Last Updated: 09/26/2026
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Found 7 publications
Characterizing Parental Use of a HIPAA-Compliant Large Language Model Chatbot in Rare Pediatric Diseases: Insights from Think-Aloud Sessions.
Journal: Applied clinical informatics
Published: June 09, 2026
Clinical, Psychosocial, and Care Coordination Concerns in Macrocephaly Capillary Malformation Syndrome: Insights From a Large International Survey.
Journal: Pediatric blood & cancer
Published: September 11, 2025
Impact of social vulnerability on glycemic control and diabetes technology use in youth with type 1 diabetes.
Journal: BMC endocrine disorders
Published: August 24, 2025
Pediatric diabetes mellitus hospitalizations and COVID-19 pandemic response measures.
Journal: Diabetes research and clinical practice
Published: June 28, 2023
Clinical and molecular phenotyping of a child with Hermansky-Pudlak syndrome-7, an uncommon genetic type of HPS.
Journal: Molecular genetics and metabolism
Published: November 22, 2016
Cystic cerebellar dysplasia and biallelic LAMA1 mutations: a lamininopathy associated with tics, obsessive compulsive traits and myopia due to cell adhesion and migration defects.
Journal: Journal of medical genetics
Published: July 25, 2015
A clinical report of Chediak-Higashi syndrome in infancy with a novel genotype from the Indian subcontinent.
Journal: International journal of dermatology
Published: September 06, 2014
Showing 1-7 of 7
Last Updated: 09/26/2026