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ÉPILEPSIE DE L'ENFANT ET DE L'ADULTE: Partie 1 / Épilepsie de l'enfant = Epilepsy of the childDE SAINT-MARTIN, Anne; LAUGEL, Vincent.La Revue du praticien (Paris). 2014, Vol 64, Num 5, pp 701-705, issn 0035-2640, 5 p.Article

Épilepsies de l'enfant : choix des antiépileptiques et surveillanceDE SAINT-MARTIN, Anne; LAUGEL, Vincent; HIRSCH, Edouard et al.MTP. Médecine thérapeutique pédiatrie. 2006, Vol 9, Num 5-6, pp 313-324, issn 1286-5494, 12 p.Article

Daily on-line haemodiafiltration: a pilot trial in childrenFISCHBACH, Michel; TERZIC, Joëlle; LAUGEL, Vincent et al.Nephrology, dialysis, transplantation (Print). 2004, Vol 19, Num 9, pp 2360-2367, issn 0931-0509, 8 p.Article

Effect of peritoneal dialysis fluid composition on peritoneal area available for exchange in childrenFISCHBACH, Michel; TERZIC, Joëlle; CHAUVE, Sylvie et al.Nephrology, dialysis, transplantation (Print). 2004, Vol 19, Num 4, pp 925-932, issn 0931-0509, 8 p.Article

A Pediatric Case of Fisher-Bickerstaff SpectrumTSAPIS, Michael; LAUGEL, Vincent; KOOB, Meriam et al.Pediatric neurology. 2010, Vol 42, Num 2, pp 147-150, issn 0887-8994, 4 p.Article

Myotubular myopathy caused by multiple abnormal splicing variants in the MTM1 RNA in a patient with a mild phenotypeVASLI, Nasim; LAUGEL, Vincent; BÖHM, Johann et al.European journal of human genetics. 2012, Vol 20, Num 6, pp 701-704, issn 1018-4813, 4 p.Article

The influence of peritoneal surface area on dialysis adequacyFISCHBACH, Michel; DHEU, Céline; HELMS, Pauline et al.Peritoneal dialysis international. 2005, Vol 25, pp S137-S140, issn 0896-8608, SUP3Article

Early-onset ophthalmoplegia in leigh-like syndrome due to NDUFV1 mutationsLAUGEL, Vincent; THIS-BERND, Valérie; CORMIER-DAIRE, Valérie et al.Pediatric neurology. 2007, Vol 36, Num 1, pp 54-57, issn 0887-8994, 4 p.Article

ARX Polyalanine Expansions Are Highly Implicated in Familial Cases of Mental Retardation With Infantile Epilepsy and/or Hand DystoniaCOSSEE, Mireille; FAIVRE, Laurence; DEMEER, Bénédicte et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 1, pp 98-105, issn 1552-4825, 8 p.Article

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorderLEEN, Wilhelmina G; KLEPPER, Joerg; BEKHOF, Jolita et al.Brain. 2010, Vol 133, pp 655-670, issn 0006-8950, 16 p., 3Article

The onset of acute oxcarbazepine toxicity related to prescription of clarithromycin in a child with refractory epilepsySANTUCCI, Raoul; FOTHERGILL, Helen; LAUGEL, Vincent et al.British journal of clinical pharmacology. 2010, Vol 69, Num 3, pp 314-316, issn 0306-5251, 3 p.Article

Deletion of 5' sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndromeLAUGEL, Vincent; DALLOZ, Cecile; DOLLFUS, Helene et al.European journal of human genetics. 2008, Vol 16, Num 3, pp 320-327, issn 1018-4813, 8 p.Article

Incidence of DNA repair deficiency disorders in western Europe : Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophyKLEIJER, Wim J; LAUGEL, Vincent; BERNEBURG, Mark et al.DNA repair. 2008, Vol 7, Num 5, pp 744-750, issn 1568-7864, 7 p.Article

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