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Two affected boys in a Rett syndrome family: clinical and molecular findings

Neurology, 2000-10, Vol.55 (8), p.1188-1193

2000

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Cell cloning‐based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes

Journal of cellular and molecular medicine, 2010-07, Vol.14 (7), p.1962-1974

2010

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AP4M1 mutations in patients with epilepsy

European journal of paediatric neurology, 2017-06, Vol.21, p.e105-e105

2017

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A new anterior approach to the Sciatic nerve block

Anesthesiology (Philadelphia), 1999-12, Vol.91 (6), p.1655-1660

1999

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Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia

Neurology, 2005-11, Vol.65 (9), p.1364-1369

2005

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Causes génétiques des retards mentaux : aspects génétiques et moléculaires des syndromes de Prader-Willi/Angelman et du syndrome X fragile

Revue neurologique, 2007-04, Vol.163 (4), p.248-248

Chelly, J.

2007

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Impact de la notion d’allergie à la pénicilline sur le pronostic des patients hospitalisés en réanimation pour une infection sévère

Médecine et maladies infectieuses, 2017-06, Vol.47 (4), p.S56-S56

2017

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Doublecortin, a Stabilizer of Microtubules

Human molecular genetics, 1999-09, Vol.8 (9), p.1599-1610

1999

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Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)

Human molecular genetics, 1998-07, Vol.7 (7), p.1063-1070

1998

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Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH

Journal of medical genetics, 2006-04, Vol.43 (4), p.362-370

2006

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Maternal origin of a novel C-terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome

Clinical genetics, 2006-07, Vol.70 (1), p.29-33

2006

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The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome

Neurology, 2008-05, Vol.70 (22 Pt 2), p.2145-2151

2008

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Continuous femoral blocks improve recovery and outcome of patients undergoing total knee arthroplasty

The Journal of arthroplasty, 2001-06, Vol.16 (4), p.436-445

2001

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Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathy

Journal of medical genetics, 2008-03, Vol.45 (3), p.172-178

2008

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Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia

Journal of medical genetics, 2007-11, Vol.44 (11), p.739-744

2007

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Clonage du gène responsable de la maladie de Menkes

M.S. Médecine sciences, 1993, Vol.9 (3), p.316

Chelly, J.

1993

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Stimulating or conventional perineural catheters after hallux valgus repair: a double-blind, pharmaco-economic evaluation

Acta anaesthesiologica Scandinavica, 2006-11, Vol.50 (10), p.1284-1289

2006

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Lidocaine versus ropivacaine for continuous interscalene brachial plexus block after open shoulder surgery

Acta anaesthesiologica Scandinavica, 2003-03, Vol.47 (3), p.355-360

2003

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The onset time of rocuronium is slowed by esmolol and accelerated by ephedrine

Anesthesia and analgesia, 2000-05, Vol.90 (5), p.1217-1219

2000

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Epidemiology of Weaning Outcome according to a New Definition. The WIND Study

American journal of respiratory and critical care medicine, 2017-03, Vol.195 (6), p.772-783

2017

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Intravascular Complications of Central Venous Catheterization by Insertion Site

The New England journal of medicine, 2015-09, Vol.373 (13), p.1220-1229

2015

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G.P.281

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.901-902

2014

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Illegitimate Transcription: Transcription of Any Gene in Any Cell Type

Proceedings of the National Academy of Sciences - PNAS, 1989-04, Vol.86 (8), p.2617-2621

1989

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The safety and efficacy of a fentanyl patient-controlled transdermal system for acute postoperative analgesia: A multicenter, placebo-controlled trial

Anesthesia and analgesia, 2004-02, Vol.98 (2), p.427-433

2004

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Identification du gène DYNC1H1 impliqué dans les malformations corticales grâce à l’étude de l’exome de 11 patients

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2013-04, Vol.20 (4), p.424-424

2013

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Two affected boys in a Rett syndrome family: clinical and molecular findings

Cell cloning‐based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes

AP4M1 mutations in patients with epilepsy

A new anterior approach to the Sciatic nerve block

Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia

Causes génétiques des retards mentaux : aspects génétiques et moléculaires des syndromes de Prader-Willi/Angelman et du syndrome X fragile

Impact de la notion d’allergie à la pénicilline sur le pronostic des patients hospitalisés en réanimation pour une infection sévère

Doublecortin, a Stabilizer of Microtubules

Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)

Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH

Maternal origin of a novel C-terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome

The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome

Continuous femoral blocks improve recovery and outcome of patients undergoing total knee arthroplasty

Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathy

Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia

Clonage du gène responsable de la maladie de Menkes

Stimulating or conventional perineural catheters after hallux valgus repair: a double-blind, pharmaco-economic evaluation

Lidocaine versus ropivacaine for continuous interscalene brachial plexus block after open shoulder surgery

The onset time of rocuronium is slowed by esmolol and accelerated by ephedrine

Epidemiology of Weaning Outcome according to a New Definition. The WIND Study

Intravascular Complications of Central Venous Catheterization by Insertion Site

G.P.281

Illegitimate Transcription: Transcription of Any Gene in Any Cell Type

The safety and efficacy of a fentanyl patient-controlled transdermal system for acute postoperative analgesia: A multicenter, placebo-controlled trial

Identification du gène DYNC1H1 impliqué dans les malformations corticales grâce à l’étude de l’exome de 11 patients

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