R. Gómez

发表

Biological variation in HbA1c predicts risk of retinopathy and nephropathy in type 1 diabetes.

R. McCarter, S. Chalew, J. Hempe, 2004, Diabetes care.

The human leukocyte antigen HLA DRB3*020/DQA1*0501 haplotype is associated with Graves' disease in African Americans.

M. Lan, Y. Tomer, N. Maclaren, 2000, The Journal of clinical endocrinology and metabolism.

Type 1 Diabetes Mellitus Helicobacter pylori Infection and Insulin Requirement Among Children With

R. Bégué, A. Mirza, R. Gómez, 2013 .

Predictors of glycemic control in children with type 1 diabetes: the importance of race.

D. Mercante, A. Butler, A. Vargas, 2000, Journal of diabetes and its complications.

Relationship of body mass index and GAD65 antibody status on β-cell secretion at diabetes onset in African-American children

A. Vargas, S. Chalew, Metin Balikcioğlu, 2013, Journal of pediatric endocrinology & metabolism : JPEM.

The Relationship of Insulin Secretion and GAD65 Antibody Levels at Diagnosis on Glycemic Control in Type 2 Diabetes

A. Vargas, S. Chalew, Pinar Gumus, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Mean blood glucose‐independent HbA1c racial disparity and iron status in youth with Type 1 DM

S. Chalew, R. Gómez, M. Hamdan, 2019, Pediatric diabetes.

Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three African‐American brothers

S. Aradhya, L. Messiaen, A. Vargas, 2013, American journal of medical genetics. Part A.

Association between Helicobacter felis-induced gastritis and elevated glycated hemoglobin levels in a mouse model of type 1 diabetes.

H. Correa, A. Vargas, R. Bégué, 2002, The Journal of infectious diseases.

A Rare Case of Painful Goiter Secondary to Pediatric Hashimoto’s Thyroiditis Requiring Thyroidectomy for Pain Control

R. Walvekar, Abdulhameed AlSaheel, R. Gómez, 2015, Pediatric reports.

Poor glycemic control is associated with increased diastolic blood pressure and heart rate in children with Type 1 diabetes.

D. Mercante, A. Vargas, S. Chalew, 2004, Journal of diabetes and its complications.

Metformin Adjunctive Therapy with Insulin Improves Glycemic Control in Patients with Type 1 Diabetes Mellitus: A Pilot Study

R. McCarter, A. Vargas, S. Chalew, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Chronic inflammatory demyelinating polyradiculoneuropathy and Graves' disease in an adolescent with Crohn's disease

J. England, A. Shetty, A. Gedalia, 1999 .

HERV-K10s and Immune-Mediated (Type 1) Diabetes

M. Lan, R. Garry, N. Maclaren, 1998, Cell.

High and low hemoglobin glycation phenotypes in type 1 diabetes: a challenge for interpretation of glycemic control.

R. McCarter, James M Hempe, Ricardo Gomez, 2002, Journal of diabetes and its complications.

Racial Disparity in Type 1 Diabetes Outcomes

A. Delamater, S. Chalew, Dania L. Felipe, 2021 .

A labile form of hemoglobin A1c is higher in African‐American youth with type 1 diabetes compared to Caucasian patients at similar glucose levels

S. Chalew, Gomez-Huelgas Ricardo, R. Gómez, 2019, Pediatric diabetes.

Differences in Red Blood Cell Indices Do Not Explain Racial Disparity in Hemoglobin A1c in Children with Type 1 Diabetes.

A. Vargas, S. Chalew, C. Velasco-Gonzalez, 2016, The Journal of pediatrics.

Intima‐media thickness at different arterial segments in pediatric type 1 diabetes patients and its relationship with advanced glycation end products

S. Chalew, S. Stender, C. Lilje, 2018, Pediatric diabetes.

Another Undiagnosed Pheochromocytoma Causes Hypertensive Crisis in the Operating Room—What about a Rapid Blood Metanephrine Test?

R. Gómez, C. Rosenberg, 2013 .

Helicobacter pylori Infection and Insulin Requirement Among Children With Type 1 Diabetes Mellitus

A. Vargas, R. Bégué, A. Mirza, 1999, Pediatrics.

Neonatal severe hyperparathyroidism caused by homozygous mutation in CASR: A rare cause of life-threatening hypercalcemia.

A. Vargas, Y. Lacassie, Regina M. Zambrano, 2016, European journal of medical genetics.

Hemoglobin A1c, frequency of glucose testing and social disadvantage: Metrics of racial health disparity in youth with type 1 diabetes.

R. Scribner, A. Vargas, S. Chalew, 2018, Journal of diabetes and its complications.

The relationship of glycemic control, insulin dose, and race with hypoglycemia in youth with type 1 diabetes.

S. Chalew, Jodi L. Kamps, J. Hempe, 2020, Journal of diabetes and its complications.

Simultaneous Occurrence of Diabetes Mellitus and Juvenile Dermatomyositis: Report of Two Cases

L. Espinoza, R. Cuchacovich, Ranju Singh, 2003, Clinical pediatrics.

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

S. Aradhya, F. Cortés, R. Sorensen, 2020, American journal of medical genetics. Part A.

Pediatric thyroid nodules: A single center experience.

A. Jeyakumar, P. Prasad, E. Chang, 2016, International journal of pediatric otorhinolaryngology.

Racial differences in neighborhood disadvantage, inflammation and metabolic control in black and white pediatric type 1 diabetes patients

R. Scribner, A. Vargas, S. Chalew, 2017, Pediatric diabetes.

Biological Variation in HbA 1 c Predicts Risk of Retinopathy and Nephropathy in Type 1 Diabetes

R. McCarter, S. Chalew, J. Hempe, 2004 .

Demyelinating Peripheral Neurophaty and Graves Disease in an Adolescent with Crohn's Disease 428

J. England, A. Shetty, A. Gedalia, 1998, Pediatric Research.

New ocular finding in Baraitser-Winter syndrome (BWS).

Y. Lacassie, A. Leon, R. Gómez, 2018, European journal of medical genetics.

Can Innovative Technologies Overcome HbA1c Disparity for African-American Youth with Type 1 Diabetes?

A. Delamater, S. Chalew, Dania L. Felipe, 2021, Journal of diabetes science and technology.

Chronic inflammatory demyelinating polyradiculoneurophathy and Graves' disease in an adolescent with Crohn's disease.

J. England, A. Shetty, A. Gedalia, 1999, Journal of pediatric gastroenterology and nutrition.

Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three African‐American brothers

S. Aradhya, L. Messiaen, A. Vargas, 2013, American journal of medical genetics. Part A.