Zeina M. Nabhan

ORCID: 0000-0003-2160-2708
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About
Contact & Profiles
Research Areas
  • Sexual Differentiation and Disorders
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Innovations in Medical Education
  • Growth Hormone and Insulin-like Growth Factors
  • Hypothalamic control of reproductive hormones
  • Hormonal and reproductive studies
  • Diversity and Career in Medicine
  • Urological Disorders and Treatments
  • Medical Education and Admissions
  • Diabetes Management and Research
  • Diabetes and associated disorders
  • Child and Adolescent Health
  • Hyperglycemia and glycemic control in critically ill and hospitalized patients
  • Thyroid Disorders and Treatments
  • Obesity, Physical Activity, Diet
  • Testicular diseases and treatments
  • Pituitary Gland Disorders and Treatments
  • Pancreatic function and diabetes
  • Adrenal Hormones and Disorders
  • Childhood Cancer Survivors' Quality of Life
  • Birth, Development, and Health
  • Pediatric Urology and Nephrology Studies
  • Simulation-Based Education in Healthcare
  • Histiocytic Disorders and Treatments
  • Bacillus and Francisella bacterial research

Indiana University School of Medicine
2011-2024

Indiana University – Purdue University Indianapolis
2012-2024

Riley Hospital for Children
2008-2021

Indiana University Indianapolis
2021

Diabetes Australia
2006-2021

Harvard Affiliated Emergency Medicine Residency
2018

Indiana University
2009

The optimal route of estrogen replacement in Turner syndrome (TS) is unknown.The objective the study was to compare conjugated oral vs. transdermal (TD E2) on bone accrual, uterine growth, pubertal development, IGF-I, and lipids girls with TS.Prepubertal GH-treated aged 10 yr or older TS were eligible. Subjects randomized TD E2 for 1 yr. Assessments included dual-emission x-ray absorptiometry, pelvic ultrasound, Tanner staging, growth velocity, lipid profile.Twelve (14.0 +/- 1.7 yr)...

10.1210/jc.2008-2123 article EN The Journal of Clinical Endocrinology & Metabolism 2009-03-25

To compare glycemic control, body mass index (BMI), neurocognitive function, and parenting stress for preschool-aged diabetic children randomized to treatment either with continuous subcutaneous insulin infusion (CSII) or intensive injection therapy (IIT).Children <5 yr of age diagnosed type 1 diabetes mellitus at least 12 months were CSII (n = 21) IIT 6 months. After months, the group began continued on pumps. Hemoglobin A1c (HbA1c) BMI percent collected baseline, 3, 6, 9, Neurocognitive...

10.1111/j.1399-5448.2008.00494.x article EN Pediatric Diabetes 2008-12-25

Objectives To increase diversity and inclusion in graduate medical education (GME), the Accreditation Council for Graduate Medical Education (ACGME) issued new standards requiring programs to engage practices that focus on systematic recruitment retention of a diverse workforce trainees faculty. The literature how program directors (PDs) can incorporate prepare this standard is limited. Methods We developed diversity, equity, (DEI) toolkit PDs as an example institutional GME-led effort...

10.1177/23821205231203136 article EN cc-by-nc Journal of Medical Education and Curricular Development 2023-01-01

Little is known about the comparative effects of different glucocorticoids on adrenal and growth hormone (GH) axes in children with congenital hyperplasia (CAH). We sought to compare hydrocortisone (HC), prednisone (PDN), dexamethasone (DEX) classic CAH investigate a potential role pharmacogenetics. Subjects were randomly assigned three sequential 6-week courses HC, PDN, DEX, each followed by evaluation hormones, IGF-1, GH, body mass index (BMI). Single nucleotide polymorphism (SNP) analysis...

10.1186/s13633-016-0035-5 article EN International Journal of Pediatric Endocrinology 2016-09-20

The objective of this study was to determine the incidence, specific abnormalities, and clinical significance upper-tract genitourinary malformations in girls with congenital adrenal hyperplasia.Medical charts children who received a diagnosis hyperplasia between 1985 2005 were reviewed.Of 107 patients hyperplasia, 66 identified. Of these, 14 found have abnormalities. anomalies consisted vesicoureteral reflux grades 1 3 (9), hydronephrosis (4), duplicated collecting system (1). Two boys...

