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Human Mutation|January 1, 1994
Time-resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathyK Huoponen, V Juvonen, A Iitiä, et al.European Journal of Human Genetics : EJHG|December 31, 1997
mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathyT Lamminen, K Huoponen, P Sistonen, et al.Journal of Inherited Metabolic Disease|January 1, 1993
Applications of a new fluorimetric enzyme assay for the diagnosis of aspartylglucosaminuriaVoznyi YaV, J L Keulemans, W J Kleijer, et al.Neurology|October 24, 2001
Hematopoietic stem cell transplantation in infantile neuronal ceroid lipofuscinosisT Lönnqvist, S L Vanhanen, K Vettenranta, et al.Neurology|May 20, 1999
A new metabolite contributing to N-acetyl signal in 1H MRS of the brain in Salla diseaseT Varho, M Komu, P Sonninen, et al.British Journal of Obstetrics and Gynaecology|April 1, 1981
Measurement of placental protein 5, placental lactogen and pregnancy-specific beta 1 glycoprotein in mid-trimester as a predictor of outcome of pregnancyH T Salem, J N Lee, M Seppälä, et al.Clinical Genetics|March 1, 1997
Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantationA Laitinen, M Hietala, J C Haworth, et al.Atherosclerosis|May 1, 1987
Effect of repeated endotoxin treatment and hypercholesterolemia on preatherosclerotic lesions in weaned pigs. Part 1. Scanning and transmission electron microscopic studyE Pesonen, E Kaprio, J Rapola, et al.Acta Obstetricia Et Gynecologica Scandinavica|January 1, 1991
Serum lipids and lipoproteins during therapeutic amenorrhea induced by lynestrenol and depot-medroxyprogesterone acetateK Huovinen, M J Tikkanen, S Autio, et al.Journal of Inherited Metabolic Disease|January 1, 1984
Metabolism of collagen in aspartylglycosaminuria: urinary excretion of hydroxyprolineK Näntö-Salonen, S Autio, E Härö, et al.Pageof 27