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Nina-Maria Wilpert

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Neuropsychiatric Disease and Treatment|October 26, 2023
Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature ReviewNina-Maria Wilpert, Davide Tonduti, Ylenia Vaia, et al.
International Journal of Molecular Sciences|August 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 DelayNina-Maria Wilpert, Roma Thamm, Michael Thamm, et al.
European Journal of Medical Genetics|July 20, 2021
Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndromeNina-Maria Wilpert, Florent Marguet, Camille Maillard, et al.
Journal of Neurology|July 29, 2023
Pediatric de novo movement disorders and ataxia in the context of SARS-CoV-2Nina-Maria Wilpert, Ana Luísa de Almeida Marcelino, Ellen Knierim, et al.
Thyroid : Official Journal of the American Thyroid Association|March 8, 2020
Spatiotemporal Changes of Cerebral Monocarboxylate Transporter 8 ExpressionNina-Maria Wilpert, Martin Krueger, Robert Opitz, et al.
Molecular Genetics and Metabolism|December 31, 2021
Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley SyndromeSilvia Masnada, Catherine Sarret, Clara Eleonora Antonello, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2025
Patients with Allan-Herndon-Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa TreatmentNina-Maria Wilpert, Angela L Hewitt, Roser Pons, et al.
Plos Computational Biology|January 5, 2023
Ten simple rules for implementing open and reproducible research practices after attending a training courseVerena Heise, Constance Holman, Hung Lo, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2025
MCT8 Deficiency in FemalesStefan Groeneweg, Ferdy S van Geest, Floor van der Most, et al.
Research Square|June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Neuropsychiatric Disease and Treatment|October 26, 2023
Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature ReviewNina-Maria Wilpert, Davide Tonduti, Ylenia Vaia, et al.
International Journal of Molecular Sciences|August 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 DelayNina-Maria Wilpert, Roma Thamm, Michael Thamm, et al.
European Journal of Medical Genetics|July 20, 2021
Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndromeNina-Maria Wilpert, Florent Marguet, Camille Maillard, et al.
Journal of Neurology|July 29, 2023
Pediatric de novo movement disorders and ataxia in the context of SARS-CoV-2Nina-Maria Wilpert, Ana Luísa de Almeida Marcelino, Ellen Knierim, et al.
Thyroid : Official Journal of the American Thyroid Association|March 8, 2020
Spatiotemporal Changes of Cerebral Monocarboxylate Transporter 8 ExpressionNina-Maria Wilpert, Martin Krueger, Robert Opitz, et al.
Molecular Genetics and Metabolism|December 31, 2021
Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley SyndromeSilvia Masnada, Catherine Sarret, Clara Eleonora Antonello, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2025
Patients with Allan-Herndon-Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa TreatmentNina-Maria Wilpert, Angela L Hewitt, Roser Pons, et al.
Plos Computational Biology|January 5, 2023
Ten simple rules for implementing open and reproducible research practices after attending a training courseVerena Heise, Constance Holman, Hung Lo, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2025
MCT8 Deficiency in FemalesStefan Groeneweg, Ferdy S van Geest, Floor van der Most, et al.
Research Square|June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Pageof 2