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H Pihko

Showing results (41-50 of 98) with videos related to

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British Medical Journal|June 8, 1974
Serum alpha-fetoprotein: diagnostic significance in liver diseaseE Ruoslahti, M Salaspuro, H Pihko, et al.
Pediatric Research|November 1, 1994
Infantile onset spinocerebellar ataxia represents an allelic disease distinct from other hereditary ataxiasK Nikali, T Koskinen, A Suomalainen, et al.
Brain & Development|May 1, 1993
Brain perfusion SPECT in children with frequent fitsH Heiskala, J Launes, H Pihko, et al.
Neurology|October 25, 2006
Lipids detected by brain MRS during coma caused by carnitine palmitoyltransferase 1 deficiencyE Roomets, N Lundbom, H Pihko, et al.
Neuropediatrics|June 1, 1996
Laminar cortical necrosis in MELAS syndrome: MR and neuropathological observationsL Valanne, A Paetau, A Suomalainen, et al.
AJNR. American Journal of Neuroradiology|March 21, 1998
Neuroradiologic findings in children with mitochondrial disordersL Valanne, L Ketonen, A Majander, et al.
Developmental Medicine and Child Neurology|January 1, 1990
Single-photon emission computed tomography of brain perfusion: analysis of 60 paediatric casesM Iivanainen, J Launes, H Pihko, et al.
Lancet (London, England)|March 3, 1998
Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduriaV Fellman, J Rapola, H Pihko, et al.
Journal of the Neurological Sciences|January 8, 1999
Infantile onset spinocerebellar ataxia with sensory neuropathy (IOSCA): neuropathological featuresT Lönnqvist, A Paetau, K Nikali, et al.
Human Molecular Genetics|May 1, 1993
Quantification of tRNA3243(Leu) point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcriptionA Suomalainen, A Majander, H Pihko, et al.
Pageof 10

Showing results (41-50 of 98) with videos related to

Sort By:
Pageof 10
British Medical Journal|June 8, 1974
Serum alpha-fetoprotein: diagnostic significance in liver diseaseE Ruoslahti, M Salaspuro, H Pihko, et al.
Pediatric Research|November 1, 1994
Infantile onset spinocerebellar ataxia represents an allelic disease distinct from other hereditary ataxiasK Nikali, T Koskinen, A Suomalainen, et al.
Brain & Development|May 1, 1993
Brain perfusion SPECT in children with frequent fitsH Heiskala, J Launes, H Pihko, et al.
Neurology|October 25, 2006
Lipids detected by brain MRS during coma caused by carnitine palmitoyltransferase 1 deficiencyE Roomets, N Lundbom, H Pihko, et al.
Neuropediatrics|June 1, 1996
Laminar cortical necrosis in MELAS syndrome: MR and neuropathological observationsL Valanne, A Paetau, A Suomalainen, et al.
AJNR. American Journal of Neuroradiology|March 21, 1998
Neuroradiologic findings in children with mitochondrial disordersL Valanne, L Ketonen, A Majander, et al.
Developmental Medicine and Child Neurology|January 1, 1990
Single-photon emission computed tomography of brain perfusion: analysis of 60 paediatric casesM Iivanainen, J Launes, H Pihko, et al.
Lancet (London, England)|March 3, 1998
Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduriaV Fellman, J Rapola, H Pihko, et al.
Journal of the Neurological Sciences|January 8, 1999
Infantile onset spinocerebellar ataxia with sensory neuropathy (IOSCA): neuropathological featuresT Lönnqvist, A Paetau, K Nikali, et al.
Human Molecular Genetics|May 1, 1993
Quantification of tRNA3243(Leu) point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcriptionA Suomalainen, A Majander, H Pihko, et al.
Pageof 10