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Refinado por: Base de dados/Biblioteca: BMJ Journals - NESLi2 remover assunto: Life Sciences & Biomedicine remover
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1
Massive congenital depression of neonate’s skull
Massive congenital depression of neonate’s skull
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Massive congenital depression of neonate’s skull

Letouzey, Mathilde ; Berveiller, Paul

Archives of disease in childhood. Fetal and neonatal edition, 2018-07, Vol.103 (4), p.F316-F316 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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2
Helmet therapy in infants with positional skull deformation: randomised controlled trial
Helmet therapy in infants with positional skull deformation: randomised controlled trial
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Helmet therapy in infants with positional skull deformation: randomised controlled trial

van Wijk, Renske M ; van Vlimmeren, Leo A ; Groothuis-Oudshoorn, Catharina G M ; Van der Ploeg, Catharina P B ; IJzerman, Maarten J ; Boere-Boonekamp, Magda M

BMJ (Online), 2014-05, Vol.348 (may01 8), p.g2741-g2741 [Periódico revisado por pares]

England: British Medical Journal Publishing Group

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3
Imaging in craniosynostosis
Imaging in craniosynostosis
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Imaging in craniosynostosis

Rodgers, Anna ; Hopper, Neil

Archives of disease in childhood, 2014-01, Vol.99 (1), p.73-73 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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4
Holoprosencephaly with premaxillary agenesis in a prehistoric skull
Holoprosencephaly with premaxillary agenesis in a prehistoric skull
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Holoprosencephaly with premaxillary agenesis in a prehistoric skull

Pachajoa, Harry ; Rodriguez, Carlos A

Archives of disease in childhood. Fetal and neonatal edition, 2013-05, Vol.98 (3), p.264-264 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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5
WTX mutations can occur both early and late in the pathogenesis of Wilms tumour
WTX mutations can occur both early and late in the pathogenesis of Wilms tumour
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WTX mutations can occur both early and late in the pathogenesis of Wilms tumour

Fukuzawa, Ryuji ; Holman, Sarah K ; Chow, C W ; Savarirayan, Ravi ; Reeve, Anthony E ; Robertson, Stephen P

Journal of medical genetics, 2010-11, Vol.47 (11), p.791-794 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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6
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)
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The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)

Wuyts, Wim ; Cleiren, Erna ; Homfray, Tessa ; Rasore-Quartino, Alberto ; Vanhoenacker, Filip ; Van Hul, Wim

Journal of medical genetics, 2000-12, Vol.37 (12), p.916-920 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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7
Helmet therapy for positional plagiocephaly and brachycephaly
Helmet therapy for positional plagiocephaly and brachycephaly
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Helmet therapy for positional plagiocephaly and brachycephaly

Collett, Brent R

BMJ (Online), 2014-05, Vol.348 (may01 8), p.g2906-g2906 [Periódico revisado por pares]

England: British Medical Journal Publishing Group

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8
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain
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Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain

McGillivray, G ; Savarirayan, R ; Cox, T C ; Stojkoski, C ; McNeil, R ; Bankier, A ; Bateman, J F ; Roscioli, T ; Gardner, R J M ; Lamandé, S R

Journal of medical genetics, 2005-08, Vol.42 (8), p.656-662 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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9
Plagiocephaly and head binding
Plagiocephaly and head binding
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Plagiocephaly and head binding

Bridges, S J ; Chambers, T L ; Pople, I K

Archives of disease in childhood, 2002-03, Vol.86 (3), p.144-145 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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10
A cloverleaf skull associated with Crouzon syndrome
A cloverleaf skull associated with Crouzon syndrome
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A cloverleaf skull associated with Crouzon syndrome

Chen, C-P ; Lin, S-P ; Su, Y-N ; Huang, J-K ; Wang, W

Archives of disease in childhood. Fetal and neonatal edition, 2006-03, Vol.91 (2), p.F98-F98 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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