Opladen, Thomas Prof. Dr. med.Universität HeidelbergHeidelberg
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Co-Autoren (Uni Heidelberg)
- Garbade, Sven (11)
- Blau, Nenad (10)
- Okun, Jürgen G. (10)
- Schröter, Julian (7)
- Syrbe, Steffen (5)
- Staufner, Christian (5)
- Hübschmann, Daniel (4)
- Gleich, Florian (4)
- Harting, Inga (4)
- Burgard, Peter (3)
- Moog, Ute (3)
- Zielonka, Matthias (3)
- Hörster, Friederike (3)
- Mütze, Ulrike (3)
- Eils, Roland (2)
- Paramasivam, Nagarajan (2)
- Haas, Dorothea (2)
- Lenz, Dominic (2)
- Posset, Roland (2)
- Bürger, Friederike (2)
- Himmelreich, Nastassja (2)
- Feyh, Patrik (2)
- Rossmann, Julia (2)
- Richter, Petra (2)
- Hinderhofer, Katrin (2)
- Granzow, Martin (2)
- Meyburg, Jochen (2)
- Thiel, Christian (2)
- Dattner, Tal (2)
- Fischer, Christine (2)
- Kiening, Karl (2)
- Evers, Christina (2)
- Boy, Nikolas (2)
- (weitere Einträge vorhanden...)
Co-Autoren (extern)
- Blau, Nenad (3)
- Burlina, Alberto (3)
- Yildiz, Yilmaz (3)
- Mastrangelo, Mario (3)
- Cortès-Saladelafont, Elisenda (3)
- Artuch, Rafael (3)
- Syring, Hanna (3)
- García-Cazorla, Àngels (3)
- Gibson, K. Michael (2)
- López-Laso, Eduardo (2)
- Göhring, Gudrun (2)
- Manti, Filippo (2)
- Thöny, Beat (2)
- Didiášová, Miroslava (2)
- Bao, Xinhua (2)
- Zeman, Jiri (2)
- Thöny, Beat (2)
- Tabarki, Brahim (2)
- Porta, Francesco (2)
- Pearson, Toni S. (2)
- López-Laso, Eduardo (2)
- Horvath, Gabriella (2)
- Anikster, Yair (2)
- Mercimek-Andrews, Saadet (2)
- Flint, Lisa (2)
- Klein, Christine (2)
- Pearl, Phillip L. (2)
- Juliá-Palacios, Natalia (2)
- Tokatly Latzer, Itay (2)
- Roullet, Jean-Baptiste (2)
- Rotenberg, Alexander (2)
- Lee, Henry H. C. (2)
- DiBacco, Melissa L. (2)
- (weitere Einträge vorhanden...)
Neueste Publikationen in heiBIB 
(ingesamt sind 80 Publikationen erfasst)
- Küper, Katharina: Dipeptides in CSF and plasma : diagnostic and therapeutic potential in neurological diseases / Katharina Küper, Gernot Poschet, Julia Rossmann, Sven F. Garbade, Alexander Spiegelhalter, Dan Wen, … , 2025. - 9 S. : Illustrationen
In: Amino acids, ISSN 1438-2199. 57(2025), Artikel-ID 2, Seite 1-9
DOI: 10.1007/s00726-024-03434-1
- Tokatly Latzer, Itay: Clinical and molecular outcomes from the 5-Year natural history study of SSADH deficiency, a model metabolic neurodevelopmental disorder / Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar-Saber, Henry H.C. Lee, Mariarita Bertoldi… , 24 April 2024. - 15 S. : Illustrationen
In: Journal of neurodevelopmental disorders, ISSN 1866-1955. 16(2024), 1, Artikel-ID 21, Seite 1-15
DOI: 10.1186/s11689-024-09538-9
- Opladen, Thomas: Neurotransmitters : it is all about communication! / Thomas Opladen, Mariarita Bertoldi, 15 May 2024. - 2 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 47(2024), 3 vom: März, Seite 409-410
DOI: 10.1002/jimd.12748
- Reischl-Hajiabadi, Anna Theresa: Newborn screening for aromatic l-amino acid decarboxylase deficiency : strategies, results, and implication for prevalence calculations / Anna T. Reischl-Hajiabadi, Jürgen G. Okun, Dirk Kohlmüller, Georgi Manukjan, Sebastian Hegert, Jürge… , 31 January 2024. - 7 S.
In: Molecular genetics and metabolism, ISSN 1096-7206. 141(2024), 3, Artikel-ID 108148, Seite 108148-1-108148-7
DOI: 10.1016/j.ymgme.2024.108148
- Julià-Palacios, Natalia: The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency / Natalia Alexandra Julia-Palacios, Oya Kuseyri Hübschmann, Mireia Olivella, Roser Pons, Gabriella Hor… , May 2024. - 16 S. : Illustrationen
In: Journal of inherited metabolic disease, ISSN 1573-2665. 47(2024), 3 vom: Mai, Seite 447-462
DOI: 10.1002/jimd.12723
- Deininger, Luca: An AI-based segmentation and analysis pipeline for high-field MR monitoring of cerebral organoids / Luca Deininger, Sabine Jung-Klawitter, Ralf Mikut, Petra Richter, Manuel Fischer, Kianush Karimian-J… , 01 December 2023. - 9 S. : Illustrationen
In: Scientific reports, ISSN 2045-2322. 13(2023), Artikel-ID 21231, Seite 1-9
DOI: 10.1038/s41598-023-48343-7
- Tokatly Latzer, Itay: Phenotypic correlates of structural and functional protein impairments resultant from ALDH5A1 variants / Itay Tokatly Latzer, Jean-Baptiste Roullet, Samuele Cesaro, Melissa L. DiBacco, Erland Arning, Alexa… , 14 November 2023. - 22 S.
In: Human genetics, ISSN 1432-1203. 142(2023), 12, Seite 1755-1776
DOI: 10.1007/s00439-023-02613-6
- Jung-Klawitter, Sabine: Tyrosine hydroxylase variants influence protein expression, cellular localization, stability, enzymatic activity and the physical interaction between tyrosine hydroxylase and GTP cyclohydrolase 1 / Sabine Jung-Klawitter, Petra Richter, Yuheng Yuan, Karin Welzel, Marie Kube, Stella Bähr, Alexander … , 12 December 2023. - 16 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. (2023), online version of record, Seite 1-16
DOI: 10.1002/jimd.12690
- Badnjarević, Ivana: Navigating the rare neurotransmitter disease diagnosis : Insights from patients and health care professionals / Ivana Badnjarevic, Kelly Moyer, Mariarita Bertoldi, Thomas Opladen, Lisa Flint, 2023. - 4 S. : Illustrationen
In: Journal of inherited metabolic disease, ISSN 1573-2665. (2023), online ahead of print
DOI: 10.1002/jimd.12675
- Himmelreich, Nastassja: Corrigendum to : Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes / Nastassja Himmelreich, Mariarita Bertoldi, Majid Alfadhel, Malak Ali Alghamdi, Yair Anikster, Xinhua… , 7 July 2023. - 5 S.
In: Molecular genetics and metabolism, ISSN 1096-7206. 139(2023), 4, Artikel-ID 107647, Seite 1-5
DOI: 10.1016/j.ymgme.2023.107647
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