Renata Stawerska

Prof of Institute

Polish Mother’s Memorial Hospital Research Institute

Poland

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Renata Stawerska is a Professor at the Polish Mother's Memorial Hospital Research Institute in Poland. Her research areas include pediatric inflammatory bowel disease, endocrine disorders, and growth hormone deficiency, as showcased in her recent articles. She has contributed significantly to understanding the relationship between bone mineral density, insulin resistance, and growth processes in children. Professor Stawerska's work addresses critical diagnostic challenges in pediatric endocrinology and metabolism.

Articles (18)

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2025

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2022

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2021

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2021

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2021

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2021

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2021

Collaborators (11)

Marcin Tkaczyk

head

Medical University of Lodz

POLAND

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Małgorzata Karbownik-Lewińska

Medical University of Lodz

POLAND

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Agnieszka Lecka- Ambroziak

Instytut Pomnik -Centrum Zdrowia Dziecka

POLAND

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Łukasz Kępczyński

assistant professor

Polish Mother’s Memorial Hospital Research Institute

POLAND

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Anna Fedorczak

Polish Mother’s Memorial Hospital Research Institute

POLAND

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Elżbieta Petriczko

Pomeranian Medical University

POLAND

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Andrzej Lewinski

Head of Department/Professor

Polish Mother’s Memorial Hospital Research Institute

POLAND

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Marta Wysocka-Mincewicz

Chief of Diabetology Subdepartment

Children's Memorial Health Institute

POLAND

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Zuzanna Gaj

Polish Mother’s Memorial Hospital Research Institute

POLAND

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Grzegorz Zielinski

Military Institute of Medicine

POLAND

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Joanna Smyczynska

Ass. Prof.

Medical University of Lodz

POLAND

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Renata Stawerska

Research Interests

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Articles (18)

RANKL/OPG Axis and Bone Mineral Density in Pediatric Inflammatory Bowel Disease

The Prevalence of Reduced Bone Mineral Density and the Impact of Specific Auxological Factors and Hormones on Bone Mass in Children with Endocrine Disorders

Resistance to Thyroid Hormone in a Boy with a Severe, Complex, Congenital Heart Defect (CHD) Requiring Multiple Cardiac Surgeries—Whether and How to Prepare Child for the Surgery

Transient Isolated, Idiopathic Growth Hormone Deficiency—A Self-Limiting Pediatric Disease with Male Predominance or a Diagnosis Based on Uncertain Criteria? Lesson from 20 Years’ Real-World Experience with Retesting at One Center

Comparison of the clinical picture and hormonal test results in children with growth hormone deficiency and idiopathic short stature – diagnostic difficulties and brief overview

Relationship between Serum Sirtuin 1 and Growth Hormone/Insulin-like Growth Factor 1 Concentrations in Children with Growth Hormone Deficiency and Idiopathic Short Stature

Comparison of the Clinical Utility of Two Insulin Resistance Indices: IRI-HOMA and IRI-Belfiore in Diagnosing Insulin Resistance and Metabolic Complications in Children Based on the Results Obtained for the Polish Population

The Variability of Vitamin D Concentrations in Short Children with Short Stature from Central Poland—The Effects of Insolation, Supplementation, and COVID-19 Pandemic Isolation

Osteoporosis as the First Sign of Cushing’s Disease in a Thin 16-Year-Old Boy—A Case Report

Involvement of Sirtuin 1 in the Growth Hormone/Insulin-like Growth Factor 1 Signal Transduction and Its Impact on Growth Processes in Children

Management of Prader-Labhart-Willi syndrome in children and in adults, with particular emphasis on the treatment with recombinant human growth hormone

Effects of Recombinant Human Growth Hormone Treatment, Depending on the Therapy Start in Different Nutritional Phases in Paediatric Patients with Prader–Willi Syndrome: A Polish Multicentre Study

Correlation of Genotype and Perinatal Period, Time of Diagnosis and Anthropometric Data before Commencement of Recombinant Human Growth Hormone Treatment in Polish Patients with Prader–Willi Syndrome

Effectiveness, economical and safety aspects of growth hormone (GH) therapy in growth promoting doses in patients with isolated GH deficiency after the attainment of near-final height. Is there a need to modify the criteria of therapy withdrawal?

Karyotype Abnormalities in the X Chromosome Predict Response to the Growth Hormone Therapy in Turner Syndrome

Contribution of Ghrelin to the Pathogenesis of Growth Hormone Deficiency

Contribution of ghrelin to the pathogenesis of growth hormone deficiency

Transient Hyperthyrotropinemia in Outpatient Children with Acute Infections of the Respiratory System

Collaborators (11)

Marcin Tkaczyk

Małgorzata Karbownik-Lewińska

Agnieszka Lecka- Ambroziak

Łukasz Kępczyński

Anna Fedorczak

Elżbieta Petriczko

Andrzej Lewinski

Marta Wysocka-Mincewicz

Zuzanna Gaj

Grzegorz Zielinski

Joanna Smyczynska

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