of the protocerebral bridge catalog
Neuroarchitecture of the Drosophila central complex: A catalog of nodulus and asymmetrical body neurons and a revision of the protocerebral bridge catalog
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Neuroarchitecture of the Drosophila central complex: A catalog of nodulus and asymmetrical body neurons and a revision of the protocerebral bridge catalog

Wolff, Tanya ; Rubin, Gerald M.

Journal of comparative neurology (1911), 2018-11, Vol.526 (16), p.2585-2611 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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