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 *

161 related articles for article (PubMed ID: 30508964)

  • 1. Hemangiomas of the tongue and the oral cavity in a myotonic dystrophy type 1 patient: A case report.
    Portaro S; Naro A; Guarneri C; Di Toro G; Manuli A; Calabrò RS
    Medicine (Baltimore); 2018 Nov; 97(48):e13448. PubMed ID: 30508964
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Myotonic dystrophies.
    Huang CC; Kuo HC
    Chang Gung Med J; 2005 Aug; 28(8):517-26. PubMed ID: 16265841
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Idiopathic ventricular fibrillation and the V1764fsX1786 frameshift mutation of the SCN5A gene in a myotonic dystrophy type 1 patient.
    Shimoyama T; Hayashi H; Suzuki F; Nishiyama Y; Miyamoto Y; Aiba T; Shimizu W; Kimura K
    J Clin Neurosci; 2020 Apr; 74():242-244. PubMed ID: 32063450
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of early onset diabetes with myotonic dystrophy type 1.
    Wan J; Zhao L; Jin P
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2023 Jun; 48(6):930-934. PubMed ID: 37587079
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Progressive conduction disturbance in myotonic dystrophy.
    Palazzolo J; Trucco E; Arce M; Riera AR; Femenía F
    Cardiol J; 2011; 18(3):322-5. PubMed ID: 21660927
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Myotonic dystrophy type 1 patient-derived iPSCs for the investigation of CTG repeat instability.
    Ueki J; Nakamori M; Nakamura M; Nishikawa M; Yoshida Y; Tanaka A; Morizane A; Kamon M; Araki T; Takahashi MP; Watanabe A; Inagaki N; Sakurai H
    Sci Rep; 2017 Feb; 7():42522. PubMed ID: 28211918
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and genetic characteristics of childhood-onset myotonic dystrophy.
    Stokes M; Varughese N; Iannaccone S; Castro D
    Muscle Nerve; 2019 Dec; 60(6):732-738. PubMed ID: 31520483
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan: implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1.
    Pan H; Lin HM; Ku WY; Li TC; Li SY; Lin CC; Hsiao KM
    Eur J Hum Genet; 2001 Aug; 9(8):638-41. PubMed ID: 11528511
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comparisons of intellectual capacities between mild and classic adult-onset phenotypes of myotonic dystrophy type 1 (DM1).
    Jean S; Richer L; Laberge L; Mathieu J
    Orphanet J Rare Dis; 2014 Nov; 9():186. PubMed ID: 25424323
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans.
    Kim SY; Kim JY; Kim GP; Sung JJ; Lim KS; Lee KW; Chae JH; Hong YH; Seong MW; Park SS
    Korean J Lab Med; 2008 Dec; 28(6):483-92. PubMed ID: 19127114
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fuchs' Endothelial Corneal Dystrophy in Patients With Myotonic Dystrophy, Type 1.
    Winkler NS; Milone M; Martinez-Thompson JM; Raja H; Aleff RA; Patel SV; Fautsch MP; Wieben ED; Baratz KH
    Invest Ophthalmol Vis Sci; 2018 Jun; 59(7):3053-3057. PubMed ID: 30025114
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Late complication of congenital hemangioma of the tongue.
    Brown DA; Smith JD
    Head Neck Surg; 1987; 9(5):299-304. PubMed ID: 3623953
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Risk of skin cancer among patients with myotonic dystrophy type 1 based on primary care physician data from the U.K. Clinical Practice Research Datalink.
    Wang Y; Pfeiffer RM; Alsaggaf R; Meeraus W; Gage JC; Anderson LA; Bremer RC; Nikolenko N; Lochmuller H; Greene MH; Gadalla SM
    Int J Cancer; 2018 Mar; 142(6):1174-1181. PubMed ID: 29114849
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MBNL1 gene variants as modifiers of disease severity in myotonic dystrophy type 1.
    Huin V; Vasseur F; Schraen-Maschke S; Dhaenens CM; Devos P; Dupont K; Sergeant N; Buée L; Lacour A; Hofmann-Radvanyi H; Sablonnière B
    J Neurol; 2013 Apr; 260(4):998-1003. PubMed ID: 23161457
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Myotonic dystrophy type 1 presenting with stroke-like episodes: a case report.
    Rollnik JD; Heinz U; Lenz O
    BMC Res Notes; 2013 Jun; 6():243. PubMed ID: 23803495
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Myotonic dystrophies: clinical presentation, pathogenesis, diagnostics and therapy].
    Finsterer J; Rudnik-Schöneborn S
    Fortschr Neurol Psychiatr; 2015 Jan; 83(1):9-17. PubMed ID: 25602187
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Overview of the Complex Relationship between Epigenetics Markers, CTG Repeat Instability and Symptoms in Myotonic Dystrophy Type 1.
    de Pontual L; Tomé S
    Int J Mol Sci; 2022 Mar; 23(7):. PubMed ID: 35408837
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Polypoidal choroidal vasculopathy in a patient with DMPK-associated myotonic dystrophy.
    Iida Y; Hayashi T; Tokuhisa T; Mizobuchi K; Omoto S; Nakano T
    Doc Ophthalmol; 2022 Jun; 144(3):217-226. PubMed ID: 35284965
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Investigation of molecular diagnosis in Chinese patients with myotonic dystrophy type 1.
    Li M; Wang Z; Cui F; Yang F; Chen Z; Ling L; Pu C; Huang X
    Chin Med J (Engl); 2014; 127(6):1084-8. PubMed ID: 24622439
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1.
    Salvatori S; Fanin M; Trevisan CP; Furlan S; Reddy S; Nagy JI; Angelini C
    Neurol Sci; 2005 Oct; 26(4):235-42. PubMed ID: 16193250
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.