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A New Tool to Identify Pediatric Patients with Atypical Diabetes Associated with Gene Polymorphisms

Diabetes & metabolism journal, 2024-03

2024

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Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

American journal of human genetics, 2024-03, Vol.111 (3), p.509-528

2024

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Pancreas Imaging of Children with Type 1 Diabetes Reveals New Patterns and Correlations with Pancreatic Functions

Pediatric diabetes, 2023-09, Vol.2023, p.1-13

2023

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Case Report: Aggressive neural crest tumors in a child with familial von Hippel Lindau syndrome associated with a germline VHL mutation (c.414A>G) and a novel KIF1B gene mutation

Frontiers in endocrinology (Lausanne), 2023-07, Vol.14, p.1204793

2023

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Congenital hyperinsulinemic hypoglycemia (HH) requiring treatment as the presenting feature of Kabuki syndrome

Clinical case reports, 2023-06, Vol.11 (6), p.e7336-n/a

2023

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Congenital hyperinsulinemic hypoglycemia (HH) requiring treatment as the presenting feature of Kabuki syndrome

Clinical case reports, 2023, Vol.11 (6), p.e7336-e7336

2023

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Always a Bridesmaid: A Machine Learning Approach to Minor Party Identity in Multi-Party Systems

Statistics, politics, and policy, 2023-03, Vol.14 (1), p.91-112

2023

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Characterization, evolution and risk factors of diabetes and prediabetes in a pediatric cohort of renal and liver transplant recipients

Frontiers in pediatrics, 2023-02, Vol.11, p.1080905-1080905

2023

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Case Report: Aggressive neural crest tumors in a child with familial von Hippel Lindau syndrome associated with a germline VHL mutation (c.414A>G) and a novel KIF1B gene mutation

Frontiers in endocrinology, 2023, Vol.14, p.1204793-1204793

2023

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Influence of the occurrence and duration of partial remission on short-term metabolic control in type 1 diabetes: the DIABHONEY pediatric study

Therapeutic advances in endocrinology and metabolism, 2023-01, Vol.14, p.20420188221145550-20420188221145550

2023

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Once-Weekly Semaglutide in Adolescents with Obesity

The New England journal of medicine, 2022-12, Vol.387 (24), p.2245-2257

2022

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OR03-5 Identification of Four New Glucotypes during the First Year after Type 1 Diabetes Onset Using Continuous Glucose Monitoring Metrics

Journal of the Endocrine Society, 2022-11, Vol.6 (Supplement_1), p.A349-A350

2022

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RF16 | PSUN203 Deep Characterization of Pancreas Volume of New-Onset Type 1 Diabetes Patients Reveals Puberty-Specific Patterns and New Topographic Correlations with Pancreatic Functions

Journal of the Endocrine Society, 2022-11, Vol.6 (Supplement_1), p.A424-A425

2022

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Effect of nationwide reimbursement of real-time continuous glucose monitoring on HbA1c, hypoglycemia and quality of life in a pediatric type 1 diabetes population: The RESCUE-pediatrics study

Frontiers in pediatrics, 2022-10, Vol.10, p.991633-991633

2022

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Glycemic Variability Patterns Strongly Correlate With Partial Remission Status in Children With Newly Diagnosed Type 1 Diabetes

Diabetes care, 2022-10, Vol.45 (10), p.2360-2368

2022

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662-P: Glycemic Variability Patterns Strongly Correlate with Partial Remission Status in Children with Newly Diagnosed Type 1 Diabetes

Diabetes (New York, N.Y.), 2022-06, Vol.71 (Supplement_1)

2022

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Intra‐amniotic levothyroxine infusions in a case of fetal goiter due to novel Thyroglobulin gene variants

Clinical case reports, 2021-09, Vol.9 (9), p.e04565-n/a

2021

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Intra-amniotic levothyroxine infusions in a case of fetal goiter due to novel Thyroglobulin gene variants

Clinical case reports, 2021, Vol.9 (9), p.e04565-e04565

2021

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Early Treatment with Empagliflozin and GABA Improves [beta]-Cell Mass and Glucose Tolerance in Streptozotocin-Treated Mice.(Research Article)

