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W Sperl

Showing results (41-50 of 112) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1994
Parenteral administration of amino acids in disorders of branched-chain amino acid metabolismW Sperl, D Skladal, W Endres, et al.
Padiatrie Und Padologie|January 1, 1985
[Lactic acid acidosis with mitochondrial myopathy due to a pyruvate dehydrogenase deficiency]W Sperl, H Maurer, E Dworschak, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
Mitochondrial respiratory chain succinate-cytochrome-c oxidoreductase deficiency and hepatic cirrhosisA C Sewell, J Herwig, H J Böhles, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 30, 2001
Poor storage and handling of tissue mimics mitochondrial DNA depletionA Berger, M Bruschek, C Grethen, et al.
Neuropediatrics|September 13, 2006
Acute flaccid paralysis as initial symptom in 4 patients with novel E1alpha mutations of the pyruvate dehydrogenase complexH M Strassburg, J Koch, J Mayr, et al.
Annals of Neurology|April 1, 1993
Maple syrup urine disease: metabolic decompensation monitored by proton magnetic resonance imaging and spectroscopyS R Felber, W Sperl, A Chemelli, et al.
Wiener Klinische Wochenschrift|March 10, 2001
Epidemiology of sudden infant death syndrome (SIDS) in the Tyrol before and after an intervention campaignU Kiechl-Kohlendorfer, U P Peglow, S Kiechl, et al.
Biology of the Neonate|January 1, 1994
Identification of CD34+ cord blood cells and their subpopulations in preterm and term neonates using three-color flow cytometryB Meister, M Tötsch, A Mayr, et al.
Wiener Klinische Wochenschrift|January 1, 1994
[Myoglobinuria and carnitine palmitoyltransferase deficiency. Diagnostic procedure and differential diagnosis]S Kiechl, U Kohlendorfer, I Paetzke, et al.
Klinische Padiatrie|September 17, 2005
[Menkes' disease: heterozygosity testing by quantitative real-time PCR and the dilemma of therapeutic support]O Rittinger, G Sander, A Schaller, et al.
Pageof 12

Showing results (41-50 of 112) with videos related to

Sort By:
Pageof 12
Journal of Inherited Metabolic Disease|January 1, 1994
Parenteral administration of amino acids in disorders of branched-chain amino acid metabolismW Sperl, D Skladal, W Endres, et al.
Padiatrie Und Padologie|January 1, 1985
[Lactic acid acidosis with mitochondrial myopathy due to a pyruvate dehydrogenase deficiency]W Sperl, H Maurer, E Dworschak, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
Mitochondrial respiratory chain succinate-cytochrome-c oxidoreductase deficiency and hepatic cirrhosisA C Sewell, J Herwig, H J Böhles, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 30, 2001
Poor storage and handling of tissue mimics mitochondrial DNA depletionA Berger, M Bruschek, C Grethen, et al.
Neuropediatrics|September 13, 2006
Acute flaccid paralysis as initial symptom in 4 patients with novel E1alpha mutations of the pyruvate dehydrogenase complexH M Strassburg, J Koch, J Mayr, et al.
Annals of Neurology|April 1, 1993
Maple syrup urine disease: metabolic decompensation monitored by proton magnetic resonance imaging and spectroscopyS R Felber, W Sperl, A Chemelli, et al.
Wiener Klinische Wochenschrift|March 10, 2001
Epidemiology of sudden infant death syndrome (SIDS) in the Tyrol before and after an intervention campaignU Kiechl-Kohlendorfer, U P Peglow, S Kiechl, et al.
Biology of the Neonate|January 1, 1994
Identification of CD34+ cord blood cells and their subpopulations in preterm and term neonates using three-color flow cytometryB Meister, M Tötsch, A Mayr, et al.
Wiener Klinische Wochenschrift|January 1, 1994
[Myoglobinuria and carnitine palmitoyltransferase deficiency. Diagnostic procedure and differential diagnosis]S Kiechl, U Kohlendorfer, I Paetzke, et al.
Klinische Padiatrie|September 17, 2005
[Menkes' disease: heterozygosity testing by quantitative real-time PCR and the dilemma of therapeutic support]O Rittinger, G Sander, A Schaller, et al.
Pageof 12