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F Hanefeld

Showing results (121-130 of 197) with videos related to

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Journal of Inherited Metabolic Disease|March 1, 1997
Progression of X-linked adrenoleukodystrophy under interferon-beta therapyG C Korenke, H J Christen, B Kruse, et al.
European Journal of Pediatrics|August 1, 1984
Slight impairment of psychomotor skills in children after treatment of acute lymphoblastic leukemiaG Harten, U Stephani, G Henze, et al.
Neuropediatrics|April 1, 1995
Cerebral proton magnetic resonance spectroscopy in Rett syndromeF Hanefeld, H J Christen, U Holzbach, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|October 1, 1996
Localized proton magnetic resonance spectroscopy of a cerebellar tumor in a two-year-old childB Wilken, G Helms, H J Christen, et al.
Journal of Medical Genetics|September 1, 1992
Identification of a new DMD gene deletion by ectopic transcript analysisF Rininsland, A Hahn, S Niemann-Seyde, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 13, 2007
Chronic relapsing opsoclonus-myoclonus syndrome: combination of cyclophosphamide and dexamethasone pulsesB Wilken, M Baumann, C G Bien, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Carbohydrate-deficient glycoprotein syndrome type V: deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferaseC Körner, R Knauer, U Holzbach, et al.
Neuropediatrics|February 7, 2003
Successful management of drooling with botulinum toxin A in neurologically disabled childrenM Ellies, S Rohrbach-Volland, C Arglebe, et al.
Metabolism: Clinical and Experimental|October 10, 1997
Guanidino compounds in guanidinoacetate methyltransferase deficiency, a new inborn error of creatine synthesisS Stöckler, B Marescau, P P De Deyn, et al.
Neuropediatrics|October 1, 1993
Diffuse white matter disease in three children: an encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopyF Hanefeld, U Holzbach, B Kruse, et al.
Pageof 20

Showing results (121-130 of 197) with videos related to

Sort By:
Pageof 20
Journal of Inherited Metabolic Disease|March 1, 1997
Progression of X-linked adrenoleukodystrophy under interferon-beta therapyG C Korenke, H J Christen, B Kruse, et al.
European Journal of Pediatrics|August 1, 1984
Slight impairment of psychomotor skills in children after treatment of acute lymphoblastic leukemiaG Harten, U Stephani, G Henze, et al.
Neuropediatrics|April 1, 1995
Cerebral proton magnetic resonance spectroscopy in Rett syndromeF Hanefeld, H J Christen, U Holzbach, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|October 1, 1996
Localized proton magnetic resonance spectroscopy of a cerebellar tumor in a two-year-old childB Wilken, G Helms, H J Christen, et al.
Journal of Medical Genetics|September 1, 1992
Identification of a new DMD gene deletion by ectopic transcript analysisF Rininsland, A Hahn, S Niemann-Seyde, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 13, 2007
Chronic relapsing opsoclonus-myoclonus syndrome: combination of cyclophosphamide and dexamethasone pulsesB Wilken, M Baumann, C G Bien, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Carbohydrate-deficient glycoprotein syndrome type V: deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferaseC Körner, R Knauer, U Holzbach, et al.
Neuropediatrics|February 7, 2003
Successful management of drooling with botulinum toxin A in neurologically disabled childrenM Ellies, S Rohrbach-Volland, C Arglebe, et al.
Metabolism: Clinical and Experimental|October 10, 1997
Guanidino compounds in guanidinoacetate methyltransferase deficiency, a new inborn error of creatine synthesisS Stöckler, B Marescau, P P De Deyn, et al.
Neuropediatrics|October 1, 1993
Diffuse white matter disease in three children: an encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopyF Hanefeld, U Holzbach, B Kruse, et al.
Pageof 20