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European Psychiatry : the Journal of the Association of European Psychiatrists|August 7, 2012
Health services and the treatment of immigrants: data on service use, interpreting services and immigrant staff members in services across EuropeU Kluge, M Bogic, W Devillé, et al.
Biochemical and Molecular Medicine|April 1, 1996
Guidelines for the retention, storage, and use of residual dried blood spot samples after newborn screening analysis: statement of the Council of Regional Networks for Genetic ServicesB L Therrell, W H Hannon, K A Pass, et al.
Genomics|December 9, 2000
Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiencyL Bartoloni, M Wattenhofer, J Kudoh, et al.
Cell Metabolism|October 8, 2013
Canonical Nlrp3 inflammasome links systemic low-grade inflammation to functional decline in agingYun-Hee Youm, Ryan W Grant, Laura R McCabe, et al.
The Journal of Infectious Diseases|May 23, 2018
Novel Treatment of Cryptococcal Meningitis via Neurapheresis TherapyGordon J Smilnak, Lefko T Charalambous, Drew Cutshaw, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|October 23, 2010
How to improve clinical practice on involuntary hospital admissions of psychiatric patients: suggestions from the EUNOMIA studyA Fiorillo, C De Rosa, V Del Vecchio, et al.
JIMD Reports|April 23, 2013
A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth SyndromeYuxin Fan, Jon Steller, Iris L Gonzalez, et al.
Frontiers in Immunology|November 7, 2022
Comparative effects of human-equivalent low, moderate, and high dose oral prednisone intake on autoimmunity and glucocorticoid-related toxicity in a murine model of environmental-triggered lupusLauren K Heine, Abby D Benninghoff, Elizabeth A Ross, et al.
Human Mutation|December 19, 2001
Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenitaY H Zhang, B L Huang, K Anyane-Yeboa, et al.
American Journal of Human Genetics|June 13, 1998
DAX1 mutations map to putative structural domains in a deduced three-dimensional modelY H Zhang, W Guo, R L Wagner, et al.
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