Similar articles for PMID: 19112063

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1

Abnormal basiocciput development in CHARGE syndrome.

Fujita K, Aida N, Asakura Y, Kurosawa K, Niwa T, Muroya K, Adachi M, Nishimura G, Inoue T. Fujita K, et al. AJNR Am J Neuroradiol. 2009 Mar;30(3):629-34. doi: 10.3174/ajnr.A1380. Epub 2008 Dec 26. AJNR Am J Neuroradiol. 2009. PMID: 19112063 Free PMC article.

2

CHARGE syndrome: 2005.

Carey JC. Carey JC. Am J Med Genet A. 2005 Mar 15;133A(3):227. doi: 10.1002/ajmg.a.30540. Am J Med Genet A. 2005. PMID: 15633196 No abstract available.

3

CHARGE syndrome.

Blake KD, Prasad C. Blake KD, et al. Orphanet J Rare Dis. 2006 Sep 7;1:34. doi: 10.1186/1750-1172-1-34. Orphanet J Rare Dis. 2006. PMID: 16959034 Free PMC article. Review.

4

Imaging of Clival Hypoplasia in CHARGE Syndrome and Hypothesis for Development: A Case-Control Study.

de Geus CM, Bergman JEH, van Ravenswaaij-Arts CMA, Meiners LC. de Geus CM, et al. AJNR Am J Neuroradiol. 2018 Oct;39(10):1938-1942. doi: 10.3174/ajnr.A5810. Epub 2018 Sep 20. AJNR Am J Neuroradiol. 2018. PMID: 30237300 Free PMC article.

5

Endocrine and radiological studies in patients with molecularly confirmed CHARGE syndrome.

Asakura Y, Toyota Y, Muroya K, Kurosawa K, Fujita K, Aida N, Kawame H, Kosaki K, Adachi M. Asakura Y, et al. J Clin Endocrinol Metab. 2008 Mar;93(3):920-4. doi: 10.1210/jc.2007-1419. Epub 2007 Dec 18. J Clin Endocrinol Metab. 2008. PMID: 18089695

6

CHARGE syndrome includes hypogonadotropic hypogonadism and abnormal olfactory bulb development.

Pinto G, Abadie V, Mesnage R, Blustajn J, Cabrol S, Amiel J, Hertz-Pannier L, Bertrand AM, Lyonnet S, Rappaport R, Netchine I. Pinto G, et al. J Clin Endocrinol Metab. 2005 Oct;90(10):5621-6. doi: 10.1210/jc.2004-2474. Epub 2005 Jul 19. J Clin Endocrinol Metab. 2005. PMID: 16030162

7

CHARGE (coloboma, heart defect, atresia choanae, retarded growth and development, genital hypoplasia, ear anomalies/deafness) syndrome and chromosome 22q11.2 deletion syndrome: a comparison of immunologic and nonimmunologic phenotypic features.

Jyonouchi S, McDonald-McGinn DM, Bale S, Zackai EH, Sullivan KE. Jyonouchi S, et al. Pediatrics. 2009 May;123(5):e871-7. doi: 10.1542/peds.2008-3400. Pediatrics. 2009. PMID: 19403480 Free PMC article.

8

Olfactory anomalies in CHARGE syndrome: imaging findings of a potential major diagnostic criterion.

Blustajn J, Kirsch CF, Panigrahy A, Netchine I. Blustajn J, et al. AJNR Am J Neuroradiol. 2008 Aug;29(7):1266-9. doi: 10.3174/ajnr.A1099. Epub 2008 Apr 16. AJNR Am J Neuroradiol. 2008. PMID: 18417599 Free PMC article.

9

Speculations on the pathogenesis of CHARGE syndrome.

Williams MS. Williams MS. Am J Med Genet A. 2005 Mar 15;133A(3):318-25. doi: 10.1002/ajmg.a.30561. Am J Med Genet A. 2005. PMID: 15637730

10

Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.

Lalani SR, Safiullah AM, Fernbach SD, Harutyunyan KG, Thaller C, Peterson LE, McPherson JD, Gibbs RA, White LD, Hefner M, Davenport SL, Graham JM, Bacino CA, Glass NL, Towbin JA, Craigen WJ, Neish SR, Lin AE, Belmont JW. Lalani SR, et al. Am J Hum Genet. 2006 Feb;78(2):303-14. doi: 10.1086/500273. Epub 2005 Dec 29. Am J Hum Genet. 2006. PMID: 16400610 Free PMC article.

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