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Specificity of Histological Markers of Long‐Term CNI Nephrotoxicity in Kidney‐Transplant Recipients Under Low‐Dose Cyclosporine Therapy

American journal of transplantation, 2011-12, Vol.11 (12), p.2635-2646

2011

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ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism

Journal of medical genetics, 2010-11, Vol.47 (11), p.752-759

2010

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Congenital hyperinsulinism and mosaic abnormalities of the ploidy

Journal of medical genetics, 2006-03, Vol.43 (3), p.248-254

2006

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Role of Lipid Emulsions in Cholestasis Associated with Long-Term Parenteral Nutrition in Children

JPEN. Journal of parenteral and enteral nutrition, 2000-11, Vol.24 (6), p.345-350

2000

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Fetal urinoma: two new cases and a review of the literature

Ultrasound in obstetrics & gynecology, 2006-11, Vol.28 (6), p.848-852

2006

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Clinical Features of 52 Neonates with Hyperinsulinism

The New England journal of medicine, 1999-04, Vol.340 (15), p.1169-1175

1999

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Fetal lung volume measurement by magnetic resonance imaging in congenital diaphragmatic hernia

BJOG : an international journal of obstetrics and gynaecology, 2001-08, Vol.108 (8), p.863-868

2001

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Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia

The Journal of clinical investigation, 1998-10, Vol.102 (7), p.1286-1291

1998

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Fatal diffuse capillaritis after hematopoietic stem-cell transplantation for dyskeratosis congenita despite low-intensity conditioning regimen

Bone marrow transplantation (Basingstoke), 2005-12, Vol.36 (12), p.1103-1105

2005

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Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy

The Journal of clinical investigation, 1997-08, Vol.100 (4), p.802-807

1997

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Invasive Pulmonary Infection Due to Scedosporium apiospermum in Two Children with Chronic Granulomatous Disease

Clinical infectious diseases, 1998-12, Vol.27 (6), p.1437-1441

1998

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A novel CLTC-TFE3 gene fusion in pediatric renal adenocarcinoma with t(X;17)(p11.2;q23)

Oncogene, 2003-08, Vol.22 (34), p.5374-5378

2003

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Interaction of Neisseria meningitidis with the Components of the Blood-Brain Barrier Correlates with an Increased Expression of PilC

The Journal of infectious diseases, 1997-11, Vol.176 (5), p.1285-1292

1997

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Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's role

Histopathology, 1998-01, Vol.32 (1), p.15-19

1998

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Eosinophilic Esophagitis in Children: Symptoms, Histology and pH Probe Results

Journal of pediatric gastroenterology and nutrition, 2004-10, Vol.39 (4), p.373-377

2004

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Value of open lung biopsy in immunocompromised children

The Journal of pediatrics, 2000-08, Vol.137 (2), p.165-171

2000

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Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother

Pediatrics (Evanston), 2002-06, Vol.109 (6), p.e97-e97

2002

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Eosinophilic Esophagitis in Children: Symptoms, Histology and pH Probe Results

Journal of pediatric gastroenterology and nutrition, 2004-10, Vol.39 (4), p.373-377

2004

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Pulmonary alveolar proteinosis: experience with eight pediatric cases and a review

Pediatrics (Evanston), 1996-01, Vol.97 (1), p.117

1996

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Fatty acid β-oxidation deficiency masquerading as fulminant myocarditis

International journal of cardiology, 1998-08, Vol.65 (3), p.287-289

1998

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Clinical utility of liver biopsy in children with acquired immunodeficiency syndrome

The Pediatric infectious disease journal, 1999-02, Vol.18 (2), p.143-147

1999

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Glioblastoma multiforme in a mature ovarian teratoma with recurring brain tumours

Histopathology, 1999-08, Vol.35 (2), p.170-173

1999

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Pédagogie et originalité

Annales de pathologie, 2010-06, Vol.30 (3), p.167-167

2010

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Foxl-2 in gonad development and pathology

Arkhiv patologii, 2011-07, Vol.73 (4), p.10

2011

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Clinical Biological and Genetic Heterogeneity of the Inborn Errors of Pulmonary Surfactant Metabolism

Clinical chemistry and laboratory medicine, 2001-02, Vol.39 (2), p.90-108

2001

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Specificity of Histological Markers of Long‐Term CNI Nephrotoxicity in Kidney‐Transplant Recipients Under Low‐Dose Cyclosporine Therapy

ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism

Congenital hyperinsulinism and mosaic abnormalities of the ploidy

Role of Lipid Emulsions in Cholestasis Associated with Long-Term Parenteral Nutrition in Children

Fetal urinoma: two new cases and a review of the literature

Clinical Features of 52 Neonates with Hyperinsulinism

Fetal lung volume measurement by magnetic resonance imaging in congenital diaphragmatic hernia

Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia

Fatal diffuse capillaritis after hematopoietic stem-cell transplantation for dyskeratosis congenita despite low-intensity conditioning regimen

Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy

Invasive Pulmonary Infection Due to Scedosporium apiospermum in Two Children with Chronic Granulomatous Disease

A novel CLTC-TFE3 gene fusion in pediatric renal adenocarcinoma with t(X;17)(p11.2;q23)

Interaction of Neisseria meningitidis with the Components of the Blood-Brain Barrier Correlates with an Increased Expression of PilC

Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's role

Eosinophilic Esophagitis in Children: Symptoms, Histology and pH Probe Results

Value of open lung biopsy in immunocompromised children

Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother

Eosinophilic Esophagitis in Children: Symptoms, Histology and pH Probe Results

Pulmonary alveolar proteinosis: experience with eight pediatric cases and a review

Fatty acid β-oxidation deficiency masquerading as fulminant myocarditis

Clinical utility of liver biopsy in children with acquired immunodeficiency syndrome

Glioblastoma multiforme in a mature ovarian teratoma with recurring brain tumours

Pédagogie et originalité

Foxl-2 in gonad development and pathology

Clinical Biological and Genetic Heterogeneity of the Inborn Errors of Pulmonary Surfactant Metabolism

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