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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 29, 2013
Newborn screening for cystic fibrosis in Switzerland--consequences after analysis of a 4 months pilot studyToni Torresani, Ralph Fingerhut, Corina S Rueegg, et al.
Blood|April 15, 1993
Relationship between tissue factor expression and deposition of fibrin, platelets, and leukocytes on cultured endothelial cells under venous blood flow conditionsD Kirchhofer, K S Sakariassen, M Clozel, et al.
Human Genetics|June 1, 1994
Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemiaK Nanao, K Okamura-Ikeda, Y Motokawa, et al.
Magnetic Resonance Imaging|March 21, 2000
A wavelet-based method for improving signal-to-noise ratio and contrast in MR imagesM E Alexander, R Baumgartner, A R Summers, et al.
Metabolism: Clinical and Experimental|August 25, 1999
Longitudinal changes in serum 25-hydroxyvitamin D in older peopleH M Perry, M Horowitz, J E Morley, et al.
Gynakologisch-Geburtshilfliche Rundschau|January 1, 1995
[Use of photodynamic laser therapy in gynecology]M Korell, M Untch, C Abels, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|October 25, 2016
Methionine synthase and methionine synthase reductase interact with MMACHC and with MMADHCChristine Bassila, Rose Ghemrawi, Justine Flayac, et al.
Molecular Genetics and Metabolism|January 24, 2012
A single mutation in MCCC1 or MCCC2 as a potential cause of positive screening for 3-methylcrotonyl-CoA carboxylase deficiencyRaphael J Morscher, Sarah Catharina Grünert, Céline Bürer, et al.
European Journal of Pediatrics|May 1, 1996
Atypical vitamin B12-unresponsive methylmalonic aciduria in sibship with severe progressive encephalomyelopathy: a new genetic disease?E Mayatepek, G F Hoffmann, R Baumgartner, et al.
Molecular Genetics and Metabolism|October 26, 2019
Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduriaParith Wongkittichote, Gary Cunningham, Marshall L Summar, et al.
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