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Clinical Physiology (Oxford, England)|April 25, 2001
Tracheal sounds and airflow dynamics in surgically treated unilateral vocal fold paralysisA Saarinen, H Rihkanen, L P Malmberg, et al.
Clinical Physiology (Oxford, England)|November 28, 2001
Disturbances in airflow dynamics and tracheal sounds during forced and quiet breathing in subjects with unilateral vocal fold paralysisA Saarinen, H Rihkanen, L P Malmberg, et al.
Biotechnology Progress|August 2, 2003
Monitoring and controlling the dissolved oxygen (DO) concentration within the high aspect ratio vessel (HARV)Mark A Saarinen, Julie S Reece, Mark A Arnold, et al.
Resuscitation|January 3, 2012
Does appropriate treatment of the primary underlying cause of PEA during resuscitation improve patients' survival?Sini Saarinen, Jouni Nurmi, Tuukka Toivio, et al.
Radiation Oncology (London, England)|January 30, 2022
Radiotherapy treatment modification for prostate cancer patients based on PSMA-PET/CTVasileios Karagiannis, Viktor Wichmann, Juha Saarinen, et al.
Molecular Genetics & Genomic Medicine|March 5, 2022
Pulmonary manifestations and the effectiveness of enzyme replacement therapy in Fabry Disease with the p. Arg227Ter (p.R227*) mutationPäivi Pietilä-Effati, Johan Söderström, Jukka T Saarinen, et al.
Applied Occupational and Environmental Hygiene|March 24, 2000
Working conditions and health in hairdressing salonsT Leino, E Kähkönen, L Saarinen, et al.
The Journal of Infectious Diseases|December 1, 1996
Mechanism of antibody-mediated reduction of nasopharyngeal colonization by Haemophilus influenzae type b studied in an infant rat modelM Kauppi-Korkeila, L van Alphen, D Madore, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 2009
Body composition and bone mineral density in children with premature adrenarche and the association of LRP5 gene polymorphisms with bone mineral densityPauliina Utriainen, Jarmo Jääskeläinen, Anne Saarinen, et al.
Human Mutation|March 3, 1998
Molecular genetics of the long QT syndrome: two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindredK Saarinen, H Swan, K Kainulainen, et al.
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