| Nome |
# |
|
Antibodies to neurofascin, contactin-1, and contactin-associated protein 1 in CIDP: Clinical relevance of IgG isotype, file e0feeaa9-8461-44d2-e053-6605fe0a8db0
|
143
|
|
Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study, file e0feeaa5-6d67-44d2-e053-6605fe0a8db0
|
133
|
|
Protein misfolding, amyotrophic lateral sclerosis and guanabenz: Protocol for a phase II RCT with futility design (ProMISe trial), file e0feeaa7-00b5-44d2-e053-6605fe0a8db0
|
130
|
|
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis, file e0feeaa9-359b-44d2-e053-6605fe0a8db0
|
105
|
|
Functioning and quality of life in patients with neuropathy associated with anti-MAG antibodies, file e0feeaa9-4347-44d2-e053-6605fe0a8db0
|
98
|
|
The MITOS system predicts long-term survival in amyotrophic lateral sclerosis, file e0feeaa8-c6c8-44d2-e053-6605fe0a8db0
|
92
|
|
C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten, file e0feeaa9-d1fb-44d2-e053-6605fe0a8db0
|
86
|
|
Next-generation sequencing approach to hyperCKemia: A 2-year cohort study, file e0feeaa8-a0b3-44d2-e053-6605fe0a8db0
|
84
|
|
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis, file e0feeaab-29d1-44d2-e053-6605fe0a8db0
|
77
|
|
Frequency and time to relapse after discontinuing 6-month therapy with IVIg or pulsed methylprednisolone in CIDP, file e0feeaab-c811-44d2-e053-6605fe0a8db0
|
66
|
|
A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation, file e0feeaab-27af-44d2-e053-6605fe0a8db0
|
57
|
|
Primary antiphospholipid syndrome during aromatase inhibitors therapy: A case report and review of the literature, file e0feeaa9-8e4e-44d2-e053-6605fe0a8db0
|
52
|
|
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients, file e0feeaab-d5cb-44d2-e053-6605fe0a8db0
|
41
|
|
Rare POMC Mutation in a Patient With Myotonic Dystrophy Type 1 and Adrenocorticotropin Hyperresponse to Corticotropin-Releasing Hormone, file e0feeaa7-f4b9-44d2-e053-6605fe0a8db0
|
37
|
|
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis, file e0feeaab-21a0-44d2-e053-6605fe0a8db0
|
34
|
|
BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration, file 2988c75e-1bce-4484-9fa3-64d30ae94126
|
18
|
|
Genetic architecture of ALS in Sardinia, file e0feeaa5-59c5-44d2-e053-6605fe0a8db0
|
14
|
|
Electrodiagnosis in cranial botulism, file e0feeaa5-b75a-44d2-e053-6605fe0a8db0
|
12
|
|
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene, file e0feeaab-c8b8-44d2-e053-6605fe0a8db0
|
11
|
|
Sporadic hereditary motor and sensory neuropathies: Advances in the diagnosis using next generation sequencing technology, file e0feeaa6-2181-44d2-e053-6605fe0a8db0
|
9
|
|
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients, file e0feeaab-be38-44d2-e053-6605fe0a8db0
|
9
|
|
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations, file c9114381-b1e5-44d0-bbee-25b70246a747
|
7
|
|
Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort, file e0feeaa6-21c0-44d2-e053-6605fe0a8db0
|
7
|
|
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients, file e0feeaa5-5d14-44d2-e053-6605fe0a8db0
|
6
|
|
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study, file e0feeaa4-eb15-44d2-e053-6605fe0a8db0
|
4
|
|
Treatment for ulnar neuropathy at the elbow, file e0feeaa5-923a-44d2-e053-6605fe0a8db0
|
4
|
|
Oxidative stress-induced apoptosis in peripheral blood lymphocytes from patients with POLG-related disorders, file e0feeaa6-2eb9-44d2-e053-6605fe0a8db0
|
4
|
|
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene, file e0feeaa7-5b31-44d2-e053-6605fe0a8db0
|
4
|
|
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD, file e0feeaa7-9a05-44d2-e053-6605fe0a8db0
|
4
|
|
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation, file e0feeaa8-14ba-44d2-e053-6605fe0a8db0
|
4
|
|
Skeletal-Muscle Metabolic Reprogramming in ALS-SOD1G93A Mice Predates Disease Onset and Is A Promising Therapeutic Target, file efcc9038-2506-4ec6-a6d6-feaa7fb2a691
|
4
|
|
CT and MRI of Wernicke's encephalopathy, file e0feeaa4-d05e-44d2-e053-6605fe0a8db0
