A Joannard

The WHO Classification of Tumors of the Nervous System

A Comparison of Brain Gene Expression Levels in Domesticated and Wild Animals

Hepatitis C virus replication in ‘autoimmune’ chronic hepatitis

Penicillin G sodium and ceftriaxone in the treatment of neuroborreliosis in children — A prospective study

Chronic active hepatitis associated with antiliver/kidney microsome antibody type 1: A second type of “autoimmune” hepatitis

Defects in maintenance of mitochondrial DNA are associated with intramitochondrial nucleotide imbalances

Mutations in the human Delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis

Repertoires of Autophagy in the Pathogenesis of Ocular Diseases

Molecular aspects of fructose metabolism and metabolic disease

Epidemiology and Estimated Population Burden of Selected Autoimmune Diseases in the United States

Inflammation in obesity, diabetes, and related disorders

Primitive Neuroectodermal Tumors of the Central Nervous System

Human disorders of cortical development: from past to present

Advances in the Diagnosis, Molecular Genetics, and Treatment of Pediatric Embryonal CNS Tumors

The Clinical Assessment, Treatment, and Prevention of Lyme Disease, Human Granulocytic Anaplasmosis, and Babesiosis: Clinical Practice Guidelines by the Infectious Diseases Society of America

Human UDP-Glucuronosyltransferases: Metabolism, Expression, and Disease

Fluorescent Chemosensors Based on Spiroring-Opening of Xanthenes and Related Derivatives

Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal

The copper transporter CTR1 provides an essential function in mammalian embryonic development

Cancerous stem cells can arise from pediatric brain tumors

Classification of chronic hepatitis: Diagnosis, grading and staging

[Spondylo-vertebral and spondylo-thoracic dysostosis. Clinical, radiological and genetic study, apropos of 7 observations].

Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome

So-called ‘cryptogenic’ partial seizures resulting from a subtle cortical dysgenesis due to adoublecortin gene mutation

Clinical expression of Menkes syndrome in females

M4 protocol for cerebellar medulloblastoma: Supratentorial radiotherapy may not be avoided

[Primary cirrhosis of the child and antimicrosome antibodies. New serological label?].

[Gycogenolysis disorders in the hereditary intolerance to fructose. Study of 2 cases in children].

[Meningo-encephalomyelitis in Lyme disease].