Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities von Vissers, Lisenka E.L.M., de Vries, Bert B.A., Osoegawa, Kazutoyo, Janssen, Irene M., Feuth, Ton, Choy, Chik On, Straatman, Huub, van der Vliet, Walter, Huys, Erik H.L.P.G., van Rijk, Anke, Smeets, Dominique, van Ravenswaaij-Arts, Conny M.A., Knoers, Nine V., van der Burgt, Ineke, de Jong, Pieter J., Brunner, Han G., van Kessel, Ad Geurts, Schoenmakers, Eric F.P.M., Veltman, Joris A.

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MO071NPHP1 DELETIONS CAUSE ESRD IN 0.9% OF ADULT-ONSET CASES von Snoek, R, van Setten, J, Keating, BJ, van der Zwaag, A, Knoers, NV, de Borst, MH, van Eerde, AM

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Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine von Peter M. T. Deen, Marian A. J. Verdijk, Nine V. A. M. Knoers, Wieringa, Bé, Leo A. H. Monnens, van Os, Carel H., van Oost, Bernard A.

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Decreased bone density and treatment in patients with autosomal recessive cutis laxa von Noordam, C, Funke, S, Knoers, NV, Jira, P, Wevers, RA, Urban, Z, Morava, E

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Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus von Shalev, Hanna, Romanovsky, Igor, Knoers, Nine V., Lupa, Salomon, Landau, Daniel

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Rare but Relevant Kidney Disorders von Glaudemans, B, van der Wijst, J, Scola, R, Lorenzoni, PJ, Heister, A, van der Kemp, A, Knoers, NV, Hoenderop, JG, Bindels, RJ

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Partial iris hypoplasia in a patient with an interstitial subtelomeric 6p deletion not including the forkhead transcription factor gene FOXC1 von Koolen, David A, Knoers, Nine V A M, Nillesen, Willy M, Slabbers, Gordon H P R, Smeets, Dominique, de Leeuw, Nicole, Sistermans, Erik A, de Vries, Bert B A

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Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference von Blanchard, A, Bockenhauer, D, Bolignano, D, Calò, LA, Cosyns, E, Devuyst, O, Ellison, DH, Karet Frankl, FE, Knoers, NV, Konrad, M, Lin, SH, Vargas-Poussou, R

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DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport von Hartill, VL, Van de Hoek, G, Patel, MP, Little, R, Watson, CM, Berry, IR, Shoemark, A, Abdelmottaleb, D, Parkes, E, Bacchelli, C, Szymanska, K, Knoers, NV, Scambler, PJ, Ueffing, M, Boldt, K, Yates, R, Winyard, PJ, Adler, B, Moya, E, Hattingh, L, Shenoy, A, Hogg, C, Sheridan, E, Roepman, R, Norris, D, Mitchison, HM, Giles, RH, Johnson, CA

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DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport von Hartill, VL, van de Hoek, G, Patel, MP, Little, R, Watson, CM, Berry, IR, Shoemark, A, Abdelmottaleb, D, Parkes, E, Bacchelli, C, Szymanska, K, Knoers, NV, Scambler, PJ, Ueffing, M, Boldt, K, Yates, R, Winyard, PJ, Adler, B, Moya, E, Hattingh, L, Shenoy, A, Hogg, C, Sheridan, E, Roepman, R, Norris, D, Mitchison, HM, Giles, RH, Johnson, CA

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Screen-based identification and validation of four new ion channels as regulators of renal ciliogenesis von Slaats, GG, Wheway, G, Foletto, V, Szymanska, K, van Balkom, BWM, Logister, I, Den Ouden, K, Keijzer-Veen, MG, Lilien, MR, Knoers, NV, Johnson, CA, Giles, RH

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Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement von Schmidts, M, Arts, HH, Bongers, EM, Yap, Z, Oud, MM, Antony, D, Duijkers, L, Emes, RD, Stalker, J, Yntema, JB, Plagnol, V, Hoischen, A, Gilissen, C, Forsythe, E, Lausch, E, Veltman, JA, Roeleveld, N, Superti-Furga, A, Kutkowska-Kazmierczak, A, Kamsteeg, EJ, Elçioglu, N, van Maarle, MC, Graul-Neumann, LM, Devriendt, K, Smithson, SF, Wellesley, D, Verbeek, NE, Hennekam, RC, Kayserili, H, Scambler, PJ, Beales, PL, UK10K, Knoers, NV, Roepman, R, Mitchison, HM

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