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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.Journal of the Neurological Sciences|December 1, 1995
Diagnosis of fatal infantile defects of the mitochondrial respiratory chain: age dependence and postmortem analysis of enzyme activitiesA Majander, J Rapola, H Sariola, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Muscle-eye-brain disease: clinical features, visual evoked potentials and brain imaging in 20 patientsP Santavuori, L Valanne, T Autti, et al.Neuromuscular Disorders : NMD|May 1, 1995
Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelicS Ranta, H Pihko, P Santavuori, et al.Journal of the Neurological Sciences|September 1, 1989
Lymphocytic beta-adrenergic receptors in X-linked muscular dystrophyT Mäki, H Somer, H Pihko, et al.Neuroradiology|August 1, 1994
MRI of the brain in muscle-eye-brain (MEB) diseaseL Valanne, H Pihko, K Katevuo, et al.Clinical Dysmorphology|July 12, 2001
Hirschsprung disease, mental retardation and dysmorphic facial features in five unrelated childrenH Kääriäinen, C Wallgren-Pettersson, A Clarke, et al.Pageof 8