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S Autio

Showing results (21-30 of 66) with videos related to

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Acta Neuropathologica|January 1, 1975
Aspartylglycosaminuria: a generalized storage disease. Morphological and histochemical studiesM Haltia, J Palo, S Autio
Pediatric Research|June 1, 1976
Enzymatic diagnosis and carrier detection of aspartylglucosaminuria using blood samplesP Aula, K Raivio, S Autio
Birth Defects Original Article Series|January 1, 1974
Aspartylglycosaminuria: a gargoyle-like syndrome with autosomal recessive inheritanceS Autio, J Palo, J Perheentupa
Archives of Disease in Childhood|October 30, 2010
Experience with nalidixic Acid in the treatment of urinary tract infections of childrenS Autio, P Mäkelä, R Sunila
Annals of Clinical Research|April 1, 1982
The clinical course of mannosidosisS Autio, T Louhimo, M Helenius
Developmental Medicine and Child Neurology|June 1, 1974
Cultured skin fibroblasts in disorders of glycoprotein catabolism and I-cell diseaseS Autio, P Aula, V Näntö
Annals of Clinical Research|June 1, 1973
Aspartylglycosaminuria (AGU). Further aspects on its clinical picture, mode of inheritance and epidemiology based on a series of 57 patientsS Autio, J K Visakorpi, H Järvinen
Acta Pharmacologica Et Toxicologica|January 1, 1977
Effect of acetylated derivatives of some sympathomimetic amines on the isolated auricles and tracheal chain of the guinea-pigM Marvola, L Piirainen, S Autio, et al.
The Journal of Pediatrics|July 1, 1974
Lymphotic inclusions in I-cell diseaseJ Rapola, S Autio, P Aula, et al.
Humangenetik|January 1, 1974
Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblastsP Aula, S Autio, K Raivio, et al.
Pageof 7

Showing results (21-30 of 66) with videos related to

Sort By:
Pageof 7
Acta Neuropathologica|January 1, 1975
Aspartylglycosaminuria: a generalized storage disease. Morphological and histochemical studiesM Haltia, J Palo, S Autio
Pediatric Research|June 1, 1976
Enzymatic diagnosis and carrier detection of aspartylglucosaminuria using blood samplesP Aula, K Raivio, S Autio
Birth Defects Original Article Series|January 1, 1974
Aspartylglycosaminuria: a gargoyle-like syndrome with autosomal recessive inheritanceS Autio, J Palo, J Perheentupa
Archives of Disease in Childhood|October 30, 2010
Experience with nalidixic Acid in the treatment of urinary tract infections of childrenS Autio, P Mäkelä, R Sunila
Annals of Clinical Research|April 1, 1982
The clinical course of mannosidosisS Autio, T Louhimo, M Helenius
Developmental Medicine and Child Neurology|June 1, 1974
Cultured skin fibroblasts in disorders of glycoprotein catabolism and I-cell diseaseS Autio, P Aula, V Näntö
Annals of Clinical Research|June 1, 1973
Aspartylglycosaminuria (AGU). Further aspects on its clinical picture, mode of inheritance and epidemiology based on a series of 57 patientsS Autio, J K Visakorpi, H Järvinen
Acta Pharmacologica Et Toxicologica|January 1, 1977
Effect of acetylated derivatives of some sympathomimetic amines on the isolated auricles and tracheal chain of the guinea-pigM Marvola, L Piirainen, S Autio, et al.
The Journal of Pediatrics|July 1, 1974
Lymphotic inclusions in I-cell diseaseJ Rapola, S Autio, P Aula, et al.
Humangenetik|January 1, 1974
Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblastsP Aula, S Autio, K Raivio, et al.
Pageof 7