Nitash Zwaveling-Soonawala

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 5

Top Topics

Peritoneal Dialysis

Replacement Therapy

Machine Learning

Top Venues

The Journal of clinical endocrinology and metabolism

American journal of medical genetics. Part A

European journal of pediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Christiaan F Mooij, Nitash Zwaveling-Soonawala, Jacquelien J Hillebrand, Adrianus Sarinus Paulus van Trotsenburg
Approach to the Patient: Challenging Cases of Pediatric Thyrotoxicosis. The Journal of clinical endocrinology and metabolism (2024)
Kevin Stroek, An Ruiter, Annelieke van der Linde, Mariëtte T Ackermans, Marelle J Bouva, Henk Engel, Bernadette Jakobs, Evelien A Kemper, Erica L T van den Akker, Mirjam E van Albada, Gianni Bocca, Martijn J J Finken, Sabine Elisabeth Hannema, E C A Mieke Houdijk, Hetty J van der Kamp, Vera van Tellingen, Adrianus Sarinus Paulus van Trotsenburg, Nitash Zwaveling-Soonawala, Annet M Bosch, Robert de Jonge, Annemieke C Heijboer, Hedi L Claahsen-van der Grinten, Anita Boelen
Second-tier Testing for 21-Hydroxylase Deficiency in the Netherlands: A Newborn Screening Pilot Study. The Journal of clinical endocrinology and metabolism 106 (11) (2021)
Peter Lauffer, A S Paul van Trotsenburg, Nitash Zwaveling-Soonawala
Low free thyroxine and normal thyroid-stimulating hormone in infants and children: possible causes and diagnostic work-up. European journal of pediatrics 180 (7) (2021)
Jolanda C Naafs, Jan Pieter Marchal, Paul H Verkerk, Eric Fliers, Adrianus Sarinus Paulus van Trotsenburg, Nitash Zwaveling-Soonawala
Health-Related Quality of Life in Patients With Early-Detected Central Congenital Hypothyroidism. The Journal of clinical endocrinology and metabolism 106 (10) (2021)
Nitash Zwaveling-Soonawala, Saskia M Maas, Marielle Alders, Charles B Majoie, Eric Fliers, A S Paul van Trotsenburg, Raoul C M Hennekam
Variants in KAT6A and pituitary anomalies. American journal of medical genetics. Part A 173 (9) (2017)