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 *

209 related articles for article (PubMed ID: 34046427)

  • 21. Natural History, Trial Readiness and Gene Discovery: Advances in Patient Registries for Neuromuscular Disease.
    Thompson R; Robertson A; Lochmüller H
    Adv Exp Med Biol; 2017; 1031():97-124. PubMed ID: 29214567
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Global Single Clustering of Phenotype-Associated Human Aging Genes in the Co-Expression and Physical Interaction Networks: An OMIM-Based Investigative Review.
    M R; M A; H B; M O
    Arch Gerontol Geriatr; 2021; 96():104461. PubMed ID: 34171756
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Neuromuscular Diseases and Bone.
    Iolascon G; Paoletta M; Liguori S; Curci C; Moretti A
    Front Endocrinol (Lausanne); 2019; 10():794. PubMed ID: 31824418
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield.
    Ankala A; da Silva C; Gualandi F; Ferlini A; Bean LJ; Collins C; Tanner AK; Hegde MR
    Ann Neurol; 2015 Feb; 77(2):206-14. PubMed ID: 25380242
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Left ventricular hypertrabeculation/noncompaction, cardiac phenotype, and neuromuscular disorders.
    Stöllberger C; Wegner C; Finsterer J
    Herz; 2019 Nov; 44(7):659-665. PubMed ID: 29626229
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Emergency room visits and admission rates of children with neuromuscular disorders: A 10-year experience in a medical center in Taiwan.
    Kao WT; Tseng YH; Jong YJ; Chen TH
    Pediatr Neonatol; 2019 Aug; 60(4):405-410. PubMed ID: 30482624
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Gene- and Disease-Based Expansion of the Knowledge on Inborn Errors of Immunity.
    Salnikova LE; Chernyshova EV; Anastasevich LA; Larin SS
    Front Immunol; 2019; 10():2475. PubMed ID: 31695696
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The predictive value of models of neuromuscular disorders to potentiate clinical translation.
    van Putten M
    Dis Model Mech; 2022 Jul; 15(7):. PubMed ID: 35912512
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Systematic identification of phenotypically enriched loci using a patient network of genomic disorders.
    Reyes-Palomares A; Bueno A; Rodríguez-López R; Medina MÁ; Sánchez-Jiménez F; Corpas M; Ranea JA
    BMC Genomics; 2016 Mar; 17():232. PubMed ID: 26980139
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Illness Perceptions and Illness Identity in Adolescents and Emerging Adults With Neuromuscular Disorders.
    Geuens S; Leyen K; Raymaekers K; Prikken S; Willen J; Goemans N; De Waele L; Lemiere J; Luyckx K
    Clin Child Psychol Psychiatry; 2023 Jul; 28(3):983-996. PubMed ID: 36112900
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Management of Cardiac Involvement Associated With Neuromuscular Diseases: A Scientific Statement From the American Heart Association.
    Feingold B; Mahle WT; Auerbach S; Clemens P; Domenighetti AA; Jefferies JL; Judge DP; Lal AK; Markham LW; Parks WJ; Tsuda T; Wang PJ; Yoo SJ;
    Circulation; 2017 Sep; 136(13):e200-e231. PubMed ID: 28838934
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular biomarkers for neuromuscular disorders - challenges and future perspectives.
    Mroczek M; Machoń L; Filipczyńska I
    Neurol Neurochir Pol; 2019; 53(3):173-180. PubMed ID: 31180130
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Diversity and molecular network patterns of symptom phenotypes.
    Shu Z; Wang J; Sun H; Xu N; Lu C; Zhang R; Li X; Liu B; Zhou X
    NPJ Syst Biol Appl; 2021 Nov; 7(1):41. PubMed ID: 34848731
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Neurological comorbidity affects prognosis in left ventricular hypertrabeculation/noncompaction.
    Stöllberger C; Blazek G; Wegner C; Finsterer J
    Heart Lung; 2012; 41(6):594-8. PubMed ID: 22515930
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Sudden cardiac death in neuromuscular disorders.
    Finsterer J; Stöllberger C; Maeztu C
    Int J Cardiol; 2016 Jan; 203():508-15. PubMed ID: 26551884
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prognostic indicators of neuromuscular disorders for palliative care referral.
    Chang RS; Wong YK
    Ann Palliat Med; 2018 Jul; 7(3):335-338. PubMed ID: 29156911
    [TBL] [Abstract][Full Text] [Related]  

  • 37. An Extended Targeted Copy Number Variation Detection Array Including 187 Genes for the Diagnostics of Neuromuscular Disorders.
    Sagath L; Lehtokari VL; Välipakka S; Udd B; Wallgren-Pettersson C; Pelin K; Kiiski K
    J Neuromuscul Dis; 2018; 5(3):307-314. PubMed ID: 30040739
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Gene-Focused Networks Underlying Phenotypic Convergence in a Systematically Phenotyped Cohort With Heterogeneous Intellectual Disability.
    Wang Y; Zhu LN; Ma XW; Yang F; Xu XL; Yang Y; Yang X; Peng W; Zhang WQ; Liang JY; Zhu WD; Jiang TJ; Zhang XL; Feng ZC
    Front Bioeng Biotechnol; 2020; 8():45. PubMed ID: 32117926
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Linkage of Stress with Neuromuscular Disorders.
    Ashraf GM; Ali A; Tabrez S; Zaidi SK; Shakil S; Alam MZ; Rehan M; Aliev G
    CNS Neurol Disord Drug Targets; 2016; 15(3):321-8. PubMed ID: 26831261
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Muscular dystrophies and myopathies: the spectrum of mutated genes in the Czech Republic.
    Stehlíková K; Skálová D; Zídková J; Haberlová J; Voháňka S; Mazanec R; Mrázová L; Vondráček P; Ošlejšková H; Zámečník J; Honzík T; Zeman J; Magner M; Šišková D; Langová M; Gregor V; Godava M; Smolka V; Fajkusová L
    Clin Genet; 2017 Mar; 91(3):463-469. PubMed ID: 27447704
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.