Dr. Rachel I Gafni MD
Endocronologist (Pediatric) | Pediatric Endocrinology
National Institutes Of Health 30 Convent Dr. Msc 4 Bethesda MD, 20892About
Dr. Rachel Gafni is a pediatric endocrinologist practicing in Bethesda, MD. Dr. Gafni specializes in growth, puberty, diabetes or other disorders related to hormones that produce certain conditions in children and growing young adults. Pediatric endocrinologists possess copious knowledge on hormone chemicals and how they can affect other parts of the body and their functions.
Education and Training
Temple Univ Sch of Med, Philadelphia Pa 1992
Board Certification
PediatricsAmerican Board of PediatricsABP- Pediatric Endocrinology
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Nighttime salivary cortisol measurement as a simple, noninvasive, outpatient screening test for Cushing's syndrome in children and adolescents.
- Catch-up growth: possible mechanisms.
- Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S4
- Effects of estrogen on growth plate senescence and epiphyseal fusion.
- The role of the resting zone in growth plate chondrogenesis.
- Overdiagnosis of osteoporosis in children due to misinterpretation of dual-energy x-ray absorptiometry (DEXA).
- Childhood bone mass acquisition and peak bone mass may not be important determinants of bone mass in late adulthood.
- Decreased bone mineral density with off-label use of tenofovir in children and adolescents infected with human immunodeficiency virus.
- Motherhood in medical school.
- Approach to the child with fractures.
- Mechanism of FGF23 processing in fibrous dysplasia.
- Fibroblast growth factor 23: state of the field and future directions.
- Ultrasound is superior to computed tomography for assessment of medullary nephrocalcinosis in hypoparathyroidism.
- Mutations in NOTCH2 in patients with Hajdu-Cheney syndrome.
- Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy: genotypic overlap with pseudoxanthoma elasticum.
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