Editorial for Clinical Endocrinology special issue on "Genetics in Endocrinology".

Szczegóły

Tytuł:: Editorial for Clinical Endocrinology special issue on "Genetics in Endocrinology".
Autorzy:: Casey RT; Department of Medical Genetics, Cambridge University, Cambridge, UK.; Department of Endocrinology, Cambridge University Hospitals Foundation Trust, Cambridge, UK.
Źródło:: Clinical endocrinology [Clin Endocrinol (Oxf)] 2022 Oct; Vol. 97 (4), pp. 387. Date of Electronic Publication: 2022 Sep 05.
Typ publikacji:: Letter
Język:: English
Imprint Name(s):: Publication: <2003->: Oxford : Blackwell Publishing
Original Publication: Oxford, Blackwell Scientific Publications.
MeSH Terms:: Endocrinology*
Humans
References:: Izatt L, Owens MM, Pierce H, Wilcox S, Park SM. A practical guide to genetic testing in endocrinology. Clin Endocrinol. 2021. doi:10.1111/cen.14596.
Newey P. Approach to the patient with a variant of uncertain significance on genetic testing. Clin Endocrinol. 2022. doi:10.1111/cen.14818.
Pieterman CRC, Valk GD. Update on the clinical management of multiple endocrine neoplasia type 1. Clin Endocrinol. 2022. doi:10.1111/cen.14727.
Coopmans EC, Korbonits M. Molecular genetic testing in the management of pituitary disease. Clin Endocrinol. 2022. doi:10.1111/cen.14706.
Colclough K, Patel K. How do I diagnose Maturity Onset Diabetes of the Young in my patients? Clin Endocrinol. 2022. doi:10.1111/cen.14744.
Winzeler B, Tufton N, Lim S, et al. Investigating the role of somatic sequencing platforms for phaeochromocytoma and paraganglioma in a large UK cohort. Clin Endocrinol. 2021. doi:10.1111/cen.14639.
Lippert J, Fassnacht M, Ronchi CL. The role of molecular profiling in adrenocortical carcinoma. Clin Endocrinol. 2021. doi:10.1111/cen.14629.
Saengkaew T, Howard SR. Genetics of pubertal delay. Clin Endocrinol. 2021. doi:10.1111/cen.14606.
Newey PJ, Hannan FM, Wilson A, Thakker RV. Genetics of monogenic disorders of calcium and bone metabolism. Clin Endocrinol. 2021. doi:10.1111/cen.14644.
Moran C, Schoenmakers N, Visser WE, Schoenmakers E, Agostini M, Chatterjee K. Genetic disorders of thyroid development, hormonebiosynthesis and signalling. Clin Endocrinol. 2022. doi:10.1111/cen.14817.
Entry Date(s):: Date Created: 20220804 Date Completed: 20220913 Latest Revision: 20221004
Update Code:: 20240104
DOI:: 10.1111/cen.14808
PMID:: 35922964
: Opinia redakcyjna

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