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F J Hansen

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Journal of Medical Genetics|January 15, 2003
No correlation between phenotype and genotype in boys with a truncating MECP2 mutationK Ravn, J B Nielsen, P Uldall, et al.
American Journal of Medical Genetics|June 5, 1995
Pigment variant of neuronal ceroid-lipofuscinosisH H Goebel, F Gullotta, T Bajanowski, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndromeK Ravn, F Wibrand, F J Hansen, et al.
Der Nervenarzt|August 19, 2007
[Integrated treatment of depression in Aachen]T Kirchner, F Bergmann, J Engels, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 17, 2000
Gait disturbance interpreted as cerebellar ataxia after MMR vaccination at 15 months of age: a follow-up studyA M Plesner, F J Hansen, K Taudorf, et al.
Human Molecular Genetics|January 1, 1997
Quantification, by solid-phase minisequencing, of the telomeric and centromeric copies of the survival motor neuron gene in families with spinal muscular atrophyM Schwartz, N Sørensen, F J Hansen, et al.
International Disability Studies|April 1, 1990
The handicap code of the ICIDH, adapted for children aged 6-7 years. Classification Group of the Nordic Neuropediatric AssociationJ Diderichsen, H Ferngren, F J Hansen, et al.
Ugeskrift for Laeger|October 15, 1998
[Guidelines on antiepileptic treatment of children]P V Uldall, F J Hansen, B Beck, et al.
Human Molecular Genetics|October 1, 1994
Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletionJ Poulton, K Morten, C Freeman-Emmerson, et al.
Neuromuscular Disorders : NMD|November 1, 1995
A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysisC Wallgren-Pettersson, K Avela, S Marchand, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Journal of Medical Genetics|January 15, 2003
No correlation between phenotype and genotype in boys with a truncating MECP2 mutationK Ravn, J B Nielsen, P Uldall, et al.
American Journal of Medical Genetics|June 5, 1995
Pigment variant of neuronal ceroid-lipofuscinosisH H Goebel, F Gullotta, T Bajanowski, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndromeK Ravn, F Wibrand, F J Hansen, et al.
Der Nervenarzt|August 19, 2007
[Integrated treatment of depression in Aachen]T Kirchner, F Bergmann, J Engels, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 17, 2000
Gait disturbance interpreted as cerebellar ataxia after MMR vaccination at 15 months of age: a follow-up studyA M Plesner, F J Hansen, K Taudorf, et al.
Human Molecular Genetics|January 1, 1997
Quantification, by solid-phase minisequencing, of the telomeric and centromeric copies of the survival motor neuron gene in families with spinal muscular atrophyM Schwartz, N Sørensen, F J Hansen, et al.
International Disability Studies|April 1, 1990
The handicap code of the ICIDH, adapted for children aged 6-7 years. Classification Group of the Nordic Neuropediatric AssociationJ Diderichsen, H Ferngren, F J Hansen, et al.
Ugeskrift for Laeger|October 15, 1998
[Guidelines on antiepileptic treatment of children]P V Uldall, F J Hansen, B Beck, et al.
Human Molecular Genetics|October 1, 1994
Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletionJ Poulton, K Morten, C Freeman-Emmerson, et al.
Neuromuscular Disorders : NMD|November 1, 1995
A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysisC Wallgren-Pettersson, K Avela, S Marchand, et al.
Pageof 2