MON-518 Osteoporosis in a Young Adult with Trisomy 13

por Wynn, Anne, Mak, Daniel, Diaz-Thomas, Alicia
Publicado 2019

Low prevalence of organic pathology in a predominantly black population with premature adrenarche: need to stratify definitions and screening protocols

por Foster, Christy, Diaz-Thomas, Alicia, Lahoti, Amit
Publicado 2020

Cushing syndrome as a failed cardiac screen in a patient with McCune–Albright syndrome: a case report

por Foster, Christy, Al Zubeidi, Hiba, Diaz-Thomas, Alicia
Publicado 2022

Transition of young adults with metabolic bone diseases to adult care

por Ross, Jordan, Bowden, Michelle R., Yu, Christine, Diaz-Thomas, Alicia
Publicado 2023

SAT-081 Hidden in Plain Sight: Rethinking Our Approach to Allan-Herndon-Dudley Syndrome

por Dye, Alyssa M, Nelson, Grace Bazan, Diaz-Thomas, Alicia Marie
Publicado 2020

Evidence Limitations in Determining Sexually Dimorphic Outcomes in Pediatric Post-Traumatic Hypopituitarism and the Path Forward

por West, Alina Nico, Diaz-Thomas, Alicia M., Shafi, Nadeem I.
Publicado 2020

SAT-LB084 Persistent Cushing Disease in a Prepubertal Pediatric Patient after Gross Total Resection: What to Expect

por Mak, Daniel, Nelson, Grace, Foster, Christy, Al-Zubeidi, Hiba, Diaz-Thomas, Alicia
Publicado 2019

Chemoenzymatic synthesis of glycopeptides bearing rare N-glycan sequences with or without bisecting GlcNAc

por Yang, Weizhun, Ramadan, Sherif, Orwenyo, Jared, Kakeshpour, Tayeb, Diaz, Thomas, Eken, Yigitcan, Sanda, Miloslav, Jackson, James E., Wilson, Angela K., Huang, Xuefei
Publicado 2018

Gestational Vitamin 25(OH)D Status as a Risk Factor for Receptive Language Development: A 24-Month, Longitudinal, Observational Study

por Tylavsky, Frances A., Kocak, Mehmet, Murphy, Laura E., Graff, J. Carolyn, Palmer, Frederick B., Völgyi, Eszter, Diaz-Thomas, Alicia M., Ferry, Robert J.
Publicado 2015

Mid-infrared III–V semiconductor lasers epitaxially grown on Si substrates

por Tournié, Eric, Monge Bartolome, Laura, Rio Calvo, Marta, Loghmari, Zeineb, Díaz-Thomas, Daniel A., Teissier, Roland, Baranov, Alexei N., Cerutti, Laurent, Rodriguez, Jean-Baptiste
Publicado 2022

OR18-3 Case Series of 16 Patients With 17β-Hydroxysteroid Dehydrogenase Type 3 Deficiency at Five Children's Hospitals in the United States

por Endocrine & Genetics Working Groups, DSD-TRN, Finlayson, Courtney, Keegan, Catherine, Mohnach, Lauren, Speiser, Phyllis, Mathew, Deepa, Rutter, Meilan, Schafer-Kalkhoff, Tara, Diaz-Thomas, Alicia, Whitehead, J
Publicado 2022

Newborn Screening Protocols and Positive Predictive Value for Congenital Adrenal Hyperplasia Vary across the United States

por Speiser, Phyllis W., Chawla, Reeti, Chen, Ming, Diaz-Thomas, Alicia, Finlayson, Courtney, Rutter, Meilan M., Sandberg, David E., Shimy, Kim, Talib, Rashida, Cerise, Jane, Vilain, Eric, Délot, Emmanuèle C.
Publicado 2020