1. "Building bridges"—An opportunity to connect, inspire, and innovate. SSIEM 2019 Annual Symposium in Rotterdam, The Netherlands. Issue 1 (11th January 2021) Authors: van der Ploeg, Ans T. Journal: Journal of inherited metabolic disease Issue: Volume 44:Issue 1(2021) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. "Crossing borders" SSIEM 2014 annual symposium in Innsbruck. Issue 4 (20th June 2015) Authors: Karall, Daniela; Scholl‐Bürgi, Sabine; Zschocke, Johannes Journal: Journal of inherited metabolic disease Issue: Volume 38:Issue 4(2015) Page Start: 619 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. "Old Roads—New Connections" SSIEM 2018 Annual Symposium in Athens. Issue 1 (20th January 2020) Authors: Michelakakis, Helen Journal: Journal of inherited metabolic disease Issue: Volume 43:Issue 1(2020) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. "Transcriptomics": molecular diagnosis of inborn errors of metabolism via RNA‐sequencing. Issue 3 (25th January 2018) Authors: Kremer, Laura S.; Wortmann, Saskia B.; Prokisch, Holger Journal: Journal of inherited metabolic disease Issue: Volume 41:Issue 3(2018) Page Start: 525 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. 100 years of inherited metabolic disorders in Austria—A national registry of minimal birth prevalence, diagnosis, and clinical outcome of inborn errors of metabolism in Austria between 1921 and 2021. Issue 2 (17th October 2021) Authors: Ramoser, Gabriele; Caferri, Federica; Radlinger, Bernhard; Brunner‐Krainz, Michaela; Herbst, Sybille; Huemer, Martina; Hufgard‐Leitner, Miriam; Kircher, Susanne G.; Konstantopoulou, Vassiliki; Löscher, Wolfgang; Möslinger, Dorothea; Plecko, Barbara; Spenger, Johannes; Stulnig, Thomas; Sunder‐Plas... Journal: Journal of inherited metabolic disease Issue: Volume 45:Issue 2(2022) Page Start: 144 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. 12th international congress of inborn errors of metabolism, 3rd–6th September, 2013. Issue 4 (26th June 2014) Authors: Campistol, Jaime; Ribes, Antonia Journal: Journal of inherited metabolic disease Issue: Volume 37:Issue 4(2014) Page Start: 481 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. 1H‐MRS in glutaric aciduria type 1: impact of biochemical phenotype and age on the cerebral accumulation of neurotoxic metabolites. Issue 5 (10th April 2015) Authors: Harting, Inga; Boy, Nikolas; Heringer, Jana; Seitz, Angelika; Bendszus, Martin; Pouwels, Petra J.W.; Kölker, Stefan Journal: Journal of inherited metabolic disease Issue: Volume 38:Issue 5(2015) Page Start: 829 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. 3‐Hydroxyisobutyrate dehydrogenase (HIBADH) deficiency—A novel disorder of valine metabolism. Issue 6 (5th July 2021) Authors: Meyer, Melanie; Hollenbeck, Jana C.; Reunert, Janine; Seelhöfer, Anja; Rust, Stephan; Fobker, Manfred; Biskup, Saskia; Och, Ulrike; Linden, Mechthild; Sass, Jörn Oliver; Marquardt, Thorsten Journal: Journal of inherited metabolic disease Issue: Volume 44:Issue 6(2021) Page Start: 1323 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. 3‐Hydroxyisobutyric acid dehydrogenase deficiency: Expanding the clinical spectrum and quantitation of D‐ and L‐3‐Hydroxyisobutyric acid by an LC–MS/MS method. Issue 3 (7th March 2022) Authors: Sasarman, Florin; Ferdinandusse, Sacha; Sinasac, David S.; Fung, Ernest; Sparkes, Rebecca; Reeves, Melanie; Rombough, Catherine; Sass, Jörn Oliver; Voit, Renate; Ruiter, Jos P. N.; Koster, Janet; Waterham, Hans R.; Pasquini, Elisabetta; Donati, Maria A.; Marquardt, Thorsten; Wanders, Ronald J. A.... Journal: Journal of inherited metabolic disease Issue: Volume 45:Issue 3(2022) Page Start: 445 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. 3‐Methylcrotonyl‐CoA carboxylase deficiency: to screen or not to screen?. Issue 2 (11th December 2015) Authors: Wilcken, Bridget Journal: Journal of inherited metabolic disease Issue: Volume 39:Issue 2(2016) Page Start: 171 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