These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
38 related articles for article (PubMed ID: 10347735)
1. Next-generation sequencing through multi-gene panel testing for the diagnosis of a Chinese patient with atypical Cockayne syndrome. Wang X; Li Y; Zhao A; Wang Y; Cao Q; Pan C; Li M Mol Genet Genomic Med; 2023 Nov; 11(11):e2254. PubMed ID: 37592445 [TBL] [Abstract][Full Text] [Related]
2. Siblings with Cockayne Syndrome B Type III Presenting with Slowly Progressive Cerebellar Ataxia. Takahashi N; Mishima T; Fujioka S; Izumi K; Ando M; Higuchi Y; Takashima H; Tsuboi Y Intern Med; 2023; 62(15):2253-2259. PubMed ID: 37532514 [TBL] [Abstract][Full Text] [Related]
3. Atypical features in two adult patients with Cockayne syndrome and analysis of genotype-phenotype correlation. Cheng H; Chen D; Wu Z; Wang N Chin Med J (Engl); 2023 Sep; 136(17):2110-2112. PubMed ID: 37106549 [No Abstract] [Full Text] [Related]
4. A Rare Case of Cockayne Syndrome-MRI Features. Mundaganur P J Clin Diagn Res; 2012 Nov; 6(9):1582-3. PubMed ID: 23285467 [TBL] [Abstract][Full Text] [Related]
5. Diagnostic and severity scores for Cockayne syndrome. Spitz MA; Severac F; Obringer C; Baer S; Le May N; Calmels N; Laugel V Orphanet J Rare Dis; 2021 Feb; 16(1):63. PubMed ID: 33536051 [TBL] [Abstract][Full Text] [Related]
6. Cockayne Syndrome: The many challenges and approaches to understand a multifaceted disease. Vessoni AT; Guerra CCC; Kajitani GS; Nascimento LLS; Garcia CCM Genet Mol Biol; 2020; 43(1 suppl. 1):e20190085. PubMed ID: 32453336 [TBL] [Abstract][Full Text] [Related]
7. [Cockayne syndrome in Lebanon. Description of 3 cases and review of the literature]. Jabre P; Mezzina M; Megarbane A J Med Liban; 1999; 47(2):144-7. PubMed ID: 10410472 [TBL] [Abstract][Full Text] [Related]