Search Results

Display Settings
Results per page: 10
Sort By: Relevance
Filter
  • 1-10 of  24,448 results for ""Muscular Dystrophy, Duchenne""

Your Filters

Reset filters
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

Deletion of exons 45 to 55 in the DMD gene: from the therapeutic perspective to the in vitro model.

  • Authors : Poyatos-García J; Neuromuscular and Ataxias Research Group, Health Research Institute Hospital La Fe (IIS La Fe), Valencia, Spain. .; Centre for Biomedical Network Research on Rare Diseases (CIBERER), CB23/07/00005, Madrid, Spain. .

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/therapy ; Dystrophin*/Dystrophin*/Dystrophin*/genetics

  • Source: Skeletal muscle [Skelet Muscle] 2024 Oct 01; Vol. 14 (1), pp. 21. Date of Electronic Publication: 2024 Oct 01.Publisher: BioMed Central Ltd Country of Publication: England NLM ID: 101561193 Publication Model: Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

Diarylpropionitrile-stimulated ERβ nuclear accumulation promotes MyoD-induced muscle regeneration in mdx mice by interacting with FOXO3A.

  • Authors : Tong H; New drug screening center, Jiangsu Center for Pharmacodynamics Research and Evaluation, State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China.; Fan S

Subjects: Mice, Inbred mdx* ; Estrogen Receptor beta*/Estrogen Receptor beta*/Estrogen Receptor beta*/genetics ; Estrogen Receptor beta*/Estrogen Receptor beta*/Estrogen Receptor beta*/metabolism

  • Source: Pharmacological research [Pharmacol Res] 2024 Oct; Vol. 208, pp. 107376. Date of Electronic Publication: 2024 Aug 30.Publisher: Elsevier Country of Publication: Netherlands NLM ID: 8907422 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

Equitable Access of Delandistrogene Moxeparvovec for Patients With Duchenne Muscular Dystrophy: A Call for Discussion.

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/drug therapy; Humans

  • Source: Pediatric neurology [Pediatr Neurol] 2024 Oct; Vol. 159, pp. 33-34. Date of Electronic Publication: 2024 Jul 30.Publisher: Elsevier Science Publishing Country of Publication: United States NLM ID: 8508183 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

A case of Duchenne muscular dystrophy recovered from prolonged ischemic kidney injury which emerged with a normal creatinine level.

  • Authors : Daikoku K; Department of Nephrology and Endocrinology, Osaki Citizen Hospital, 3-8-1, Furukawahonami, Osaki, Miyagi, 989-6183, Japan. .; Kondo H

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/complications ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/diagnosis ; Creatinine*/Creatinine*/Creatinine*/blood

  • Source: CEN case reports [CEN Case Rep] 2024 Oct; Vol. 13 (5), pp. 397-402. Date of Electronic Publication: 2024 Mar 04.Publisher: Springer Japan Country of Publication: Japan NLM ID: 101636244 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Editorial & Opinion

Whether tamoxifen is beneficial for cardiac dysfunction in Duchenne muscular dystrophy requires appropriately designed studies.

  • Authors : Finsterer J; Neurology Dpt, Neurology & Neurophysiology Center, Postfach 20, 1180, Vienna, Austria. .; Stollberger C

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/drug therapy ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/complications ; Tamoxifen*/Tamoxifen*/Tamoxifen*/therapeutic use

  • Source: European journal of pediatrics [Eur J Pediatr] 2024 Oct; Vol. 183 (10), pp. 4585-4586. Date of Electronic Publication: 2024 Aug 05.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7603873 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

A Case Report of Becker Muscular Dystrophy and Stroke Who Successfully Regained Mobility With Robot-Assisted Gait Training.

  • Authors : Tay SS; From the Department of Rehabilitation Medicine, Changi General Hospital, Singapore.; Zainul Abideen AB

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/rehabilitation ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/complications ; Stroke Rehabilitation*/Stroke Rehabilitation*/Stroke Rehabilitation*/methods

  • Source: American journal of physical medicine & rehabilitation [Am J Phys Med Rehabil] 2024 Oct 01; Vol. 103 (10), pp. e137-e140. Date of Electronic Publication: 2024 Apr 29.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 8803677 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

The relationship between lower urinary system symptoms and the level of independence and quality of life in children with Duchenne muscular dystrophy.

  • Authors : Öztürk D; Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Lokman Hekim University, 06530, Ankara, Turkey. .; Faculty of Physical Therapy and Rehabilitation, Hacettepe University, Ankara, Turkey. .

Subjects: Lower Urinary Tract Symptoms*/Lower Urinary Tract Symptoms*/Lower Urinary Tract Symptoms*/etiology ; Lower Urinary Tract Symptoms*/Lower Urinary Tract Symptoms*/Lower Urinary Tract Symptoms*/diagnosis ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/complications

  • Source: Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2024 Oct; Vol. 39 (10), pp. 3005-3012. Date of Electronic Publication: 2024 Jun 01.Publisher: Springer International Country of Publication: Germany NLM ID: 8708728 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

Chimeric Cell Therapy Transfers Healthy Donor Mitochondria in Duchenne Muscular Dystrophy.

  • Authors : Siemionow M; Chair and Department of Traumatology, Orthopedics and Surgery of the Hand, Poznan University of Medical Sciences, Poznan, 61‑545, Poland. .; Dystrogen Therapeutics Technology Polska z o.o., Warsaw, 00-777, Poland. .

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/therapy ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/metabolism

  • Source: Stem cell reviews and reports [Stem Cell Rev Rep] 2024 Oct; Vol. 20 (7), pp. 1819-1829. Date of Electronic Publication: 2024 Jul 17.Publisher: Springer Country of Publication: United States NLM ID: 101752767 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

Predictors of cardiac disease in duchenne muscular dystrophy: a systematic review and evidence grading.

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/drug therapy ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics; Humans

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Sep 28; Vol. 19 (1), pp. 359. Date of Electronic Publication: 2024 Sep 28.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

Record details

Read More Add to Saved list
×
Academic Journal

CRISPR-mediated megabase-scale transgene de-duplication to generate a functional single-copy full-length humanized DMD mouse model.

  • Authors : Chey YCJ; School of Biomedicine and Robinson Research Institute, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, SA, Australia.; Genome Editing Program, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/therapy ; Mice, Transgenic*

  • Source: BMC biology [BMC Biol] 2024 Sep 27; Vol. 22 (1), pp. 214. Date of Electronic Publication: 2024 Sep 27.Publisher: BioMed Central Country of Publication: England NLM ID: 101190720 Publication Model: Electronic Cited Medium: Internet ISSN: 1741-7007

Record details

Read Online Read More Add to Saved list
×
  • 1-10 of  24,448 results for ""Muscular Dystrophy, Duchenne""