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Incremental Value of Continuous Glucose Monitoring When Starting Pump Therapy in Patients With Poorly Controlled Type 1 Diabetes: The RealTrend study

Diabetes care, 2009-12, Vol.32 (12), p.2245-2250

2009

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Characteristics of newly diagnosed type 1 diabetes in paediatric and adult population from Reims University Hospital, France from 1997 to 2019

Diabetes & metabolism, 2022-09, Vol.48 (5), p.101346-101346, Article 101346

2022

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Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: a report from the French ND (Neonatal Diabetes) Study Group

Diabetes (New York, N.Y.), 2008-04, Vol.57 (4), p.1115-1119

2008

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Apparent mineralocorticoid excess : Report of six new cases and extensive personal experience

Journal of the American Society of Nephrology, 2006-11, Vol.17 (11), p.3176-3184

2006

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Congenital goitre with hypothyroidism caused by a novel compound heterozygous mutations in the thyroglobulin gene

Clinical endocrinology (Oxford), 2010-05, Vol.72 (5), p.716-718

2010

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Incremental Value of Continuous Glucose Monitoring When Starting Pump Therapy in Patients With Poorly Controlled Type 1 Diabetes

Diabetes care, 2009-12, Vol.32 (12), p.2245-2250

2009

Volltextzugriff (PDF)

Heterozygous Missense Mutations in the Insulin Gene Are Linked to Permanent Diabetes Appearing in the Neonatal Period or in Early Infancy

Diabetes (New York, N.Y.), 2008-04, Vol.57 (4), p.1115-1119

2008

Volltextzugriff (PDF)

Deletion 2q36.2q36.3 with multiple renal cysts and severe mental retardation

European journal of medical genetics, 2008-11, Vol.51 (6), p.598-607

2008

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Metabolic Control in Children with Diabetes Mellitus Who are Younger than 6 Years at Diagnosis: Continuous Subcutaneous Insulin Infusion as a First Line Treatment?

The Journal of pediatrics, 2010-07, Vol.157 (1), p.103-107

2010

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Subtle Health Impairment and Socioeducational Attainment in Young Adult Patients with Congenital Hypothyroidism Diagnosed by Neonatal Screening: A Longitudinal Population-Based Cohort Study

The journal of clinical endocrinology and metabolism, 2011-06, Vol.96 (6), p.1771-1782

2011

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SHOX point mutations in dyschondrosteosis

Journal of medical genetics, 2001-05, Vol.38 (5), p.323-323

2001

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Assessment of patient-led or physician-driven continuous glucose monitoring in patients with poorly controlled type 1 diabetes using basal-bolus insulin regimens: a 1-year multicenter study

Diabetes care, 2012-05, Vol.35 (5), p.965-971

2012

Volltextzugriff (PDF)

Congenital goitre with hypothyroidism caused by a novel compound heterozygous mutations in the thyroglobulin gene

Clinical endocrinology (Oxford), 2009-09

2009

Volltextzugriff (PDF)

Heterozygous Missense Mutations in the Insulin Gene Are Linked to Permanent Diabetes Appearing in the Neonatal Period or in Early Infancy : A Report From the French ND (Neonatal Diabetes) Study Group. Commentary

Diabetes (New York, N.Y.), 2008, Vol.57 (4)

2008

Volltextzugriff (PDF)

Androgenic Activity in Autism

The American journal of psychiatry, 1997-11, Vol.154 (11), p.1626-a-1627

1997

Volltextzugriff (PDF)

Congenital goitre with hypothyroidism caused by a novel compound heterozygous mutations in the thyroglobulin gene

Clinical endocrinology, 2010, Vol.72 (5), p.716-718

2010

Volltextzugriff (PDF)

Food perception, lifestyle, nutritional and health status in the older people: Typologies and factors associated with aging well

Appetite, 2021-09, Vol.164, p.105223-105223, Article 105223

2021

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Food perception, lifestyle, nutritional and health status in the older people: Typologies and factors associated with aging well

Appetite, 2021-09, Vol.164

2021

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Incremental Value of Continuous Glucose Monitoring When Starting Pump Therapy in Patients With Poorly Controlled Type 1 Diabetes: The RealTrend study

Characteristics of newly diagnosed type 1 diabetes in paediatric and adult population from Reims University Hospital, France from 1997 to 2019

Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: a report from the French ND (Neonatal Diabetes) Study Group

Apparent mineralocorticoid excess : Report of six new cases and extensive personal experience

Assessment of Patient-Led or Physician-Driven Continuous Glucose Monitoring in Patients With Poorly Controlled Type 1 Diabetes Using Basal-Bolus Insulin Regimens: A 1-year multicenter study

Congenital goitre with hypothyroidism caused by a novel compound heterozygous mutations in the thyroglobulin gene

Assessment of Patient-Led or Physician-Driven Continuous Glucose Monitoring in Patients With Poorly Controlled Type 1 Diabetes Using Basal-Bolus Insulin Regimens

Incremental Value of Continuous Glucose Monitoring When Starting Pump Therapy in Patients With Poorly Controlled Type 1 Diabetes

Heterozygous Missense Mutations in the Insulin Gene Are Linked to Permanent Diabetes Appearing in the Neonatal Period or in Early Infancy

Is there an optimal strategy for real‐time continuous glucose monitoring in pediatrics? A 12‐month French multi‐center, prospective, controlled randomized trial (Start‐In!)

Deletion 2q36.2q36.3 with multiple renal cysts and severe mental retardation

Metabolic Control in Children with Diabetes Mellitus Who are Younger than 6 Years at Diagnosis: Continuous Subcutaneous Insulin Infusion as a First Line Treatment?

Subtle Health Impairment and Socioeducational Attainment in Young Adult Patients with Congenital Hypothyroidism Diagnosed by Neonatal Screening: A Longitudinal Population-Based Cohort Study

SHOX point mutations in dyschondrosteosis

Assessment of patient-led or physician-driven continuous glucose monitoring in patients with poorly controlled type 1 diabetes using basal-bolus insulin regimens: a 1-year multicenter study

Assessment of Patient-Led or Physician-Driven Continuous Glucose Monitoring in Patients With Poorly Controlled Type 1 Diabetes Using Basal-Bolus Insulin Regiments: A 1-year multicenter study

Congenital goitre with hypothyroidism caused by a novel compound heterozygous mutations in the thyroglobulin gene

Heterozygous Missense Mutations in the Insulin Gene Are Linked to Permanent Diabetes Appearing in the Neonatal Period or in Early Infancy : A Report From the French ND (Neonatal Diabetes) Study Group. Commentary

Androgenic Activity in Autism

Congenital goitre with hypothyroidism caused by a novel compound heterozygous mutations in the thyroglobulin gene

Food perception, lifestyle, nutritional and health status in the older people: Typologies and factors associated with aging well

Food perception, lifestyle, nutritional and health status in the older people: Typologies and factors associated with aging well

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