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Muscle & Nerve|January 1, 1993
Progressive unilateral hypertrophic myopathy: a case studyH Pihko, I Lehtinen, H Tikkanen, et al.Proceedings of the National Academy of Sciences of the United States of America|December 15, 1991
Spectrum of mutations in aspartylglucosaminuriaE Ikonen, P Aula, K Grön, et al.Social Science & Medicine (1982)|July 17, 1998
Attitudes towards genetic testing: analysis of contradictionsP Jallinoja, A Hakonen, A R Aro, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 1, 1996
In vivo purging of bone marrow in children with poor-risk neuroblastoma for marrow collection and autologous bone marrow transplantationU M Saarinen, S Wikström, A Mäkipernaa, et al.American Journal of Human Genetics|August 19, 2000
The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlationN Aula, P Salomäki, R Timonen, et al.The EMBO Journal|January 1, 1991
Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the diseaseE Ikonen, M Baumann, K Grön, et al.Experimental Hematology|September 10, 1999
Correction of peripheral lysosomal accumulation in mice with aspartylglucosaminuria by bone marrow transplantationM Laine, J Richter, C Fahlman, et al.Acta Diabetologica|January 1, 1992
Cyclosporin reduces renal prostanoid excretion in type 1 diabetic patientsV A Koivisto, M Leirisalo-Repo, R Pelkonen, et al.Neuropediatrics|May 1, 1991
The spectrum of Jansky-Bielschowsky diseaseP Santavuori, J Rapola, A Nuutila, et al.American Journal of Human Genetics|June 1, 1997
Lysinuric protein intolerance (LPI) gene maps to the long arm of chromosome 14T Lauteala, P Sistonen, M L Savontaus, et al.Pageof 27