Cargando…

MON-065 Prevention of 6-Mercaptopurine-Induced Hypoglycemia by Levocarnitine Replacement

Background: Symptomatic hypoglycemia has been reported in children less than 6 years of age receiving 6-Mercaptopurine for acute lymphoblastic anemia (ALL); however, the mechanism of 6-Mercaptopurine-induced hypoglycemia has been unclear. Objective: The objective was to investigate the metabolism in...

Descripción completa

Detalles Bibliográficos
Autores principales:	Torchinsky, Michael Yuri, Miller, Mark, Benavides, Valeria
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2020
Materias:	Pediatric Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207991/ http://dx.doi.org/10.1210/jendso/bvaa046.012

Ejemplares similares

MON-073 Hyperinsulinemic Hypoglycemia Responsive to Diazoxide Due to a Previously Unknown ABCC8 Dominant Mutation
por: Figueredo, Veronica M, et al.
Publicado: (2020)

MON-083 Childhood Diabetic Ketoacidosis (DKA) in New-Onset and Established Patients in Central Illinois: Contributing Factors and Risk Stratification
por: Szymczuk, Vivian, et al.
Publicado: (2020)

MON-068 The First Case in Korea, ZC4H2 Gene Mutation in Wieacker-Wolff Syndrome with Recurrent Hypoglycemia
por: Lee, Gahyun, et al.
Publicado: (2020)

MON-089 Discovery and Identification of Late Stage Selective Nonpeptide Somatostatin Subtype 5 (sst5) Agonists for the Treatment of Hyperinsulinemic Hypoglycemia
por: Fowler, Melissa A, et al.
Publicado: (2020)

SAT-065 A Novel De Novo GATA3 Gene Mutation in an Adolescent with HDR Syndrome
por: Cruz-Aviles, Lisa Michelle, et al.
Publicado: (2020)

SUN-065 Bone Health Outcomes in a Large, Diverse Pediatric Cohort Undergoing Hematopoietic Stem Cell Transplant
por: Swauger, Sarah, et al.
Publicado: (2020)

MON-082 The Neonatal Screen That Cried Wolff
por: D’Ambrosio, Fabiola, et al.
Publicado: (2020)

MON-087 Natural History and Neurodevelopmental Outcomes in Perinatal Stress Induced Hyperinsulinism
por: Sigal, Winnie M, et al.
Publicado: (2020)

Allopurinol reverses mercaptopurine-induced hypoglycemia in patients with acute lymphoblastic leukemia
por: Zhang, Melissa, et al.
Publicado: (2019)

MON-LB015 Sporadic MTC in Children: Characterization of a Rare Disease
por: Gammons, Sarah, et al.
Publicado: (2020)

MON-253 Severe Infantile Hypercalcemia in Williams-Beuren Syndrome
por: Nasir, Hamza, et al.
Publicado: (2019)

MON-258 Toddler with Hypercalcemia: Diagnosis of Familial Hypocalciuric Hypercalcemia
por: Kochanski, Justin, et al.
Publicado: (2019)

MON-067 A Perplexing Case of Hyponatremia and Abdominal Pain
por: Yeliosof, Olga, et al.
Publicado: (2020)

MON-062 46 XX DSD Due to POR Deficiency
por: Reddy, Nithin Modhugu, et al.
Publicado: (2020)

MON-058 Precocious Puberty and Hypothyroidism in a Pediatric Case
por: Sea, Jessica L, et al.
Publicado: (2020)

MON-079 Prepubertal Gynecomastia Secondary to Excessive Soy Consumption
por: Sea, Jessica, et al.
Publicado: (2020)

MON-270 Diagnostic Exome Sequencing in Children with Permanent Congenital Hypothyroidism
por: Kim, Jisun, et al.
Publicado: (2019)

MON-268 A Rare Case of Primary Hypoaldosteronism in a Newborn
por: Mody, Armaiti, et al.
Publicado: (2019)

