ArticleThyroid : official journal of the American Thyroid Association2021
Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by
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In one paragraph
Article in Thyroid : official journal of the American Thyroid Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.
0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 11% of its field
What it found
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Who cites it
20 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.
- 2024 European Thyroid Association Guidelines on diagnosis and management of genetic disorders of thyroid hormone transport, metabolism and action.European thyroid journal · 2024Guideline
- Reduced thyroid hormone transport in a human placental model with inhibited MCT8.European thyroid journal · 2026Article
- Novel Variants in the SLC16A2 Gene Associated With Allan-Herndon-Dudley Syndrome in China.Human mutation · 2026Article
- Peripheral manifestations of monocarboxylate transporter 8 deficiency: hepatic and skeletal muscle involvement.Frontiers in pediatrics · 2026Review
- Is It Time to Expand Newborn Screening for Congenital Hypothyroidism to Other Rare Thyroid Diseases?International journal of neonatal screening · 2025Review
- Maternal thyroid hormone is required to develop the hindbrain vasculature in zebrafish.Communications biology · 2025Article
- Patients with Allan-Herndon-Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa Treatment.Movement disorders : official journal of the Movement Disorder Society · 2025Observational
- Toward a treatment for thyroid hormone transporter MCT8 deficiency - achievements and challenges.European thyroid journal · 2024Review
- Combined Levothyroxine and Propylthiouracil Treatment in Children with Monocarboxylate Transporter 8 Deficiency: A Multicenter Case Series of 12 Patients.Thyroid : official journal of the American Thyroid Association · 2024Article
- Mapping Thyroid Hormone Action in the Human Brain.Thyroid : official journal of the American Thyroid Association · 2024Review
- Impaired T3 uptake and action in MCT8-deficient cerebral organoids underlie Allan-Herndon-Dudley syndrome.JCI insight · 2024Article
- Role and Clinical Significance of Monocarboxylate Transporter 8 (MCT8) During Pregnancy.Reproductive sciences (Thousand Oaks, Calif.) · 2023Review
- Maternal Administration of the CNS-Selective Sobetirome Prodrug Sob-AM2 Exerts Thyromimetic Effects in Murine MCT8-Deficient Fetuses.Thyroid : official journal of the American Thyroid Association · 2023Article
- Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review.Neuropsychiatric disease and treatment · 2023Article
- In a zebrafish biomedical model of human Allan-Herndon-Dudley syndrome impaired MTH signaling leads to decreased neural cell diversity.Frontiers in endocrinology · 2023Article
- Thyroid Hormone Transporters in Pregnancy and Fetal Development.International journal of molecular sciences · 2022Review
- Ganglioglioma with novel molecular features presenting in a child with Allan-Herndon-Dudley syndrome.BMJ case reports · 2022Article
- Measurement of Reverse Triiodothyronine Level and the Triiodothyronine to Reverse Triiodothyronine Ratio in Dried Blood Spot Samples at Birth May Facilitate Early Detection of Monocarboxylate Transporter 8 Deficiency.Thyroid : official journal of the American Thyroid Association · 2021Article
- Monocarboxylate Transporter 8 Deficiency: From Pathophysiological Understanding to Therapy Development.Frontiers in endocrinology · 2021Review
- Regional Difference in Myelination in Monocarboxylate Transporter 8 Deficiency: Case Reports and Literature Review of Cases in Japan.Frontiers in neurology · 2021Article
Corrections and comments
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Authors and funding
14 authors at 8 institutions in 2 countries.
Samuel RefetoffDepartment of Medicine, The University of Chicago, Chicago, Illinois, USA.
Theodora PappaDepartment of Molecular Metabolism and Nutrition, The University of Chicago, Chicago, Illinois, USA.
Meredith K WilliamsNorthwest Perinatal Center, Portland, Oregon, USA.
M Gisele MatheusDepartment of Radiology and Radiological Science, Medical University of South Carolina, Charleston, South Carolina, USA.
Xiao-Hui LiaoDepartment of Medicine, The University of Chicago, Chicago, Illinois, USA.
Karen HansenNorthwest Perinatal Center, Portland, Oregon, USA.
Lindsey NicolDepartment of Pediatrics-Endocrinology and Oregon Health & Science University, Portland, Oregon, USA.
Melinda PierceDepartment of Pediatrics-Endocrinology and Oregon Health & Science University, Portland, Oregon, USA.
Peter A BlascoNeurodevelopmental Disabilities Doernbacher Children's Hospital, Oregon Health & Science University, Portland, Oregon, USA.
Mandie Wiebers JensenNeurodevelopmental Disabilities Doernbacher Children's Hospital, Oregon Health & Science University, Portland, Oregon, USA.
Juan BernalInstituto de Investigaciones Biomedicas, Consejo Superior de Investigaciones Cientificas, Universidad Autonoma de Madrid and Center for Biomedical Research on Rare Diseases, Madrid, Spain.
Roy E WeissDepartment of Medicine, University of Miami Miller School of Medicine, Miami, Florida, USA.
Alexandra M DumitrescuDepartment of Medicine, The University of Chicago, Chicago, Illinois, USA.
Stephen LaFranchiDepartment of Pediatrics-Endocrinology and Oregon Health & Science University, Portland, Oregon, USA.
Oregon Health & Science University · USDoernbecher Children's Hospital · USEducation Northwest · USUniversity of Chicago · USUniversity of Illinois Chicago · USInstituto de Investigaciones Biomédicas Sols-Morreale · ESMedical University of South Carolina · USUniversity of Miami · US
Funding
THYROID PHYSIOLOGY STUDIES OF INHERITED DISORDERSR01DK015070 · NIDDK · UNIVERSITY OF CHICAGO · PI ANTONIO C BIANCO, Alexandra Mihaela Dumitrescu · 1986 to 2026
$8.1MMouse Sbp2 deficiency models the multi-system syndrome of human SBP2 defectsR01DK110322 · NIDDK · UNIVERSITY OF CHICAGO · PI DUMITRESCU, ALEXANDRA MIHAELA · 2016 to 2020
$1.8MNIDDK NIH HHS R01 DK015070NIDDK NIH HHS R01 DK110322
Abstract
PubMed holds no abstract for this paper.
Indexed as
AdultAmniotic FluidAntithyroid AgentsBrainCase-Control StudiesFemaleFetal TherapiesHumansMagnetic Resonance ImagingMaleMonocarboxylic Acid TransportersMuscle HypotoniaMuscular AtrophyPregnancyPropylthiouracilSymportersAntithyroid AgentsMonocarboxylic Acid TransportersPropylthiouracilSLC16A2 protein, humanSymportersThyrotropinThyroxineTriiodothyronineAllan–Herndon–Dudley syndromeamniotic fluidgeneticshypothyroidismMCT8prenatal treatmentTH membrane transporterthyroid hormone action
Identifiers
What OpenQuestion holds
Textmetadata
Read underepoch 390
Registered trials
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.