[Acute pyogenic sacroiliac arthritis in the child]

First set of gated x-ray imaging diagnostics for the Laser Megajoule facility.

The Review of scientific instruments·2016

Inverted duplication with deletion: first interstitial case suggesting a novel undescribed mechanism of formation.

American journal of medical genetics. Part A·2014

Phenotype determining alleles in GM1 gangliosidosis patients bearing novel GLB1 mutations.

Clinical genetics·2010

Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum.

Brain : a journal of neurology·2008

[Management of acute visual loss in children].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2004

[Study of visual field and vigabatrin treatment in children].

Journal francais d'ophtalmologie·2002

[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

Persistent Periorbital Edema as the Initial Manifestation of Probable Systemic Lupus Erythematosus With Suspected Protein-Losing Enteropathy or Lupus Serositis in an Adolescent: A Case Report.

Cureus·2026

Differences in body composition and physical activity in youth with obesity who report pain.

Obesity pillars·2026

Related Experiment Videos

[Acute pyogenic sacroiliac arthritis in the child]

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First set of gated x-ray imaging diagnostics for the Laser Megajoule facility.

Inverted duplication with deletion: first interstitial case suggesting a novel undescribed mechanism of formation.

Phenotype determining alleles in GM1 gangliosidosis patients bearing novel GLB1 mutations.

Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum.

[Management of acute visual loss in children].

[Study of visual field and vigabatrin treatment in children].

[Natal and neonatal teeth. Management].

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

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

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

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

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

Persistent Periorbital Edema as the Initial Manifestation of Probable Systemic Lupus Erythematosus With Suspected Protein-Losing Enteropathy or Lupus Serositis in an Adolescent: A Case Report.

Differences in body composition and physical activity in youth with obesity who report pain.

Related Experiment Videos

[Acute pyogenic sacroiliac arthritis in the child]

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