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.
209 related articles for article (PubMed ID: 34046427)
1. Decoding Neuromuscular Disorders Using Phenotypic Clusters Obtained From Co-Occurrence Networks. Díaz-Santiago E; Claros MG; Yahyaoui R; de Diego-Otero Y; Calvo R; Hoenicka J; Palau F; Ranea JAG; Perkins JR Front Mol Biosci; 2021; 8():635074. PubMed ID: 34046427 [TBL] [Abstract][Full Text] [Related]
2. HPO2Vec+: Leveraging heterogeneous knowledge resources to enrich node embeddings for the Human Phenotype Ontology. Shen F; Peng S; Fan Y; Wen A; Liu S; Wang Y; Wang L; Liu H J Biomed Inform; 2019 Aug; 96():103246. PubMed ID: 31255713 [TBL] [Abstract][Full Text] [Related]
3. Phenotype-genotype comorbidity analysis of patients with rare disorders provides insight into their pathological and molecular bases. Díaz-Santiago E; Jabato FM; Rojano E; Seoane P; Pazos F; Perkins JR; Ranea JAG PLoS Genet; 2020 Oct; 16(10):e1009054. PubMed ID: 33001999 [TBL] [Abstract][Full Text] [Related]
4. PhenPath: a tool for characterizing biological functions underlying different phenotypes. Babbi G; Martelli PL; Casadio R BMC Genomics; 2019 Jul; 20(Suppl 8):548. PubMed ID: 31307376 [TBL] [Abstract][Full Text] [Related]
5. Expanding genotype/phenotype of neuromuscular diseases by comprehensive target capture/NGS. Tian X; Liang WC; Feng Y; Wang J; Zhang VW; Chou CH; Huang HD; Lam CW; Hsu YY; Lin TS; Chen WT; Wong LJ; Jong YJ Neurol Genet; 2015 Aug; 1(2):e14. PubMed ID: 27066551 [TBL] [Abstract][Full Text] [Related]
6. Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential Falzarano MS; Rossi R; Grilli A; Fang M; Osman H; Sabatelli P; Antoniel M; Lu Z; Li W; Selvatici R; Al-Khalili C; Gualandi F; Bicciato S; Torelli S; Ferlini A Front Physiol; 2021; 12():716471. PubMed ID: 34744760 [No Abstract] [Full Text] [Related]
9. An evaluation of clinical presentation and genetic testing approaches for patients with neuromuscular disorders. Rosenberg A; Tian C; He H; Ulm E; Collins Ruff K; B Nagaraj C Am J Med Genet A; 2023 Nov; 191(11):2679-2692. PubMed ID: 37503964 [TBL] [Abstract][Full Text] [Related]
10. Shared Regulatory Pathways Reveal Novel Genetic Correlations Between Grip Strength and Neuromuscular Disorders. Gokuladhas S; Schierding W; Cameron-Smith D; Wake M; Scotter EL; O'Sullivan J Front Genet; 2020; 11():393. PubMed ID: 32391060 [TBL] [Abstract][Full Text] [Related]
17. Molecular diagnosis of myopathies. Gomez-Vargas A; Baker SK Rheum Dis Clin North Am; 2011 May; 37(2):269-87, vii. PubMed ID: 21444025 [TBL] [Abstract][Full Text] [Related]
18. Exercise biology of neuromuscular disorders. Ng SY; Manta A; Ljubicic V Appl Physiol Nutr Metab; 2018 Nov; 43(11):1194-1206. PubMed ID: 29944848 [TBL] [Abstract][Full Text] [Related]
19. Survey on patients' organisations' knowledge and position paper on screening for inherited neuromuscular diseases in Europe. Lamy F; Ferlini A; ; Evangelista T Orphanet J Rare Dis; 2021 Feb; 16(1):75. PubMed ID: 33568176 [TBL] [Abstract][Full Text] [Related]
20. Respiratory management of acute respiratory failure in neuromuscular diseases. Racca F; Del Sorbo L; Mongini T; Vianello A; Ranieri VM Minerva Anestesiol; 2010 Jan; 76(1):51-62. PubMed ID: 20125073 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]