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Annals of Neurology|December 11, 2007
Long-term course and mutational spectrum of spatacsin-linked spastic paraplegiaUte Hehr, Peter Bauer, Beate Winner, et al.
Human Mutation|September 18, 2010
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficitsDenise Horn, Johannes Kapeller, Núria Rivera-Brugués, et al.
Endoscopy|August 8, 2014
Core needle versus standard needle for endoscopic ultrasound-guided biopsy of solid pancreatic masses: a randomized crossover studyGeoffroy Vanbiervliet, Bertrand Napoléon, Marie Christine Saint Paul, et al.
Molecular Vision|March 25, 2015
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani originZeinab Ravesh, Mohammed E El Asrag, Nicole Weisschuh, et al.
The American Journal of Pathology|September 17, 2023
Resolvin D2-G-Protein Coupled Receptor 18 Enhances Bone Marrow Function and Limits Steatosis and Hepatic Collagen Accumulation in AgingHannah Fitzgerald, Jesse L Bonin, Sayeed Khan, et al.
Molecular Psychiatry|January 27, 2016
Mast cells' involvement in inflammation pathways linked to depression: evidence in mastocytosisS Georgin-Lavialle, D S Moura, A Salvador, et al.
Journal of Animal Physiology and Animal Nutrition|November 18, 2024
Fibre Sources on Performance and Carcass and Meat Characteristics of Feedlot Nellore Young BullsMarcus Vinicius Garcia Niwa, Luís Carlos Vinhas Ítavo, Camila Celeste Brandão Ferreira Ítavo, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1Lars R Jensen, Wei Chen, Bettina Moser, et al.
Internet Interventions|February 19, 2019
Web-based indicated prevention of common mental disorders in university students in four European countries - Study protocol for a randomised controlled trialPeter Musiat, Rachel Potterton, Gemma Gordon, et al.
Cancers|August 28, 2025
Clinical, Histopathological, Dermoscopic Features, and BRAF, NRAS, and Cell Cycle Genes' Mutation Status in Cutaneous MelanomaMaria A Pizzichetta, Jerry Polesel, Maria C Sini, et al.
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