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Neuropsychiatric Disease and Treatment
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October 26, 2023
Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review
Nina-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 Delay
Nina-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 syndrome
Nina-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-2
Nina-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 Expression
Nina-Maria Wilpert, Martin Krueger, Robert Opitz, et al.
Molecular Genetics and Metabolism
|
December 31, 2021
Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome
Silvia 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 Treatment
Nina-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 course
Verena Heise, Constance Holman, Hung Lo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 27, 2025
MCT8 Deficiency in Females
Stefan 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 diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
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Search research articles
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Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Neuropsychiatric Disease and Treatment
|
October 26, 2023
Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review
Nina-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 Delay
Nina-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 syndrome
Nina-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-2
Nina-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 Expression
Nina-Maria Wilpert, Martin Krueger, Robert Opitz, et al.
Molecular Genetics and Metabolism
|
December 31, 2021
Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome
Silvia 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 Treatment
Nina-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 course
Verena Heise, Constance Holman, Hung Lo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 27, 2025
MCT8 Deficiency in Females
Stefan 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 diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
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of 2