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 *

158 related articles for article (PubMed ID: 30506906)

  • 1. A novel EMD mutation in a Chinese family with initial diagnosis of conduction cardiomyopathy.
    Zhou J; Li H; Li X; Li Y; Yang M; Shi G; Xu D; Shi X
    Brain Behav; 2019 Jan; 9(1):e01167. PubMed ID: 30506906
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole exome sequencing identifies a novel EMD mutation in a Chinese family with dilated cardiomyopathy.
    Zhang M; Chen J; Si D; Zheng Y; Jiao H; Feng Z; Hu Z; Duan R
    BMC Med Genet; 2014 Jul; 15():77. PubMed ID: 24997722
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A mutation in the X-linked Emery-Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy.
    Vohanka S; Vytopil M; Bednarik J; Lukas Z; Kadanka Z; Schildberger J; Ricotti R; Bione S; Toniolo D
    Neuromuscul Disord; 2001 May; 11(4):411-3. PubMed ID: 11369194
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cardiac Emerinopathy: A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction.
    Ishikawa T; Mishima H; Barc J; Takahashi MP; Hirono K; Terada S; Kowase S; Sato T; Mukai Y; Yui Y; Ohkubo K; Kimoto H; Watanabe H; Hata Y; Aiba T; Ohno S; Chishaki A; Shimizu W; Horie M; Ichida F; Nogami A; Yoshiura KI; Schott JJ; Makita N
    Circ Arrhythm Electrophysiol; 2020 Oct; 13(10):e008712. PubMed ID: 32755394
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Emery-Dreifuss muscular dystrophy.
    Helbling-Leclerc A; Bonne G; Schwartz K
    Eur J Hum Genet; 2002 Mar; 10(3):157-61. PubMed ID: 11973618
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Emery-Dreifuss muscular dystrophy.
    Zacharias AS; Wagener ME; Warren ST; Hopkins LC
    Semin Neurol; 1999; 19(1):67-79. PubMed ID: 10711990
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X-linked form of Emery-Dreifuss muscular dystrophy.
    Hayashi YK
    Acta Myol; 2005 Oct; 24(2):98-103. PubMed ID: 16550925
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Emery-Dreifuss humeroperoneal muscular dystrophy: cardiac manifestations.
    Parmar MS; Parmar KS
    Can J Cardiol; 2012; 28(4):516.e1-3. PubMed ID: 22480903
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel emerin gene mutation in Emery Dreifuss muscular dystrophy patient with spontaneous chordae tendinae rupture.
    Pancheri E; Bozzetti S; Rimessi P; Macchione F; Barillari M; Venturoli A; Guglielmi V; Fortunato F; Tonin P; Vattemi G
    Clin Neurol Neurosurg; 2019 Nov; 186():105536. PubMed ID: 31574358
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dilated, arrhythmogenic cardiomyopathy in emery-dreifuss muscular dystrophy due to the emerin splice-site mutation c.449 + 1G>A.
    Finsterer J; Stöllberger C; Sehnal E; Rehder H; Laccone F
    Cardiology; 2015; 130(1):48-51. PubMed ID: 25502304
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Emerin and cardiomyopathy in Emery-Dreifuss muscular dystrophy.
    Funakoshi M; Tsuchiya Y; Arahata K
    Neuromuscul Disord; 1999 Mar; 9(2):108-14. PubMed ID: 10220866
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot.
    Brown CA; Scharner J; Felice K; Meriggioli MN; Tarnopolsky M; Bower M; Zammit PS; Mendell JR; Ellis JA
    J Hum Genet; 2011 Aug; 56(8):589-94. PubMed ID: 21697856
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A case of Emery-Dreifuss muscular dystrophy with slight joint contracture].
    Fujii S; Eguchi K; Sato C; Saito Y; Indrawati LA; Shirai S; Nishino I; Yabe I
    Rinsho Shinkeigaku; 2020 Aug; 60(8):554-559. PubMed ID: 32641626
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?
    Ben Yaou R; Toutain A; Arimura T; Demay L; Massart C; Peccate C; Muchir A; Llense S; Deburgrave N; Leturcq F; Litim KE; Rahmoun-Chiali N; Richard P; Babuty D; Récan-Budiartha D; Bonne G
    Neurology; 2007 May; 68(22):1883-94. PubMed ID: 17536044
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Emery-Dreifuss muscular dystrophy].
    Kubo S; Tsukahara T; Arahata K
    Nihon Rinsho; 1997 Dec; 55(12):3186-9. PubMed ID: 9436433
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Emery-Dreifuss muscular dystrophy.
    Heller SA; Shih R; Kalra R; Kang PB
    Muscle Nerve; 2020 Apr; 61(4):436-448. PubMed ID: 31840275
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery-Dreifuss muscular dystrophy caused by an LMNA gene mutation.
    Wada E; Matsumoto K; Susumu N; Kato M; Hayashi YK
    J Physiol Sci; 2023 Nov; 73(1):27. PubMed ID: 37940872
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up study.
    Yunisova G; Ceylaner S; Oflazer P; Deymeer F; Parman YG; Durmus H
    Neuromuscul Disord; 2022 Sep; 32(9):718-727. PubMed ID: 35922275
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Emery dreifuss muscular dystrophy: a clinico-pathological study.
    Gayathri N; Taly AB; Sinha S; Suresh TG; Gorai D
    Neurol India; 2006 Jun; 54(2):197-9. PubMed ID: 16804269
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cardiac dysrhythmias,cardiomyopathy and muscular dystrophy in patients with Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B.
    Hong JS; Ki CS; Kim JW; Suh YL; Kim JS; Baek KK; Kim BJ; Ahn KJ; Kim DK
    J Korean Med Sci; 2005 Apr; 20(2):283-90. PubMed ID: 15832002
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.