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Journal of Medical Genetics|January 11, 2000
Identification of cathepsin C mutations in ethnically diverse papillon-Lefèvre syndrome patientsP S Hart, Y Zhang, E Firatli, et al.Lancet (London, England)|February 24, 1999
Angiotensin-converting-enzyme gene insertion/deletion polymorphism and response to physical trainingH Montgomery, P Clarkson, M Barnard, et al.Bioorganic & Medicinal Chemistry Letters|January 13, 2006
Imidazo[1,2-a]pyrimidines as functionally selective GABA(A) ligandsWesley P Blackaby, John R Atack, Frances Bromidge, et al.Brain : a Journal of Neurology|May 15, 2023
Comprehension of acoustically degraded speech in Alzheimer's disease and primary progressive aphasiaJessica Jiang, Jeremy C S Johnson, Maï-Carmen Requena-Komuro, et al.The Journal of Clinical Endocrinology and Metabolism|June 14, 2021
Mild Idiopathic Infantile Hypercalcemia-Part 1: Biochemical and Genetic FindingsNina Lenherr-Taube, Edwin J Young, Michelle Furman, et al.BMC Nephrology|February 3, 2019
Outcomes and practice patterns with hemodiafiltration in Shanghai: a longitudinal cohort studyWeiming Zhang, Changlin Mei, Nan Chen, et al.Alzheimer'S Research & Therapy|July 27, 2018
Retained capacity for perceptual learning of degraded speech in primary progressive aphasia and Alzheimer's diseaseChris J D Hardy, Charles R Marshall, Rebecca L Bond, et al.Journal of Medicinal Chemistry|February 16, 1996
Controlled modification of acidity in cholecystokinin B receptor antagonists: N-(1,4-benzodiazepin-3-yl)-N'-[3-(tetrazol-5-ylamino) phenyl]ureasJ L Castro, R G Ball, H B Broughton, et al.Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|July 17, 2021
Laughter as a paradigm of socio-emotional signal processing in dementiaHarri Sivasathiaseelan, Charles R Marshall, Elia Benhamou, et al.Clinical Genetics|December 1, 2010
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorderM T Carter, S M Nikkel, B A Fernandez, et al.Pageof 201