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Nature Medicine|April 4, 2006
Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1Marion G Ott, Manfred Schmidt, Kerstin Schwarzwaelder, et al.
Plos One|August 6, 2014
Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thicknessAlice E Davidson, Sek-Shir Cheong, Pirro G Hysi, et al.
Journal of the American Heart Association|June 1, 2018
Effect of Vitamin D Supplementation on Markers of Vascular Function: A Systematic Review and Individual Participant Meta-AnalysisLouise A Beveridge, Faisel Khan, Allan D Struthers, et al.
Autoimmunity Reviews|July 6, 2010
Vitamin D and musculoskeletal health, cardiovascular disease, autoimmunity and cancer: Recommendations for clinical practiceJean-Claude Souberbielle, Jean-Jacques Body, Joan M Lappe, et al.
PLOS Global Public Health|May 5, 2025
Wastewater-integrated pathogen surveillance dashboards enable real-time, transparent, and interpretable public health risk assessment and disseminationNosihle S Msomi, Joshua I Levy, Nathaniel L Matteson, et al.
Cells|October 14, 2022
Circulating Microparticles Are Differentially Increased in Lowlanders and Highlanders with High Altitude Induced Pulmonary Hypertension during the Cold SeasonAkylbek Sydykov, Aleksandar Petrovic, Abdirashit M Maripov, et al.
European Journal of Neurology|January 14, 2025
Lyme neuroborreliosis in Japan: Borrelia burgdorferi sensu lato as a cause of meningitis of previously undetermined etiology in hospitalized patients outside of the island of Hokkaido, 2010-2021Masayuki Ohira, Ai Takano, Kentaro Yoshi, et al.
Methods of Information in Medicine|March 9, 2017
On Teaching International Courses on Health Information Systems. Lessons Learned during 16 Years of Frank - van Swieten Lectures on Strategic Information Management in Health Information SystemsElske Ammenwerth, Petra Knaup, Alfred Winter, et al.
Journal of Medical Genetics|September 27, 2005
Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patientsH L Archer, S D Whatley, J C Evans, et al.
BMC Medical Genetics|April 27, 2016
Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsyAndrew E Fry, Elliott Rees, Rose Thompson, et al.
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