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 *

247 related articles for article (PubMed ID: 38791328)

  • 21. Early cardiac rehabilitation after heart transplantation in a patient with limb-girdle muscular dystrophy: A case report.
    Kim Y; Park MK; Shin MJ; Shin YB; Lee HW; Yun RY; Lee BJ
    Medicine (Baltimore); 2022 Jul; 101(30):e29180. PubMed ID: 35905204
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Compound Heterozygous
    Gaertner A; Burr L; Klauke B; Brodehl A; Laser KT; Klingel K; Tiesmeier J; Schulz U; Knyphausen EZ; Gummert J; Milting H
    Int J Mol Sci; 2022 Jun; 23(12):. PubMed ID: 35743126
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Heart transplantation in muscular dystrophy: Single-center analysis.
    Visrodia P; Patel NJ; Burford M; Hamilton MA; Patel JK; Kobashigawa JA; Kittleson MM
    Clin Transplant; 2022 Jun; 36(6):e14645. PubMed ID: 35293038
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genotype-phenotype correlations in alpha-sarcoglycanopathy: a systematic review.
    Carson L; Merrick D
    Ir J Med Sci; 2022 Dec; 191(6):2743-2750. PubMed ID: 35040091
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Orthotopic Heart Transplantation in Manifesting Carrier of Duchenne Muscular Dystrophy.
    Cullom C; Vo V; McCabe MD
    J Cardiothorac Vasc Anesth; 2022 Aug; 36(8 Pt A):2593-2599. PubMed ID: 34670720
    [No Abstract]   [Full Text] [Related]  

  • 26. Life Expectancy in Duchenne Muscular Dystrophy: Reproduced Individual Patient Data Meta-analysis.
    Broomfield J; Hill M; Guglieri M; Crowther M; Abrams K
    Neurology; 2021 Dec; 97(23):e2304-e2314. PubMed ID: 34645707
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.
    Alonso-Pérez J; González-Quereda L; Bruno C; Panicucci C; Alavi A; Nafissi S; Nilipour Y; Zanoteli E; Isihi LMA; Melegh B; Hadzsiev K; Muelas N; Vílchez JJ; Dourado ME; Kadem N; Kutluk G; Umair M; Younus M; Pegorano E; Bello L; Crawford TO; Suárez-Calvet X; Töpf A; Guglieri M; Marini-Bettolo C; Gallano P; Straub V; Díaz-Manera J
    Brain; 2022 Apr; 145(2):596-606. PubMed ID: 34515763
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Expanding Spectrum of Desmin-Related Myopathy, Long-term Follow-up, and Cardiac Transplantation.
    Shelly S; Talha N; Pereira NL; Engel AG; Johnson JN; Selcen D
    Neurology; 2021 Sep; 97(11):e1150-e1158. PubMed ID: 34315782
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy.
    Restrepo-Cordoba MA; Wahbi K; Florian AR; Jiménez-Jáimez J; Politano L; Arad M; Climent-Paya V; Garcia-Alvarez A; Hansen RB; Larrañaga-Moreira JM; Kubanek M; Lopes LR; Ros A; Jurcut R; Rasmussen TB; Ruiz-Guerrero L; Pribe-Wolferts R; Palomino-Doza J; Bilinska Z; Rodríguez-Palomares JF; Van Loon RLE; Basurte Elorz MT; Quarta G; Robledo Iñarritu M; Verdonschot JAJ; Stojkovic T; Shomanova Z; Bermudez-Jimenez F; Palladino A; Freimark D; García-Álvarez MI; Jorda P; Dominguez F; Ochoa JP; Girolami F; Brugada R; Meder B; Barriales-Villa R; Mogensen J; Laforêt P; Yilmaz A; Elliott P; Garcia-Pavia P;
    Eur J Heart Fail; 2021 Aug; 23(8):1276-1286. PubMed ID: 34050592
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Skeletal and Cardiac Muscle Disorders Caused by Mutations in Genes Encoding Intermediate Filament Proteins.
    Maggi L; Mavroidis M; Psarras S; Capetanaki Y; Lattanzi G
    Int J Mol Sci; 2021 Apr; 22(8):. PubMed ID: 33923914
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cardiac Arrhythmias in Muscular Dystrophies Associated with Emerinopathy and Laminopathy: A Cohort Study.
    Marchel M; Madej-Pilarczyk A; Tymińska A; Steckiewicz R; Ostrowska E; Wysińska J; Russo V; Grabowski M; Opolski G
    J Clin Med; 2021 Feb; 10(4):. PubMed ID: 33673224
    [TBL] [Abstract][Full Text] [Related]  

