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Thomas Opladen

Showing results (11-20 of 95) with videos related to

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Stem Cell Research|April 12, 2017
Generation of an iPSC line from a patient with GTP cyclohydrolase 1 (GCH1) deficiency: HDMC0061i-GCH1Sabine Jung-Klawitter, Juliane Ebersold, Gudrun Göhring, et al.
Pediatric Neurology|May 29, 2012
Dyskinesias as a limiting factor in the treatment of Segawa diseaseEduardo López-Laso, Katrin Beyer, Thomas Opladen, et al.
Journal of Inherited Metabolic Disease|July 30, 2010
Phenylalanine loading in pediatric patients with dopa-responsive dystonia: revised test protocol and pediatric cutoff valuesThomas Opladen, Jürgen G Okun, Peter Burgard, et al.
JIMD Reports|May 27, 2015
Dopamine-Responsive Growth-Hormone Deficiency and Central Hypothyroidism in Sepiapterin Reductase DeficiencyMatthias Zielonka, Nawal Makhseed, Nenad Blau, et al.
Stem Cell Research|March 23, 2019
Generation of 2 iPSC clones from a patient with DNAJC12 deficiency: DHMCi003-A and DHMCi003-BSabine Jung-Klawitter, Selina Wächter, Maike Hagedorn, et al.
Stem Cell Research|December 10, 2016
Generation of an iPSC line from a patient with tyrosine hydroxylase (TH) deficiency: TH-1 iPSCSabine Jung-Klawitter, Nenad Blau, Attila Sebe, et al.
Pathology, Research and Practice|December 12, 2003
Flow cytometric cerebrospinal fluid analysis in childrenMartin Häusler, Bernd Sellhaus, Klaus Schweizer, et al.
Journal of Inherited Metabolic Disease|March 19, 2011
Diagnosis of tetrahydrobiopterin deficiency using filter paper blood spots: further development of the method and 5 years experienceThomas Opladen, Bettina Abu Seda, Anahita Rassi, et al.
Molecular Genetics and Metabolism|July 9, 2011
Cerebral folate deficiency: a neurometabolic syndrome?Sarah Mangold, Nenad Blau, Thomas Opladen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2010
Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemiaThomas Opladen, Georg Hoffmann, Friederike Hörster, et al.
Pageof 10

Showing results (11-20 of 95) with videos related to

Sort By:
Pageof 10
Stem Cell Research|April 12, 2017
Generation of an iPSC line from a patient with GTP cyclohydrolase 1 (GCH1) deficiency: HDMC0061i-GCH1Sabine Jung-Klawitter, Juliane Ebersold, Gudrun Göhring, et al.
Pediatric Neurology|May 29, 2012
Dyskinesias as a limiting factor in the treatment of Segawa diseaseEduardo López-Laso, Katrin Beyer, Thomas Opladen, et al.
Journal of Inherited Metabolic Disease|July 30, 2010
Phenylalanine loading in pediatric patients with dopa-responsive dystonia: revised test protocol and pediatric cutoff valuesThomas Opladen, Jürgen G Okun, Peter Burgard, et al.
JIMD Reports|May 27, 2015
Dopamine-Responsive Growth-Hormone Deficiency and Central Hypothyroidism in Sepiapterin Reductase DeficiencyMatthias Zielonka, Nawal Makhseed, Nenad Blau, et al.
Stem Cell Research|March 23, 2019
Generation of 2 iPSC clones from a patient with DNAJC12 deficiency: DHMCi003-A and DHMCi003-BSabine Jung-Klawitter, Selina Wächter, Maike Hagedorn, et al.
Stem Cell Research|December 10, 2016
Generation of an iPSC line from a patient with tyrosine hydroxylase (TH) deficiency: TH-1 iPSCSabine Jung-Klawitter, Nenad Blau, Attila Sebe, et al.
Pathology, Research and Practice|December 12, 2003
Flow cytometric cerebrospinal fluid analysis in childrenMartin Häusler, Bernd Sellhaus, Klaus Schweizer, et al.
Journal of Inherited Metabolic Disease|March 19, 2011
Diagnosis of tetrahydrobiopterin deficiency using filter paper blood spots: further development of the method and 5 years experienceThomas Opladen, Bettina Abu Seda, Anahita Rassi, et al.
Molecular Genetics and Metabolism|July 9, 2011
Cerebral folate deficiency: a neurometabolic syndrome?Sarah Mangold, Nenad Blau, Thomas Opladen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2010
Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemiaThomas Opladen, Georg Hoffmann, Friederike Hörster, et al.
Pageof 10