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 *

447 related articles for article (PubMed ID: 23650303)

  • 41. Nemaline Myopathy Initially Diagnosed as Right Heart Failure with Type 2 Respiratory Failure.
    Ito M; Shima S; Nagao R; Nakano S; Esaka K; Ueda A; Maeda S; Moriya R; Kondo M; Imaizumi K; Noda S; Katsuno M; Nishino I; Watanabe H
    Intern Med; 2022 Jun; 61(12):1897-1901. PubMed ID: 34776486
    [TBL] [Abstract][Full Text] [Related]  

  • 42. An infant with congenital nemaline myopathy and hypertrophic cardiomyopathy.
    Nakajima M; Shima Y; Kumasaka S; Kuwabara K; Migita M; Fukunaga Y
    J Nippon Med Sch; 2008 Dec; 75(6):350-3. PubMed ID: 19155574
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Fetal akinesia sequence caused by nemaline myopathy.
    Lammens M; Moerman P; Fryns JP; Lemmens F; van de Kamp GM; Goemans N; Dom R
    Neuropediatrics; 1997 Apr; 28(2):116-9. PubMed ID: 9208412
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Identification of a novel nemaline myopathy-causing mutation in the troponin T1 (TNNT1) gene: a case outside of the old order Amish.
    Marra JD; Engelstad KE; Ankala A; Tanji K; Dastgir J; De Vivo DC; Coffee B; Chiriboga CA
    Muscle Nerve; 2015 May; 51(5):767-72. PubMed ID: 25430424
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Nemaline myopathy with exclusively intranuclear rods and a novel mutation in ACTA1 (Q139H).
    Koy A; Ilkovski B; Laing N; North K; Weis J; Neuen-Jacob E; Mayatepek E; Voit T
    Neuropediatrics; 2007 Dec; 38(6):282-6. PubMed ID: 18461503
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy.
    Nguyen MA; Joya JE; Kee AJ; Domazetovska A; Yang N; Hook JW; Lemckert FA; Kettle E; Valova VA; Robinson PJ; North KN; Gunning PW; Mitchell CA; Hardeman EC
    Brain; 2011 Dec; 134(Pt 12):3516-29. PubMed ID: 22067542
    [TBL] [Abstract][Full Text] [Related]  

  • 47. A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions.
    Gommans IM; Davis M; Saar K; Lammens M; Mastaglia F; Lamont P; van Duijnhoven G; ter Laak HJ; Reis A; Vogels OJ; Laing N; van Engelen BG; Kremer H
    Brain; 2003 Jul; 126(Pt 7):1545-51. PubMed ID: 12805120
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Acquired noncompaction associated with myopathy.
    Hofer M; Stöllberger C; Finsterer J
    Int J Cardiol; 2007 Oct; 121(3):296-7. PubMed ID: 17109978
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Nemaline (actin) myopathy with myofibrillar dysgenesis and abnormal ossification.
    Arai A; Mitsuhashi S; Saito Y; Komaki H; Sakuma H; Nakagawa E; Sugai K; Sasaki M; Robertson SP; Nishimura G; Yamamoto T; Nonaka I; Nishino I
    Neuromuscul Disord; 2009 Jul; 19(7):485-8. PubMed ID: 19553121
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Nemaline myopathy with stiffness and hypertonia associated with an ACTA1 mutation.
    Jain RK; Jayawant S; Squier W; Muntoni F; Sewry CA; Manzur A; Quinlivan R; Lillis S; Jungbluth H; Sparrow JC; Ravenscroft G; Nowak KJ; Memo M; Marston SB; Laing NG
    Neurology; 2012 Apr; 78(14):1100-3. PubMed ID: 22442437
    [No Abstract]   [Full Text] [Related]  

  • 51. [Nemaline congenital myopathy:clinical features and histopathological findings in nine patients].
    Botelho CH; Carod-Artal FJ; Kalil RK
    Rev Neurol; 2001 Feb 16-28; 32(4):309-14. PubMed ID: 11333383
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Sporadic late onset nemaline myopathy and immunoglobulin deposition disease.
    Doppler K; Knop S; Einsele H; Sommer C; Wessig C
    Muscle Nerve; 2013 Dec; 48(6):983-8. PubMed ID: 23873431
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report].
    Oya Y; Segawa M; Ogawa M; Goto Y; Nonaka I; Kawai M
    Rinsho Shinkeigaku; 2000 May; 40(5):452-8. PubMed ID: 11002727
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Adult-onset nemaline myopathy: a case report and review of the literature.
    Gyure KA; Prayson RA; Estes ML
    Arch Pathol Lab Med; 1997 Nov; 121(11):1210-3. PubMed ID: 9372751
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Congenital rapidly fatal form of nemaline myopathy with fetal hydrops and arthrogryposis. A case report and review.
    Vardon D; Chau C; Sigodi S; Figarella-Branger D; Boubli L
    Fetal Diagn Ther; 1998; 13(4):244-9. PubMed ID: 9784647
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Intranuclear rods myopathy with autonomic dysfunction.
    Chou PC; Liang WC; Nonaka I; Mitsuhashi S; Nishino I; Jong YJ
    Brain Dev; 2013 Aug; 35(7):686-9. PubMed ID: 23102861
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Nemaline myopathy: an unusual cause of ophthalmoparesis.
    Wright RA; Plant GT; Landon DN; Morgan-Hughes JA
    J Neuroophthalmol; 1997 Mar; 17(1):39-43. PubMed ID: 9093960
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Heart failure and dilated cardiomyopathy associated with severe longstanding untreated hypothyroidism.
    Stănescu C; Branidou K; Ranetti EA
    Rom J Intern Med; 2007; 45(1):77-83. PubMed ID: 17966446
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 68-year old man with progressive weakness and ventilator dependent respiratory failure: a case report of sporadic late onset nemaline myopathy.
    Kirupaharan P; Kramer D; Gandler A; Kenyon L; Summer R
    BMC Pulm Med; 2022 Mar; 22(1):97. PubMed ID: 35305606
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Adult-onset nemaline myopathy with distal muscle atrophy--case report].
    Niwa F; Shiga K; Kimura M; Yamaguchi T; Kondo M; Nakagawa M
    Brain Nerve; 2009 Jun; 61(6):695-9. PubMed ID: 19526838
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 23.