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Pediatric Diabetes|June 10, 2018
β-Cell secretory defects are present in pancreatic insufficient cystic fibrosis with 1-hour oral glucose tolerance test glucose ≥155 mg/dLSarah C Nyirjesy, Saba Sheikh, Denis Hadjiliadis, et al.
Annals of Neurology|August 12, 1999
Rapid-onset dystonia-parkinsonism: linkage to chromosome 19q13P L Kramer, M Mineta, C Klein, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 1994
Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystoniaS B Bressman, A L Hunt, G A Heiman, et al.
American Journal of Human Genetics|March 1, 1992
Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi JewsL J Ozelius, P L Kramer, D de Leon, et al.
The Journal of Clinical Endocrinology and Metabolism|December 15, 2016
Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2Christine T Ferrara, Kara E Boodhansingh, Eleonora Paradies, et al.
The Journal of Clinical Endocrinology and Metabolism|August 19, 2020
Management and Appropriate Use of Diazoxide in Infants and Children with HyperinsulinismPreneet Cheema Brar, Ryan Heksch, Kristina Cossen, et al.
Hormone Research in Paediatrics|March 8, 2026
Double trouble: When focal and diffuse hyperinsulinism occur simultaneouslyVictoria R Sanders, Katherine Lord, Winnie Sigal, et al.
Neurology|February 1, 1994
A study of idiopathic torsion dystonia in a non-Jewish family: evidence for genetic heterogeneityS B Bressman, G A Heiman, T G Nygaard, et al.
Neurology|October 23, 2002
Clinical findings of a myoclonus-dystonia family with two distinct mutationsD Doheny, F Danisi, C Smith, et al.
Neuroscience|December 17, 2009
Functional recovery of stepping in rats after a complete neonatal spinal cord transection is not due to regrowth across the lesion siteN J K Tillakaratne, J J Guu, R D de Leon, et al.
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