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J Puranen

Showing results (81-90 of 84) with videos related to

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Annals of Neurology|June 9, 1999
Extensive cerebral white matter abnormality without clinical symptoms: a new hereditary condition?T Autti, M Muttilainen, R Raininko, et al.
Neuropediatrics|March 6, 2004
Neuroradiological findings (MRS, MRI, SPECT) in infantile neuronal ceroid-lipofuscinosis (infantile CLN1) at different stages of the diseaseS-L Vanhanen, J Puranen, T Autti, et al.
Endocrinology|June 29, 1999
Characterization of molecular and catalytic properties of intact and truncated human 17beta-hydroxysteroid dehydrogenase type 2 enzymes: intracellular localization of the wild-type enzyme in the endoplasmic reticulumT J Puranen, R M Kurkela, J T Lakkakorpi, et al.
Neurology|February 5, 1999
Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosisL Lauronen, P B Munroe, I Järvelä, et al.
Pageof 9

Showing results (81-90 of 84) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 84 results.
Annals of Neurology|June 9, 1999
Extensive cerebral white matter abnormality without clinical symptoms: a new hereditary condition?T Autti, M Muttilainen, R Raininko, et al.
Neuropediatrics|March 6, 2004
Neuroradiological findings (MRS, MRI, SPECT) in infantile neuronal ceroid-lipofuscinosis (infantile CLN1) at different stages of the diseaseS-L Vanhanen, J Puranen, T Autti, et al.
Endocrinology|June 29, 1999
Characterization of molecular and catalytic properties of intact and truncated human 17beta-hydroxysteroid dehydrogenase type 2 enzymes: intracellular localization of the wild-type enzyme in the endoplasmic reticulumT J Puranen, R M Kurkela, J T Lakkakorpi, et al.
Neurology|February 5, 1999
Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosisL Lauronen, P B Munroe, I Järvelä, et al.
Pageof 9