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Multivariable Prediction Model for Biochemical Response to First-Generation Somatostatin Receptor Ligands in Acromegaly

The journal of clinical endocrinology and metabolism, 2020-09, Vol.105 (9), p.2964-2974

2020

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Comment on Moriconi et al. Very-Low-Calorie Ketogenic Diet as a Safe and Valuable Tool for Long-Term Glycemic Management in Patients with Obesity and Type 2 Diabetes. Nutrients 2021, 13, 758

Nutrients, 2021-10, Vol.13 (10), p.3613

2021

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The Fascinating Interplay between Growth Hormone, Insulin-Like Growth Factor-1, and Insulin

Endocrinology and Metabolism, 2024, 39(1), , pp.83-89

2024

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Pegvisomant for acromegaly: does it always works?

Archives of Endocrinology and Metabolism, 2019-08, Vol.63 (4), p.318-319

2019

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Health Problems in Adults with Prader-Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the Literature

Journal of clinical medicine, 2022-07, Vol.11 (14), p.4033

2022

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How to Position Pasireotide LAR Treatment in Acromegaly

The journal of clinical endocrinology and metabolism, 2019-06, Vol.104 (6), p.1978-1988

2019

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The Diagnostic Journey of a Patient with Prader–Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature

Genes, 2021-06, Vol.12 (6), p.875

2021

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Bariatric Surgery for Hypothalamic Obesity in Craniopharyngioma Patients: A Retrospective, Matched Case-Control Study

The journal of clinical endocrinology and metabolism, 2021-11, Vol.106 (11), p.e4734-e4745

2021

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Efficacy and Safety of Switching to Pasireotide in Patients With Acromegaly Controlled With Pegvisomant and First-Generation Somatostatin Analogues (PAPE Study)

The journal of clinical endocrinology and metabolism, 2018-02, Vol.103 (2), p.586-595

2018

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Effects of Childhood Multidisciplinary Care and Growth Hormone Treatment on Health Problems in Adults with Prader-Willi Syndrome

Journal of clinical medicine, 2021-07, Vol.10 (15), p.3250

2021

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Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review

The journal of clinical endocrinology and metabolism, 2023-12, Vol.108 (12), p.e1720-e1730

2023

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Growth Hormone Treatment for Adults With Prader-Willi Syndrome: A Meta-Analysis

The journal of clinical endocrinology and metabolism, 2021-10, Vol.106 (10), p.3068-3091

2021

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What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of ‘Internal Medicine for Rare Genetic Syndromes’

Journal of clinical medicine, 2021-11, Vol.10 (22), p.5457

2021

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Associations Between Fatigue and Endocrine and Non-endocrine Health Problems in Turner Syndrome: Cohort Study and Review

The journal of clinical endocrinology and metabolism, 2023-11, Vol.108 (12), p.e1649-e1659

2023

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Eucaloric Very-Low-Carbohydrate Ketogenic Diet in Acromegaly Treatment

The New England journal of medicine, 2020-05, Vol.382 (22), p.2161-2162

2020

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The acylated (AG) to unacylated (UAG) ghrelin ratio in esterase inhibitor-treated blood is higher than previously described

Clinical endocrinology (Oxford), 2015-01, Vol.82 (1), p.142-146

2015

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ACRODAT® and AcroVoice: an insight into a holistic approach to the management of acromegaly

Pituitary, 2019-12, Vol.22 (6), p.647-648

2019

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Body Composition and Bone Mineral Density in Craniopharyngioma Patients: A Longitudinal Study Over 10 Years

The journal of clinical endocrinology and metabolism, 2020-12, Vol.105 (12), p.1-e4637

2020

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Fractures, Bone Mineral Density, and Final Height in Craniopharyngioma Patients with a Follow-up of 16 Years

The journal of clinical endocrinology and metabolism, 2020-04, Vol.105 (4), p.e1397-e1407

2020

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Risk factors and management of pasireotide-associated hyperglycemia in acromegaly

Endocrine Connections, 2020-12, Vol.9 (12), p.1178-1190

2020

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Towards an Earlier Diagnosis of Acromegaly and Gigantism

Journal of clinical medicine, 2021-03, Vol.10 (7), p.1363

2021

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Corrigendum: Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review

Frontiers in endocrinology (Lausanne), 2024, Vol.15, p.1357219-1357219

2024

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Endocrine and non-endocrine causes of fatigue in adults with Neurofibromatosis type 1

Frontiers in endocrinology (Lausanne), 2023, Vol.14, p.1119159-1119159

2023

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The position of combined medical treatment in acromegaly

Archives of Endocrinology and Metabolism, 2019-11, Vol.63 (6), p.646-652

2019

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Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review

Frontiers in endocrinology (Lausanne), 2023, Vol.14, p.1168648-1168648

2023

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Multivariable Prediction Model for Biochemical Response to First-Generation Somatostatin Receptor Ligands in Acromegaly

Comment on Moriconi et al. Very-Low-Calorie Ketogenic Diet as a Safe and Valuable Tool for Long-Term Glycemic Management in Patients with Obesity and Type 2 Diabetes. Nutrients 2021, 13, 758

The Fascinating Interplay between Growth Hormone, Insulin-Like Growth Factor-1, and Insulin

Pegvisomant for acromegaly: does it always works?

Health Problems in Adults with Prader-Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the Literature

How to Position Pasireotide LAR Treatment in Acromegaly

The Diagnostic Journey of a Patient with Prader–Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature

Bariatric Surgery for Hypothalamic Obesity in Craniopharyngioma Patients: A Retrospective, Matched Case-Control Study

Efficacy and Safety of Switching to Pasireotide in Patients With Acromegaly Controlled With Pegvisomant and First-Generation Somatostatin Analogues (PAPE Study)

Effects of Childhood Multidisciplinary Care and Growth Hormone Treatment on Health Problems in Adults with Prader-Willi Syndrome

Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review

Growth Hormone Treatment for Adults With Prader-Willi Syndrome: A Meta-Analysis

What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of ‘Internal Medicine for Rare Genetic Syndromes’

Associations Between Fatigue and Endocrine and Non-endocrine Health Problems in Turner Syndrome: Cohort Study and Review

Eucaloric Very-Low-Carbohydrate Ketogenic Diet in Acromegaly Treatment

The acylated (AG) to unacylated (UAG) ghrelin ratio in esterase inhibitor-treated blood is higher than previously described

ACRODAT® and AcroVoice: an insight into a holistic approach to the management of acromegaly

Body Composition and Bone Mineral Density in Craniopharyngioma Patients: A Longitudinal Study Over 10 Years

Fractures, Bone Mineral Density, and Final Height in Craniopharyngioma Patients with a Follow-up of 16 Years

Risk factors and management of pasireotide-associated hyperglycemia in acromegaly

Towards an Earlier Diagnosis of Acromegaly and Gigantism

Corrigendum: Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review

Endocrine and non-endocrine causes of fatigue in adults with Neurofibromatosis type 1

The position of combined medical treatment in acromegaly

Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review

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