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Journal of inherited metabolic disease : JIMD ; official journal of the Society for the Study of Inborn Errors of Metabolism

ISSNs: 0141-8955

Additional searchable ISSN (electronic): 1573-2665

Springer, Dordrecht [u. a.], United States of America

Scopus rating (2025): CiteScore 6.4 SJR 1.401 SNIP 1.592

Journal

Titles	Journal of inherited metabolic disease : JIMD ; official journal of the Society for the Study of Inborn Errors of Metabolism(1978 → …) Journal of Inherited Metabolic Disease
Additional searchable titles	J Inherited Metab Dis, J. INHERIT. METAB. DIS., J. Inher. Metab. Dis.
ISSNs	0141-8955
Additional searchable ISSN (electronic)	1573-2665
Publisher	Springer, Dordrecht [u. a.]
Country/Territory	United States of America
Scopus ID	15106
ZDB-ID	2006875-X

Keywords

ASJC Scopus subject areas

Genetics
Genetics (clinical)

Library keywords

610 Medicine and health

Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revision

Boy, N., Mühlhausen, C., Maier, E. M., Ballhausen, D., Baumgartner, M. R., Beblo, S. & Burgard, P. & 27 others, Chapman, K. A., Dobbelaere, D., Heringer-Seifert, J., Fleissner, S., Grohmann-Held, K., Hahn, G., Harting, I., Hoffmann, G. F., Jochum, F., Karall, D., Konstantopoulous, V., Krawinkel, M. B., Lindner, M., Märtner, E. M. C., Nuoffer, J. M., Okun, J. G., Plecko, B., Posset, R., Sahm, K., Scholl-Bürgi, S., Thimm, E., Walter, M., Williams, M., vom Dahl, S., Ziagaki, A., Zschocke, J. & Kölker, S., May 2023, In: Journal of inherited metabolic disease : JIMD ; official journal of the Society for the Study of Inborn Errors of Metabolism. 46, 3, p. 482-519 38 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

Human heterologous liver cells transiently improve hyperammonemia and ureagenesis in individuals with severe urea cycle disorders

Meyburg, J., Opladen, T., Spiekerkötter, U., Schlune, A., Schenk, J. P., Schmidt, J. & Weitz, J. & 10 others, Okun, J., Bürger, F., Omran, T. B., Abdoh, G., Al Rifai, H., Monavari, A., Konstantopoulou, V., Kölker, S., Yudkoff, M. & Hoffmann, G. F., 1 Jan 2018, In: Journal of Inherited Metabolic Disease. 41, 1, p. 81-90 10 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

Aromatic l-amino acid decarboxylase deficiency: Clinical features, drug therapy and follow-up

Manegold, C., Hoffmann, G. F., Degen, I., Ikonomidou, H., Knust, A., Laaß, M. W. & Pritsch, M. & 2 others, Wilichowski, E. & Hörster, F., 2009, In: Journal of Inherited Metabolic Disease. 32, 3, p. 371-380 10 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

Three-generational alkaptonuria in a non-consanguineous family

Oexle, K., Engel, K., Tinschert, S., Haas, D. & Lee-Kirsch, M. A., Dec 2008, In: Journal of Inherited Metabolic Disease. 31, Suppl 2, p. S425-S430

Research output: Contribution to journal › Research article › Contributed › peer-review

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Research Portal of the TU Dresden

Keywords

ASJC Scopus subject areas

Library keywords

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