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 *

120 related articles for article (PubMed ID: 34595143)

  • 1. Case Report: The Genetic Diagnosis of Duchenne Muscular Dystrophy in the Middle East.
    Alghamdi F; Al-Tawari A; Alrohaif H; Alshuaibi W; Mansour H; Aartsma-Rus A; Mégarbané A
    Front Pediatr; 2021; 9():716424. PubMed ID: 34595143
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond.
    Elbashir H; Fathalla W; Mundada V; Iqbal M; Al Tawari AA; Chandratre S; Bastaki L; Romany I; Ismayl O; Abou Tayoun A
    J Neuromuscul Dis; 2022; 9(6):787-801. PubMed ID: 36245386
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comprehensive genetic analysis of 961 unrelated Duchenne Muscular Dystrophy patients: Focus on diagnosis, prevention and therapeutic possibilities.
    Kumar SH; Athimoolam K; Suraj M; Das Christu Das MS; Muralidharan A; Jeyam D; Ashokan J; Karthikeyan P; Krishna R; Khanna-Gupta A; Bremadesam Raman L
    PLoS One; 2020; 15(6):e0232654. PubMed ID: 32559196
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Current management of Duchenne muscular dystrophy in the Middle East: expert report.
    Jumah MA; Muhaizea MA; Rumayyan AA; Saman AA; Shehri AA; Cupler E; Jan M; Madani AA; Fathalla W; Kashyape P; Kodavooru G; Thihli KA; Bastaki L; Megarbane A; Skrypnyk C; Zamani G; Tuffery-Giraud S; Urtizberea A; Ortez González CI
    Neurodegener Dis Manag; 2019 Jun; 9(3):123-133. PubMed ID: 31166138
    [No Abstract]   [Full Text] [Related]  

  • 5. Reliability and validity of the Thai version of the Pediatric Quality of Life inventory™ 3.0 Duchenne Muscular Dystrophy module in Thai children with Duchenne Muscular Dystrophy.
    Thongsing A; Likasitwattanakul S; Sanmaneechai O
    Health Qual Life Outcomes; 2019 May; 17(1):76. PubMed ID: 31046775
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A comparative study of care practices for young boys with Duchenne muscular dystrophy between Japan and European countries: Implications of early diagnosis.
    Takeuchi F; Komaki H; Yamagata Z; Maruo K; Rodger S; Kirschner J; Kubota T; Kimura E; Takeda S; Gramsch K; Vry J; Bushby K; Lochmüller H; Wada K; Nakamura H
    Neuromuscul Disord; 2017 Oct; 27(10):894-904. PubMed ID: 28807665
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic diagnosis as a tool for personalized treatment of Duchenne muscular dystrophy.
    Bello L; Pegoraro E
    Acta Myol; 2016 Dec; 35(3):122-127. PubMed ID: 28484312
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.
    Zhang J; Ma D; Liu G; Wang Y; Liu A; Li L; Luo C; Hu P; Xu Z
    BMC Med Genet; 2019 Nov; 20(1):180. PubMed ID: 31727011
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Clinical practice guidelines for Duchenne muscular dystrophy].
    Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association ; Tan H; Liang D; Wu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Mar; 37(3):258-262. PubMed ID: 32128741
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Progress in treatment and newborn screening for Duchenne muscular dystrophy and spinal muscular atrophy.
    Ke Q; Zhao ZY; Mendell JR; Baker M; Wiley V; Kwon JM; Alfano LN; Connolly AM; Jay C; Polari H; Ciafaloni E; Qi M; Griggs RC; Gatheridge MA
    World J Pediatr; 2019 Jun; 15(3):219-225. PubMed ID: 30904991
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dysphagia in Duchenne muscular dystrophy: practical recommendations to guide management.
    Toussaint M; Davidson Z; Bouvoie V; Evenepoel N; Haan J; Soudon P
    Disabil Rehabil; 2016 Oct; 38(20):2052-62. PubMed ID: 26728920
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identifying Non-Duchenne Muscular Dystrophy-Positive and False Negative Results in Prior Duchenne Muscular Dystrophy Newborn Screening Programs: A Review.
    Gatheridge MA; Kwon JM; Mendell JM; Scheuerbrandt G; Moat SJ; Eyskens F; Rockman-Greenberg C; Drousiotou A; Griggs RC
    JAMA Neurol; 2016 Jan; 73(1):111-6. PubMed ID: 26594870
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Anesthetic complications. The incidence of severe anesthetic complications in patients and families with progressive muscular dystrophy of the Duchenne and Becker types].
    Breucking E; Reimnitz P; Schara U; Mortier W
    Anaesthesist; 2000 Mar; 49(3):187-95. PubMed ID: 10788987
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical management of Duchenne muscular dystrophy: the state of the art.
    Messina S; Vita GL
    Neurol Sci; 2018 Nov; 39(11):1837-1845. PubMed ID: 30218397
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy].
    Zhao W; Jiang N; Li S; Li JS; Miao Y; Liang SY; Yu DY
    Zhonghua Fu Chan Ke Za Zhi; 2019 Apr; 54(4):226-231. PubMed ID: 31006187
    [No Abstract]   [Full Text] [Related]  

