المؤلفون: Noemi Pellegrino, Daniela Pietrobon, Marianna Gabriella Rispoli, Filippo Brighina, Vincenzo Di Stefano, Eleonora Rotondo, Christian Napoli, Pasquale Parisi, Alessandro Graziosi

المساهمون: Di Stefano V., Rispoli M.G., Pellegrino N., Graziosi A., Rotondo E., Napoli C., Pietrobon D., Brighina F., Parisi P.

المصدر: Journal of Neurology, Neurosurgery, and Psychiatry

مصطلحات موضوعية: Weakness, medicine.medical_specialty, Migraine with Aura, Electroencephalography, Motor symptoms, Diagnosis, Differential, clinical neurology, EEG, headache, ion transport, 03 medical and health sciences, 0302 clinical medicine, Physical medicine and rehabilitation, Intellectual disability, medicine, Humans, Migraine, 030304 developmental biology, 0303 health sciences, Cerebellar ataxia, medicine.diagnostic_test, business.industry, Disease Management, medicine.disease, Pedigree, Clinical neurology, Impaired consciousness, Psychiatry and Mental health, Mutation, Hemiplegic migraine, Settore MED/26 - Neurologia, Surgery, Calcium Channels, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbcdb78bdd31a48f81520a207b3dc13bTest
https://doi.org/10.1136/jnnp-2020-322850Test

المؤلفون: Maria Vittoria De Angelis, Vincenzo Di Stefano, Marianna Gabriella Rispoli, Elide Mantuano

المساهمون: Rispoli M.G., Di Stefano V., Mantuano E., De Angelis M.V.

المصدر: BMJ case reports 12 (2019). doi:10.1136/bcr-2019-231129.
info:cnr-pdr/source/autori:Rispoli M.G; Di Stefano V.; Mantuano E.; De Angelis M.V./titolo:Novel missense mutation in the ATP1A2 gene associated with atypical sporapedic hemiplegic migraine/doi:10.1136%2Fbcr-2019-231129./rivista:BMJ case reports/anno:2019/pagina_da:/pagina_a:/intervallo_pagine:/volume:12
BMJ Case Rep

مصطلحات موضوعية: Male, Weakness, Pediatrics, medicine.medical_specialty, Ataxia, Neurology, Migraine with Aura, Mutation, Missense, Neuroimaging, neuro genetics, Diagnosis, Differential, 03 medical and health sciences, 0302 clinical medicine, Rare Disease, ATP1A2, medicine, Humans, Missense mutation, genetic screening / counselling, 030212 general & internal medicine, Migraine, Aged, Neurologic Examination, Genetic counselling, Cerebellar ataxia, business.industry, Headache, General Medicine, Magnetic Resonance Imaging, Migraine with aura, Pedigree, Hemiparesis, Settore MED/26 - Neurologia, Sodium-Potassium-Exchanging ATPase, medicine.symptom, business, headache (including migraines), 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39c559960227e4156cddbc5830b94a6eTest
https://casereports.bmj.com/content/12/10/e231129Test