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

per Admoni, Osnat, Rath, Shoshana, Almagor, Tal, Elias-Assad, Ghadir, Tenenbaum-Rakover, Yardena
Publicat a Front Endocrinol (Lausanne) (2020)

Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation

per Majdoub, Hussein, Amselem, Serge, Legendre, Marie, Rath, Shoshana, Bercovich, Dani, Tenenbaum-Rakover, Yardena
Publicat a Front Endocrinol (Lausanne) (2019)

Case Report: Severe Hypocalcemic Episodes Due to Autoimmune Enteropathy

per Halabi, Inbal, Barohom, Marie Noufi, Peleg, Sarit, Trougouboff, Phillippe, Elias-Assad, Ghadir, Agbaria, Rhania, Tenenbaum-Rakover, Yardena
Publicat a Front Endocrinol (Lausanne) (2021)

Loss-of-Function Mutations in the Thyrotropin Receptor Gene as a Major Determinant of Hyperthyrotropinemia in a Consanguineous Community

per Tenenbaum-Rakover, Yardena, Grasberger, Helmut, Mamanasiri, Sunee, Ringkananont, Usanee, Montanelli, Lucia, Barkoff, Marla S., Dahood, Ahmad Mahameed-Hag, Refetoff, Samuel
Publicat 2009

Case Report: Neonatal Diabetes Mellitus Caused by a Novel GLIS3 Mutation in Twins

per London, Shira, De Franco, Elisa, Elias-Assad, Ghadir, Barhoum, Marie Noufi, Felszer, Clari, Paniakov, Marina, Weiner, Scott A., Tenenbaum-Rakover, Yardena
Publicat a Front Endocrinol (Lausanne) (2021)

A Novel Loss-of-Function Mutation, Gln459Arg, of the Calcium-Sensing Receptor Gene Associated with Apparent Autosomal Recessive Inheritance of Familial Hypocalciuric Hypercalcemia

per Lietman, Steven A., Tenenbaum-Rakover, Yardena, Jap, Tjin Shing, Yi-Chi, Wu, De-Ming, Yang, Ding, Changlin, Kussiny, Najat, Levine, Michael A.
Publicat 2009

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

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

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

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

High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism

per Almagor, Tal, Rath, Shoshana, Nachtigal, Dan, Sharroni, Zohara, Elias-Assad, Ghadir, Hess, Ora, Havazelet, Gilad, Zehavi, Yoav, Spiegel, Ronen, Bercovich, Dani, Almashanu, Shlomo, Tenenbaum-Rakover, Yardena
Publicat a Eur Thyroid J (2021)

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

per 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
Publicat a Endocr Connect (2021)

Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3

per Lorenz-Depiereux, Bettina, Benet-Pages, Anna, Eckstein, Gertrud, Tenenbaum-Rakover, Yardena, Wagenstaller, Janine, Tiosano, Dov, Gershoni-Baruch, Ruth, Albers, Norbert, Lichtner, Peter, Schnabel, Dirk, Hochberg, Ze’ev, Strom, Tim M.
Publicat 2006

Microcephaly, Epilepsy and Neonatal Diabetes Due to Compound Heterozygous Mutations in IER3IP1: Insights into the Natural History of a Rare Disorder

per Shalev, Stavit A., Tenenbaum-Rakover, Yardena, Horovitz, Yoseph, Paz, Veronica P., Ye, Honggang, Carmody, David, Highland, Heather M., Boerwinkle, Eric, Hanis, Craig L., Muzny, Donna M., Gibbs, Richard A., Bell, Graeme I., Philipson, Louis H., Greeley, Siri Atma W.
Publicat 2013