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Mashup Score: 78Clinical Reasoning: A 24-Year-Old Man With Gait Impairment, Hearing Loss, and Recurrent Fever | Neurology - 1 day(s) ago
We present a case study of a 24-year-old man who reported mild balance and walking difficulties for 2 years. He had a history of recurrent fever, skin lesions, headache, and elbow pain, but most of these events resolved spontaneously. There was no …
Source: www.neurology.orgCategories: General Medicine News, NeurologyTweet
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Mashup Score: 14
Dr. Derek Stitt talks with Dr. Adam de Havenon about the burden of neurologic health care and incident neurologic diagnoses in the year after COVID-19 vs influenza. Read the related article in . This podcast is sponsored by argenx. Visit for more information. Disclosures can be found at .
Source: directory.libsyn.comCategories: General Medicine News, NeurologyTweet-
Neurology Podcast: Dr. Derek Stitt and Dr. Adam de Havenon discuss the burden of neurologic health care and incident neurologic diagnoses in the year after COVID-19 vs influenza. Listen now: https://t.co/N6QdJZzy2F Article: https://t.co/ZTPdhzbtWE #NeuroTwitter @brainsnthingz https://t.co/ms2FyMMd9L
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Mashup Score: 59Neurology: Vol 102, No 9 - 1 day(s) ago
Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’ Choice Disputes & Debates: Editors’
Source: www.neurology.orgCategories: General Medicine News, NeurologyTweet
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Mashup Score: 64Clinical and Genetic Characterization of a Cohort of Brazilian Patients With Congenital Ataxia | Neurology Genetics - 2 day(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 …
Source: www.neurology.orgCategories: General Medicine News, NeurologyTweet
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Mashup Score: 43Resident & Fellow Section Recruiting | Neurology® Journals - 2 day(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
Source: www.neurology.orgCategories: General Medicine News, NeurologyTweet
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Mashup Score: 48Reversibility of Cognitive Deficits and Functional Connectivity With Transfusion in Children With Sickle Cell Disease | Neurology - 2 day(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 …
Source: www.neurology.orgCategories: General Medicine News, NeurologyTweet
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Mashup Score: 113Radiologic Lag and Brain MRI Lesion Dynamics During Attacks in MOG Antibody–Associated Disease | Neurology - 2 day(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: 96
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: 95
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 …
Source: www.neurology.orgCategories: General Medicine News, NeurologyTweet
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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
Source: www.neurology.orgCategories: General Medicine News, NeurologyTweet
Test your clinical reasoning with this case of a 24-year-old man with gait impairment, hearing loss, and recurrent fever: https://t.co/wsisKfRkoI #NeurologyRF #NeuroTwitter https://t.co/aTCW1KIJyM