Τρίτη 5 Μαΐου 2020

The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD
Abstract Purpose Mutations in the gene HSD17B3 encoding the 17-beta hydroxysteroid dehydrogenase 3 enzyme cause testosterone insufficiency leading to XY disorders of sex development. In this study the clinical and molecular characteristics of three patients from consanguineous families are elucidated. Methods We identified three patients from two unrelated...
International journal of basic and clinical endocrinology
Tue May 05, 2020 03:00
Lymphocyte-to-monocyte ratio prior to radioiodine ablation in low- and intermediate-risk, papillary thyroid cancer
Abstract Purpose We aimed to investigate inflammation indices based on preablation hematological parameter of the lymphocyte-to-monocyte ratio (LMR) to predict the clinical outcome in papillary thyroid cancer (PTC) patients with low- and intermediate-risk stratification. Methods This retrospective study analyzed 772 patients with low- and intermediate-risk...
International journal of basic and clinical endocrinology
Tue May 05, 2020 03:00
Periprostatic paraganglioma causing occult Cushing’s syndrome
International journal of basic and clinical endocrinology
Tue May 05, 2020 03:00

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