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F Hanefeld

Showing results (131-140 of 197) with videos related to

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Human Genetics|February 1, 1996
Identification of mutations in the ALD-gene of 20 families with adrenoleukodystrophy/adrenomyeloneuropathyE W Krasemann, V Meier, G C Korenke, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 1, 1997
Aromatic L-amino acid decarboxylase deficiency: an extrapyramidal movement disorder with oculogyric crisesG C Korenke, H J Christen, K Hyland, et al.
Artificial Organs|November 1, 1982
Advantages of bicarbonate hemodialysisH Hampl, H Klopp, M Wolfgruber, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. I. Clinical reviewD Rating, F Hanefeld, H Siemes, et al.
Brain & Development|November 1, 1991
Multiple sclerosis in childhood: report of 15 casesF Hanefeld, H J Bauer, H J Christen, et al.
Pediatric Neurology|August 30, 2000
Quantitative proton magnetic resonance spectroscopy of focal brain lesionsB Wilken, P Dechent, J Herms, et al.
Journal of Medical Genetics|December 24, 1998
Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28T Webb, A Clarke, F Hanefeld, et al.
European Journal of Endocrinology|July 1, 1997
Variability of endocrinological dysfunction in 55 patients with X-linked adrenoleucodystrophy: clinical, laboratory and genetic findingsG C Korenke, C Roth, E Krasemann, et al.
Human Mutation|February 6, 1998
First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathyG C Korenke, E Krasemann, V Meier, et al.
Neuropediatrics|October 9, 2002
Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patientsM Meins, K Brockmann, S Yadav, et al.
Pageof 20

Showing results (131-140 of 197) with videos related to

Sort By:
Pageof 20
Human Genetics|February 1, 1996
Identification of mutations in the ALD-gene of 20 families with adrenoleukodystrophy/adrenomyeloneuropathyE W Krasemann, V Meier, G C Korenke, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 1, 1997
Aromatic L-amino acid decarboxylase deficiency: an extrapyramidal movement disorder with oculogyric crisesG C Korenke, H J Christen, K Hyland, et al.
Artificial Organs|November 1, 1982
Advantages of bicarbonate hemodialysisH Hampl, H Klopp, M Wolfgruber, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. I. Clinical reviewD Rating, F Hanefeld, H Siemes, et al.
Brain & Development|November 1, 1991
Multiple sclerosis in childhood: report of 15 casesF Hanefeld, H J Bauer, H J Christen, et al.
Pediatric Neurology|August 30, 2000
Quantitative proton magnetic resonance spectroscopy of focal brain lesionsB Wilken, P Dechent, J Herms, et al.
Journal of Medical Genetics|December 24, 1998
Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28T Webb, A Clarke, F Hanefeld, et al.
European Journal of Endocrinology|July 1, 1997
Variability of endocrinological dysfunction in 55 patients with X-linked adrenoleucodystrophy: clinical, laboratory and genetic findingsG C Korenke, C Roth, E Krasemann, et al.
Human Mutation|February 6, 1998
First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathyG C Korenke, E Krasemann, V Meier, et al.
Neuropediatrics|October 9, 2002
Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patientsM Meins, K Brockmann, S Yadav, et al.
Pageof 20