10.1542/peds.2006-2993 article EN PEDIATRICS 2007-08-01

OBJECTIVE A diverse physician workforce ensures equitable care. The holistic review of residency applications is one strategy to enhance diversity; however, little known about current adoption and the factors that facilitate/impede recruitment practices (HRPs) by graduate medical education (GME) residency, fellowship program directors (PDs). To describe state explore, barriers/facilitators HRPs at our institution. METHODS We disseminated information HRP within between 2021 2022. In May 2022,...

10.1177/23821205241260243 article EN cc-by-nc Journal of Medical Education and Curricular Development 2024-01-01

To investigate the incidence of urinary tract infections (UTIs) in children with congenital adrenal hyperplasia (CAH), and to determine whether there was a correlation between UTIs timing type genital surgery girls.Medical records patients CAH < or = 15 years were reviewed. A parent questionnaire regarding history completed.Seventy-one classic (41 girls, 30 boys) aged 8.3 +/- 4.2 identified. Thirty-five (85%) girls had undergone feminizing genitoplasty at 1.1 0.8 years, while six (15%) not....

10.1515/jpem.2006.19.6.815 article EN Journal of Pediatric Endocrinology and Metabolism 2006-01-01

Issue: Resident teachers play an essential role in medical education and can support broader efforts to advance anti-racism health equity medicine. The Accreditation Council for Graduate Medical Education requires programs provide about care disparities so residents contribute lead work this area. However, the literature includes few examples, frameworks, or strategies preparing develop knowledge skills needed promote equity, including their as clinical teachers. Evidence: In article,...

10.1080/10401334.2022.2147529 article EN Teaching and Learning in Medicine 2022-11-21

Article Normal Adult Height Among Girls Treated for Central Precocious Puberty with Gonadotropin-Releasing Hormone Analog Therapy was published on April 1, 2009 in the journal Journal of Pediatric Endocrinology and Metabolism (volume 22, issue 4).

10.1515/jpem.2009.22.4.309 article EN Journal of Pediatric Endocrinology and Metabolism 2009-01-01

Efforts toward achieving diversity, equity, inclusion, and justice (DEIJ) within graduate medical education (GME) often begin with the formation of a DEIJ committee that steers work. Little is known about experiences challenges faced by those serving on such committees. We sought to describe members our institutional GME gain knowledge would propel this work forward. An open-ended survey was electronically administered committee. Responses were analyzed using rapid qualitative analytical...

10.3389/fpubh.2022.867035 article EN cc-by Frontiers in Public Health 2022-04-27

Problem: Learner mistreatment has remained an ongoing challenge in academic medicine despite accreditation requirements mandating that every program systems place to prevent and respond mistreatment. While efforts vary across institutions, much remains unanswered the literature about best practices. Additionally, for foreseeable future, challenges learning environment will likely continue potentially worsen, given confluence of multiple external stressors including COVID-19 pandemic, faculty...

10.1080/10401334.2022.2122979 article EN Teaching and Learning in Medicine 2022-09-15

Monozygotic twins with Turner syndrome have rarely been reported. An increased incidence of slipped capital femoral epiphysis has associated growth hormone therapy, as well syndrome, but never described in syndrome. We report the first case monozygotic a 46,Xi(Xq) karyotype, both whom developed during therapy. This adds to existing reports and contributes recognition potential clinical course such patients. In addition, association between epiphysis, is emphasized.

10.1542/peds.2006-0955 article EN PEDIATRICS 2006-11-07

To describe an unusual case of familial male precocious puberty (FMPP) characterized by periodic remission compared to a series boys with typical testotoxicosis.Medical records FMPP followed at our institution from 2001-2017 were reviewed. Variables analyzed included age, family history, physical exam, hormone levels, bone and treatment.A boy age 2 years 10 months presented growth acceleration masturbatory behaviors. On he had 6-mL testes, enlarged phallus (10.5 × 2.5 cm), Tanner pubic hair....

10.4158/accr-2018-0246 article EN cc-by-nc-nd AACE Clinical Case Reports 2018-08-17

Short stature is a common reason for referral to the pediatric endocrine clinic. In 2003, US Food and Drug Administration (FDA) approved use of growth hormone (GH) treatment children with idiopathic short (ISS).To explore if this indication changed referrals (SS).A retrospective chart review seen SS in clinic between July 1998 June 1999 (interval one, n=138) 2005-June 2006 two, n=268) was performed. Variables collected included age, gender, height (h), parental heights.Average standard...

10.1515/jpem.2011.120 article EN Journal of Pediatric Endocrinology and Metabolism 2011-01-01
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