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Neurology|April 1, 2026
Diagnostic Value of the Kappa Free Light Chain Index to Distinguish MOGAD, NMOSD, and MSApolline Tournier, Antoine Gavoille, Julie Pique, et al.
EMBO Molecular Medicine|November 15, 2023
LKB1-SIK2 loss drives uveal melanoma proliferation and hypersensitivity to SLC8A1 and ROS inhibitionSarah Proteau, Imène Krossa, Chrystel Husser, et al.
Nature Communications|March 14, 2026
Hypusination of the translation factor eIF5A regulates mitochondrial tRNA processing to promote prostate cancer aggressivenessMichel Kahi, Abigail Mazzu, Ludovic Batistic, et al.
The Journal of Pediatrics|June 18, 2010
Age-dependent Mendelian predisposition to herpes simplex virus type 1 encephalitis in childhoodLaurent Abel, Sabine Plancoulaine, Emmanuelle Jouanguy, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 10, 2011
Cardiac magnetic resonance assessment of left ventricular mass in autosomal dominant polycystic kidney diseaseRonald D Perrone, Kaleab Z Abebe, Robert W Schrier, et al.
Kidney International|December 30, 2011
Analysis of baseline parameters in the HALT polycystic kidney disease trialsVicente E Torres, Arlene B Chapman, Ronald D Perrone, et al.
Journal of the American Heart Association|June 8, 2021
Contemporary Outcomes in Tetralogy of Fallot With Absent Pulmonary Valve After Fetal DiagnosisAnjali Chelliah, Anita J Moon-Grady, Shabnam Peyvandi, et al.
Sensors (Basel, Switzerland)|December 14, 2011
Transport infrastructure surveillance and monitoring by electromagnetic sensing: the ISTIMES projectMonica Proto, Massimo Bavusi, Romeo Bernini, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 25, 2014
Invasive pneumococcal disease in children can reveal a primary immunodeficiencyJean Gaschignard, Corinne Levy, Maya Chrabieh, et al.
Journal of Clinical Immunology|May 8, 2012
Clinical, functional and genetic analysis of twenty-four patients with chronic granulomatous disease - identification of eight novel mutations in CYBB and NCF2 genesCécile Martel, Michelle Mollin, Sylvain Beaumel, et al.
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