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Mashup Score: 26Clinical and Genetic Characterization of a Cohort of Brazilian Patients With Congenital Ataxia | Neurology Genetics - 10 hour(s) ago
Background and ObjectivesCongenital ataxias are rare hereditary disorders characterized by hypotonia and developmental motor delay in the first few months of life, followed by cerebellar ataxia in early childhood. The course of the disease is …
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Mashup Score: 43Resident & Fellow Section Recruiting | Neurology® Journals - 10 hour(s) ago
The Neurology Resident & Fellow Editors are seeking applications from neurology residents to serve a three-year term on the Neurology Resident & Fellow Section Editorial Board. Responsibilities will begin in September 2024 and include reviewing manuscripts, generating ideas for the section, and participating in monthly conference calls. New members are expected to dedicate an estimated 3 hours per month to the section. Residents should have excellent communication and interpersonal skills with demonstrated
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Mashup Score: 26Reversibility of Cognitive Deficits and Functional Connectivity With Transfusion in Children With Sickle Cell Disease | Neurology - 12 hour(s) ago
Background and ObjectivesPeople with sickle cell disease (SCD) are at risk of cognitive dysfunction independent of stroke. Diminished functional connectivity in select large-scale networks and white matter integrity reflect the neurologic consequences of …
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Mashup Score: 41Diagnosis and Treatment of Spontaneous Intracranial Hypotension: Role of Epidural Blood Patching: Neurology Clinical Practice: Vol 14, No 3 - 15 hour(s) ago
Purpose of ReviewThis review focuses on the challenges of diagnosing and treating spontaneous intracranial hypotension (SIH), a condition caused by spinal CSF leakage. It emphasizes the need for increased awareness and advocates for early and thoughtful …
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Mashup Score: 60Radiologic Lag and Brain MRI Lesion Dynamics During Attacks in MOG Antibody–Associated Disease | Neurology - 16 hour(s) ago
Background and ObjectivesKnowledge of the evolution of CNS demyelinating lesions within attacks could assist diagnosis. We evaluated intra-attack lesion dynamics in patients with myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD) vs …
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Mashup Score: 89
ObjectivesMyelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD) is an autoimmune demyelinating disease rarely associated with malignancy. We report the clinical, MRI, immunopathology, and treatment response in a person with MOGAD and …
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Mashup Score: 3
ObjectivesHeterozygous missense variants in MYBPC1 have been recently identified in 13 patients from 6 families with congenital myopathy with tremor. All the patients had mild skeletal myopathy invariably associated with a distinctive myogenic tremor and …
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Mashup Score: 3
Objective: To report interim results of a TREM2 (triggering receptor expressed on myeloid cells 2) agonist from the first interventional study in ALSP. Background: ALSP is a rare, fatal, inherited, autosomal-dominant, rapidly progressing …
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Mashup Score: 92
Background and ObjectivesPathogenic variants in NOTCH3 are the main cause of hereditary cerebral small vessel disease (SVD). SVD-associated NOTCH3 variants have recently been categorized into high risk (HR), moderate risk (MR), or low risk (LR) for …
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Mashup Score: 100
View all available purchase options and get full access to this article. DeLorey DS. Sympathetic vasoconstriction in skeletal muscle: modulatory effects of aging, exercise training, and sex. Appl Physiol Nutr Metab. 2021;46(12):1437-1447. Barker D, Saito M. Autonomic innerva tion of receptors and muscle fibres in cat skeletal muscle. Proc R Soc Lond B Biol Sci. 1981;212(1188):317-332. Roatta S, Windhorst U, Ljubisavljevic M, Johansson H, Passatore M. Sympathetic modulation of muscle spindle afferent
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Clinical and Genetic Characterization of a Cohort of Brazilian Patients With Congenital Ataxia: https://t.co/rxpTy2sXgg #NeuroTwitter #NeuroGenetics https://t.co/FXEr0TlkaM