A Novel Mutation (S54C) of the PAX8 Gene in a Family with Congenital Hypothyroidism and High Proportion of Affected Individuals

gan Srichomkwun, Panudda, Admoni, Osnat, Refetoff, Samuel, de Vries, Liat
Cyhoeddwyd yn Horm Res Paediatr (2016)

Long-Term Follow-Up and Outcomes of Autoimmune Thyroiditis in Childhood

gan Admoni, Osnat, Rath, Shoshana, Almagor, Tal, Elias-Assad, Ghadir, Tenenbaum-Rakover, Yardena
Cyhoeddwyd yn Front Endocrinol (Lausanne) (2020)

The Coexistence of a Novel Inactivating Mutant Thyrotropin Receptor Allele with Two Thyroid Peroxidase Mutations: A Genotype-Phenotype Correlation

gan Sriphrapradang, Chutintorn, Tenenbaum-Rakover, Yardena, Weiss, Mia, Barkoff, Marla S., Admoni, Osnat, Kawthar, Dallasheh, Caltabiano, Gianluigi, Pardo, Leonardo, Dumitrescu, Alexandra M., Refetoff, Samuel
Cyhoeddwyd 2011

Long-Term Outcome of Loss-of-Function Mutations in Thyrotropin Receptor Gene

gan Tenenbaum-Rakover, Yardena, Almashanu, Shlomo, Hess, Ora, Admoni, Osnat, Hag-Dahood Mahameed, Ahmad, Schwartz, Naama, Allon-Shalev, Stavit, Bercovich, Dani, Refetoff, Samuell
Cyhoeddwyd yn Thyroid (2015)

OR15-07 Novel Genes Involved in Sex Differentiation Identified by Whole-Exome Sequencing in a Cohort of Children with Disorders of Sex Development

gan Rakover, Yardena Tenenbaum, Admoni, Osnat, Assad, Ghadir Elias, London, Shira, Barhoum, Marie Noufi, Ludar, Hana, Almagor, Tal, Bertalan, Rita, Bashamboo, Anu, McElreavey, Prof, Kenneth
Cyhoeddwyd yn J Endocr Soc (2020)

The evolving role of whole-exome sequencing in the management of disorders of sex development

gan Tenenbaum-Rakover, Yardena, Admoni, Osnat, Elias-Assad, Ghadir, London, Shira, Noufi-Barhoum, Marie, Ludar, Hanna, Almagor, Tal, Zehavi, Yoav, Sultan, Charles, Bertalan, Rita, Bashamboo, Anu, McElreavey, Kenneth
Cyhoeddwyd yn Endocr Connect (2021)