Einas Alkhatib | Medical Services
Programs & Services
Languages
- Arabic
- English
Einas Alkhatib | Education
Undergraduate School
St. Cloud State University
2014, St. Cloud, MN
Medical School
Oakland University William Beaumont School of Medicine
2018, Rochester, MI
Internship
Pediatrics
Helen Devos Children's Hospital (Michigan State University)
2019, Grand Rapids, MI
Residency
Pediatrics
Helen Devos Children's Hospital (Michigan State University)
2021, Grand Rapids, MI
Fellowship
Pediatric Endocrinology
Children's National Hospital
2024, Washington, DC
Einas Alkhatib | Certifications
- American Board of Pediatrics (General)
Einas Alkhatib | Publications
Feasibility of a multidisciplinary pilot intervention for parent/caregiver diabetes distress. Diabet Med. 2025 May; 42(5):e70006. View Feasibility of a multidisciplinary pilot intervention for parent/caregiver diabetes distress. Abstract
Feasibility of caregiver diabetes distress screening in routine clinical care of youth with type 1 diabetes. Diabet Med. 2024 Dec; 41(12):e15416. View Feasibility of caregiver diabetes distress screening in routine clinical care of youth with type 1 diabetes. Abstract
Case report: Early molecular confirmation and sodium polystyrene sulfonate management of systemic pseudohypoaldosteronism type I. Front Endocrinol (Lausanne). 2023; 14:1297335. View Case report: Early molecular confirmation and sodium polystyrene sulfonate management of systemic pseudohypoaldosteronism type I. Abstract
Case Report: Insulin hypersensitivity in youth with type 1 diabetes. Front Endocrinol (Lausanne). 2023; 14:1226231. View Case Report: Insulin hypersensitivity in youth with type 1 diabetes. Abstract
Weekly Growth Hormone (Lonapegsomatropin) Causes Severe Transient Hyperglycemia in a Child with Obesity. Horm Res Paediatr. 2023; 96(5):542-546. View Weekly Growth Hormone (Lonapegsomatropin) Causes Severe Transient Hyperglycemia in a Child with Obesity. Abstract
Case of an unreported genetic variant of salt losing 3-ß-hydroxysteroid dehydrogenase deficiency. Oxf Med Case Reports. 2021 May; 2021(5):omab021. View Case of an unreported genetic variant of salt losing 3-ß-hydroxysteroid dehydrogenase deficiency. Abstract