Nina-Maria Wilpert

7PUBLICATIONS
130CO-AUTHORS
Microelectromechanical systems (MEMS)Child and adolescent developmentInfant and child healthGene expression (incl. microarray and other genome-wide approaches)Gene and molecular therapy
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (7)

|May 27, 2025
MCT8 Deficiency in Females.

Stefan Groeneweg, Ferdy S van Geest, Floor van der Most

|Mar 15, 2025
Patients with Allan-Herndon-Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa Treatment.

Nina-Maria Wilpert, Angela L Hewitt, Roser Pons

|Aug 29, 2024
Normal Values for the fT3/fT4 Ratio: Centile Charts (0-29 Years) and Their Application for the Differential Diagnosis of Children with Developmental Delay.

Nina-Maria Wilpert, Roma Thamm, Michael Thamm

|Jun 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.

Hellen Lesmann, Alexander Hustinx, Shahida Moosa

|Oct 26, 2023
Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review.

Nina-Maria Wilpert, Davide Tonduti, Ylenia Vaia

|Jul 29, 2023
Pediatric de novo movement disorders and ataxia in the context of SARS-CoV-2.

Nina-Maria Wilpert, Ana Luísa de Almeida Marcelino, Ellen Knierim

Pageof 2

Frequent Collaborators

5 joint publications

Markus Schuelke

4 joint publications

Heiko Krude

2 joint publications

Angela M Kaindl

1 joint publications

W Edward Visser