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The American Journal of Cardiology|September 1, 1992
Exclusion of coronary artery disease by exercise thallium-201 tomography in patients with aortic valve stenosisM Kupari, K S Virtanen, H Turto, et al.
International Journal of Tissue Reactions|January 1, 1989
Non-proteolytic activation of latent human neutrophil collagenase and its role in matrix destruction in periodontal diseasesT Sorsa, H Saari, Y T Konttinen, et al.
Proceedings of the Finnish Dental Society. Suomen Hammaslaakariseuran Toimituksia|January 1, 1989
Identification of protease(s) capable of further degrading native 3/4- and 1/4-collagen fragments generated by collagenase from native type I collagen in human neutrophilsT Sorsa, K Suomalainen, Y T Konttinen, et al.
Matrix (Stuttgart, Germany)|August 1, 1991
Collagenase reserves in polymorphonuclear neutrophil leukocytes from synovial fluid and peripheral blood of patients with rheumatoid arthritisY T Konttinen, O Lindy, P Kemppinen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2017
High frequency of mosaic pathogenic variants in genes causing epilepsy-related neurodevelopmental disordersMary Beth Stosser, Amanda S Lindy, Elizabeth Butler, et al.
American Journal of Medical Genetics. Part A|June 14, 2014
Truncating mutations in LRP4 lead to a prenatal lethal form of Cenani-Lenz syndromeAmanda S Lindy, Caleb P Bupp, Stephen J McGee, et al.
American Journal of Medical Genetics. Part A|March 31, 2016
Identification of a novel insertion mutation in FGFR3 that causes thanatophoric dysplasia type 1Amanda S Lindy, Monica J Basehore, Mumingjiang Munisha, et al.
Development (Cambridge, England)|June 23, 2006
An antagonistic role for the C. elegans Schnurri homolog SMA-9 in modulating TGFbeta signaling during mesodermal patterningMarisa L Foehr, Amanda S Lindy, Rachel C Fairbank, et al.
Epilepsia|April 15, 2018
Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disordersAmanda S Lindy, Mary Beth Stosser, Elizabeth Butler, et al.
Brain : a Journal of Neurology|March 14, 2020
A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variantsJavier A López-Rivera, Eduardo Pérez-Palma, Joseph Symonds, et al.
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