Results 151 to 160 of about 73,992 (251)

Pan-immune-inflammation value as a predictor of loss of ambulation in duchenne muscular dystrophy: a retrospective cohort study. [PDF]

BMC Pediatr
Özgör B, Bıçakcıoğlu I, Tan M, Yücel G, Karadağ M, Güngör S.   +5 more
europepmc   +1 more source

The Achievement of Duchenne [PDF]

Proceedings of the Royal Society of Medicine, 1973
openaire   +2 more sources

Targeting autophagy in Duchenne muscular dystrophy: mechanistic insights and emerging therapeutic strategies. [PDF]

J Med Genet
Krishna L, Srivathsa A, Anand R, Rao A, Karnik M, Vishwanath P, Dharmashekar C, Kumar Honnavalli Y, Prashant A.   +8 more
europepmc   +1 more source

Neonatal screening for Duchenne muscular dystrophy in eastern China: a closed prospective study. [PDF]

Transl Pediatr
Qian G, Yang R, Huang X, Wu D, Fang K, Zhao Z.   +5 more
europepmc   +1 more source

Potential benefits of Ayurveda in Duchenne muscular Dystrophy: A case based analysis. [PDF]

J Ayurveda Integr Med
Puja MS, Jyothy KB, Kulkarni V, Srihari S.   +3 more
europepmc   +1 more source

Patient reported outcome measures in spinal muscular atrophy and duchenne muscular dystrophy: review of instruments and their inclusion in clinical and regulatory processes. [PDF]

Neurol Sci
Malandrini F, Spataro C, Meregaglia M, Sansone V, D'amico A, Scopinaro A, Ciani O.   +6 more
europepmc   +1 more source

Dystrophin-Deficient Cardiomyopathy Due to a Novel Hemizygous DMD Indel Variant. [PDF]

JACC Case Rep
Albrecht K, Averbuch T, Huculak C, Marcadier J, Oudit G, van Landeghem FKH, Adam B, Lyons KJ, Kiamanesh O.   +8 more
europepmc   +1 more source

Smiling and first impressions in ad hoc entrustment decisions: An avatar-based simulation study. [PDF]

GMS J Med Educ
Bauermann M, Schindler AK, Kuchenbaur M, Rühl J, Reinert P, Kunz M, Friedrich-Welz S, André E, Rotthoff T.   +8 more
europepmc   +1 more source

Dystrophic Skeletal Muscle Phenotypes Can Be Horizontally Transferred via Fecal Microbiome Transplantations. [PDF]

FASEB J
Butcher J, Gosse JT, Gobin J, Ravel-Chapuis A, Jasmin BJ, Stintzi A.   +5 more
europepmc   +1 more source

A Rare Co-occurrence of Duchenne Muscular Dystrophy and Glycerol Kinase Deficiency Associated With Xp21 Contiguous Gene Deletion Syndrome: A Case Report. [PDF]

Cureus
Marques L, Lipari Pinto P, Coelho J, Florindo C, Soeiro E Sá M, Rodrigues R, Sousa A, Gaspar A.   +7 more
europepmc   +1 more source