ODP380 Case of Skeletal Dysplasia in Post-Menarchal Pediatric Patient due to Novel Mutation of CSGALNACT1

por Baby, Merilyn, Breidbart, Emily, Kohn, Brenda, Pappas, John
Publicado 2022

Pancreatic Neuroendocrine Tumor in a Young Child With Tuberous Sclerosis Complex 1

por Mehta, Shilpa, Rusyn, Larisa, Ginsburg, Howard, Hajdu, Cristina, Kohn, Brenda
Publicado 2019

SAT-176 Cellular Mechanisms of Impaired Bone Remodeling in Type 1 Diabetes Mellitus

por Mehta, Shilpa, Yildirim, Gina, Liu, Zhongbo, Kohn, Brenda, Yakar, Shoshana
Publicado 2019

Genotype - phenotype correlation in an adolescent girl with pathogenic PPARy genetic variation that caused severe hypertriglyceridemia and early onset type 2 diabetes

por Gutierrez Alvarez, Ana, Yachelevich, Naomi, Kohn, Brenda, Brar, Preneet Cheema
Publicado 2021

Pitfalls of Prenatal Diagnosis guiding Postnatal Management in Congenital Adrenal Hyperplasia(CAH)

por Murthy, Deepa Badrinath, Litao, Melissa Kaori, Shah, Bina Cherryl, Kohn, Brenda, Breidbart, Emily Nicole
Publicado 2021

SAT-463 Familial X-Linked Acrogigantism: Postnatal Outcomes and Tumor Pathology in a Prenatally Diagnosed Infant and His Affected Mother

por Wise-Oringer, Brittany, Zanazzi, George, Gordon, Rebecca, Wardlaw, Sharon, William, Christopher, Kohn, Brenda, Wisoff, Jeffrey, Oberfield, Sharon
Publicado 2019

SARS‐CoV‐2 infection and paediatric endocrine disorders: Risks and management considerations

por Miller, Ryan, Ashraf, Ambika P., Gourgari, Evgenia, Gupta, Anshu, Kamboj, Manmohan K., Kohn, Brenda, Lahoti, Amit, Mak, Daniel, Mehta, Shilpa, Mitchell, Deborah, Patel, Neha, Raman, Vandana, Reynolds, Danielle G., Yu, Christine, Krishnan, Sowmya
Publicado 2021