Alexandra M Dumitresu
10PUBLICATIONS
13CO-AUTHORS
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Publications (10)
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|Sep 16, 2024
Combined Levothyroxine and Propylthiouracil Treatment in Children with Monocarboxylate Transporter 8 Deficiency: A Multicenter Case Series of 12 Patients.Roy E Weiss, Joana R N Lemos, Alexandra M Dumitrescu
|May 07, 2024
STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179.Helmut Grasberger, Alexandra M Dumitrescu, Xiao-Hui Liao
|Aug 19, 2023
The Relationship Between Fetal THRB Genotype and Maternal Thyroid Function.Federico Salas-Lucia, Xiao-Hui Liao, Hanzi Jiang
|Jan 12, 2023
Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).Reham Shareef, Aryel Furman, Yui Watanabe
|May 25, 2022
A Novel Pathogenic Variant in PAX8 Leads to Familial Congenital Hypothyroidism.Monica Malheiros França, Lucy Reeve, Alexandra M Dumitrescu
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Frequent Collaborators
8 joint publications
Samuel Refetoff
2 joint publications
Monica Malheiros França
1 joint publications
Roy E Weiss
1 joint publications
Matthew Ettleson
1 joint publications
Antonio C Bianco
1 joint publications
Jean-Philippe Vit
1 joint publications
Xiao-Hui Liao
1 joint publications
Elliott G Swanson
1 joint publications
Junfeng Chen
1 joint publications
Takashi Yoshimura
