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Effect of intermittent glutamine supplementation on skeletal muscle is not long-lasting in very old rats

The Journal of nutrition, health & aging, 2013, Vol.17 (10), p.876-879

2013

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Prenatal diagnosis of thrombosis of the dural sinuses: report of six cases, review of the literature and suggested management

Ultrasound in obstetrics & gynecology, 2008-08, Vol.32 (2), p.188-198

2008

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Long-term intermittent glutamine supplementation repairs intestinal damage (structure and functional mass) with advanced age: Assessment with plasma citrulline in a rodent model

The Journal of nutrition, health & aging, 2014, Vol.18 (9), p.814-819

2014

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Contribution of immature muscle precursors to myositis pathogenesis: a source of type I interferon and a possible target of the immune attack

Annals of the rheumatic diseases, 2012-02, Vol.71 (Suppl 1), p.A43-A43

2012

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The challenge of prenatal identification of congenital diaphragmatic hernia in the context of hydrops

European Journal of Obstetrics & Gynecology and Reproductive Biology, 2014-11, Vol.182, p.238-239

2014

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Long-term intermittent glutamine supplementation repairs intestinal damage (structure and functional mass) with advanced age: Assessment with plasma citrulline in a rodent model

The Journal of nutrition, health & aging, 2014-11, Vol.18 (9), p.814-819

2014

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Recurrent congenital pulmonary lymphangiectasia

Ultrasound in obstetrics & gynecology, 2008-04, Vol.31 (4), p.479-481

2008

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Fetal umbilical cord ligation under ultrasound guidance

Ultrasound in obstetrics & gynecology, 1994-09, Vol.4 (5), p.399-401

1994

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Prenatal detection of mosaic isochromosome 20q: a fourth report with abnormal phenotype

Prenatal diagnosis, 2005-08, Vol.25 (8), p.653-655

2005

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Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p

Prenatal diagnosis, 2008-02, Vol.28 (2), p.131-134

2008

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First‐trimester features of Fowler syndrome (hydrocephaly–hydranencephaly proliferative vasculopathy)

Ultrasound in obstetrics & gynecology, 2002-12, Vol.20 (6), p.612-615

2002

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OP03.16: Prenatal detection of thromboses of the dural sinuses: report of five cases, diagnosis and outcome

Ultrasound in obstetrics & gynecology, 2006-09, Vol.28 (4), p.437-437

2006

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Pancreatic involvement in Wegener's granulomatosis: a rare and difficult diagnosis

La revue de medecine interne, 2006-02, Vol.27 (2), p.144-147

2006

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X-linked myopathy with excessive autophagy: a clinicopathological study of five new families

Neuromuscular disorders : NMD, 2001-05, Vol.11 (4), p.376-388

2001

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Congenital Adrenal Hypoplasia Due to Isolated Familial ACTH Deficiency

Fetal and pediatric pathology, 1994, Vol.14 (2), p.377-380

1994

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Sudden unexpected death in an infant due to a ruptured coronary aneurysm revealing Kawasaki disease

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2002-12, Vol.9 (12), p.1248-1251

2002

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Diagnostic anténatal des tumeurs cérébrales fœtales et diagnostics différentiels

Journal de gynécologie, obstétrique et biologie de la reproduction, 2013-05, Vol.42 (3), p.290-296

2013

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Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease

Kidney international, 2010-02, Vol.77 (4), p.350-358

2010

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Prenatal diagnosis of cerebral tumors and differential diagnosis

Journal de gynecologie, obstetrique et biologie de la reproduction, 2013-05, Vol.42 (3), p.290

2013

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P009: Corpus callosum or not corpus callosum? Lobar holoprosencephaly associated with a mimicking corpus callosum: value of “the anterior cerebral artery crawling under the skull”

Ultrasound in obstetrics & gynecology, 2003, Vol.22 (S1), p.73-73

2003

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P345: Twin to twin transfusion syndrome (TTTS) in momoamniotic monochorionic pregnancies (MAMC) does exist: proposition of antenatal surveillance

Ultrasound in obstetrics & gynecology, 2003, Vol.22 (S1), p.164-164

2003

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Les atteintes pancréatiques au cours de la granulomatose de Wegener : une localisation rare et un diagnostic difficile

La revue de medecine interne, 2006-02, Vol.27 (2), p.144-147

2006

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Mort subite chez un nourrisson par rupture d’anévrisme coronarien révélatrice d’une maladie de Kawasaki

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2002-12, Vol.9 (12), p.1248-1251

2002

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Une observation familiale d'ophtalmoplégie externe chronique progressive liée à une mitochondriopathie

Journal français d'ophtalmologie, 2001, Vol.24 (9), p.961-965

2001

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Trois bonnes raisons de révéler un déficit en CPT2. À propos d’une observation

La revue de medecine interne, 2010-12, Vol.31, p.S443-S443

2010

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Effect of intermittent glutamine supplementation on skeletal muscle is not long-lasting in very old rats

Prenatal diagnosis of thrombosis of the dural sinuses: report of six cases, review of the literature and suggested management

Long-term intermittent glutamine supplementation repairs intestinal damage (structure and functional mass) with advanced age: Assessment with plasma citrulline in a rodent model

Contribution of immature muscle precursors to myositis pathogenesis: a source of type I interferon and a possible target of the immune attack

The challenge of prenatal identification of congenital diaphragmatic hernia in the context of hydrops

Long-term intermittent glutamine supplementation repairs intestinal damage (structure and functional mass) with advanced age: Assessment with plasma citrulline in a rodent model

Recurrent congenital pulmonary lymphangiectasia

Fetal umbilical cord ligation under ultrasound guidance

Prenatal detection of mosaic isochromosome 20q: a fourth report with abnormal phenotype

Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p

First‐trimester features of Fowler syndrome (hydrocephaly–hydranencephaly proliferative vasculopathy)

OP03.16: Prenatal detection of thromboses of the dural sinuses: report of five cases, diagnosis and outcome

Pancreatic involvement in Wegener's granulomatosis: a rare and difficult diagnosis

X-linked myopathy with excessive autophagy: a clinicopathological study of five new families

Congenital Adrenal Hypoplasia Due to Isolated Familial ACTH Deficiency

Sudden unexpected death in an infant due to a ruptured coronary aneurysm revealing Kawasaki disease

Diagnostic anténatal des tumeurs cérébrales fœtales et diagnostics différentiels

Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease

Prenatal diagnosis of cerebral tumors and differential diagnosis

P009: Corpus callosum or not corpus callosum? Lobar holoprosencephaly associated with a mimicking corpus callosum: value of “the anterior cerebral artery crawling under the skull”

P345: Twin to twin transfusion syndrome (TTTS) in momoamniotic monochorionic pregnancies (MAMC) does exist: proposition of antenatal surveillance

Les atteintes pancréatiques au cours de la granulomatose de Wegener : une localisation rare et un diagnostic difficile

Mort subite chez un nourrisson par rupture d’anévrisme coronarien révélatrice d’une maladie de Kawasaki

Une observation familiale d'ophtalmoplégie externe chronique progressive liée à une mitochondriopathie

Trois bonnes raisons de révéler un déficit en CPT2. À propos d’une observation

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