Dubai Hospital

Hospital


Location: Dubai, United Arab Emirates (AE) AE

ISNI: 0000000417967314

ROR: https://ror.org/04czxss33

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

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Abstract

Journal

Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions (2024) Deutsch K, Klämbt V, Kitzler TM, Jobst-Schwan T, Schneider R, Buerger F, Seltzsam S, et al. Journal article Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract (2022) Wu CHW, Lim TY, Wang C, Seltzsam S, Zheng B, Schierbaum L, Schneider S, et al. Journal article EARLY CHILDHOOD HEIGHT-ADJUSTED TOTAL KIDNEY VOLUME AS A RISK MARKER OF KIDNEY SURVIVAL IN AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE (ARPKD) (2021) Burgmaier K, Kilian S, Arbeiter K, Atmis B, Buescher A, Derichs U, Dursun I, et al. Conference contribution Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD) (2020) Burgmaier K, Ariceta G, Bald M, Buescher AK, Burgmaier M, Erger F, Gessner M, et al. Journal article Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract (2018) Van Der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, et al. Journal article Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease. (2018) Burgmaier K, Kunzmann K, Ariceta G, Bergmann C, Buescher AK, Burgmaier M, Dursun I, et al. Journal article The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase? (2017) Azukaitis K, Simkova E, Majid MA, Galiano M, Benz K, Amann KU, Bockmeyer C, et al. Journal article