Keyword Connections

amyotrophic lateral sclerosis

Journals

10

1 Scientific reports

2 Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

3 acta neuropathologica communications

4 Journal of Alzheimer's disease : JAD

5 frontiers in neurology

6 Biochemistry and biophysics reports

7 Regenerative therapy

8 current alzheimer research

9 journal of neurology, neurosurgery, and psychiatry

10 neurotherapeutics : the journal of the american society for experimental neurotherapeutics

Research Groups

0

No Research Group Connected

Bibliographies

62

1 Development and assessment of the inter-rater and intra-rater reproducibility of a self-administration version of the ALSFRS-R.

2 Sarm1 deletion suppresses TDP-43-linked motor neuron degeneration and cortical spine loss.

3 Ropinirole hydrochloride remedy for amyotrophic lateral sclerosis - Protocol for a randomized, double-blind, placebo-controlled, single-center, and open-label continuation phase I/IIa clinical trial (ROPALS trial).

4 Elevated cerebrospinal fluid homocysteine is associated with blood-brain barrier disruption in amyotrophic lateral sclerosis patients.

5 A model for gain of function in superoxide dismutase.

6 risk agents related to work and amyotrophic lateral sclerosis: an occupational medicine focus

7 survival prediction in amyotrophic lateral sclerosis based on mri measures and clinical characteristics

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

9 epidural anesthesia combined with sedation with dexmedetomidine for appendectomy in a patient with amyotrophic lateral sclerosis: a case report

10 skeletal muscle satellite cells, mitochondria and micrornas: their involvement in the pathogenesis of als

11 molecular diagnostics of neurodegenerative disorders

12 the split hand sign

13 alterations in the stomatognathic system due to amyotrophic lateral sclerosis

14 sialorrhoea: how to manage a frequent complication of motor neuron disease

15 two case reports of an unusual association between klippel-feil syndrome and amyotrophic lateral sclerosis: do they share same genetic defect?

16 Withaferin-A Treatment Alleviates TAR DNA-Binding Protein-43 Pathology and Improves Cognitive Function in a Mouse Model of FTLD.

17 Molecular docking study of potential phytochemicals and their effects on the complex of SARS-CoV2 spike protein and human ACE2.

18 circadian rhythm dysfunction accelerates disease progression in a mouse model with amyotrophic lateral sclerosis

19 the involvement of micrornas in neurodegenerative diseases

20 lessons of als imaging: pitfalls and future directions — a critical review

21 the role of the innate immune system in als

22 vascular endothelial growth factor (vegf) prevents the downregulation of the cholinergic phenotype in axotomized motoneurons of the adult rat

23 Spinal cord pathology is ameliorated by P2X7 antagonism in a SOD1-mutant mouse model of amyotrophic lateral sclerosis

24 The multidimensional nature of dyspnoea in amyotrophic lateral sclerosis patients with chronic respiratory failure: Air hunger, anxiety and fear

25 Predicting Development of Amyotrophic Lateral Sclerosis in Frontotemporal Dementia.

26 Amyotrophic Lateral Sclerosis and Primary Biliary Cirrhosis Overlap Syndrome: Two Cases Report.

27 Autopsy findings in the early stage of amyotrophic lateral sclerosis with "dropped head" syndrome.

28 Stability of a chronic implanted brain-computer interface in late-stage amyotrophic lateral sclerosis

29 Split-hand index in amyotrophic lateral sclerosis: an F-wave study.

30 Dysphagia in amyotrophic lateral sclerosis: Impact on patient behavior, diet adaptation, and riluzole management

31 Information-seeking behavior and information needs in patients with amyotrophic lateral sclerosis

32 Is the evidence strong enough for acupuncture ameliorates clinical symptoms in patients with amyotrophic lateral sclerosis: A protocol for a systematic review and meta-analysis.

33 The role of gut microbiota, butyrate and proton pump inhibitors in amyotrophic lateral sclerosis: a systematic review.

34 Exploring sarcasm detection in amyotrophic lateral sclerosis using ecologically valid measures.

35 Exploring sarcasm detection in Amyotrophic Lateral Sclerosis using ecologically valid measures

36 The influence of metallothionein treatment and treadmill running exercise on disease onset and survival in SOD1 amyotrophic lateral sclerosis mice.

37 Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein.

38 Multi-disciplinary clinical protocol for the diagnosis of bulbar amyotrophic lateral sclerosis.

39 The established and emerging roles of astrocytes and microglia in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia.

40 Toward in vivo determination of peripheral nervous system immune activity in amyotrophic lateral sclerosis.

41 Amyotrophic lateral sclerosis with ophthalmoplegia and multisystem degeneration in patients on long-term use of respirators

42 Ultrastructural study of chromatolytic neurons in an adult-onset sporadic case of amyotrophic lateral sclerosis

43 Immunocytochemical and ultrastructural study of pericapillary rosettes in amyotrophic lateral sclerosis

44 adeno-associated viral vector delivered rnai for gene therapy of sod1 amyotrophic lateral sclerosis

45 the relationship between depressive symptoms, disease state, and cognition in amyotrophic lateral sclerosis.

46 dipals: diaphragm pacing in patients with amyotrophic lateral sclerosis – a randomised controlled trial

47 structural and diffusion imaging versus clinical assessment to monitor amyotrophic lateral sclerosis

48 an iranian familial amyotrophic lateral sclerosis pedigree with p.val48phe causing mutation in sod1: a genetic and clinical report

49 lack of association between nuclear factor erythroid-derived 2-like 2 promoter gene polymorphisms and oxidative stress biomarkers in amyotrophic lateral sclerosis patients

50 communication of diagnosis in amyotrophic lateral sclerosis: stratification of patients for the estimation of the individual needs

51 the utility of independent component analysis and machine learning in the identification of the amyotrophic lateral sclerosis diseased brain.

52 amyotrophic lateral sclerosis and multiple sclerosis overlap: a case report

53 administration of recombinant heat shock protein 70 delays peripheral muscle denervation in the sod1g93a mouse model of amyotrophic lateral sclerosis

54 writing errors and anosognosia in amyotrophic lateral sclerosis with dementia

55 increased il-17, a pathogenic link between hepatosplenic schistosomiasis and amyotrophic lateral sclerosis: a hypothesis

56 genetic correction of sod1 mutant ipscs reveals erk and jnk activated ap1 as a driver of neurodegeneration in amyotrophic lateral sclerosis

57 blood biomarkers for amyotrophic lateral sclerosis: myth or reality?

58 early gene expression changes in spinal cord from sod1g93a amyotrophic lateral sclerosis animal model

59 cellular and molecular mechanisms of motor neuron death in amyotrophic lateral sclerosis: a perspective

60 Correction to: A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features

61 A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features

62 Small peptide CSF fingerprint of amyotrophic lateral sclerosis.