Hans Rudolf Lytchoff Eiberg

Hans Rudolf Lytchoff Eiberg

Associate Professor


  1. 1998
  2. Published

    Molecular genetic, clinical and psychiatric associations in nocturnal enuresis

    Hollmann, E., Gontard, A. V., Eiberg, Hans Rudolf Lytchoff, Rittig, S. & Lemkuhl, G., 1998, In: British Journal of Urology. 81, suppl. 3, p. 37-39

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Molecular genetics of nocturnal enuresis: Clinical and genetic heterogeneity

    Gontard, A. V., Eiberg, Hans Rudolf Lytchoff, Hollmann, E., Rittig, S. & Lehmkuhl, G., 1998, In: Acta Paediatrica. 87, p. 571-578

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    The Ala/Val98 Polymorphism of the Hepatocyte Nuclear Factor-1a Gene Contributes to the Interindividual Variation in Serum C-Peptide Response during an Oral Glucose Tolerance Test: Evidence from.....

    Urhammer, S. A., Hansen, T., Ekstrøm, C. T., Eiberg, Hans Rudolf Lytchoff & Pedersen, O., 1998, In: Journal of Clinical Endocrinology and Metabolism. Vol. 83, No 12, p. 4506-4509

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    The effect of two frequent amino acid variant of the hepatocyte nuclear fact.-1a gene on estimates of pancr.ß-cell funct. in caucasian glucose-tolerant first-degree relatives of tp.2 diabetic ptt.

    Urhammer, S. A., Møller, A. M., Nyholm, B., Ekstrøm, C. T., Eiberg, Hans Rudolf Lytchoff, Clausen, J. O., Hansen, T., Pedersen, O. & Schmitz, O., 1998, In: Journal of Clinical Endocrinology and Metabolism. Vol. 83, no. 11, p. 3992-3995

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    The g/a Nucleotide Variant at Position -30 in the *Gb-Cell-Specific Glucokinase Gene Promotor Has No Impact on the *Gb-Cell Function in Danish Caucasians

    Urhammer, S. A., Hansen, T., Clausen, J. O., Eiberg, Hans Rudolf Lytchoff & Pedersen, O., 1998, In: Diabetes. 47, p. 1359-1361

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Total Genome Scan Analysis in a Single Extended Family for Primary Nocturnal Enuresis: Evidence for a New Locus (ENUR3) for Primary Nocturnal Enuresis on Chromosome 22q11

    Eiberg, Hans Rudolf Lytchoff, 1998, In: European Urology. 33 (suppl 3), p. 34-36

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. 1997
  9. Published

    (1997) Clinical enuresis phenotypes in familial nocturnal enuresis

    Gontard, A. V., Hollmann, E., Benden, B., Eiberg, Hans Rudolf Lytchoff, Rittig, S. & Lehmkuhl, G., 1997, In: Scandinavian Journal of Urology and Nephrology. 31 (suppl.183), p. 11-16

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    A Survey of the Newborn Populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey and Japan for the G985 Variant Allele with Haplotype Analysis at the Medium Chain Acyl-CoA Dehydrogenase Gene. Locus: Clinical and Evol.Con.

    Tanaka, K., Gregersen, N., Ribes, A., Kim, J., Kølvraa, S., Winter, V. S., Eiberg, Hans Rudolf Lytchoff, Martinez, G., Deufel, T., Leifert, B., Santer, R., Francois, B., Pronicka, E., Laszlo, A., Kmoch, S., Kremensky, I., Kalaydjicva, L., Ozalp, I. & Ito, M., 1997, In: Pediatric Research. vol 41, 2, p. 201-209

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Assignment of human plasma methylumbelliferyl-tetra-N-acetylchitotetraoside hydrolase or chitinase to chromosome 1 q by a linkage study

    Eiberg, Hans Rudolf Lytchoff & Tandt, W. R. D., 1997, In: Human Genetics. 101, p. 205-207

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24

    Nielsen, J. E., Koefoed, P., Abell, K., Eiberg, Hans Rudolf Lytchoff, Fenger, K., Niebuhr, E. & Sørensen, S. A., 1997, In: Human Molecular Genetics. Vol. 6, No. 11, p. 1811-1816

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 5291