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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1969 1
1970 1
1981 1
1982 2
1984 1
1985 4
1988 1
1992 4
1993 1
1994 1
1995 4
1996 9
1997 8
1998 5
1999 6
2000 8
2001 11
2002 6
2003 8
2004 8
2005 4
2006 8
2007 9
2008 8
2009 5
2010 7
2011 11
2012 13
2013 14
2014 24
2015 26
2016 21
2017 24
2018 25
2019 32
2020 15
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Similar Articles for PMID: 11039354

302 results
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Page 1
Prominent basal emissary foramina in syndromic craniosynostosis: correlation with phenotypic and molecular diagnoses.
Robson CD, Mulliken JB, Robertson RL, Proctor MR, Steinberger D, Barnes PD, McFarren A, Müller U, Zurakowski D. Robson CD, et al. AJNR Am J Neuroradiol. 2000 Oct;21(9):1707-17. AJNR Am J Neuroradiol. 2000. PMID: 11039354 Free article.
Molecular diagnosis of bilateral coronal synostosis.
Mulliken JB, Steinberger D, Kunze S, Müller U. Mulliken JB, et al. Plast Reconstr Surg. 1999 Nov;104(6):1603-15. doi: 10.1097/00006534-199911000-00001. Plast Reconstr Surg. 1999. PMID: 10541159 Review.
Abnormal venous drainage in syndromic craniosynostosis and the role of CT venography.
Jeevan DS, Anlsow P, Jayamohan J. Jeevan DS, et al. Childs Nerv Syst. 2008 Dec;24(12):1413-20. doi: 10.1007/s00381-008-0667-8. Epub 2008 Jun 25. Childs Nerv Syst. 2008. PMID: 18575870
Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis.
Kan SH, Elanko N, Johnson D, Cornejo-Roldan L, Cook J, Reich EW, Tomkins S, Verloes A, Twigg SR, Rannan-Eliya S, McDonald-McGinn DM, Zackai EH, Wall SA, Muenke M, Wilkie AO. Kan SH, et al. Am J Hum Genet. 2002 Feb;70(2):472-86. doi: 10.1086/338758. Epub 2002 Jan 4. Am J Hum Genet. 2002. PMID: 11781872 Free PMC article.
Phenotypic diversity in patients with craniosynostoses unrelated to Apert syndrome: the role of fibroblast growth factor receptor gene mutations.
Ito S, Sekido K, Kanno H, Sato H, Tanaka M, Yamaguchi K, Yamamoto I. Ito S, et al. J Neurosurg. 2005 Jan;102(1 Suppl):23-30. doi: 10.3171/ped.2005.102.1.0023. J Neurosurg. 2005. PMID: 16206730
Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings.
Agochukwu NB, Solomon BD, Muenke M. Agochukwu NB, et al. Int J Pediatr Otorhinolaryngol. 2014 Dec;78(12):2037-47. doi: 10.1016/j.ijporl.2014.09.019. Epub 2014 Sep 28. Int J Pediatr Otorhinolaryngol. 2014. PMID: 25441602 Review.
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses.
Passos-Bueno MR, Sertié AL, Richieri-Costa A, Alonso LG, Zatz M, Alonso N, Brunoni D, Ribeiro SF. Passos-Bueno MR, et al. Am J Med Genet. 1998 Jul 7;78(3):237-41. Am J Med Genet. 1998. PMID: 9677057
Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review.
Nur BG, Pehlivanoğlu S, Mıhçı E, Calışkan M, Demir D, Alper OM, Kayserili H, Lüleci G. Nur BG, et al. Pediatr Neurol. 2014 May;50(5):482-90. doi: 10.1016/j.pediatrneurol.2014.01.023. Epub 2014 Jan 11. Pediatr Neurol. 2014. PMID: 24656465 Review.
Expanding the phenotype for the recurrent p.Ala391Glu variant in FGFR3: Beyond crouzon syndrome and acanthosis nigricans.
Rymer K, Shiang R, Hsiung A, Pandya A, Bigdeli T, Webb BT, Rhodes J. Rymer K, et al. Mol Genet Genomic Med. 2019 Jun;7(6):e656. doi: 10.1002/mgg3.656. Epub 2019 Apr 23. Mol Genet Genomic Med. 2019. PMID: 31016899 Free PMC article.
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