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Items: 6

1.
Cognitive Impairment and Brain Imaging Characteristics of Patients with Congenital Cataracts, Facial Dysmorphism, Neuropathy Syndrome
Teodora Chamova, Dora Zlatareva, Margarita Raycheva, Stoyan Bichev, Luba Kalaydjieva, Ivailo Tournev
Behav Neurol. 2015; 2015: 639539. Published online 2015 Apr 28. doi: 10.1155/2015/639539
PMCID:
PMC4427823
ArticlePDF–1.8M
2.
Congenital cataract, facial dysmorphism and demyelinating neuropathy (CCFDN) in 10 Czech gypsy children – frequent and underestimated cause of disability among Czech gypsies
Petra Lassuthova, Dana Šišková, Jana Haberlová, Iva Sakmaryová, Aleš Filouš, Pavel Seeman
Orphanet J Rare Dis. 2014; 9: 46. Published online 2014 Apr 1. doi: 10.1186/1750-1172-9-46
PMCID:
PMC3976362
ArticlePDF–1.8M
3.
Carrier Rates of Four Single-Gene Disorders in Croatian Bayash Roma
Ana Barešić, Marijana Peričić Salihović
Genet Test Mol Biomarkers. 2014 Feb 1; 18(2): 83–87. doi: 10.1089/gtmb.2013.0323
PMCID:
PMC3926160
ArticlePDF–160K
4.
Congenital Cataracts – Facial Dysmorphism – Neuropathy
Luba Kalaydjieva
Orphanet J Rare Dis. 2006; 1: 32. Published online 2006 Aug 29. doi: 10.1186/1750-1172-1-32
PMCID:
PMC1563997
ArticlePDF–230K
5.
Anesthesia of a patient with congenital cataract, facial dysmorphism, and neuropathy syndrome for posterior scoliosis: A case report
Jan Hudec, Martina Kosinova, Tereza Prokopova, Milan Filipovic, Martin Repko, Petr Stourac
World J Clin Cases. 2022 May 6; 10(13): 4207–4213. Published online 2022 May 6. doi: 10.12998/wjcc.v10.i13.4207
PMCID:
PMC9131212
ArticlePDF–989K
6.
Ctdp1 deficiency leads to early embryonic lethality in mice and defects in cell cycle progression in MEFs
Fangfang Qiao, Henry C.-H. Law, Kimiko L. Krieger, Emalie J. Clement, Yi Xiao, Shannon M. Buckley, Nicholas T. Woods
Biol Open. 2021 Jan 15; 10(1): bio057232. Published online 2021 Jan 6. doi: 10.1242/bio.057232
PMCID:
PMC7803460
ArticlePDF–2.7M

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