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A centennial review of discoveries and advances in diabetes: Children and youth

Pediatric diabetes, 2022-11, Vol.23 (7), p.926-943

2022

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Use of glucagon‐like peptide‐1 receptor agonists for pediatric patients with obesity and diabetes: The providers' perspectives

Pediatric diabetes, 2021-09, Vol.22 (6), p.872-875

2021

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Gender Bias in U.S. Pediatric Growth Hormone Treatment

Scientific reports, 2015-06, Vol.5 (1), p.11099-11099, Article 11099

2015

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El impacto de la pandemia del COVID-19 en la educación médica:: adaptabilidad y experiencia con enseñanza a distancia de la Sociedad Médica Peruano Americana

Anales de la Facultad de Medicina (Lima, Peru : 1990), 2023, Vol.84 (1), p.117-122

2023

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Efficacy and safety of the SGLT2 inhibitor empagliflozin versus placebo and the DPP-4 inhibitor linagliptin versus placebo in young people with type 2 diabetes (DINAMO): a multicentre, randomised, double-blind, parallel group, phase 3 trial

The lancet. Diabetes & endocrinology, 2023-03, Vol.11 (3), p.169-181

2023

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1323006: Cardiometabolic Risk Factors and Insulin Therapy Requirement in Youth with New Onset Type 2 Diabetes during the COVID-19 Pandemic

Endocrine practice, 2022-12, Vol.28 (12), p.S9-S9

2022

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ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic

Journal of the Endocrine Society, 2022-11, Vol.6 (Supplement_1), p.A608-A608

2022

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Tap or Bottled Water: Drinking Preferences Among Urban Minority Children and Adolescents

Journal of community health, 2012-02, Vol.37 (1), p.54-58

2012

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Do Mindfulness Interventions Improve Obesity Rates in Children and Adolescents: A Review of the Evidence

Diabetes, metabolic syndrome and obesity, 2021-01, Vol.14, p.4621-4629

2021

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Challenging diagnosis of congenital hyperinsulinism in two infants of diabetic mothers with rare pathogenic KCNJ11 and HNF4A gene variants

International journal of pediatric endocrinology, 2018-07, Vol.2018 (1), p.5, Article 5

2018

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A Novel Variant in NR5A1 Presenting as 46,XY Difference of Sex Development

JCEM case reports, 2023-09, Vol.1 (5), p.luad103

2023

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Novel Heterozygous Calcium Sensing Receptor (CASR ) Genetic Variant in Child with Unique Phenotype: Hypocalcemia, Mandibular Hypoplasia, Renal Cysts and Type E Brachydactyly

Journal of the Endocrine Society, 2021-05, Vol.5 (Supplement_1), p.A703-A703

2021

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National congenital hypothyroidism screening in Peru: a broken program

Revista peruana de medicina experimental y salud pública, 2015-07, Vol.32 (3), p.579-585

2015

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Non-Gastric Extranodal Marginal Zone MALT B-Cell Lymphoma In a Peruvian Cancer Referral Center (Instituto Nacional de Enfermedades Neoplasicas)

Blood, 2010-11, Vol.116 (21), p.5099-5099

2010

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8765 Assessment of the Social Vulnerability Index of a 10-Year Retrospective Cohort of Youth with Prediabetes

Journal of the Endocrine Society, 2024-10, Vol.8 (Supplement_1)

2024

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Approaching High-Metabolic Risk Youth During a Pandemic: Severe Presentations of New Onset Type 2 Diabetes

Journal of the Endocrine Society, 2021-05, Vol.5 (Supplement_1), p.A696-A696

2021

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A Novel Variant in NR5A1 Presenting as 46,XY Difference of Sex Development

JCEM case reports, 2023, Vol.1 (5), p.luad103-luad103

2023

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Challenging diagnosis of congenital hyperinsulinism in two infants of diabetic mothers with rare pathogenic KCNJ11 and HNF4A gene variants

International journal of pediatric endocrinology, 2018, Vol.2018, p.5-5

2018

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Tamizaje nacional unificado de hipotiroidismo congénito en el Perú: un programa inexistente

Revista peruana de medicina experimental y salud pública, 2015-09, Vol.32 (3), p.579-585

2015

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Tamizaje nacional unificado de hipotiroidismo congénito en el Perú: un programa inexistente

Revista peruana de medicina experimental y salud pública, 2015-09, Vol.32 (3), p.579

2015

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A centennial review of discoveries and advances in diabetes: Children and youth

Use of glucagon‐like peptide‐1 receptor agonists for pediatric patients with obesity and diabetes: The providers' perspectives

Gender Bias in U.S. Pediatric Growth Hormone Treatment

El impacto de la pandemia del COVID-19 en la educación médica:: adaptabilidad y experiencia con enseñanza a distancia de la Sociedad Médica Peruano Americana

Efficacy and safety of the SGLT2 inhibitor empagliflozin versus placebo and the DPP-4 inhibitor linagliptin versus placebo in young people with type 2 diabetes (DINAMO): a multicentre, randomised, double-blind, parallel group, phase 3 trial

1323006: Cardiometabolic Risk Factors and Insulin Therapy Requirement in Youth with New Onset Type 2 Diabetes during the COVID-19 Pandemic

The Coronavirus Disease 2019 Pandemic is Associated with a Substantial Rise in Frequency and Severity of Presentation of Youth-Onset Type 2 Diabetes

ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic

Tap or Bottled Water: Drinking Preferences Among Urban Minority Children and Adolescents

Do Mindfulness Interventions Improve Obesity Rates in Children and Adolescents: A Review of the Evidence

Challenging diagnosis of congenital hyperinsulinism in two infants of diabetic mothers with rare pathogenic KCNJ11 and HNF4A gene variants

A Novel Variant in NR5A1 Presenting as 46,XY Difference of Sex Development

Novel Heterozygous Calcium Sensing Receptor (CASR ) Genetic Variant in Child with Unique Phenotype: Hypocalcemia, Mandibular Hypoplasia, Renal Cysts and Type E Brachydactyly

National congenital hypothyroidism screening in Peru: a broken program

Non-Gastric Extranodal Marginal Zone MALT B-Cell Lymphoma In a Peruvian Cancer Referral Center (Instituto Nacional de Enfermedades Neoplasicas)

8765 Assessment of the Social Vulnerability Index of a 10-Year Retrospective Cohort of Youth with Prediabetes

Approaching High-Metabolic Risk Youth During a Pandemic: Severe Presentations of New Onset Type 2 Diabetes

A Novel Variant in NR5A1 Presenting as 46,XY Difference of Sex Development

Challenging diagnosis of congenital hyperinsulinism in two infants of diabetic mothers with rare pathogenic KCNJ11 and HNF4A gene variants

Tamizaje nacional unificado de hipotiroidismo congénito en el Perú: un programa inexistente

Tamizaje nacional unificado de hipotiroidismo congénito en el Perú: un programa inexistente

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