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Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).
Thyroid. 2023 Feb;33(2):261-266. doi: 10.1089/thy.2022.0492.
Thyroid. 2023.
PMID: 36633921
Free PMC article.
A Perspective Of Intestinal Immune-Microbiome Interactions In Alcohol-Associated Liver Disease.
Bruellman R, Llorente C.
Bruellman R, et al.
Int J Biol Sci. 2021 Jan 1;17(1):307-327. doi: 10.7150/ijbs.53589. eCollection 2021.
Int J Biol Sci. 2021.
PMID: 33390852
Free PMC article.
Review.
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Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ.
Ebrhim RS, Bruellman RJ, Watanabe Y, Creech MK, Abdullah MA, Dumitrescu AM, Refetoff S, Weiss RE.
Ebrhim RS, et al. Among authors: bruellman rj.
Horm Res Paediatr. 2019;92(6):390-394. doi: 10.1159/000504981. Epub 2020 Jan 8.
Horm Res Paediatr. 2019.
PMID: 31914441
Free PMC article.
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Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism.
Bruellman R, Watanabe Y, Shareef R, Abdullah MA, Dumitrescu A, Strauss BS, Refetoff S, Weiss RE.
Bruellman R, et al.
Thyroid. 2020 May;30(5):780-782. doi: 10.1089/thy.2019.0636. Epub 2020 Feb 3.
Thyroid. 2020.
PMID: 31868128
Free PMC article.
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Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
Bruellman RJ, Watanabe Y, Ebrhim RS, Creech MK, Abdullah MA, Dumitrescu AM, Refetoff S, Weiss RE.
Bruellman RJ, et al.
J Clin Endocrinol Metab. 2020 May 1;105(5):1564-72. doi: 10.1210/clinem/dgz297.
J Clin Endocrinol Metab. 2020.
PMID: 31867598
Free PMC article.
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Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families.
Watanabe Y, Bruellman RJ, Ebrhim RS, Abdullah MA, Dumitrescu AM, Refetoff S, Weiss RE.
Watanabe Y, et al. Among authors: bruellman rj.
Thyroid. 2019 Feb;29(2):302-304. doi: 10.1089/thy.2018.0295. Epub 2018 Dec 18.
Thyroid. 2019.
PMID: 30375286
Free PMC article.
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