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J Weglage

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Neuropediatrics|August 1, 1997
Progression of cerebral white matter abnormalities in early treated patients with phenylketonuria during adolescenceJ Weglage, U Bick, G Schuierer, et al.
Journal of Inherited Metabolic Disease|September 3, 1999
Regression of neuropsychological deficits in early-treated phenylketonurics during adolescenceJ Weglage, M Pietsch, J Denecke, et al.
European Journal of Pediatrics|July 1, 1992
Psychological and social findings in adolescents with phenylketonuriaJ Weglage, B Fünders, B Wilken, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Behavioural and emotional problems in early-treated adolescents with phenylketonuria in comparison with diabetic patients and healthy controlsJ Weglage, M Grenzebach, M Pietsch, et al.
Neuropediatrics|August 1, 1995
In-vivo NMR spectroscopy in patients with phenylketonuria: changes of cerebral phenylalanine levels under dietary treatmentH E Möller, P Vermathen, K Ullrich, et al.
European Journal of Pediatrics|November 1, 1995
Therapy of complex I deficiency: peripheral neuropathy during dichloroacetate therapyG Kurlemann, I Paetzke, H Möller, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1989
[Aspartylglucosaminuria. Clinical description of 2 German patients]R Ziegler, H Schmidt, A C Sewell, et al.
Neuropediatrics|October 1, 1994
Cranial MRI in PKU: evaluation of a critical threshold for blood phenylalanineK Ullrich, J Weglage, G Schuierer, et al.
European Journal of Pediatrics|July 1, 1996
Effect of L-dopa on visual evoked potentials and neuropsychological tests in adult phenylketonuria patientsK Ullrich, J Weglage, C Oberwittler, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Individual blood-brain barrier phenylalanine transport in siblings with classical phenylketonuriaJ Weglage, D Wiedermann, J Denecke, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Neuropediatrics|August 1, 1997
Progression of cerebral white matter abnormalities in early treated patients with phenylketonuria during adolescenceJ Weglage, U Bick, G Schuierer, et al.
Journal of Inherited Metabolic Disease|September 3, 1999
Regression of neuropsychological deficits in early-treated phenylketonurics during adolescenceJ Weglage, M Pietsch, J Denecke, et al.
European Journal of Pediatrics|July 1, 1992
Psychological and social findings in adolescents with phenylketonuriaJ Weglage, B Fünders, B Wilken, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Behavioural and emotional problems in early-treated adolescents with phenylketonuria in comparison with diabetic patients and healthy controlsJ Weglage, M Grenzebach, M Pietsch, et al.
Neuropediatrics|August 1, 1995
In-vivo NMR spectroscopy in patients with phenylketonuria: changes of cerebral phenylalanine levels under dietary treatmentH E Möller, P Vermathen, K Ullrich, et al.
European Journal of Pediatrics|November 1, 1995
Therapy of complex I deficiency: peripheral neuropathy during dichloroacetate therapyG Kurlemann, I Paetzke, H Möller, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1989
[Aspartylglucosaminuria. Clinical description of 2 German patients]R Ziegler, H Schmidt, A C Sewell, et al.
Neuropediatrics|October 1, 1994
Cranial MRI in PKU: evaluation of a critical threshold for blood phenylalanineK Ullrich, J Weglage, G Schuierer, et al.
European Journal of Pediatrics|July 1, 1996
Effect of L-dopa on visual evoked potentials and neuropsychological tests in adult phenylketonuria patientsK Ullrich, J Weglage, C Oberwittler, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Individual blood-brain barrier phenylalanine transport in siblings with classical phenylketonuriaJ Weglage, D Wiedermann, J Denecke, et al.
Pageof 5