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 *

119 related articles for article (PubMed ID: 38881774)

  • 21. Sporadic late-onset nemaline myopathy: a case report of a treatable cause of cardiac failure.
    Turnquist C; Grogono JC; Hofer M; Pitcher A
    Eur Heart J Case Rep; 2021 Jan; 5(1):ytaa480. PubMed ID: 33554019
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Nemaline Myopathy in a Hypotonic Neonate: Diagnostic Approach for Early Detection and Management.
    Vu A; Nanda S; Chassee T
    Cureus; 2024 Mar; 16(3):e56866. PubMed ID: 38659511
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Congenital Nemaline Myopathy in Two Neonates With Different Mutations: A Case Series and Literature Review.
    Mohtisham F; Al Thaqafi M; Shawli A; Sallam A
    Cureus; 2023 Sep; 15(9):e45197. PubMed ID: 37720117
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance (SLONM-MGUS): An alternative treatment using cyclophosphamide-thalidomide-dexamethasone (CTD) regimen.
    Kumutpongpanich T; Owattanapanich W; Tanboon J; Nishino I; Boonyapisit K
    Neuromuscul Disord; 2018 Jul; 28(7):610-613. PubMed ID: 29910095
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Late-onset sporadic nemaline myopathy presenting as hypercapnic respiratory failure.
    García Estévez DA; Juanatey-García A; San Millán Tejado B; Barros Angueira F
    Neurologia (Engl Ed); 2024; 39(1):99-101. PubMed ID: 38056594
    [No Abstract]   [Full Text] [Related]  

  • 26. A case of nemaline myopathy with associated dilated cardiomyopathy and respiratory failure.
    Nagata R; Kamimura D; Suzuki Y; Saito T; Toyama H; Dejima T; Inada H; Miwa Y; Uchino K; Umemura S; Shimizu M
    Int Heart J; 2011; 52(6):401-5. PubMed ID: 22188717
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort.
    Monforte M; Primiano G; Silvestri G; Mirabella M; Luigetti M; Cuccagna C; Ricci E; Servidei S; Tasca G
    J Neurol; 2018 Mar; 265(3):542-551. PubMed ID: 29356967
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Nemaline rod myopathy: a rare form of myopathy.
    Sharma MC; Gulati S; Atri S; Seth R; Kalra V; Das TK; Sarkar C
    Neurol India; 2007; 55(1):70-4. PubMed ID: 17272906
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases.
    Schnitzler LJ; Schreckenbach T; Nadaj-Pakleza A; Stenzel W; Rushing EJ; Van Damme P; Ferbert A; Petri S; Hartmann C; Bornemann A; Meisel A; Petersen JA; Tousseyn T; Thal DR; Reimann J; De Jonghe P; Martin JJ; Van den Bergh PY; Schulz JB; Weis J; Claeys KG
    Orphanet J Rare Dis; 2017 May; 12(1):86. PubMed ID: 28490364
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Nemaline myopathy as a cause of neonatal hypotonia - with emphasis on personal experiences. Report of a family with two brothers affected].
    Bojdo A; Obersztyn E; Wallgren-Pettersson C; Lehtokari V; Laing N; Davis M; Kułakowska Z
    Med Wieku Rozwoj; 2009; 13(1):5-10. PubMed ID: 19648653
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A childhood-onset nemaline myopathy caused by novel heterozygote variants in the nebulin gene with literature review.
    Wen Q; Chang X; Guo J
    Acta Neurol Belg; 2020 Dec; 120(6):1351-1360. PubMed ID: 31696431
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Nemaline myopathy with dilated cardiomyopathy in childhood.
    Gatayama R; Ueno K; Nakamura H; Yanagi S; Ueda H; Yamagishi H; Yasui S
    Pediatrics; 2013 Jun; 131(6):e1986-90. PubMed ID: 23650303
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy.
    Miyatake S; Mitsuhashi S; Hayashi YK; Purevjav E; Nishikawa A; Koshimizu E; Suzuki M; Yatabe K; Tanaka Y; Ogata K; Kuru S; Shiina M; Tsurusaki Y; Nakashima M; Mizuguchi T; Miyake N; Saitsu H; Ogata K; Kawai M; Towbin J; Nonaka I; Nishino I; Matsumoto N
    Am J Hum Genet; 2017 Jan; 100(1):169-178. PubMed ID: 28017374
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Nemaline myopathy in newly diagnosed systemic lupus erythematosus and Sjögren's overlap syndrome complicated by macrophage activation syndrome.
    Vogel C; Manwani P; Cornford ME; Heinze ER
    BMC Rheumatol; 2022 Mar; 6(1):21. PubMed ID: 35287748
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hypertrophic cardiomyopathy in a neonate associated with nemaline myopathy.
    Mir A; Lemler M; Ramaciotti C; Blalock S; Ikemba C
    Congenit Heart Dis; 2012; 7(4):E37-41. PubMed ID: 22067214
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Sporadic Late-Onset Nemaline Myopathy: Current Landscape.
    Nicolau S; Milone M
    Curr Neurol Neurosci Rep; 2023 Nov; 23(11):777-784. PubMed ID: 37856049
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Respiratory failure in nemaline myopathy.
    Sasaki M; Takeda M; Kobayashi K; Nonaka I
    Pediatr Neurol; 1997 May; 16(4):344-6. PubMed ID: 9258972
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Case report: Homozygous variants of
    Skrypnyk C; Husain AA; Hassan HY; Ahmed J; Darwish A; Almusalam L; Ben Khalaf N; Al Qashar F
    Front Genet; 2023; 14():1098102. PubMed ID: 37025449
    [No Abstract]   [Full Text] [Related]  

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