Journal of Diabetes Research, 2019-08

2019

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Novel insights into glucocorticoid replacement therapy for pediatric and adult adrenal insufficiency

Therapeutic Advances in Endocrinology and Metabolism, 2019, Vol.10, p.2042018818821294-2042018818821294

2019

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Early Treatment with Empagliflozin and GABA Improves β-Cell Mass and Glucose Tolerance in Streptozotocin-Treated Mice

Journal of diabetes research, 2019, Vol.2019, p.2813489-14

2019

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Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

Case reports in orthopedics, 2018, Vol.2018, p.7698052-5

2018

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Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

Case reports in orthopedics, 2018, Vol.2018, p.7698052-7698052

2018

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Familial Forms of Cushing Syndrome in Primary Pigmented Nodular Adrenocortical Disease Presenting with Short Stature and Insidious Symptoms: A Clinical Series

Hormone research in paediatrics, 2018-01, Vol.89 (6), p.423-433

2018

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Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2–p13.12/13 deletion

American journal of hematology, 2017-01, Vol.92 (1), p.E2-E3

2017

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A New Tool to Identify Pediatric Patients with Atypical Diabetes Associated with Gene Polymorphisms

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

Pancreas Imaging of Children with Type 1 Diabetes Reveals New Patterns and Correlations with Pancreatic Functions

Case Report: Aggressive neural crest tumors in a child with familial von Hippel Lindau syndrome associated with a germline VHL mutation (c.414A>G) and a novel KIF1B gene mutation

Congenital hyperinsulinemic hypoglycemia (HH) requiring treatment as the presenting feature of Kabuki syndrome

Congenital hyperinsulinemic hypoglycemia (HH) requiring treatment as the presenting feature of Kabuki syndrome

Always a Bridesmaid: A Machine Learning Approach to Minor Party Identity in Multi-Party Systems

Characterization, evolution and risk factors of diabetes and prediabetes in a pediatric cohort of renal and liver transplant recipients

Case Report: Aggressive neural crest tumors in a child with familial von Hippel Lindau syndrome associated with a germline VHL mutation (c.414A>G) and a novel KIF1B gene mutation

Influence of the occurrence and duration of partial remission on short-term metabolic control in type 1 diabetes: the DIABHONEY pediatric study

Once-Weekly Semaglutide in Adolescents with Obesity

OR03-5 Identification of Four New Glucotypes during the First Year after Type 1 Diabetes Onset Using Continuous Glucose Monitoring Metrics

RF16 | PSUN203 Deep Characterization of Pancreas Volume of New-Onset Type 1 Diabetes Patients Reveals Puberty-Specific Patterns and New Topographic Correlations with Pancreatic Functions

Effect of nationwide reimbursement of real-time continuous glucose monitoring on HbA1c, hypoglycemia and quality of life in a pediatric type 1 diabetes population: The RESCUE-pediatrics study

Glycemic Variability Patterns Strongly Correlate With Partial Remission Status in Children With Newly Diagnosed Type 1 Diabetes

662-P: Glycemic Variability Patterns Strongly Correlate with Partial Remission Status in Children with Newly Diagnosed Type 1 Diabetes

Intra‐amniotic levothyroxine infusions in a case of fetal goiter due to novel Thyroglobulin gene variants

Intra-amniotic levothyroxine infusions in a case of fetal goiter due to novel Thyroglobulin gene variants

Early Treatment with Empagliflozin and GABA Improves [beta]-Cell Mass and Glucose Tolerance in Streptozotocin-Treated Mice.(Research Article)

Novel insights into glucocorticoid replacement therapy for pediatric and adult adrenal insufficiency

Early Treatment with Empagliflozin and GABA Improves β-Cell Mass and Glucose Tolerance in Streptozotocin-Treated Mice

Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

Familial Forms of Cushing Syndrome in Primary Pigmented Nodular Adrenocortical Disease Presenting with Short Stature and Insidious Symptoms: A Clinical Series

Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2–p13.12/13 deletion

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