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

Diabetes and Metabolism Journal, 2024, 48(5), 205, pp.949-959

2024

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Policy for transitioning childhood-onset growth hormone deficiency from pediatric to adult endocrine care in Belgium

Frontiers in endocrinology (Lausanne), 2024-09, Vol.15

2024

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β-cell replacement sources for type 1 diabetes: a focus on pancreatic ductal cells

Therapeutic Advances in Endocrinology and Metabolism, 2016-08, Vol.7 (4), p.182-199

2016

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Islet neogenesis: a possible pathway for beta-cell replenishment

The review of diabetic studies, 2012, Vol.9 (4), p.407-416

2012

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Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

Case reports in orthopedics, 2018, Vol.2018 (2018), p.1-5

2018

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Growth hormone releasing hormone excess and blockade in X-LAG syndrome

Endocrine-related cancer, 2016, Vol.23 (3), p.161-170

2016

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La thérapie cellulaire du diabète: Le point sur les actualités

M.S. Médecine sciences, 2016-04, Vol.32 (4), p.401-407

Lysy, Philippe A.

2016

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Cellular therapy of diabetes: focus on the latest developments

M.S. Médecine sciences, 2016-04, Vol.32 (4), p.401

Lysy, Philippe A

2016

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Update on Genetic Determinants of Type1 Diabetes

Journal of molecular and genetic medicine, 2016, Vol.8 (3)

Lysy, Philippe A

2016

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

Journal of Diabetes Research, 2019-08

2019

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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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Making [beta] Cells from Adult Cells Within the Pancreas

Current diabetes reports, 2013-10, Vol.13 (5), p.695

2013

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

Diabetes & metabolism journal, 2024-09, Vol.48 (5), p.949

2024

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Blood urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study

Therapeutic advances in endocrinology and metabolism, 2017-01, Vol.8

2017

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Human skin fibroblasts: From mesodermal to hepatocyte-like differentiation

Hepatology (Baltimore, Md.), 2007-11, Vol.46 (5), p.1574-1585

2007

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RNA-based MAFA overexpression is sufficient to drive human pancreatic duct-derived cells toward a [Beta]-cell-like phenotype

Acta clinica belgica (English ed. Online), 2016-03, Vol.71 (S2), p.8

2016

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Characterization of patients stopping GH therapy for childhood-onset growth hormone deficiency in belgium - luxemburg

Endocrine Abstracts, 2024-05

2024

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Partial proximal 10q trisomy: a new case associated with biliary atresia: Proximal 10q trisomy and biliary atresia

Hereditas, 2007-10, Vol.144 (5), p.191-194

2007

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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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Post-Hypoglycemic Hyperglycemia Are Highly Relevant Markers For Stratification Of Glycemic Variability and Remission Status Of Pediatric Patients With New-Onset Type 1 Diabetes

Endocrine Abstracts, 2023-11

2023

Volltextzugriff (PDF)

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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Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

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

2018

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The clinical characteristics of X-linked acro-gigantism syndrome

Endocrine Abstracts, 2015-05

2015

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

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

Policy for transitioning childhood-onset growth hormone deficiency from pediatric to adult endocrine care in Belgium

β-cell replacement sources for type 1 diabetes: a focus on pancreatic ductal cells

Islet neogenesis: a possible pathway for beta-cell replenishment

Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

Growth hormone releasing hormone excess and blockade in X-LAG syndrome

La thérapie cellulaire du diabète: Le point sur les actualités

Cellular therapy of diabetes: focus on the latest developments

Update on Genetic Determinants of Type1 Diabetes

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

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

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

Making [beta] Cells from Adult Cells Within the Pancreas

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

Blood urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study

Human skin fibroblasts: From mesodermal to hepatocyte-like differentiation

RNA-based MAFA overexpression is sufficient to drive human pancreatic duct-derived cells toward a [Beta]-cell-like phenotype

Characterization of patients stopping GH therapy for childhood-onset growth hormone deficiency in belgium - luxemburg

Partial proximal 10q trisomy: a new case associated with biliary atresia: Proximal 10q trisomy and biliary atresia

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

Post-Hypoglycemic Hyperglycemia Are Highly Relevant Markers For Stratification Of Glycemic Variability and Remission Status Of Pediatric Patients With New-Onset Type 1 Diabetes

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

Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

The clinical characteristics of X-linked acro-gigantism syndrome

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