Violetta Csákváry

Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium‐sensing receptor gene

Judit Tõke, Gábor Czirják, Attila Patócs et al. · Clinical Endocrinology · 2007 · 30 citations

Relation between biomarkers and clinical severity in patients with Smith–Lemli–Opitz syndrome

Anna V. Oláh, Gabriella P. Szabó, József Varga et al. · European Journal of Pediatrics · 2013 · 22 citations · Full text

Clinical Disorders, Smith–lemli–opitz Syndrome, Diagnosis +2

Mutational Spectrum of Smith-Lemli-Opitz Syndrome Patients in Hungary

István Balogh, Katalin Koczok, György Szabó et al. · Molecular Syndromology · 2012 · 18 citations · Full text

Association of Lean and Fat Body Mass, Bone Biomarkers and Gonadal Steroids with Bone Mass during Pre- and Midpuberty

Violetta Csákváry, Éva Erhardt, P. Vargha et al. · Hormone Research in Paediatrics · 2012 · 17 citations

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Macimorelin in Children with Suspected Growth Hormone Deficiency: An Open-Label, Group Comparison, Dose-Escalation Trial

Violetta Csákváry, Nicola Ammer, Ekaterine Bakhtadze Bagci et al. · Hormone Research in Paediatrics · 2021 · 14 citations · Full text