Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Lucille Rodriguez"'
Autor:
Ashok Balasubramanyam, E. O'Brian Smith, Maria J. Redondo, Lucille Rodriguez, Nidhi Bansal, Christiane S. Hampe, Jake A. Kushner
Publikováno v:
Diabetic Medicine. 34:641-646
Aim To study whether DPD epitope-specific glutamate decarboxylase autoantibodies are found more frequently in children with milder forms of Type 1 diabetes. Methods We prospectively evaluated 75 children with new-onset autoimmune Type 1 diabetes, in
Autor:
Lucille Rodriguez, Maria J. Redondo, EO Smith, Ashok Balasubramanyam, Christiane S. Hampe, Morey W. Haymond, Sridevi Devaraj
Publikováno v:
Pediatric Diabetes. 15:543-549
Obesity increases the risk of cardiovascular disease and diabetic complications in type 1 diabetes. Adipokines, which regulate obesity-induced inflammation, may contribute to this association. We compared serum adipokines and inflammatory cytokines i
Autor:
Åke Lernmark, Ramaswami Nalini, Gilberto Garza, Lakshmi K. Gaur, Lucille Rodriguez, Christiane S. Hampe, Ashok Balasubramanyam, Mario Maldonado
Publikováno v:
Diabetes Care
OBJECTIVE—Ketosis-prone diabetes (KPD) comprises four subgroups based on the presence or absence of β-cell autoantibodies (A+ or A−) and β-cell functional reserve (β+ or β−). Genetic factors could contribute to their distinctive phenotypes.
Publikováno v:
Diabetic Medicine. 22:1744-1750
Aim To evaluate factors predictive of insulin discontinuation in subjects with ketosis-prone Type 2 diabetes. Methods One hundred and six subjects with ketosis-prone Type 2 diabetes were recruited during the index episode of diabetic ketoacidosis (DK
Autor:
Gilberto Garza, Christiane S. Hampe, Lucille Rodriguez, Åke Lernmark, Lakshmi K. Gaur, Ashok Balasubramanyam, Mario Maldonado
Publikováno v:
Diabetes care. 29(12)
OBJECTIVE—Ketosis-prone diabetes (KPD) is an emerging, heterogeneous syndrome. A sound classification scheme for KPD is essential to guide clinical practice and pathophysiologic studies. Four schemes have been used and are based on immunologic crit
Autor:
Mario R, Maldonado, Max E, Otiniano, Rebekah, Lee, Lucille, Rodriguez, Ashok, Balasubramanyam
Publikováno v:
Ethnicitydisease. 14(2)
To compare demographic and clinical characteristics among 3 ethnic groups of indigent patients exhibiting diabetic ketoacidosis (DKA), in Houston, Texas.Over a span of 3.5 years, 321 patients were interviewed at the time of admission for DKA. Demogra
Autor:
Arun S. Rajan, Mario Maldonado, Christiane S. Hampe, Lucille Rodriguez, Douglas Bolgiano, Lakshmi K. Gaur, Susana D'Amico, Ashok Balasubramanyam, Dinakar Iyer, Lisa P. Hammerle, Åke Lernmark
Publikováno v:
The Journal of clinical endocrinology and metabolism. 88(11)
Ketosis-prone diabetes is heterogeneous. Its causes could include novel beta-cell functional defects. To characterize such defects, 103 patients with diabetic ketoacidosis were evaluated for beta-cell autoimmunity and human leukocyte antigen (HLA) cl
Publikováno v:
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists. 9(1)
To investigate whether a specialized intervention program could improve diabetes-related health outcomes in indigent patients with type 1 diabetes who were prone to occurrence of diabetic ketoacidosis (DKA).Patients with type 1 diabetes mellitus admi
Publikováno v:
Diabetes care. 26(8)
Diabetic ketoacidosis (DKA) has been reported in subjects who lack the clinical characteristics of type 1 diabetes (1–3). In a preliminary analysis of the “types” of diabetes in patients presenting with DKA, we found that Hispanic patients had