Universitäts-Kinderspital Zürich

Hospital


Location: Zürich, Switzerland (CH) CH

ISNI: 0000000107264330

ROR: https://ror.org/035vb3h42

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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Unpublished / Preprint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

Isolated nocturnal and isolated daytime hypertension associate with altered cardiovascular morphology and function in children with chronic kidney disease: findings from the Cardiovascular Comorbidity in Children with Chronic Kidney Disease study (2019) Düzova A, Karabay Bayazit A, Canpolat N, Niemirska A, Kaplan Bulut I, Azukaitis K, Karagoz T, et al. Journal article Secondary prevention measures in anaphylaxis patients: Data from the anaphylaxis registry (2019) Kraft M, Knop MP, Renaudin JM, Scherer Hofmeier K, Pfoehler C, Bilo MB, Lang R, et al. Journal article Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly (2019) Boonsawat P, Joset P, Steindl K, Oneda B, Gogoll L, Azzarello-Burri S, Sheth F, et al. Conference contribution Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly (2019) Boonsawat P, Joset P, Steindl K, Oneda B, Gogoll L, Azzarello-Burri S, Sheth F, et al. Journal article The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and high-resolution copy number study (2019) Papuc S, Abela L, Steindl K, Begemann A, Simmons T, Schmitt B, Zweier M, et al. Conference contribution The functional consequences of SCN2A mutations determine the phenotype (2019) Begemann A, Acuna M, Zweier M, Sticht H, Steindl K, Besnard M, Hackenberg A, et al. Conference contribution The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study (2019) Papuc SM, Abela L, Steindl K, Begemann A, Simmons TL, Schmitt B, Zweier M, et al. Journal article Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes (2019) Begemann A, Acuna MA, Zweier M, Vincent M, Steindl K, Bachmann-Gagescu R, Hackenberg A, et al. Journal article Presence of centromeric but absence of telomeric group B KIR haplotypes in stem cell donors improve leukaemia control after HSCT for childhood ALL (2019) Babor F, Peters C, Manser AR, Glogova E, Sauer M, Pötschger U, Ahlmann M, et al. Journal article Antithrombotic therapy in pediatric ventricular assist devices: Multicenter survey of the European EXCOR Pediatric Investigator Group (2018) Miera O, Schmitt KL, Akintuerk H, Boet A, Cesnjevar R, Chilas T, Fleck T, et al. Journal article
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