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Steven A Wall

Showing results (31-40 of 72) with videos related to

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Journal of Neurosurgery. Pediatrics|September 27, 2014
The preoperative incidence of raised intracranial pressure in nonsyndromic sagittal craniosynostosis is underestimated in the literatureSteven A Wall, Gregory P L Thomas, David Johnson, et al.
Journal of Neurosurgery. Pediatrics|January 7, 2015
The incidence of raised intracranial pressure in nonsyndromic sagittal craniosynostosis following primary surgeryGregory P L Thomas, David Johnson, Jo C Byren, et al.
Journal of Neurosurgery. Pediatrics|November 11, 2015
ResponseSteven A Wall, Gregory P L Thomas, David Johnson, et al.
Journal of Neurosurgery. Pediatrics|November 11, 2015
ResponseSteven A Wall, Gregory P L Thomas, David Johnson, et al.
Human Genetics|July 9, 2004
Paternal origin of FGFR3 mutations in Muenke-type craniosynostosisSahan V Rannan-Eliya, Indira B Taylor, I Marieke De Heer, et al.
European Journal of Human Genetics : EJHG|April 16, 2015
Association of mutations in FLNA with craniosynostosisNathalie Fennell, Nicola Foulds, Diana S Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2004
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndromeStephen R F Twigg, Rui Kan, Christian Babbs, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 21, 2005
Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogoniaAnne Goriely, Gilean A T McVean, Ans M M van Pelt, et al.
Human Mutation|July 25, 2018
Disruption of TWIST1 translation by 5' UTR variants in Saethre-Chotzen syndromeYan Zhou, Nils Koelling, Aimée L Fenwick, et al.
Human Molecular Genetics|March 17, 2006
Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosisAmy E Merrill, Elena G Bochukova, Sean M Brugger, et al.
Pageof 8

Showing results (31-40 of 72) with videos related to

Sort By:
Pageof 8
Journal of Neurosurgery. Pediatrics|September 27, 2014
The preoperative incidence of raised intracranial pressure in nonsyndromic sagittal craniosynostosis is underestimated in the literatureSteven A Wall, Gregory P L Thomas, David Johnson, et al.
Journal of Neurosurgery. Pediatrics|January 7, 2015
The incidence of raised intracranial pressure in nonsyndromic sagittal craniosynostosis following primary surgeryGregory P L Thomas, David Johnson, Jo C Byren, et al.
Journal of Neurosurgery. Pediatrics|November 11, 2015
ResponseSteven A Wall, Gregory P L Thomas, David Johnson, et al.
Journal of Neurosurgery. Pediatrics|November 11, 2015
ResponseSteven A Wall, Gregory P L Thomas, David Johnson, et al.
Human Genetics|July 9, 2004
Paternal origin of FGFR3 mutations in Muenke-type craniosynostosisSahan V Rannan-Eliya, Indira B Taylor, I Marieke De Heer, et al.
European Journal of Human Genetics : EJHG|April 16, 2015
Association of mutations in FLNA with craniosynostosisNathalie Fennell, Nicola Foulds, Diana S Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2004
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndromeStephen R F Twigg, Rui Kan, Christian Babbs, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 21, 2005
Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogoniaAnne Goriely, Gilean A T McVean, Ans M M van Pelt, et al.
Human Mutation|July 25, 2018
Disruption of TWIST1 translation by 5' UTR variants in Saethre-Chotzen syndromeYan Zhou, Nils Koelling, Aimée L Fenwick, et al.
Human Molecular Genetics|March 17, 2006
Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosisAmy E Merrill, Elena G Bochukova, Sean M Brugger, et al.
Pageof 8