Duplication of chromosome 1q23.2 in congenital craniopharyngioma

Case Reports

Neha Kumar et al. Clin Neuropathol. 2020 Jan/Feb.

. 2020 Jan/Feb;39(1):40-42.

doi: 10.5414/NP301191.

No abstract available

Similar articles

[Gyrate atrophy and craniopharyngioma: a case report].
Angioï-Duprez K, Maalouf T, George JL. Angioï-Duprez K, et al. J Fr Ophtalmol. 2001 May;24(5):513-6. J Fr Ophtalmol. 2001. PMID: 11397989 French.
BRAF V600E mutation is a useful marker for differentiating Rathke's cleft cyst with squamous metaplasia from papillary craniopharyngioma.
Kim JH, Paulus W, Heim S. Kim JH, et al. J Neurooncol. 2015 May;123(1):189-91. doi: 10.1007/s11060-015-1757-6. Epub 2015 Mar 28. J Neurooncol. 2015. PMID: 25820214 No abstract available.
CCT and sonographic findings in congenital craniopharyngioma.
Helmke K, Hausdorf G, Moehrs D, Laas R. Helmke K, et al. Neuroradiology. 1984;26(6):523-6. doi: 10.1007/BF00342694. Neuroradiology. 1984. PMID: 6504322
Paediatric craniopharyngioma: a pathological review.
Nozza P, Gambini C. Nozza P, et al. J Pediatr Endocrinol Metab. 2006 Apr;19 Suppl 1:295-8. J Pediatr Endocrinol Metab. 2006. PMID: 16700304 Review. No abstract available.
ENDOCRINE TUMORS: BRAF V600E mutations in papillary craniopharyngioma.
Brastianos PK, Santagata S. Brastianos PK, et al. Eur J Endocrinol. 2016 Apr;174(4):R139-44. doi: 10.1530/EJE-15-0957. Epub 2015 Nov 12. Eur J Endocrinol. 2016. PMID: 26563980 Free PMC article. Review.