Thomas Opladen

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 17

Top Venues

Journal of inherited metabolic disease

Annals of neurology

EMBO molecular medicine

PloS one

University Childrens Hospital Heidelberg

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University Childrens Hospital Heidelberg Oct 01 2005

Germany

Prof. Dr. :: Division of Child Neurology and Metabolic Medicine

Publications

Natalia Alexandra Julia-Palacios, Oya Kuseyri Hübschmann, Mireia Olivella, Roser Pons, Gabriella Ana Horvath, Thomas Lücke, Cheuk Wing Fung, Suet-Na Wong, Elisenda Cortés-Saladelafont, M Mar Rovira-Remisa, Yılmaz Yıldız, Saadet Mercimek-Mahmutoglu, Birgit Assmann, Galina Stevanović, Filippo Manti, Heiko Brennenstuhl, Sabine Jung-Klawitter, Kathrin Jeltsch, Hatice Serap Sivri, Sven F Garbade, Àngels García-Cazorla, Thomas Opladen
The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Natalia Alexandra Julia-Palacios, Oya Kuseyri Hübschmann, Mireia Olivella, Roser Pons, Gabriella Ana Horvath, Thomas Lücke, Cheuk Wing Fung, Suet-Na Wong, Elisenda Cortés-Saladelafont, M Mar Rovira-Remisa, Yılmaz Yıldız, Saadet Mercimek-Mahmutoglu, Birgit Assmann, Galina Stevanović, Filippo Manti, Heiko Brennenstuhl, Sabine Jung-Klawitter, Kathrin Jeltsch, Hatice Serap Sivri, Sven F Garbade, Àngels García-Cazorla, Thomas Opladen
The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Thomas Opladen, Mariarita Bertoldi
Neurotransmitters … it is all about communication! Journal of inherited metabolic disease 47 (3) (2024)
Natalia Alexandra Julia-Palacios, Oya Kuseyri Hübschmann, Mireia Olivella, Roser Pons, Gabriella Ana Horvath, Thomas Lücke, Cheuk Wing Fung, Suet-Na Wong, Elisenda Cortés-Saladelafont, M Mar Rovira-Remisa, Yılmaz Yıldız, Saadet Mercimek-Mahmutoglu, Birgit Assmann, Galina Stevanović, Filippo Manti, Heiko Brennenstuhl, Sabine Jung-Klawitter, Kathrin Jeltsch, Hatice Serap Sivri, Sven F Garbade, Àngels García-Cazorla, Thomas Opladen
The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease (2024)
Thomas Opladen, Mariarita Bertoldi
Neurotransmitters … it is all about communication! Journal of inherited metabolic disease 47 (3) (2024)
Thomas Opladen, Mariarita Bertoldi
Neurotransmitters … it is all about communication! Journal of inherited metabolic disease 47 (3) (2024)
Yilmaz Yildiz, Oya Kuseyri Hübschmann, Ayça A Karaosmanoğlu, Filippo Manti, Meryem Karaca, Ida Vanessa D Schwartz, Roser Pons, Eduardo López-Laso, Natalia Alexandra Julia Palacios, Francesco Porta, Ivana I Kavecan, Mehmet Cihan Balcı, Marisela E Dy-Hollins, Suet-Na Wong, Mari Oppebøen, Leonardo Simão Medeiros, Leila Cristina Pedroso de Paula, Angeles García-Cazorla, Georg Friedrich Hoffmann, Kathrin Jeltsch, Vincenzo Leuzzi, Gülden Gökçay, Daniel Hübschmann, Inga Harting, Zeynep Alev Ozon, Hatice Serap Sivri, Thomas Opladen
Levodopa-refractory hyperprolactinemia and pituitary findings in inherited disorders of biogenic amine metabolism. Journal of inherited metabolic disease (2023)
Ivana Badnjarevic, Kelly Moyer, Mariarita Bertoldi, Thomas Opladen, Lisa Flint
Navigating the Rare Neurotransmitter Disease Diagnosis: Insights from Patients and Health Care Professionals. Journal of inherited metabolic disease (2023)
Agathe Roubertie, Thomas Opladen, Heiko Brennenstuhl, Oya Kuseyri Hübschmann, Lisa Flint, Michel A Willemsen, Vincenzo Leuzzi, Angels Garcia Cazorla, Manju A Kurian, Marie Céline François-Heude, Paul Hwu, Bruria Ben Zeev, Karl Kiening, Thomas Roujeau, Roser Pons, Toni S Pearson
