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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

Wiley, Hoboken, United States of America

Scopus rating (2023): CiteScore 9.5 SJR 1.591 SNIP 1.541

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	Wiley, Hoboken
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 othersChapman, 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 othersOkun, 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 othersWilichowski, 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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