Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 62

1.

Spatially localized phosphorous metabolism of skeletal muscle in Duchenne muscular dystrophy patients: 24-month follow-up.

Hooijmans MT, Doorenweerd N, Baligand C, Verschuuren JJGM, Ronen I, Niks EH, Webb AG, Kan HE.

PLoS One. 2017 Aug 1;12(8):e0182086. doi: 10.1371/journal.pone.0182086. eCollection 2017.

2.

Short (16-mer) locked nucleic acid splice-switching oligonucleotides restore dystrophin production in Duchenne Muscular Dystrophy myotubes.

Pires VB, Simões R, Mamchaoui K, Carvalho C, Carmo-Fonseca M.

PLoS One. 2017 Jul 24;12(7):e0181065. doi: 10.1371/journal.pone.0181065. eCollection 2017.

3.

WHOLE-BODY VIBRATION EXERCISE IS WELL TOLERATED IN PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW.

Moreira-Marconi E, Sá-Caputo DC, Dionello CF, Guedes-Aguiar EO, Sousa-Gonçalves CR, Morel DS, Paineiras-Domingos LL, Souza PL, Kütter CR, Costa-Cavalcanti RG, Costa G, Paiva PC, Figueiredo C, Brandão-Sobrinho-Neto S, Stark C, Unger M, Bernardo-Filho M.

Afr J Tradit Complement Altern Med. 2017 Jul 7;14(4 Suppl):2-10. doi: 10.21010/ajtcam.v14i4S.1. eCollection 2017. Review.

4.

Noninvasive Respiratory Care Received by Individuals With Duchenne Muscular Dystrophy Since 1979.

Bach J, Goncalves M, Chiou M, Hart N, Toussaint M.

Respir Care. 2017 Aug;62(8):1120-1121. doi: 10.4187/respcare.05635. No abstract available.

PMID:
28733320
5.

Central Arterial Function Measured by Non-invasive Pulse Wave Analysis is Abnormal in Patients with Duchenne Muscular Dystrophy.

Ryan TD, Parent JJ, Gao Z, Khoury PR, Dupont E, Smith JN, Wong B, Urbina EM, Jefferies JL.

Pediatr Cardiol. 2017 Aug;38(6):1269-1276. doi: 10.1007/s00246-017-1657-y. Epub 2017 Jun 21.

PMID:
28639151
6.

Pulmonary Endpoints in Duchenne Muscular Dystrophy. A Workshop Summary.

Finder J, Mayer OH, Sheehan D, Sawnani H, Abresch RT, Benditt J, Birnkrant DJ, Duong T, Henricson E, Kinnett K, McDonald CM, Connolly AM.

Am J Respir Crit Care Med. 2017 Aug 15;196(4):512-519. doi: 10.1164/rccm.201703-0507WS. Review.

PMID:
28636407
7.

Platelet-Derived Growth Factor BB Influences Muscle Regeneration in Duchenne Muscle Dystrophy.

Piñol-Jurado P, Gallardo E, de Luna N, Suárez-Calvet X, Sánchez-Riera C, Fernández-Simón E, Gomis C, Illa I, Díaz-Manera J.

Am J Pathol. 2017 Aug;187(8):1814-1827. doi: 10.1016/j.ajpath.2017.04.011. Epub 2017 Jun 12.

PMID:
28618254
8.

Variations in Duchenne muscular dystrophy course in a multi-ethnic UK population: potential influence of socio-economic factors.

Hufton M, Roper H.

Dev Med Child Neurol. 2017 Aug;59(8):837-842. doi: 10.1111/dmcn.13460. Epub 2017 May 16.

PMID:
28509411
9.

Potential Therapeutic Action of Adiponectin in Duchenne Muscular Dystrophy.

Abou-Samra M, Boursereau R, Lecompte S, Noel L, Brichard SM.

Am J Pathol. 2017 Jul;187(7):1577-1585. doi: 10.1016/j.ajpath.2017.02.018. Epub 2017 Apr 29.

PMID:
28463682
10.

Two Cases of Duchenne Muscular Dystrophy That Showed Different Reactions to Nerve Stimulation During Peripheral Nerve Block: A Case Report.

