1. 2011
  2. Complex III staining in blue native polyacrylamide gels.

    Smet, J., De Paepe, B., Seneca, S., Lissens, W., Kotarsky, H., De Meirleir, L., Fellman, V. & Van Coster, R., 12 Apr 2011, In : J Inherit Metab Dis. 34, p. 741-747 7 p.

    Research output: Contribution to journalArticle

  3. DETECTION OF MITOCHONDRIAL DNA DEPLETION USING RELATIVE REAL-TIME PCR

    Vancampenhout, K., Van Dooren, S., De Meirleir, L., Smet, J., Vancoster, R., Lissens, W., Bonduelle, M-L. & Seneca, S., 5 Apr 2011, Unknown.

    Research output: Chapter in Book/Report/Conference proceedingMeeting abstract (Book)Research

  4. Rapid, sensitive and discriminatory HbS and HbC mutation detection using High Resolution Melting Analysis

    Van Dooren, S., Endels, K., Keymolen, K., Seneca, S., Liebaers, I. & Lissens, W., 4 Mar 2011, Abstract book of the 11th Annual Meeting of the Belgian Society of Human Genetics. p. 98-98 1 p.

    Research output: Chapter in Book/Report/Conference proceedingMeeting abstract (Book)Research

  5. Array-CGH analysis in patients with maturation arrest of spermatogenesis

    Stouffs, K., Vandermaelen, D., Massart, A., Menten, B., Tournaye, H. & Lissens, W., 2011, In : Eur J Hum Genet. 19, p. 162-162 1 p.

    Research output: Contribution to journalEditorial

  6. Molecular basis of inherited Protein C deficiency in Belgian families

    Orlando, C., Lissens, W. & Jochmans, K., 2011, In : Belgian Journal of Hematology. p. 7-8 2 p.

    Research output: Contribution to journalMeeting abstract (Journal)

  7. Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages

    Stouffs, K., Vandermaelen, D., Tournaye, H., Liebaers, I. & Lissens, W., 2011, In : Reproductive BioMedicine Online. 22, p. 65-71 7 p.

    Research output: Contribution to journalArticle

  8. Screening for nuclear genetic defects in the ATP synthase-associated genes TMEM70, ATP12 and ATP5E in patients with 3-methylglutaconic aciduria.

    Tort, F., Del Toro, M., Lissens, W., Montoya, J., Fernandez-Burriel, M., Font, A., Bujan, N., Navarro-Sastre, A., Lopez-Gallardo, E., Arranz, J., Riudor, E., Briones, P. & Ribes, A., 2011, In : Clin Genet. 80, September, p. 297-300 4 p.

    Research output: Contribution to journalArticle

  9. TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria

    Jansen, A. C., Oostra, A., Desprechins, B., De Vlaeminck, Y., Verhelst, H., Régal, L., Verloo, P., Bockaert, N., Keymolen, K., Seneca, S., De Meirleir, L. & Lissens, W., 2011, In : Neurology. 76, 11, p. 988-92 5 p.

    Research output: Contribution to journalArticle

  10. What about gr/gr deletions and male infertility? Systematic review and meta-analysis.

    Stouffs, K., Lissens, W., Tournaye, H. & Haentjens, P., 2011, In : Human Reproduction Update. 17, March-April, p. 197-209 13 p.

    Research output: Contribution to journalArticle

  11. 2010
  12. A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and severity of hypercalcaemia

    Hannan, F. M., Nesbit, M. A., Christie, P. T., Lissens, W., Van Der Schueren, B., Bex, M., Bouillon, R. & Thakker, R. V., 16 Nov 2010, In : Clinical Endocrinology. 73, p. 715-722 8 p.

    Research output: Contribution to journalArticle

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