Gene therapy for aromatic L-amino acid decarboxylase deficiency: requirements for safe application and knowledge-generating follow-up. Journal of inherited metabolic disease (2023)
Sabine Jung-Klawitter, Petra Richter, Yuheng Yuan, Karin Welzel, Marie Kube, Stella Bähr, Alexander Leibner, Egbert Flory, Thomas Opladen
Tyrosine hydroxylase variants influence protein expression, cellular localization, stability, enzymatic activity and the physical interaction between tyrosine hydroxylase and GTP cyclohydrolase 1. Journal of inherited metabolic disease (2023)
Oya Kuseyri Hübschmann, Natalia Alexandra Juliá-Palacios, Mireia Olivella, Philipp Guder, Dimitrios I Zafeiriou, Gabriella Horvath, Jan Kulhánek, Toni S Pearson, Alice Kuster, Elisenda Cortés-Saladelafont, Salvador Ibáñez, Maria Concepción García-Jiménez, Tomáš Honzík, René Santer, Kathrin Jeltsch, Sven F Garbade, Georg F Hoffmann, Thomas Opladen, Ángeles García-Cazorla
Integrative Approach to Predict Severity in Nonketotic Hyperglycinemia. Annals of neurology 92 (2) (2022)
Mara Scharping, Heiko Brennenstuhl, Sven F Garbade, Beate Wild, Roland Posset, Matthias Zielonka, Stefan Kölker, Markus W Haun, Thomas Opladen
Unmet Needs of Parents of Children with Urea Cycle Disorders. Children (Basel, Switzerland) 9 (5) (2022)
Paul Wuh-Liang Hwu, Karl Kiening, Irina Anselm, David R Compton, Takeshi Nakajima, Thomas Opladen, Phillip L Pearl, Agathe Roubertie, Thomas Roujeau, Shin-Ichi Muramatsu
Gene therapy in the putamen for curing AADC deficiency and Parkinson's disease. EMBO molecular medicine 13 (9) (2021)
Oya Kuseyri Hübschmann, Gabriella Horvath, Elisenda Cortès-Saladelafont, Yilmaz Yildiz, Mario Mastrangelo, Roser Pons, Jennifer Friedman, Saadet Mercimek-Mahmutoglu, Suet-Na Wong, Toni S Pearson, Dimitrios I Zafeiriou, Jan Kulhánek, Manju A Kurian, Eduardo López-Laso, Mari Oppebøen, Sebile Kılavuz, Tessa Wassenberg, Helly Goez, Sabine Scholl-Bürgi, Francesco Porta, Tomáš Honzík, René Santer, Alberto Burlina, Hatice Serap Sivri, Vincenzo Leuzzi, Georg F Hoffmann, Kathrin Jeltsch, Daniel Hübschmann, Sven F Garbade, null null, Angeles García-Cazorla, Thomas Opladen
Insights into the expanding phenotypic spectrum of inherited disorders of biogenic amines. Nature communications 12 (1) (2021)
Thomas Opladen, Florian Gleich, Viktor Kozich, Maurizio Scarpa, Diego Martinelli, Franz Schaefer, Kathrin Jeltsch, Natalia Juliá-Palacios, Ángels García-Cazorla, Carlo Dionisi-Vici, Stefan Kölker
U-IMD: the first Unified European registry for inherited metabolic diseases. Orphanet journal of rare diseases 16 (1) (2021)
Heiko Brennenstuhl, Dirk Kohlmüller, Gwendolyn Gramer, Sven F Garbade, Steffen Syrbe, Patrik Feyh, Stefan Kölker, Jürgen G Okun, Georg F Hoffmann, Thomas Opladen
High throughput newborn screening for aromatic ʟ-amino-acid decarboxylase deficiency by analysis of concentrations of 3-O-methyldopa from dried blood spots. Journal of inherited metabolic disease 43 (3) (2020)
Maximilian Breuer, Luca Guglielmi, Matthias Zielonka, Verena Hemberger, Stefan Kölker, Jürgen G Okun, Georg F Hoffmann, Matthias Carl, Sven W Sauer, Thomas Opladen
QDPR homologues in Danio rerio regulate melanin synthesis, early gliogenesis, and glutamine homeostasis. PloS one 14 (4) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Thomas Opladen