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F Hanefeld

Showing results (91-100 of 197) with videos related to

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Human Molecular Genetics|May 18, 2000
Rett syndrome: analysis of MECP2 and clinical characterization of 31 patientsP Huppke, F Laccone, N Krämer, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 26, 2002
Endocrinological study on growth retardation in Rett syndromeP Huppke, C Roth, H J Christen, et al.
Journal of the Neurological Sciences|July 1, 1977
Oligoclonal gamma-globulin banding of cerebrospinal fluid in patients with subacute sclerosing panencephalitis. Comparison of the electrophoretic pattern with that in multiple sclerosis and congenital infectionsH Siemes, M Siegert, F Hanefeld, et al.
American Journal of Human Genetics|May 1, 1996
Guanidinoacetate methyltransferase deficiency: the first inborn error of creatine metabolism in manS Stöckler, D Isbrandt, F Hanefeld, et al.
Acta Paediatrica Scandinavica|December 1, 1990
Peripheral facial palsy in childhood--Lyme borreliosis to be suspected unless proven otherwiseH J Christen, N Bartlau, F Hanefeld, et al.
Acta Neuropathologica|October 1, 1975
Anoxic encephalopathy with predominant involvement of basal ganglia, brain stem and spinal cord in the perinatal period. Report on seven newbornsH Schneider, L Ballowitz, H Schachinger, et al.
Annals of Neurology|October 17, 2001
Myelinopathia centralis diffusa (vanishing white matter disease): evidence of apoptotic oligodendrocyte degeneration in early lesion developmentW Brück, J Herms, K Brockmann, et al.
The Journal of Pediatrics|March 1, 1988
Hyperphosphatasia with mental retardationK Kruse, F Hanefeld, A Kohlschütter, et al.
Lancet (London, England)|November 7, 1992
Distinct neurological syndrome in two brothers with hyperuricaemiaH J Christen, F Hanefeld, J A Duley, et al.
The American Journal of Physiology|September 14, 1999
Increase of total creatine in human brain after oral supplementation of creatine-monohydrateP Dechent, P J Pouwels, B Wilken, et al.
Pageof 20

Showing results (91-100 of 197) with videos related to

Sort By:
Pageof 20
Human Molecular Genetics|May 18, 2000
Rett syndrome: analysis of MECP2 and clinical characterization of 31 patientsP Huppke, F Laccone, N Krämer, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 26, 2002
Endocrinological study on growth retardation in Rett syndromeP Huppke, C Roth, H J Christen, et al.
Journal of the Neurological Sciences|July 1, 1977
Oligoclonal gamma-globulin banding of cerebrospinal fluid in patients with subacute sclerosing panencephalitis. Comparison of the electrophoretic pattern with that in multiple sclerosis and congenital infectionsH Siemes, M Siegert, F Hanefeld, et al.
American Journal of Human Genetics|May 1, 1996
Guanidinoacetate methyltransferase deficiency: the first inborn error of creatine metabolism in manS Stöckler, D Isbrandt, F Hanefeld, et al.
Acta Paediatrica Scandinavica|December 1, 1990
Peripheral facial palsy in childhood--Lyme borreliosis to be suspected unless proven otherwiseH J Christen, N Bartlau, F Hanefeld, et al.
Acta Neuropathologica|October 1, 1975
Anoxic encephalopathy with predominant involvement of basal ganglia, brain stem and spinal cord in the perinatal period. Report on seven newbornsH Schneider, L Ballowitz, H Schachinger, et al.
Annals of Neurology|October 17, 2001
Myelinopathia centralis diffusa (vanishing white matter disease): evidence of apoptotic oligodendrocyte degeneration in early lesion developmentW Brück, J Herms, K Brockmann, et al.
The Journal of Pediatrics|March 1, 1988
Hyperphosphatasia with mental retardationK Kruse, F Hanefeld, A Kohlschütter, et al.
Lancet (London, England)|November 7, 1992
Distinct neurological syndrome in two brothers with hyperuricaemiaH J Christen, F Hanefeld, J A Duley, et al.
The American Journal of Physiology|September 14, 1999
Increase of total creatine in human brain after oral supplementation of creatine-monohydrateP Dechent, P J Pouwels, B Wilken, et al.
Pageof 20