Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Julie Leydet"'
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Partial acute transverse myelitis is a predictor of multiple sclerosis in children
Autor: R Cheminal, Y Mikaeloff, Pierre Meyer, N. Molinari, Gilles Cambonie, Nicolas Leboucq, G. Rondouin, Julie Leydet, Ulrike Walther-Louvier, Kumaran Deiva, François Rivier, D Cuntz-Shadfar, Agathe Roubertie, B. Echenne, Maryline Carneiro
Publikováno v: Multiple Sclerosis Journal
Multiple Sclerosis Journal, SAGE Publications, 2014, 20 (11), pp.1485-1493. ⟨10.1177/1352458514526943⟩
Multiple Sclerosis Journal, 2014, 20 (11), pp.1485-1493. ⟨10.1177/1352458514526943⟩
Background: Acute transverse myelitis (ATM) in children is a rare and often severe disease for which there are few known prognostic factors, particularly the subsequent risk of multiple sclerosis (MS) diagnosis. Objectives: To determine the clinical
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2036eb22cb33aee428c75eca7ed2462d
https://hal.umontpellier.fr/hal-02544667/document
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4
Benign paroxysmal vertigo of childhood: long-term outcome
Autor: Bernard Echenne, Agathe Roubertie, Benjamin Krams, Julie Leydet, François Rivier
Publikováno v: Cephalalgia : an international journal of headache. 31(4)
Introduction Benign paroxysmal vertigo (BPV) is characterized by recurrent attacks of dizziness in a healthy child. Complete recovery typically takes place during childhood, and an epidemiological link with migraine has been pointed out. Nevertheless
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3677500243f4659345b383baa2a0217d
https://pubmed.ncbi.nlm.nih.gov/20851837
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5
Monoamine metabolism study in severe, early-onset epilepsy in childhood
Autor: Bernard, Echenne, Agathe, Roubertie, Julie, Leydet, François, Rivier, Georg Friedrich, Hoffmann
Publikováno v: Epileptic disorders : international epilepsy journal with videotape. 10(2)
To investigate the possible dysfunction of monoamine metabolism in patients with early-onset, epileptic encephalopathies.The CSF dopamine, serotonin and biopterin metabolites were studied in 37 patients with severe, mostly drug-resistant epilepsy.No
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3444e8098dc753467a508110a439bc57
https://pubmed.ncbi.nlm.nih.gov/18539563
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6
Partial epilepsy and 47,XXX karyotype: report of four cases
Autor: Bernard Echenne, Agathe Roubertie, Julie Leydet, Véronique Humbertclaude, Geneviève Lefort
Publikováno v: Pediatric neurology. 35(1)
Epilepsy is a common finding in chromosomal imbalances, but only a few chromosome abnormalities have a characteristic electro-clinical pattern. Trisomy X is one of the most common sex chromosome abnormalities in females, and is associated with consid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cb1d03a7022f02e46d14b060d3213ae
https://pubmed.ncbi.nlm.nih.gov/16814091
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7
Trouble de l’attention avec ou sans hyperactivité (TDAH) : état des lieux des ressources dédiées à la prise en charge des enfants atteints sur le territoire français. Coopération entre les différents professionnels de santé
Autor: Sagnes, Caroline
Publikováno v: Médecine humaine et pathologie. 2021
Le TDAH (Trouble de l’Attention avec ou sans Hyperactivité) est l’un des troubles du neurodéveloppement les plus fréquents chez l’enfant, avec un impact majeur sur la vie sociale et scolaire. Nous avons étudié les ressources à disposition
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2592::acee227791ee08bf7574bad599bb1f36
https://dumas.ccsd.cnrs.fr/dumas-03429613
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