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T Autti

Showing results (51-60 of 58) 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.
Neurology|August 25, 2004
Five new cases of a recently described leukoencephalopathy with high brain lactateT Linnankivi, N Lundbom, T Autti, et al.
European Journal of Neurology|March 29, 2007
Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiencyR Kälviäinen, K Eriksson, M Losekoot, et al.
Journal of Neuropathology and Experimental Neurology|December 23, 1998
Monitoring the CNS pathology in aspartylglucosaminuria miceK Tenhunen, A Uusitalo, T Autti, et al.
Human Molecular Genetics|March 21, 1998
Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patientsA Jalanko, K Tenhunen, C E McKinney, 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.
The European Respiratory Journal|October 20, 2006
Chest CT screening of asbestos-exposed workers: lung lesions and incidental findingsT Vierikko, R Järvenpää, T Autti, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 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.
Neurology|August 25, 2004
Five new cases of a recently described leukoencephalopathy with high brain lactateT Linnankivi, N Lundbom, T Autti, et al.
European Journal of Neurology|March 29, 2007
Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiencyR Kälviäinen, K Eriksson, M Losekoot, et al.
Journal of Neuropathology and Experimental Neurology|December 23, 1998
Monitoring the CNS pathology in aspartylglucosaminuria miceK Tenhunen, A Uusitalo, T Autti, et al.
Human Molecular Genetics|March 21, 1998
Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patientsA Jalanko, K Tenhunen, C E McKinney, 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.
The European Respiratory Journal|October 20, 2006
Chest CT screening of asbestos-exposed workers: lung lesions and incidental findingsT Vierikko, R Järvenpää, T Autti, et al.
Pageof 6