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Page 1
Myotonic dystrophy associated with VACTERL? A case report.
Kölker S, Degen I, Koch MC, Lindner M, Haas D, Hoffmann GF. Kölker S, et al. Among authors: haas d. Neuropediatrics. 2001 Feb;32(1):53-4. doi: 10.1055/s-2001-12220. Neuropediatrics. 2001. PMID: 11318010 No abstract available.
Inherited disorders of cholesterol biosynthesis.
Haas D, Kelley RI, Hoffmann GF. Haas D, et al. Neuropediatrics. 2001 Jun;32(3):113-22. doi: 10.1055/s-2001-16618. Neuropediatrics. 2001. PMID: 11521206 Review.
Molecular analysis of the MVK and TNFRSF1A genes in patients with a clinical presentation typical of the hyperimmunoglobulinemia D with periodic fever syndrome: a low-penetrance TNFRSF1A variant in a heterozygous MVK carrier possibly influences the phenotype of hyperimmunoglobulinemia D with periodic fever syndrome or vice versa.
Stojanov S, Lohse P, Lohse P, Hoffmann F, Renner ED, Zellerer S, Kéry A, Shin YS, Haas D, Hoffmann GF, Belohradsky BH. Stojanov S, et al. Among authors: haas d. Arthritis Rheum. 2004 Jun;50(6):1951-8. doi: 10.1002/art.20264. Arthritis Rheum. 2004. PMID: 15188372 Free article.
Quantitative acylcarnitine profiling in peripheral blood mononuclear cells using in vitro loading with palmitic and 2-oxoadipic acids: biochemical confirmation of fatty acid oxidation and organic acid disorders.
Schulze-Bergkamen A, Okun JG, Spiekerkötter U, Lindner M, Haas D, Kohlmüller D, Mayatepek E, Schulze-Bergkamen H, Greenberg CR, Zschocke J, Hoffmann GF, Kölker S. Schulze-Bergkamen A, et al. Among authors: haas d. Pediatr Res. 2005 Nov;58(5):873-80. doi: 10.1203/01.PDR.0000181378.98593.3E. Epub 2005 Sep 23. Pediatr Res. 2005. PMID: 16183823
1,307 results