The Genetics of Pituitary Adenomas

por Tatsi, Christina, Stratakis, Constantine A.
Publicado 2019

ODP618 The profile of patients with ACTH-secreting pituitary adenomas and subclinical pituitary apoplexy

por Tatsi, Christina, Saidkhodjaeva, Lola, Flippo, Chelsi, Stratakis, Constantine
Publicado 2022

ODP387 Hemihypertrophy: A Rare Clinical Presentation of Cushing's disease

por Casanova Torres, Kristine M, Relan, Shilpi, Tatsi, Christina
Publicado 2022

THU213 Posterior Reversible Encephalopathy Syndrome As A Rare Presentation Of ACTH-dependent Cushing Syndrome In A Pediatric Patient

por Bell-Sambataro, Esther Eunice, Tatsi, Christina, Chittiboina, Prashant, Bowden, Sasigarn Arunchaiya
Publicado 2023

Safety and Efficacy of Pegvisomant in Pediatric Growth Hormone Excess

por Tatsi, Christina, Wajnrajch, Michael Paul, Camacho-Hubner, Cecilia, Stratakis, Constantine A
Publicado 2021

MON-190 Telomere Length as a Novel Prognostic Marker of Cushing Complications

por Tatsi, Christina, Faucz, Fabio Rueda, Flippo, Chelsi, Sinaii, Ninet, Stratakis, Constantine A
Publicado 2020

THU478 Unchecked Kinase Activation Underlies Pituitary Adenomas Causing Cushing’s Disease

por Asuzu, David, Mullaney, Dustin, Li, Yan, Mandal, Debjani, Tatsi, Christina, Nieman, Lynnette K, Chittiboina, Prashant
Publicado 2023

Spatial Transcriptomic Analysis of Pituitary Corticotroph Tumors Unveils Intratumor Heterogeneity

por Piña, Jeremie Oliver, Faucz, Fabio R., Padilla, Cameron, Floudas, Charalampos S., Chittiboina, Prashant, Quezado, Martha, Tatsi, Christina
Publicado 2023

MON-433 The Spectrum Of Growth Hormone Excess In Carney Complex: Characterizing A Common Finding In A Rare Syndrome

por Tatsi, Christina, Karageorgiadis, Alexander, Faucz, Fabio, Nikolaos, Settas, Lyssikatos, Charalampos, Elena, Belyavskaya, Lodish, Maya, Stratakis, Constantine
Publicado 2019

A SOX5 gene variant as a possible contributor to short stature

por Gkirgkinoudis, Athanasios, Tatsi, Christina, DeWard, Stephanie J, Friedman, Bethany, Faucz, Fabio R, Stratakis, Constantine A
Publicado 2020

The complex of myxomas, spotty skin pigmentation and endocrine overactivity (Carney complex): imaging findings with clinical and pathological correlation

por Courcoutsakis, Nikos A., Tatsi, Christina, Patronas, Nicholas J., Lee, Chiy-Chia Richard, Prassopoulos, Panos K., Stratakis, Constantine A.
Publicado 2013

SUN-713 Prevalence of Renal Cysts in Patients with Carney Complex

por Kamilaris, Crystal Dawn Chrysavgi, Gkirgkinoudis, Athanasios, Tatsi, Christina, Pitsava, Georgia, Sinaii, Ninet, Hannah-Shmouni, Fady, Stratakis, Constantine A
Publicado 2020

Somatic PRKAR1A Gene Mutation in a Nonsyndromic Metastatic Large Cell Calcifying Sertoli Cell Tumor

por Tatsi, Christina, Faucz, Fabio R, Blavakis, Emmanouil, Carneiro, Benedito A, Lyssikatos, Charalampos, Belyavskaya, Elena, Quezado, Martha, Stratakis, Constantine A
Publicado 2019

OR01-02 Epigenomic Dysregulation Of PPP1R17 Drives The Cell Cycle In Adenomas Causing Cushing’s Disease

por Asuzu, David, Mullaney, Dustin, Stoica, Stefan, Mandal, Debjani, Maric, Dragan, Elkahloun, Abdel, Sisay, Bayu, Tatsi, Christina, Nieman, Lynnette K, Chittiboina, Prashant
Publicado 2023

Decreased Lymphocytes and Increased Risk for Infection are Common in Endogenous Pediatric Cushing Syndrome

por Tatsi, Christina, Boden, Rebecca, Sinaii, Ninet, Keil, Meg, Lyssikatos, Charalampos, Belyavskaya, Elena, Rosenzweig, Sergio D., Stratakis, Constantine A., Lodish, Maya B.
Publicado 2017

THU214 Exploratory Study Of The Association Of Genetic Factors With Recovery Of Hypothalamic-Pituitary-Adrenal Axis In Cushing Disease

por Nguyen, Matthew H, Zhang, Wei, Pankratz, Nathan, Lane, John, Chittiboina, Prashant, Faucz, Fabio R, Liu, Aiyi, Mills, James L, Stratakis, Constantine A, Tatsi, Christina
Publicado 2023

Aggrecan Mutations in Nonfamilial Short Stature and Short Stature Without Accelerated Skeletal Maturation

por Tatsi, Christina, Gkourogianni, Alexandra, Mohnike, Klaus, DeArment, Diana, Witchel, Selma, Andrade, Anenisia C., Markello, Thomas C., Baron, Jeffrey, Nilsson, Ola, Jee, Youn Hee
Publicado 2017

Neurofibromatosis Type 1 Has a Wide Spectrum of Growth Hormone Excess

por Hannah-Shmouni, Fady, Trivellin, Giampaolo, Beckers, Pablo, Karaviti, Lefkothea P., Lodish, Maya, Tatsi, Christina, Adesina, Adekunle M., Adamidou, Fotini, Mintziori, Gesthimani, Josefson, Jami L., Quezado, Martha, Stratakis, Constantine A.
Publicado 2022

Corticotropinoma as a Component of Carney Complex

por Hernández-Ramírez, Laura C., Tatsi, Christina, Lodish, Maya B., Faucz, Fabio R., Pankratz, Nathan, Chittiboina, Prashant, Lane, John, Kay, Denise M., Valdés, Nuria, Dimopoulos, Aggeliki, Mills, James L., Stratakis, Constantine A.
Publicado 2017

Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease

por Faucz, Fabio R., Tirosh, Amit, Tatsi, Christina, Berthon, Annabel, Hernández-Ramírez, Laura C., Settas, Nikolaos, Angelousi, Anna, Correa, Ricardo, Papadakis, Georgios Z., Chittiboina, Prashant, Quezado, Martha, Pankratz, Nathan, Lane, John, Dimopoulos, Aggeliki, Mills, James L., Lodish, Maya, Stratakis, Constantine A.
Publicado 2017