Last Updated: 09/26/2026
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Found 8 publications
Severe SOPH syndrome due to a novel NBAS mutation in a 27-year-old woman-Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decades.
Journal: American journal of medical genetics. Part A
Published: December 26, 2019
Hemoglobin A1c, frequency of glucose testing and social disadvantage: Metrics of racial health disparity in youth with type 1 diabetes.
Journal: Journal of diabetes and its complications
Published: November 13, 2017
Further evidence that variants in PPP1CB cause a rasopathy similar to Noonan syndrome with loose anagen hair.
Journal: American journal of medical genetics. Part A
Published: March 31, 2016
Racial differences in neighborhood disadvantage, inflammation and metabolic control in black and white pediatric type 1 diabetes patients.
Journal: Pediatric diabetes
Published: October 02, 2015
Differences in Red Blood Cell Indices Do Not Explain Racial Disparity in Hemoglobin A1c in Children with Type 1 Diabetes.
Journal: The Journal of pediatrics
Published: September 16, 2015
Neonatal severe hyperparathyroidism caused by homozygous mutation in CASR: A rare cause of life-threatening hypercalcemia.
Journal: European journal of medical genetics
Published: August 31, 2015
Relationship of body mass index and GAD65 antibody status on β-cell secretion at diabetes onset in African-American children.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: April 07, 2013
Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three African-American brothers.
Journal: American journal of medical genetics. Part A
Published: October 31, 2012
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Last Updated: 09/26/2026