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 *

419 related articles for article (PubMed ID: 23650303)

  • 61. Variable presentation of nemaline myopathy: novel mutation of alpha actin gene.
    Bouldin AA; Parisi MA; Laing N; Patterson K; Gospe SM
    Muscle Nerve; 2007 Feb; 35(2):254-8. PubMed ID: 16967490
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Nemaline myopathy: a clinical study of 143 cases.
    Ryan MM; Schnell C; Strickland CD; Shield LK; Morgan G; Iannaccone ST; Laing NG; Beggs AH; North KN
    Ann Neurol; 2001 Sep; 50(3):312-20. PubMed ID: 11558787
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Sporadic late-onset nemaline myopathy as a rare cause of slowly progressive muscle weakness with young adult onset.
    Maeda MH; Ohta H; Izutsu K; Shimizu J; Uesaka Y
    Muscle Nerve; 2015 May; 51(5):772-4. PubMed ID: 25381859
    [TBL] [Abstract][Full Text] [Related]  

  • 64. [A case of hypothyroid myopathy complicated with congestive heart failure simulating dilated cardiomyopathy].
    Hamashige N; Doi Y; Yonezawa Y; Ebuchi Y; Ozawa T; Myojin K; Sonobe H
    Nihon Naika Gakkai Zasshi; 1984 Jun; 73(6):876-81. PubMed ID: 6491455
    [No Abstract]   [Full Text] [Related]  

  • 65. [Two cases of nemaline myopathy presenting with hypertrophy of distal limbs with prominent asymmetry].
    Mizuno Y; Mori-Yoshimura M; Oya Y; Nishikawa A; Nishino I; Takahashi Y
    Rinsho Shinkeigaku; 2017 Nov; 57(11):691-697. PubMed ID: 29070751
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Camptocormia as the presenting symptom in sporadic late onset nemaline myopathy: a case report.
    Türk M; Nagel AM; Roemer F; Schlötzer-Schrehardt U; Thiel CT; Winterholler M; Schröder R
    BMC Musculoskelet Disord; 2019 Nov; 20(1):553. PubMed ID: 31747907
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Nemaline myopathy with dilated cardiomyopathy and severe heart failure: A case report.
    Wang Q; Hu F
    World J Clin Cases; 2021 Apr; 9(11):2569-2575. PubMed ID: 33889622
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Adult-onset nemaline myopathy and monoclonal gammopathy.
    Keller CE; Hays AP; Rowland LP; Moghadaszadeh B; Beggs AH; Bhagat G
    Arch Neurol; 2006 Jan; 63(1):132-4. PubMed ID: 16401746
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Somatic mosaicism of a heterogeneous mutation of ACTA1 in nemaline myopathy.
    Yokoi T; Sei K; Enomoto Y; Naruto T; Kurosawa K
    Pediatr Int; 2019 Nov; 61(11):1169-1171. PubMed ID: 31724238
    [No Abstract]   [Full Text] [Related]  

  • 70. Familial congestive cardiomyopathy with nemaline rods in heart and skeletal muscle.
    Jones JG; Factor SM
    Virchows Arch A Pathol Anat Histopathol; 1985; 408(2-3):307-12. PubMed ID: 3002014
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Severe nemaline myopathy associated with consecutive mutations E74D and H75Y on a single ACTA1 allele.
    Garcia-Angarita N; Kirschner J; Heiliger M; Thirion C; Walter MC; Schnittfeld-Acarlioglu S; Albrecht M; Müller K; Wieczorek D; Lochmüller H; Krause S
    Neuromuscul Disord; 2009 Jul; 19(7):481-4. PubMed ID: 19553116
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Sporadic late onset nemaline myopathy.
    Chahin N; Selcen D; Engel AG
    Neurology; 2005 Oct; 65(8):1158-64. PubMed ID: 16148261
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Severe congenital nemaline myopathy: a personal perspective.
    Marinone K
    Neonatal Netw; 1998 Feb; 17(1):29-32. PubMed ID: 9526359
    [TBL] [Abstract][Full Text] [Related]  

  • 74. A patient with slowly progressive adult-onset nemaline myopathy and novel compound heterozygous mutations in the nebulin gene.
    Tsunoda K; Yamashita T; Motokura E; Takahashi Y; Sato K; Takemoto M; Hishikawa N; Ohta Y; Nishikawa A; Nishino I; Abe K
    J Neurol Sci; 2017 Feb; 373():254-257. PubMed ID: 28131200
    [No Abstract]   [Full Text] [Related]  

  • 75. Clinical approach to the diagnosis of congenital myopathies.
    North KN
    Semin Pediatr Neurol; 2011 Dec; 18(4):216-20. PubMed ID: 22172416
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Dietary L-tyrosine supplementation in nemaline myopathy.
    Ryan MM; Sy C; Rudge S; Ellaway C; Ketteridge D; Roddick LG; Iannaccone ST; Kornberg AJ; North KN
    J Child Neurol; 2008 Jun; 23(6):609-13. PubMed ID: 18079309
    [TBL] [Abstract][Full Text] [Related]  

  • 77. [Myocarditis and dilated cardiomyopathy (an analysis of questions of etiology, pathogenesis and differential diagnosis in a clinical example)].
    Samsonov MIu; Naumov VG; Ibragimov AIu; Aleksandrova LZ; Galakhov IE
    Biull Vsesoiuznogo Kardiol Nauchn Tsentra AMN SSSR; 1988; 11(2):13-8. PubMed ID: 3233150
    [TBL] [Abstract][Full Text] [Related]  

  • 78. A case of neuromuscular mimicry.
    Bos MM; Overeem S; van Engelen BG; Scheffer H; van den Elzen C; Ter Laak H; Lammens M; Schelhaas HJ; Zwarts MJ
    Neuromuscul Disord; 2006 Aug; 16(8):510-3. PubMed ID: 16919950
    [TBL] [Abstract][Full Text] [Related]  

  • 79. The course of the dilated cardiomyopathy in three siblings - a rare case of familial non-compact left ventricle.
    Kwiatkowska J; Aleszewicz-Baranowska J; Waldoch A; Komorowska W; Wierzba J
    Georgian Med News; 2011 Apr; (193):60-3. PubMed ID: 21617277
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state.
    Kawase K; Nishino I; Sugimoto M; Togawa T; Sugiura T; Kouwaki M; Kibe T; Koyama N; Yokochi K
    Brain Dev; 2015 Oct; 37(9):887-90. PubMed ID: 25721947
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.