So M, Sugiura T, Yoshizawa S, Sobue K.

A A Case Rep. 2017 Jul 15;9(2):52-53. doi: 10.1213/XAA.0000000000000524.

PMID:
28459722
11.

Relationship Between Fragmented QRS Complexes and Cardiac Status in Duchenne Muscular Dystrophy: Multimodal Validation Using Echocardiography, Magnetic Resonance Imaging, and Holter Monitoring.

Cho MJ, Lee JW, Lee J, Shin YB, Lee HD.

Pediatr Cardiol. 2017 Jun;38(5):1042-1048. doi: 10.1007/s00246-017-1616-7. Epub 2017 Apr 29.

PMID:
28456833
12.

Sleep Disordered Breathing in Duchenne Muscular Dystrophy.

LoMauro A, D'Angelo MG, Aliverti A.

Curr Neurol Neurosci Rep. 2017 May;17(5):44. doi: 10.1007/s11910-017-0750-1. Review.

PMID:
28397169
13.

Rocuronium-induced neuromuscular block and sugammadex in pediatric patient with duchenne muscular dystrophy: A case Report.

Kim JE, Chun HR.

Medicine (Baltimore). 2017 Mar;96(13):e6456. doi: 10.1097/MD.0000000000006456.

14.

Eteplirsen in the treatment of Duchenne muscular dystrophy.

Lim KR, Maruyama R, Yokota T.

Drug Des Devel Ther. 2017 Feb 28;11:533-545. doi: 10.2147/DDDT.S97635. eCollection 2017. Review.

15.

A rare subclinical or mild type of Becker muscular dystrophy caused by a single exon 48 deletion of the dystrophin gene.

Zimowski JG, Pilch J, Pawelec M, Purzycka JK, Kubalska J, Ziora-Jakutowicz K, Dudzińska M, Zaremba J.

J Appl Genet. 2017 Aug;58(3):343-347. doi: 10.1007/s13353-017-0391-8. Epub 2017 Feb 28.

16.

Quantitative muscle ultrasound detects disease progression in Duchenne muscular dystrophy.

Zaidman CM, Wu JS, Kapur K, Pasternak A, Madabusi L, Yim S, Pacheck A, Szelag H, Harrington T, Darras BT, Rutkove SB.

Ann Neurol. 2017 May;81(5):633-640. doi: 10.1002/ana.24904. Epub 2017 May 4.

PMID:
28241384
17.

Characterization of a Blood Spot Creatine Kinase Skeletal Muscle Isoform Immunoassay for High-Throughput Newborn Screening of Duchenne Muscular Dystrophy.

Moat SJ, Korpimäki T, Furu P, Hakala H, Polari H, Meriö L, Mäkinen P, Weeks I.

Clin Chem. 2017 Apr;63(4):908-914. doi: 10.1373/clinchem.2016.268425. Epub 2017 Feb 16.

PMID:
28209627
18.

Skeletal muscle secretome in Duchenne muscular dystrophy: a pivotal anti-inflammatory role of adiponectin.

Lecompte S, Abou-Samra M, Boursereau R, Noel L, Brichard SM.

Cell Mol Life Sci. 2017 Jul;74(13):2487-2501. doi: 10.1007/s00018-017-2465-5. Epub 2017 Feb 10.

19.

Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy.

Wang H, Xu Y, Liu X, Wang L, Jiang W, Xiao B, Wei W, Chen Y, Ye W, Ji X.

Prenat Diagn. 2017 Apr;37(4):356-364. doi: 10.1002/pd.5019. Epub 2017 Mar 6.

PMID:
28181689
20.

Predictors of Health-Related Quality of Life in boys with Duchenne muscular dystrophy from six European countries.

Otto C, Steffensen BF, Højberg AL, Barkmann C, Rahbek J, Ravens-Sieberer U, Mahoney A, Vry J, Gramsch K, Thompson R, Rodger S, Bushby K, Lochmüller H, Kirschner J.

J Neurol. 2017 Apr;264(4):709-723. doi: 10.1007/s00415-017-8406-2. Epub 2017 Feb 7.

PMID:
28175989

Supplemental Content

Loading ...
Support Center