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First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.
Korenke GC, Krasemann E, Meier V, Beuche W, Hunneman DH, Hanefeld F. Korenke GC, et al. Among authors: hanefeld f. Hum Mutat. 1998;Suppl 1:S204-6. doi: 10.1002/humu.1380110166. Hum Mutat. 1998. PMID: 9452087 No abstract available.
Glyceroltrioleate/glyceroltrierucate therapy in 16 patients with X-chromosomal adrenoleukodystrophy/adrenomyeloneuropathy: effect on clinical, biochemical and neurophysiological parameters.
Korenke GC, Hunneman DH, Kohler J, Stöckler S, Landmark K, Hanefeld F. Korenke GC, et al. Among authors: hanefeld f. Eur J Pediatr. 1995 Jan;154(1):64-70. doi: 10.1007/BF01972976. Eur J Pediatr. 1995. PMID: 7895759
Intrathecal IgA synthesis in X-linked cerebral adrenoleukodystrophy.
Korenke GC, Reiber H, Hunneman DH, Hanefeld F. Korenke GC, et al. Among authors: hanefeld f. J Child Neurol. 1997 Aug;12(5):314-20. doi: 10.1177/088307389701200505. J Child Neurol. 1997. PMID: 9378899
Progression of X-linked adrenoleukodystrophy under interferon-beta therapy.
Korenke GC, Christen HJ, Kruse B, Hunneman DH, Hanefeld F. Korenke GC, et al. Among authors: hanefeld f. J Inherit Metab Dis. 1997 Mar;20(1):59-66. doi: 10.1023/a:1005361607523. J Inherit Metab Dis. 1997. PMID: 9061569
Enhanced lymphocyte proliferation in patients with adrenoleukodystrophy treated with erucic acid (22:1)-rich triglycerides.
Pour RB, Stöckler-Ipsiroglu S, Hunneman DH, Gahr M, Korenke GC, Pabst W, Hanefeld F, Peters A. Pour RB, et al. Among authors: hanefeld f. J Inherit Metab Dis. 2000 Mar;23(2):113-9. doi: 10.1023/a:1005657530372. J Inherit Metab Dis. 2000. PMID: 10801052 Clinical Trial.
Decreased platelet membrane anisotropy in patients with adrenoleukodystrophy treated with erucic acid (22:1)-rich triglycerides.
Stöckler S, Opper C, Greinacher A, Hunneman DH, Korenke GC, Unkrig CJ, Hanefeld F. Stöckler S, et al. Among authors: hanefeld f. J Inherit Metab Dis. 1997 Mar;20(1):54-8. doi: 10.1023/a:1005309623452. J Inherit Metab Dis. 1997. PMID: 9061568
Actin-related myopathy without any missense mutation in the ACTA1 gene.
Goebel HH, Brockmann K, Bönnemann CG, Warlo IA, Hanefeld F, Labeit S, Durling HJ, Laing NG. Goebel HH, et al. Among authors: hanefeld f. J Child Neurol. 2004 Feb;19(2):149-53. doi: 10.1177/08830738040190021201. J Child Neurol. 2004. PMID: 15072110
MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin.
Trappe R, Laccone F, Cobilanschi J, Meins M, Huppke P, Hanefeld F, Engel W. Trappe R, et al. Among authors: hanefeld f. Am J Hum Genet. 2001 May;68(5):1093-101. doi: 10.1086/320109. Epub 2001 Apr 17. Am J Hum Genet. 2001. PMID: 11309679 Free PMC article.
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