|
3
|
|
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72, file e0feeaa4-e2e7-44d2-e053-6605fe0a8db0
|
3
|
|
Antiangiogenic VEGF isoform in inflammatory myopathies, file e0feeaa5-2ba2-44d2-e053-6605fe0a8db0
|
3
|
|
Italian multicentre study of peroneal mononeuropathy: Multiperspective follow-up, file e0feeaa7-9248-44d2-e053-6605fe0a8db0
|
3
|
|
Major motor-functional determinants associated with poor self-reported health-related quality of life in myasthenia gravis patients, file e0feeaa9-e9c4-44d2-e053-6605fe0a8db0
|
3
|
|
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD, file e0feeaa4-cf45-44d2-e053-6605fe0a8db0
|
2
|
|
null, file e0feeaa5-b8f0-44d2-e053-6605fe0a8db0
|
2
|
|
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients, file e0feeaa6-0469-44d2-e053-6605fe0a8db0
|
2
|
|
TBK1 is associated with ALS and ALS-FTD in Sardinian patients, file e0feeaa6-0ba0-44d2-e053-6605fe0a8db0
|
2
|
|
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years, file e0feeaa6-16b4-44d2-e053-6605fe0a8db0
|
2
|
|
Polysomnographic characterization of pergolide-induced sleep attacks in idiopathic PD., file e0feeaa7-3cde-44d2-e053-6605fe0a8db0
|
2
|
|
Multicentre study of peroneal mononeuropathy: Multiperspective follow-up of nonsurgical cases, file e0feeaa7-9ae6-44d2-e053-6605fe0a8db0
|
2
|
|
Study of total duration of distal compound muscle action potential in demyelinating and axonal Guillain-Barre' syndrome, file 5db36c2c-04fc-47c7-8818-60573fc3e247
|
1
|
|
Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial, file e0feeaa4-c8ca-44d2-e053-6605fe0a8db0
|
1
|
|
Effects of immunotherapy on motor cortex excitability in Stiff Person Syndrome, file e0feeaa4-c8f2-44d2-e053-6605fe0a8db0
|
1
|
|
Prevalence and characteristics of peripheral neuropathy in hepatitis C virus population., file e0feeaa4-c927-44d2-e053-6605fe0a8db0
|
1
|
|
FUS mutations in sporadic amyotrophic lateral sclerosis, file e0feeaa4-daa8-44d2-e053-6605fe0a8db0
|
1
|
|
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay., file e0feeaa4-ea5e-44d2-e053-6605fe0a8db0
|
1
|
|
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population, file e0feeaa4-efef-44d2-e053-6605fe0a8db0
|
1
|
|
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study, file e0feeaa4-eff0-44d2-e053-6605fe0a8db0
|
1
|
|
Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies., file e0feeaa5-0266-44d2-e053-6605fe0a8db0
|
1
|
|
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis, file e0feeaa5-0952-44d2-e053-6605fe0a8db0
|
1
|
|
null, file e0feeaa5-6e51-44d2-e053-6605fe0a8db0
|
1
|
|
null, file e0feeaa5-6fbe-44d2-e053-6605fe0a8db0
|
1
|
|
Rhabdomyolysis in an elderly multitreated patient: multiple drug interactions after statin withdrawal, file e0feeaa5-9fd5-44d2-e053-6605fe0a8db0
|
1
|
|
Eosinophilia-associated muscle disorders:an immunohistological study with tissue localisation of major basic protein in distinct clinicopathological forms, file e0feeaa5-df44-44d2-e053-6605fe0a8db0
|
1
|
|
Wernicke Encephalopathy After Gastrointestinal Surgery for Cancer: Causes of Diagnostic Failure or Delay., file e0feeaa7-962a-44d2-e053-6605fe0a8db0
|
1
|
|
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation, file e0feeaa8-3c0a-44d2-e053-6605fe0a8db0
|
1
|
|
Sustained response to subcutaneous immunoglobulins in chronic ataxic neuropathy with anti-disialosyl IgM antibodies (CANDA): report of two cases and review of the literature, file e0feeaa8-cccd-44d2-e053-6605fe0a8db0
|
1
|
|
A new mutation in DNM2 gene in a large Italian family, file e0feeaa9-321d-44d2-e053-6605fe0a8db0
|
1
|
|
The Italian multicenter experience with edaravone in amyotrophic lateral sclerosis, file e0feeaa9-676b-44d2-e053-6605fe0a8db0
|
1
|
|
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients, file e0feeaaa-6321-44d2-e053-6605fe0a8db0
|
1
|
|
Different saccadic profile in bulbar versus spinal-onset 1 amyotrophic lateral sclerosis, file e0feeaab-b905-44d2-e053-6605fe0a8db0
|
1
|
| Totale |
1.406 |