Suchergebnisse - "Gitiaux, Cyril"

PubPharm (115)

91

Clinical characteristics, management and outcomes in patients with juvenile dermatomyositis requiring admission in pediatric intensive care unit

enthalten in: Pediatric rheumatology | 2014

von Besancon, A. | Gitiaux, C. | Brochard, K. | +7

92

Hemiconvulsion-hemiplegia syndrome revisited : longitudinal MRI findings in 10 children

enthalten in: Developmental medicine and child neurology | 2013

von Barcia, G. | Desguerre, I. | Carmona, O. | +7

CommentIn: Dev Med Child Neurol. 2013 Dec;55(12):1073-4. - PMID 23924305

93

Early electro-clinical features may contribute to diagnosis of the anti-NMDA receptor encephalitis in children

enthalten in: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology | 2013

von Gitiaux, C. | Simonnet, H. | Eisermann, M. | +14

ErratumIn: Clin Neurophysiol. 2014 Jun;125(6):1288

94

Hemiconvulsion–hemiplegia syndrome revisited: longitudinal MRI findings in 10 children

enthalten in: Developmental medicine & child neurology | 2013

von Barcia, G. | Desguerre, I. | Carmona, O. | +7

95

Brain magnetic resonance imaging pattern and outcome in children with haemolytic-uraemic syndrome and neurological impairment treated with eculizumab

enthalten in: Developmental medicine and child neurology | 2013

von Gitiaux, C. | Krug, P. | Grevent, D. | +7

CommentIn: Dev Med Child Neurol. 2013 Aug;55(8):687-8. - PMID 23659611

96

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

enthalten in: Nature genetics | 2013

von Poirier, K. | Lebrun, N. | Broix, L. | +32

97

Brain magnetic resonance imaging pattern and outcome in children with haemolytic‐uraemic syndrome and neurological impairment treated with eculizumab

enthalten in: Developmental medicine & child neurology | 2013

von Gitiaux, C. | Krug, P. | Grevent, D. | +7

98

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

enthalten in: Nature genetics | 2013

von Poirier, K. | Lebrun, N. | Broix, L. | +32

ErratumIn: Nat Genet. 2013 Aug;45(8):962

99

Diaphragmatic weakness with progressive sensory and motor polyneuropathy : case report of a neonatal IGHMBP2-related neuropathy

enthalten in: Journal of child neurology | 2013

von Gitiaux, C. | Bergounioux, J. | Magen, M. | +4

100

Diaphragmatic Weakness With Progressive Sensory and Motor Polyneuropathy: Case Report of a Neonatal IGHMBP2-Related Neuropathy

enthalten in: Journal of child neurology | 2013

von Gitiaux, C. | Bergounioux, J. | Magen, M. | +4

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