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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 26721046)

  • 21. Cockayne syndrome in 2 siblings.
    Hamamy HA; Daas HA; Shegem NS; Al-Hadidy AM; Ajlouni K
    Saudi Med J; 2005 May; 26(5):875-9. PubMed ID: 15951889
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ultrastructure and electrodiagnosis of peripheral neuropathy in Cockayne's syndrome.
    Grunnet ML; Zimmerman AW; Lewis RA
    Neurology; 1983 Dec; 33(12):1606-9. PubMed ID: 6316205
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cockayne syndrome--an audiologic and temporal bone analysis.
    Shemen LJ; Mitchell DP; Farkashidy J
    Am J Otol; 1984 Apr; 5(4):300-7. PubMed ID: 6720882
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Peripheral and central myelinopathy in Cockayne's syndrome. Report of 3 siblings.
    Smits MG; Gabreëls FJ; Renier WO; Joosten EM; Gabreëls-Festen AA; ter Laak HJ; Pinckers AJ; Hombergen GC; Notermans SL; Thijssen HO
    Neuropediatrics; 1982 Aug; 13(3):161-7. PubMed ID: 7133337
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Cockayne syndrome].
    Dumić M; Jasenka I; Silahić A; Kordić R
    Lijec Vjesn; 1995; 117(9-10):232-5. PubMed ID: 8643015
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Anesthesia for a patient with Cockayne's syndrome].
    Shimizu T; Inomata S; Miyabe M; Toyooka H
    Masui; 2002 Jan; 51(1):39-41. PubMed ID: 11840661
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cockayne syndrome with early onset of manifestations.
    Moyer DB; Marquis P; Shertzer ME; Burton BK
    Am J Med Genet; 1982 Oct; 13(2):225-30. PubMed ID: 7137233
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Cockayne's syndrome with unusual retinal involvement (report of one family)].
    Hamdani M; El Kettani A; Rais L; Benhaddou M; Hda N; Rachid R; El Belhadji M; Laouissi N; Zaghloul K; Benslimane A; Amraoui A
    J Fr Ophtalmol; 2000 Jan; 23(1):52-6. PubMed ID: 10660649
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome.
    Mohammadi-Asl J; Hajjari M; Tahmasebi Birgani M; Riahi K; Nasiri H; Kollaee A
    Ann Hum Genet; 2018 Sep; 82(5):304-308. PubMed ID: 30039856
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Deep intronic variation in splicing regulatory element of the ERCC8 gene associated with severe but long-term survival Cockayne syndrome.
    Schalk A; Greff G; Drouot N; Obringer C; Dollfus H; Laugel V; Chelly J; Calmels N
    Eur J Hum Genet; 2018 Apr; 26(4):527-536. PubMed ID: 29422660
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cockayne Syndrome due to a maternally-inherited whole gene deletion of ERCC8 and a paternally-inherited ERCC8 exon 4 deletion.
    Ting TW; Brett MS; Tan ES; Shen Y; Lee SP; Lim EC; Vasanwala RF; Lek N; Thomas T; Lim KW; Tan EC
    Gene; 2015 Nov; 572(2):274-8. PubMed ID: 26210811
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Infantile onset of Cockayne syndrome without photosensitivity in a Tunisian girl.
    Tinsa F; Bellalah M; Brini I; Bousnina D; Lehmann A; Boussetta K; Bousnina S
    Tunis Med; 2009 Dec; 87(12):877-9. PubMed ID: 20209858
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Atypical features and de novo heterozygous mutations in two siblings with Cockayne syndrome.
    Wu S; Liu Y; Zhang Q; Meng X; Huang L; Xu Z; Zhang C; Li Y; Chen T; Bai Z
    Mol Genet Genomic Med; 2020 May; 8(5):e1204. PubMed ID: 32160415
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Central motor pathways conduction after magnetic stimulation of the brain in Cockayne's syndrome.
    Cruz Martínez A; Anciones B
    Acta Neurol Scand; 1991 Oct; 84(4):291-4. PubMed ID: 1663306
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studies.
    Patton MA; Giannelli F; Francis AJ; Baraitser M; Harding B; Williams AJ
    J Med Genet; 1989 Mar; 26(3):154-9. PubMed ID: 2468771
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of two novel homozygous mutations in ERCC8 gene in two unrelated consanguineous families with Cockayne syndrome from Iran.
    Yousefipour F; Mahjoobi F
    Clin Chim Acta; 2021 Dec; 523():65-71. PubMed ID: 34461059
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Chronological changes of auditory brainstem responses in Cockayne's syndrome.
    Iwasaki S; Kaga K
    Int J Pediatr Otorhinolaryngol; 1994 Nov; 30(3):211-21. PubMed ID: 7836034
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cockayne syndrome--a primary defect in DNA repair, transcription, both or neither?
    Friedberg EC
    Bioessays; 1996 Sep; 18(9):731-8. PubMed ID: 8831289
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis of Cockayne's syndrome.
    Lehmann AR; Francis AJ; Giannelli F
    Lancet; 1985 Mar; 1(8427):486-8. PubMed ID: 2579301
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Progressive demyelinating neuropathy correlates with clinical severity in Cockayne syndrome.
    Gitiaux C; Blin-Rochemaure N; Hully M; Echaniz-Laguna A; Calmels N; Bahi-Buisson N; Desguerre I; Dabaj I; Wehbi S; Quijano-Roy S; Laugel V
    Clin Neurophysiol; 2015 Jul; 126(7):1435-9. PubMed ID: 25453614
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.