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H Pihko

Showing results (31-40 of 98) with videos related to

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AJNR. American Journal of Neuroradiology|July 1, 1993
PEHO syndrome (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy): neuroradiologic findingsM Somer, O Salonen, H Pihko, et al.
The Journal of Pediatrics|December 24, 1997
Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutationT Tyni, J Rapola, A Palotie, et al.
Neuropediatrics|June 1, 1992
CNS in congenital muscular dystrophy without mental retardationH Pihko, T Louhimo, L Valanne, et al.
Neuropediatrics|December 7, 2007
High-dose vitamin D supplementation in children with cerebral palsy or neuromuscular disorderP Kilpinen-Loisa, H Nenonen, H Pihko, et al.
AJNR. American Journal of Neuroradiology|August 1, 1995
Infantile-onset spinocerebellar ataxia: MR and CT findingsT Koskinen, L Valanne, L M Ketonen, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Severe hyperprostaglandin E syndrome with hyperthyroidism--studies of pathogenetic mechanismsV Fellman, H Pihko, A Majander, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency with the G1528C mutationT Tyni, A Majander, H Kalimo, et al.
Pediatric Pathology & Laboratory Medicine : Journal of the Society for Pediatric Pathology, Affiliated with the International Paediatric Pathology Association|May 1, 1997
Pathology of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutationT Tyni, J Rapola, A Paetau, et al.
Muscle & Nerve|May 1, 1994
Sensory neuropathy in infantile onset spinocerebellar ataxia (IOSCA)T Koskinen, K Sainio, J Rapola, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Mitochondrial diseases]H Pihko, A Suomalainen, H Somer, et al.
Pageof 10

Showing results (31-40 of 98) with videos related to

Sort By:
Pageof 10
AJNR. American Journal of Neuroradiology|July 1, 1993
PEHO syndrome (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy): neuroradiologic findingsM Somer, O Salonen, H Pihko, et al.
The Journal of Pediatrics|December 24, 1997
Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutationT Tyni, J Rapola, A Palotie, et al.
Neuropediatrics|June 1, 1992
CNS in congenital muscular dystrophy without mental retardationH Pihko, T Louhimo, L Valanne, et al.
Neuropediatrics|December 7, 2007
High-dose vitamin D supplementation in children with cerebral palsy or neuromuscular disorderP Kilpinen-Loisa, H Nenonen, H Pihko, et al.
AJNR. American Journal of Neuroradiology|August 1, 1995
Infantile-onset spinocerebellar ataxia: MR and CT findingsT Koskinen, L Valanne, L M Ketonen, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Severe hyperprostaglandin E syndrome with hyperthyroidism--studies of pathogenetic mechanismsV Fellman, H Pihko, A Majander, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency with the G1528C mutationT Tyni, A Majander, H Kalimo, et al.
Pediatric Pathology & Laboratory Medicine : Journal of the Society for Pediatric Pathology, Affiliated with the International Paediatric Pathology Association|May 1, 1997
Pathology of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutationT Tyni, J Rapola, A Paetau, et al.
Muscle & Nerve|May 1, 1994
Sensory neuropathy in infantile onset spinocerebellar ataxia (IOSCA)T Koskinen, K Sainio, J Rapola, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Mitochondrial diseases]H Pihko, A Suomalainen, H Somer, et al.
Pageof 10