Gajja Salomons

PROF.DR., (Principal Investigator)

20062020

Research output per year

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Research Output

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2016

2-hydroxyglutaric aciduria

Struys, EA., van der Knaap, MS. & Salomons, GS., 18 Aug 2016, Inherited Metabolic Disease in Adults: A Clinical Guide. Hollak, CEM. & Lachmann, R. (eds.). Oxford University Press, Chapter 22

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

Creatine deficiency syndromes

Stöckler-Isiroglu, S., Mercimek-Mahmutoglu, S. & Salomons, GS., 2016, Metabolic Diseases: Diagnosis and Treatment. Saudubray, J. M., Baumgartner, M. & Walter, J. H. (eds.). 6 ed. Heidelberg, Berlin, Germany: Springer-Verlag Berlin Heidelberg, p. 243-248

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

2015

Creatine Deficiency Syndromes

Mahmutoglu, S. & Salomons, G. S., 2015, GeneReviews® [internet]. Seattle (WA): University of Washington

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

2012

Creatine deficiency syndromes

Stöckler, S. & Salomons, G. S., 2012, Inborn Metabolic diseases. p. 239-247

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic