Format
Sort by

Send to

Choose Destination

Search results

Items: 5

1.

Multiple antipsychotic induced neutropenia—a possible genetic association.

Chan HS, Tibrewal P, Dhillon R, Bastiampillai T.

Asian J Psychiatr. 2014 Oct;11:81. doi: 10.1016/j.ajp.2014.06.009. Epub 2014 Jul 2. No abstract available.

PMID:
25453707
2.

Long-term follow-up in patients with CCFDN syndrome.

Walter MC, Bernert G, Zimmermann U, Müllner-Eidenböck A, Moser E, Kalaydjieva L, Lochmüller H, Müller-Felber W.

Neurology. 2014 Oct 7;83(15):1337-44. doi: 10.1212/WNL.0000000000000874. Epub 2014 Sep 3.

PMID:
25186864
3.

Congenital cataract, facial dysmorphism and demyelinating neuropathy (CCFDN) in 10 Czech Gypsy children--frequent and underestimated cause of disability among Czech Gypsies.

Lassuthova P, Sišková D, Haberlová J, Sakmaryová I, Filouš A, Seeman P.

Orphanet J Rare Dis. 2014 Apr 1;9:46. doi: 10.1186/1750-1172-9-46.

4.

Carrier rates of four single-gene disorders in Croatian Bayash Roma.

Barešić A, Peričić Salihović M.

Genet Test Mol Biomarkers. 2014 Feb;18(2):83-7. doi: 10.1089/gtmb.2013.0323. Epub 2013 Nov 4.

5.

Congenital cataracts, facial dysmorphism, and neuropathy syndrome.

Tzifi F, Pons R, Athanassaki C, Poulou M, Kanavakis E.

Pediatr Neurol. 2011 Sep;45(3):206-8. doi: 10.1016/j.pediatrneurol.2011.05.008.

PMID:
21824574

Supplemental Content

Loading ...
Support Center