  • 16. A current approach to heart failure in Duchenne muscular dystrophy.
    D'Amario D; Amodeo A; Adorisio R; Tiziano FD; Leone AM; Perri G; Bruno P; Massetti M; Ferlini A; Pane M; Niccoli G; Porto I; D'Angelo GA; Borovac JA; Mercuri E; Crea F
    Heart; 2017 Nov; 103(22):1770-1779. PubMed ID: 28668906
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements.
    D'Amico A; Catteruccia M; Baranello G; Politano L; Govoni A; Previtali SC; Pane M; D'Angelo MG; Bruno C; Messina S; Ricci F; Pegoraro E; Pini A; Berardinelli A; Gorni K; Battini R; Vita G; Trucco F; Scutifero M; Petillo R; D'Ambrosio P; Ardissone A; Pasanisi B; Vita G; Mongini T; Moggio M; Comi GP; Mercuri E; Bertini E
    Neuromuscul Disord; 2017 May; 27(5):447-451. PubMed ID: 28262469
    [TBL] [Abstract][Full Text] [Related]  

  • 18. De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in Germany.
    König K; Pechmann A; Thiele S; Walter MC; Schorling D; Tassoni A; Lochmüller H; Müller-Reible C; Kirschner J
    Orphanet J Rare Dis; 2019 Jun; 14(1):152. PubMed ID: 31234869
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular diagnosis of Duchenne muscular dystrophy.
    Nallamilli BR; Ankala A; Hegde M
    Curr Protoc Hum Genet; 2014 Oct; 83():9.25.1-29. PubMed ID: 25271841
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A checklist for clinical trials in rare disease: obstacles and anticipatory actions-lessons learned from the FOR-DMD trial.
    Crow RA; Hart KA; McDermott MP; Tawil R; Martens WB; Herr BE; McColl E; Wilkinson J; Kirschner J; King WM; Eagle M; Brown MW; Hirtz D; Lochmuller H; Straub V; Ciafaloni E; Shieh PB; Spinty S; Childs AM; Manzur AY; Morandi L; Butterfield RJ; Horrocks I; Roper H; Flanigan KM; Kuntz NL; Mah JK; Morrison L; Darras BT; von der Hagen M; Schara U; Wilichowski E; Mongini T; McDonald CM; Vita G; Barohn RJ; Finkel RS; Wicklund M; McMillan HJ; Hughes I; Pegoraro E; Bryan Burnette W; Howard JF; Thangarajh M; Campbell C; Griggs RC; Bushby K; Guglieri M
    Trials; 2018 May; 19(1):291. PubMed ID: 29793540
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.