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F Hanefeld

Showing results (181-190 of 197) with videos related to

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Journal of Chromatography|July 23, 1993
Quantitative organic acid analysis in cerebrospinal fluid and plasma: reference values in a pediatric populationG F Hoffmann, C K Seppel, B Holmes, et al.
Journal of Pediatric Hematology/Oncology|January 4, 1998
Potential prognostic value of C-erbB-2 expression in medulloblastomas in very young childrenJ W Herms, J Behnke, M Bergmann, et al.
Pediatric Research|February 1, 1997
Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndromeE Wilichowski, A Grüters, K Kruse, et al.
Epilepsia|September 1, 1994
Severe hepatotoxicity during valproate therapy: an update and report of eight new fatalitiesS A König, H Siemes, F Bläker, et al.
Neuropediatrics|March 6, 2004
CNS disease as the main manifestation of hemophagocytic lymphohistiocytosis in two childrenK Rostasy, R Kolb, D Pohl, et al.
Neurology|February 1, 1995
The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigreesP G Barth, G Blennow, H G Lenard, et al.
European Journal of Pediatrics|October 1, 1992
Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromesH Seyschab, D Schindler, R Friedl, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenaseP G Barth, G F Hoffmann, J Jaeken, et al.
European Journal of Pediatrics|December 1, 1990
Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathiesG C Korenke, H A Bentlage, W Ruitenbeek, et al.
Annals of Neurology|July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic diseaseP G Barth, G F Hoffmann, J Jaeken, et al.
Pageof 20

Showing results (181-190 of 197) with videos related to

Sort By:
Pageof 20
Journal of Chromatography|July 23, 1993
Quantitative organic acid analysis in cerebrospinal fluid and plasma: reference values in a pediatric populationG F Hoffmann, C K Seppel, B Holmes, et al.
Journal of Pediatric Hematology/Oncology|January 4, 1998
Potential prognostic value of C-erbB-2 expression in medulloblastomas in very young childrenJ W Herms, J Behnke, M Bergmann, et al.
Pediatric Research|February 1, 1997
Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndromeE Wilichowski, A Grüters, K Kruse, et al.
Epilepsia|September 1, 1994
Severe hepatotoxicity during valproate therapy: an update and report of eight new fatalitiesS A König, H Siemes, F Bläker, et al.
Neuropediatrics|March 6, 2004
CNS disease as the main manifestation of hemophagocytic lymphohistiocytosis in two childrenK Rostasy, R Kolb, D Pohl, et al.
Neurology|February 1, 1995
The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigreesP G Barth, G Blennow, H G Lenard, et al.
European Journal of Pediatrics|October 1, 1992
Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromesH Seyschab, D Schindler, R Friedl, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenaseP G Barth, G F Hoffmann, J Jaeken, et al.
European Journal of Pediatrics|December 1, 1990
Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathiesG C Korenke, H A Bentlage, W Ruitenbeek, et al.
Annals of Neurology|July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic diseaseP G Barth, G F Hoffmann, J Jaeken, et al.
Pageof 20