Results 141 to 150 of about 73,071 (237)

Corticosteroid therapy in Duchenne muscular dystrophy: Management and new insights

Developmental Medicine &Child Neurology, Volume 68, Issue 3, Page 310-311, March 2026.
Claudia Brogna, Eugenio Mercuri
wiley   +1 more source

Duchennes muskeldystrofi

Tidsskrift for Den norske legeforening, 2014
Magnhild Rasmussen, Inger Lund-Petersen, Ellen J. Annexstad   +2 more
openaire   +1 more source

Early Cardiac Manifestations as the Initial Presentation of Duchenne Muscular Dystrophy in Infancy. [PDF]

Cureus
Shatarat F, Alkasasbeh J, Shatarat R, Tarawneh S.   +3 more
europepmc   +1 more source

An Assessment of Paediatricians' Knowledge and Perspectives of Duchenne Muscular Dystrophy in Oman. [PDF]

Sultan Qaboos Univ Med J
Al Jabri Z, Alsawaie M, Saki Malehi A, Al Futaisi A, Al-Amrani F.   +4 more
europepmc   +1 more source

State-of-the-Art Research and New Pharmacological Perspectives on Renal Involvement in Duchenne Muscular Dystrophy: A Narrative Review. [PDF]

Biomedicines
Bellis M, Imbrici P, Lenti R, Liantonio A, De Luca A.   +4 more
europepmc   +1 more source

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

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

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

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

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