BMJ open

frontiers in neurology

[1] Developing a web-based patient decision aid for gastrostomy in motor neuron disease: a study protocol.

[2] Routine Cerebrospinal Fluid (CSF) Parameters in Patients With Spinal Muscular Atrophy (SMA) Treated With Nusinersen.

[3] the relationship between depressive symptoms, disease state, and cognition in amyotrophic lateral sclerosis.

[4] increasing agrin function antagonizes muscle atrophy and motor impairment in spinal muscular atrophy

[5] sialorrhoea: how to manage a frequent complication of motor neuron disease

[6] gemins: potential therapeutic targets for spinal muscular atrophy?

[7] endovascular treatment of a basilar artery dissecting aneurysm fasciculações benignas responsivas à gabapentina

[8] a systematic review and meta-analysis of the funtional mri investigation of motor neuron disease

[9] inducing chronic excitotoxicity in the mouse spinal cord to investigate lower motor neuron degeneration

[10] neuromuscular junctions as key contributors and therapeutic targets in spinal muscular atrophy

[11] Small GSK-3 Inhibitor Shows Efficacy in a Motor Neuron Disease Murine Model Modulating Autophagy.

[12] Developing a web-based patient decision aid for gastrostomy in motor neuron disease: a study protocol.

[13] Immunohistochemical identification of messenger RNA-related proteins in basophilic inclusions of adult-onset atypical motor neuron disease

[14] Heparan sulfate-like immunoreactivity in the spinal cord in motor neuron disease

[15] Gene expression analysis of frontotemporal lobar degeneration of the motor neuron disease type with ubiquitinated inclusions

[16] Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration

[17] TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease

[18] Motor neuron disease clinically limited to the lower motor neuron is a diffuse TDP-43 proteinopathy

[19] focus on the role of d-serine and d-amino acid oxidase in amyotrophic lateral sclerosis/motor neuron disease (als)

[20] sialorrhoea: how to manage a frequent complication of motor neuron disease

[21] primary hyperparathyroidism simulating motor neuron disease: case report hiperparatiroidismo primário simulando doença do neurônio motor: relato de caso

[22] natural history of motor neuron disease in adult onset gm2-gangliosidosis: a case report with 25 years of follow-up

[23] a case of camptocormia (bent spine) secondary to early motor neuron disease

[24] a systematic review and meta-analysis of the funtional mri investigation of motor neuron disease

[25] man-in-the-barrel syndrome, a symmetrical proximal brachial amyotrophic diplegia related to motor neuron diseases: a survey of nine cases síndrome do homem no barril, uma diplegia amiotrófica braquial proximal simétrica relacionada a doença do neurônio motor: a propósito de nove casos