Brigitte Llanas

The Joubert Syndrome-associated Missense Mutation (V443D) in the Abelson-helper Integration Site 1 (AHI1) Protein Alters Its Localization and Protein-Protein Interactions

A Nationwide Study ofVipera BerusBites During One Year—Epidemiology and Morbidity of 231 Cases

Management of comorbidities in older patients with cystic fibrosis

Cystic fibrosis

Interleukin-10-Producing Plasmablasts Exert Regulatory Function in Autoimmune Inflammation

The molecular basis of human retinal and vitreoretinal diseases

RPGRIP1L mutations are mainly associated with the cerebello‐renal phenotype of Joubert syndrome‐related disorders

A Wolbachia Symbiont in Aedes aegypti Limits Infection with Dengue, Chikungunya, and Plasmodium

Chikungunya Fever: An Epidemiological Review of a Re‐Emerging Infectious Disease

Leber congenital amaurosis: Genes, proteins and disease mechanisms

Updated consensus statement on biological agents for the treatment of rheumatic diseases, 2010

Long‐term effect of rituximab in maintaining remission of recurrent and plasmapheresis‐dependent nephrotic syndrome post‐renal transplantation – Case report

The Global Burden of Snakebite: A Literature Analysis and Modelling Based on Regional Estimates of Envenoming and Deaths

Update on Streptococcus pneumoniae associated hemolytic uremic syndrome

Circulating Permeability Factors in Idiopathic Nephrotic Syndrome and Focal Segmental Glomerulosclerosis

The role of primary cilia in neuronal function

The primary cilium: a signalling centre during vertebrate development

Efficacy of rituximab in acute refractory or chronic relapsing non-familial idiopathic thrombotic thrombocytopenic purpura: a systematic review with pooled data analysis

Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome

Acute Kidney Injury and Hemolytic Anemia Secondary to <b><i>Mycoplasma pneumoniae</i></b> Infection

Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue

Making sense of cilia in disease: The human ciliopathies

Cby1 promotes Ahi1 recruitment to a ring-shaped domain at the centriole–cilium interface and facilitates proper cilium formation and function

A review of the current use of rituximab in autoimmune diseases

Hemolytic uremic syndrome complicating Mycoplasma pneumoniae infection

Aspects pédiatriques de l’épidémie de Chikungunya à l’île de la Réunion

High NPHP1 and NPHP6 Mutation Rate in Patients with Joubert Syndrome and Nephronophthisis

Rituximab therapy for childhood-onset systemic lupus erythematosus

Severe transient ADAMTS13 deficiency in pneumococcal-associated hemolytic uremic syndrome

Rituximab treatment for severe steroid- or cyclosporine-dependent nephrotic syndrome: a multicentric series of 22 cases

Renal impairment in children with cystic fibrosis

Successful treatment with rituximab for acute refractory thrombotic thrombocytopenic purpura related to acquired ADAMTS13 deficiency: A pediatric report and literature review

Rhabdomyolysis in European viper bite