[Serum bile acids and liver disorders in total parenteral nutrition in children]

[French guidelines for sweat test practice and interpretation for cystic fibrosis neonatal screening].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2010

Surfactant protein C gene (SFTPC) mutation-associated lung disease: high-resolution computed tomography (HRCT) findings and its relation to histological analysis.

Pediatric pulmonology·2010

Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal form.

Clinical genetics·2010

Phenotype and genotype in females with POU3F4 mutations.

Clinical genetics·2009

The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening.

Journal of medical genetics·2009

New surfactant protein C gene mutations associated with diffuse lung disease.

Journal of medical genetics·2009

[Natal and neonatal teeth. Management].

Annales de pediatrie·1993

[Risks of failure of uncontrolled adoption of foreign children].

Annales de pediatrie·1993

[Hepatic hydatidosis and portal hypertension in children. Is it the Budd-Chiari syndrome?].

Annales de pediatrie·1993

[Neonatal testicular ischemic necrosis without torsion, associated with antithrombin III deficit].

Annales de pediatrie·1993

[Diffuse neonatal hemangiomatosis. A case with tetralogy of Fallot].

Annales de pediatrie·1993

[Fulminant pneumococcal septicemia in a splenectomized child despite vaccination and chemoprophylaxis: necessity for education of the entourage].

Annales de pediatrie·1993

Dual Urea Cycle Dysfunction Caused by Coexisting Argininosuccinic Aciduria and Citrin Deficiency: Clinical, Biochemical, and Molecular Insights From an Exceptional Case.

JIMD reports·2026

Cost-Effectiveness of Dapagliflozin in the Treatment of Patients With Chronic Kidney Disease in Denmark.

Kidney medicine·2026

Beyond Food Selectivity: Feeding Problems, Nutritional Status, and Parental Quality of Life in Autism Spectrum Disorder.

Journal of autism and developmental disorders·2026

Refractory diabetic ketoacidosis in Rabson-Mendenhall syndrome due to a novel mutation: contrasting outcomes in a sibling - case series.

Journal of pediatric endocrinology & metabolism : JPEM·2026

Timing matters: gastrostomy placement and outcomes in patients with head and neck cancer undergoing chemoradiotherapy.

Frontiers in nutrition·2026

Common Pathogens Associated with Diabetic Charcot Neuroarthropathy in the Indian Population: A Retrospective Observational Study.

Annals of African medicine·2026

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[Serum bile acids and liver disorders in total parenteral nutrition in children]

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[French guidelines for sweat test practice and interpretation for cystic fibrosis neonatal screening].

Surfactant protein C gene (SFTPC) mutation-associated lung disease: high-resolution computed tomography (HRCT) findings and its relation to histological analysis.

Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal form.

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New surfactant protein C gene mutations associated with diffuse lung disease.

[Natal and neonatal teeth. Management].

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Cost-Effectiveness of Dapagliflozin in the Treatment of Patients With Chronic Kidney Disease in Denmark.

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