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Early weaning stress impairs development of mucosal barrier function in the porcine intestine

American journal of physiology: Gastrointestinal and liver physiology, 2010-03, Vol.298 (3), p.G352-G363

2010

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Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotype

Ultrasound in obstetrics & gynecology, 2022-12, Vol.60 (6), p.805-811

2022

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Prognostic value of contrast-enhanced MRI in Guillain-Barré syndrome in children

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2022-04, Vol.29 (3), p.230-235

2022

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Comparison of somatostatin receptor agonist and antagonist for peptide receptor radionuclide therapy: a pilot study

Journal of Nuclear Medicine, 2014-08, Vol.55 (8), p.1248-1252

2014

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First clinical evidence that imaging with somatostatin receptor antagonists is feasible

Journal of Nuclear Medicine, 2011-09, Vol.52 (9), p.1412-1417

2011

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Arthrogryposis in children: Etiological assessments and preparation of a protocol for etiological investigations

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2018-07, Vol.25 (5), p.322-326

2018

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Corrigendum to “22nd International Congress of the World Muscle Society, Saint Malo, France, 3rd–7th October 2017” [Neuromuscular Disorders 27S2 (2017) S51–S270]

Neuromuscular disorders : NMD, 2017-11, Vol.27 (11), p.e1-e1

2017

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Bilateral facial nerve palsy associated with Epstein-Barr virus infection in a 3-year-old boy

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2017-06, Vol.24 (6), p.564-567

2017

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Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations

Journal of medical genetics, 2008-10, Vol.45 (10), p.647-653

2008

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Central manifestations of dystrophinopathies

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2015-12, Vol.22 (12 Suppl 1), p.12S58-12S62

2015

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Benign paroxysmal tonic upgaze, benign paroxysmal torticollis, episodic ataxia and CACNA1A mutation in a family

Journal of neurology, 2008-10, Vol.255 (10), p.1600-1602

2008

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Severe cardiopathy in a patient with a new mutation of the fukutin gene with limb girdle phenotype

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S164-S164

2016

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Partial acute transverse myelitis is a predictor of multiple sclerosis in children

Multiple sclerosis, 2014-10, Vol.20 (11), p.1485-1493

2014

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Titin gene mutations presenting as centronuclear myophathies

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S113-S113

2016

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Optic neuritis in children: Prognostic factors and evolution. A retrospective study about 28 cases

European journal of paediatric neurology, 2017-06, Vol.21, p.e112-e112

2017

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Infantile facioscapulohumeral muscular dystrophy (FSHD): A severe multi-systemic disease

European journal of paediatric neurology, 2017-06, Vol.21, p.e94-e95

2017

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Unexpected neurological sequelae following propofol anesthesia in infants: Three case reports

Brain & development (Tokyo. 1979), 2010-11, Vol.32 (10), p.872-878

2010

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Congenital neuromuscular diseases with neonatal respiratory failure excluding myotonic dystrophy type 1 and infantile spinal muscular atrophy. Diagnosis strategy according to a 19-child series

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2016-09, Vol.23 (9), p.878-886

2016

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Pediatric cerebral venous thrombosis: Description and prognosis according to the physiopathological mechanism in a population of 40 cases

European journal of paediatric neurology, 2017-06, Vol.21, p.e174-e174

2017

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Infantile systemic hyalinosis

European journal of paediatric neurology, 2017-06, Vol.21, p.e199-e199

2017

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PP05.17 – 2757: Acute acquired nontraumatic VIth cranial nerve palsies in children: about 22 cases

European journal of paediatric neurology, 2015-05, Vol.19, p.S51-S51

2015

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Bilateral idiopathic calf muscle hypertrophy: An exceptional cause of unsightly leg curvature

Annales de chirurgie plastique et esthétique, 2015-04, Vol.60 (2), p.160-163

2015

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Juvenile xanthogranuloma with bilateral optic neuritis

British journal of ophthalmology, 2011-09, Vol.95 (9), p.1331-1332

2011

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L’encéphalomyopathie neuro-gastro-intestinale mitochondriale : un tableau d’anorexie mentale atypique

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2014-12, Vol.21 (12), p.1370-1374

2014

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Early weaning stress impairs development of mucosal barrier function in the porcine intestine

Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotype

Prognostic value of contrast-enhanced MRI in Guillain-Barré syndrome in children

Comparison of somatostatin receptor agonist and antagonist for peptide receptor radionuclide therapy: a pilot study

Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression

First clinical evidence that imaging with somatostatin receptor antagonists is feasible

Arthrogryposis in children: Etiological assessments and preparation of a protocol for etiological investigations

Corrigendum to “22nd International Congress of the World Muscle Society, Saint Malo, France, 3rd–7th October 2017” [Neuromuscular Disorders 27S2 (2017) S51–S270]

Bilateral facial nerve palsy associated with Epstein-Barr virus infection in a 3-year-old boy

Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations

Central manifestations of dystrophinopathies

Benign paroxysmal tonic upgaze, benign paroxysmal torticollis, episodic ataxia and CACNA1A mutation in a family

Severe cardiopathy in a patient with a new mutation of the fukutin gene with limb girdle phenotype

Partial acute transverse myelitis is a predictor of multiple sclerosis in children

Titin gene mutations presenting as centronuclear myophathies

Optic neuritis in children: Prognostic factors and evolution. A retrospective study about 28 cases

Infantile facioscapulohumeral muscular dystrophy (FSHD): A severe multi-systemic disease

Unexpected neurological sequelae following propofol anesthesia in infants: Three case reports

Congenital neuromuscular diseases with neonatal respiratory failure excluding myotonic dystrophy type 1 and infantile spinal muscular atrophy. Diagnosis strategy according to a 19-child series

Pediatric cerebral venous thrombosis: Description and prognosis according to the physiopathological mechanism in a population of 40 cases

Infantile systemic hyalinosis

PP05.17 – 2757: Acute acquired nontraumatic VIth cranial nerve palsies in children: about 22 cases

Bilateral idiopathic calf muscle hypertrophy: An exceptional cause of unsightly leg curvature

Juvenile xanthogranuloma with bilateral optic neuritis

L’encéphalomyopathie neuro-gastro-intestinale mitochondriale : un tableau d’anorexie mentale atypique

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