MON-263 Graves’ Disease Presenting As Chronic Diarrhea In A Toddler
por: Chen, Jarreau, et al.
Publicado: (2019)

Isolated Growth Hormone Deficiency as a Cause of Hypoglycemia Past Infancy
por: Thakkar, Amruta, et al.
Publicado: (2021)

MON-254 Fragility Fracture in a Pediatric Patient with Williams-Beuren Syndrome
por: Favela, Kristin, et al.
Publicado: (2019)

MON-262 Aggrecan Is Required for Chondrocyte Differentiation in ATDC5 Chondroprogenitor Cells
por: Hodax, Juanita, et al.
Publicado: (2019)

MON-257 A Case of Primary Hyperparathyroidism Complicated by Vitamin D Deficiency
por: Robinson, Sylvia, et al.
Publicado: (2019)

MON-269 Analysis of Clinical Features of Congenital Hypothyroidism with Eutopic Thyroid Gland
por: Terashita, Shintaro
Publicado: (2019)

MON-077 A Case of Growth Hormone Deficiency in Sturge-Weber Syndrome
por: Hwang, Jeongju, et al.
Publicado: (2020)

MON-075 Autonomy and Self-Determination in a Patient with XY Gonadal Dysgenesis
por: Moryan-Blanchard, Kristen, et al.
Publicado: (2020)

MON-080 Unusual Association Between Congenital Hyperinsulinism and Neurofibromatosis Type 1
por: Marinescu, Andreea S, et al.
Publicado: (2020)

Effects of TPMT, NUDT15, and ITPA Genetic Variants on 6-Mercaptopurine Toxicity for Pediatric Patients With Acute Lymphoblastic Leukemia in Yunnan of China
por: Mao, Xiaoyan, et al.
Publicado: (2021)

THU133 Inpatient Hypoglycemia Management: Error Rates In Pediatric Diabetes Care
por: Odutayo, Daniella A, et al.
Publicado: (2023)

MON-LB016 Tyrosine Kinase Inhibitor Induced Hypothyroidism in Pediatric and Young Adult Population: An Institutional Review
por: Arora, Shruthi, et al.
Publicado: (2020)

MON-267 The Girl Who Never Cries: Allgrove Syndrome with Uncommon Cardiac Complication
por: Wahedi, Tayba, et al.
Publicado: (2019)

MON-245 Sexuality and Fertility Issues in 46,XY Disorders of Sex Development Individuals
por: Batista, Rafael, et al.
Publicado: (2019)

MON-106 Prevalence and Incidence of Obesity in Children and Young Adults in Korea: The Kangwha Study
por: Suh, Junghwan, et al.
Publicado: (2020)

MON-059 Acute Hyponatremia Following Computed Tomography Radiocontrast in a Pediatric Patient
por: Chiu, Harvey Kenn, et al.
Publicado: (2020)

MON-078 WFS1 Related Disorder in A 4-Month Old Girl
por: Kleanthous, Kleanthis, et al.
Publicado: (2020)

MON-084 Hyperosmolar Hyperglycemic State as Initial Presentation of Type 1 Diabetes in Children
por: D’Ambrosio, Fabiola, et al.
Publicado: (2020)

MON-109 Modulator of Gut Barrier, Zonulin Was Associated with Waist to Height Ratio in Adolescents
por: Kim, Ki Eun, et al.
Publicado: (2020)

MON-249 Algorithm-Driven Electronic Health Record Notification Enhances the Detection of Turner Syndrome
por: Alexandrou, Eirene, et al.
Publicado: (2019)

MON-265 Congenital Hypothyroidism and Bilateral Ptosis Due to a Novel TSHR Gene Mutation
por: Marinescu, Andreea, et al.
Publicado: (2019)

MON-056 Rare X Chromosome Pericentric Inversion Associated with Ovotesticular Disorder of Sex Development
por: Guerra-Junior, Gil, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_lkebii13itpmkg7avlk51p9n1j