  • 32. New Insights in Adherence and Survival in Myotonic Dystrophy Patients Using Home Mechanical Ventilation.
    Seijger C; Raaphorst J; Vonk J; van Engelen B; Heijerman H; Stigter N; Wijkstra P
    Respiration; 2021; 100(2):154-163. PubMed ID: 33461194
    [TBL] [Abstract][Full Text] [Related]  

  • 33. LGMD. Identification, description and classification.
    Angelini C
    Acta Myol; 2020 Dec; 39(4):207-217. PubMed ID: 33458576
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Causes of clinical variability in Duchenne and Becker muscular dystrophies and implications for exon skipping therapies.
    Hoffman EP
    Acta Myol; 2020 Dec; 39(4):179-186. PubMed ID: 33458572
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death.
    Fischer B; Dittmann S; Brodehl A; Unger A; Stallmeyer B; Paul M; Seebohm G; Kayser A; Peischard S; Linke WA; Milting H; Schulze-Bahr E
    Int J Cardiol; 2021 Apr; 329():167-174. PubMed ID: 33373648
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy.
    Protonotarios A; Brodehl A; Asimaki A; Jager J; Quinn E; Stanasiuk C; Ratnavadivel S; Futema M; Akhtar MM; Gossios TD; Ashworth M; Savvatis K; Walhorn V; Anselmetti D; Elliott PM; Syrris P; Milting H; Lopes LR
    Can J Cardiol; 2021 Jun; 37(6):857-866. PubMed ID: 33290826
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies.
    Guimarães-Costa R; Fernández-Eulate G; Wahbi K; Leturcq F; Malfatti E; Behin A; Leonard-Louis S; Desguerre I; Barnerias C; Nougues MC; Isapof A; Estournet-Mathiaud B; Quijano-Roy S; Fayssoil A; Orlikowski D; Fauroux B; Richard I; Semplicini C; Romero NB; Querin G; Eymard B; Laforêt P; Stojkovic T
    Eur J Neurol; 2021 Feb; 28(2):660-669. PubMed ID: 33051934
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Homozygous Fukutin Missense Mutation in Two Mexican Siblings with Dilated Cardiomyopathy.
    Villarreal-mMolina MT; Rosas-Madrigal S; López-Mora E; Calderón-Avila AL; Rodríguez-Zanella H; Romero-Hidalgo S; Rosendo-Gutierrez R; Carnevale A
    Rev Invest Clin; 2020 May; 73(5):. PubMed ID: 33048919
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP related.
    Libell EM; Richardson JA; Lutz KL; Ng BY; Mockler SRH; Laubscher KM; Stephan CM; Zimmerman BM; Edens ER; Reinking BE; Mathews KD
    Muscle Nerve; 2020 Nov; 62(5):626-632. PubMed ID: 32914449
    [TBL] [Abstract][Full Text] [Related]  

  • 40. LAMA2-related muscular dystrophy: Natural history of a large pediatric cohort.
    Zambon AA; Ridout D; Main M; Mein R; Phadke R; Muntoni F; Sarkozy A
    Ann Clin Transl Neurol; 2020 Oct; 7(10):1870-1882. PubMed ID: 32910545
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.