Found: 34
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Atraumatic proximal radial nerve entrapment. Illustrative cases and systematic review of literature.
- Published in:
- European Journal of Orthopaedic Surgery & Traumatology, 2022, v. 32, n. 5, p. 811, doi. 10.1007/s00590-021-03037-6
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- Publication type:
- Article
Hepatitis E Virus and Neurologic Disorders.
- Published in:
- Emerging Infectious Diseases, 2011, v. 17, n. 2, p. 173, doi. 10.3201/eid1702.100856
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- Publication type:
- Article
Type 1 FSHD with 6–10 Repeated Units: Factors Underlying Severity in Index Cases and Disease Penetrance in Their Relatives Attention.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 6, p. 2221, doi. 10.3390/ijms21062221
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- Publication type:
- Article
Hepatitis E Virus Quasispecies in Cerebrospinal Fluid with Neurological Manifestations.
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- Vaccines, 2021, v. 9, n. 10, p. 1205, doi. 10.3390/vaccines9101205
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- Publication type:
- Article
Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect.
- Published in:
- 2018
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- Publication type:
- journal article
Prognostic factors for the sequelae and severity of Guillain-Barré syndrome in children.
- Published in:
- 2019
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- Publication type:
- journal article
Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria.
- Published in:
- 2018
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- Publication type:
- journal article
Chloride channel dysfunction study in myotonic dystrophy type 1 using repeated short exercise tests.
- Published in:
- 2016
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- Publication type:
- journal article
Clinical features and follow-up of four new cases of facial-onset sensory and motor neuronopathy.
- Published in:
- Muscle & Nerve, 2011, v. 43, n. 1, p. 136, doi. 10.1002/mus.21884
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- Publication type:
- Article
One Multilocus Genomic Variation Is Responsible for a Severe Charcot–Marie–Tooth Axonal Form.
- Published in:
- Brain Sciences (2076-3425), 2020, v. 10, n. 12, p. 986, doi. 10.3390/brainsci10120986
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- Publication type:
- Article
Comparison between a novel helical and a posterior ankle–foot orthosis on gait in people with unilateral foot drop: a randomised crossover trial.
- Published in:
- Journal of NeuroEngineering & Rehabilitation (JNER), 2023, v. 20, n. 1, p. 1, doi. 10.1186/s12984-023-01184-x
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- Publication type:
- Article
A Cardio-Neurological Form of Laminopathy: Dilated Cardiomyopathy with Permanent Partial Atrial Standstill and Axonal Neuropathy.
- Published in:
- 2009
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- Publication type:
- Case Study
Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral Dystrophy.
- Published in:
- 2022
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- Publication type:
- journal article
Hepatitis E Virus Infection: Neurological Manifestations and Pathophysiology.
- Published in:
- Pathogens, 2021, v. 10, n. 12, p. 1582, doi. 10.3390/pathogens10121582
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- Publication type:
- Article
Long‐term outcomes of paediatric Guillain–Barré syndrome.
- Published in:
- Developmental Medicine & Child Neurology, 2024, v. 66, n. 2, p. 176, doi. 10.1111/dmcn.15693
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- Publication type:
- Article
Hematopoietic stem cell transplantation in chronic inflammatory demyelinating polyneuropathy: French experience about four patients, under the behalf of French society for bone marrow transplantation.
- Published in:
- 2021
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- Publication type:
- Letter
Impact of tricuspid regurgitation on survival in patients with cardiac amyloidosis.
- Published in:
- ESC Heart Failure, 2021, v. 8, n. 1, p. 438, doi. 10.1002/ehf2.13093
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- Publication type:
- Article
Gateway and journey of patients with cardiac amyloidosis.
- Published in:
- ESC Heart Failure, 2020, v. 7, n. 5, p. 2418, doi. 10.1002/ehf2.12793
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- Publication type:
- Article
Hearing loss in inherited peripheral neuropathies: Molecular diagnosis by NGS in a French series.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 9, p. N.PAG, doi. 10.1002/mgg3.839
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- Publication type:
- Article
Which Method for Diagnosing Small Fiber Neuropathy?
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00342
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- Publication type:
- Article
Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registry.
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- European Journal of Neurology, 2024, v. 31, n. 10, p. 1, doi. 10.1111/ene.16428
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- Publication type:
- Article
Real‐life effectiveness 1 year after switching to avalglucosidase alfa in late‐onset Pompe disease patients worsening on alglucosidase alfa therapy: A French cohort study.
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- European Journal of Neurology, 2024, v. 31, n. 7, p. 1, doi. 10.1111/ene.16292
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- Publication type:
- Article
Clinical and electrophysiological characteristics of women with X‐linked Charcot–Marie–Tooth disease.
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- European Journal of Neurology, 2023, v. 30, n. 10, p. 3265, doi. 10.1111/ene.15937
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- Publication type:
- Article
Anti‐disialosyl‐immunoglobulin M chronic autoimmune neuropathies: a nationwide multicenter retrospective study.
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- European Journal of Neurology, 2022, v. 29, n. 12, p. 3547, doi. 10.1111/ene.15523
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- Publication type:
- Article
Phenotypical variability and atypical presentations in a French cohort of Andersen–Tawil syndrome.
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- European Journal of Neurology, 2022, v. 29, n. 8, p. 2398, doi. 10.1111/ene.15369
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- Publication type:
- Article
Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study.
- Published in:
- PLoS ONE, 2016, v. 11, n. 2, p. 1, doi. 10.1371/journal.pone.0148264
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- Publication type:
- Article
The FLNC Ala1186Val Variant Linked to Cytoplasmic Body Myopathy and Cardiomyopathy Causes Protein Instability.
- Published in:
- Biomedicines, 2024, v. 12, n. 2, p. 322, doi. 10.3390/biomedicines12020322
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- Publication type:
- Article
Continuous Monitoring of Middle Cerebral Artery Recanalization with Transcranial Color-Coded Sonography and Levovist.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2005, v. 19, n. 1, p. 55, doi. 10.1007/s11239-005-0940-6
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- Publication type:
- Article
Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in TPM2 and TPM3 Causing Congenital Myopathies.
- Published in:
- Human Mutation, 2014, v. 35, n. 7, p. 779, doi. 10.1002/humu.22554
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- Publication type:
- Article
Transfusion-acquired hepatitis E infection misdiagnosed as severe critical illness polyneuromyopathy in a heart transplant patient.
- Published in:
- Transplant Infectious Disease, 2017, v. 19, n. 6, p. n/a, doi. 10.1111/tid.12784
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- Publication type:
- Article
An Integrated Clinical-Biological Approach to Identify Interindividual Variability and Atypical Phenotype-Genotype Correlations in Myopathies: Experience on A Cohort of 156 Families.
- Published in:
- Genes, 2021, v. 12, n. 8, p. 1199, doi. 10.3390/genes12081199
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- Publication type:
- Article
Dry immersion as a model of deafferentation: A neurophysiology study using somatosensory evoked potentials.
- Published in:
- PLoS ONE, 2018, v. 13, n. 8, p. 1, doi. 10.1371/journal.pone.0201704
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- Publication type:
- Article
HEPATITIS E VIRUS AND NEUROLOGIC DISORDERS.
- Published in:
- Romanian Journal of Infectious Diseases / Revista Romana de de Boli Infectioase, 2011, v. 14, n. 1, p. 19
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- Publication type:
- Article
A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literature.
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- Journal of the Peripheral Nervous System, 2017, v. 22, n. 2, p. 77, doi. 10.1111/jns.12216
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- Publication type:
- Article