Neuroimaging in hereditary neuromuscular disorders: a literature review and clinical case reports

Clinical features of fatigue in amyotrophic lateral sclerosis

Phenotype expansion, or double trouble: the combination of congenital disorder of glycosylation type 1i and Joubert syndrome type 17

Assessment of social emotional, cognitive and communicative development and adaptive behavior in children with spinal muscular atrophy 5q

Overlap of myasthenia gravis, myocarditis, and inflammatory myopathy secondary to immune checkpoint inhibitor (pembrolizumab) on a background of previously undiagnosed thymoma-associated acetylcholine receptor antibody-positive myasthenia gravis

Results of rehabilitation of myasthenia gravis patients with subclinical respiratory disturbances

Neuroimaging in hereditary neuromuscular disorders: a literature review and clinical case reports

Clinical features of fatigue in amyotrophic lateral sclerosis

Phenotype expansion, or double trouble: the combination of congenital disorder of glycosylation type 1i and Joubert syndrome type 17

Assessment of social emotional, cognitive and communicative development and adaptive behavior in children with spinal muscular atrophy 5q

Overlap of myasthenia gravis, myocarditis, and inflammatory myopathy secondary to immune checkpoint inhibitor (pembrolizumab) on a background of previously undiagnosed thymoma-associated acetylcholine receptor antibody-positive myasthenia gravis

Results of rehabilitation of myasthenia gravis patients with subclinical respiratory disturbances