Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S Autio

Showing results (51-60 of 66) with videos related to

Pageof 7
Sort By:
Acta Neuropathologica|January 1, 1972
Aspartylglucosaminuria. II. Biochemical studies on brain, liver, kidney and spleenJ Palo, P Riekkinen, A U Arstila, et al.
Acta Neuropathologica|January 1, 1972
Aspartylglucosaminuria. I. Fine structural studies on liver, kidney and brainA U Arstila, J Palo, M Haltia, et al.
The Journal of Biological Chemistry|September 10, 1973
A mannose-containing trisaccharide isolated from urines of three patients with mannosidosisN E Nordén, A Lundblad, S Svensson, et al.
Life Sciences|January 1, 1990
Elevated levels of serum dolichol in aspartylglucosaminuriaM Salaspuro, K Salmela, K Humaloja, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1981
[Salla disease - a new inherited Finnish disease]P Aula, M Renlund, K Raivio, et al.
Human Genetics|September 1, 1987
Prevalence of the fragile X syndrome in four birth cohorts of children of school ageM Kähkönen, T Alitalo, E Airaksinen, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 1, 1984
Abnormal collagen fibrils in aspartylglycosaminuria. Altered dermal ultrastructure in a glycoprotein storage disorderK Näntö-Salonen, L J Pelliniemi, S Autio, et al.
Acta Paediatrica Scandinavica|November 1, 1973
Mannosidosis: clinical, fine-structural and biochemical findings in three casesS Autio, N E Nordén, P A Ockerman, et al.
Monographs in Human Genetics|January 1, 1978
Four patients with a new lysosomal storage disorder (Salla disease)P Aula, K Raivio, S Autio, et al.
Neurology|January 1, 1983
Salla disease: a new lysosomal storage disorder with disturbed sialic acid metabolismM Renlund, P Aula, K O Raivio, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
Acta Neuropathologica|January 1, 1972
Aspartylglucosaminuria. II. Biochemical studies on brain, liver, kidney and spleenJ Palo, P Riekkinen, A U Arstila, et al.
Acta Neuropathologica|January 1, 1972
Aspartylglucosaminuria. I. Fine structural studies on liver, kidney and brainA U Arstila, J Palo, M Haltia, et al.
The Journal of Biological Chemistry|September 10, 1973
A mannose-containing trisaccharide isolated from urines of three patients with mannosidosisN E Nordén, A Lundblad, S Svensson, et al.
Life Sciences|January 1, 1990
Elevated levels of serum dolichol in aspartylglucosaminuriaM Salaspuro, K Salmela, K Humaloja, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1981
[Salla disease - a new inherited Finnish disease]P Aula, M Renlund, K Raivio, et al.
Human Genetics|September 1, 1987
Prevalence of the fragile X syndrome in four birth cohorts of children of school ageM Kähkönen, T Alitalo, E Airaksinen, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 1, 1984
Abnormal collagen fibrils in aspartylglycosaminuria. Altered dermal ultrastructure in a glycoprotein storage disorderK Näntö-Salonen, L J Pelliniemi, S Autio, et al.
Acta Paediatrica Scandinavica|November 1, 1973
Mannosidosis: clinical, fine-structural and biochemical findings in three casesS Autio, N E Nordén, P A Ockerman, et al.
Monographs in Human Genetics|January 1, 1978
Four patients with a new lysosomal storage disorder (Salla disease)P Aula, K Raivio, S Autio, et al.
Neurology|January 1, 1983
Salla disease: a new lysosomal storage disorder with disturbed sialic acid metabolismM Renlund, P Aula, K O Raivio, et al.
Pageof 7