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Karolina Rutkowska

Medical University of Warsaw

Poland

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Research Interests

Pediatric Nutrition

20%

Clinical Psychology

10%

Neurodevelopmental Disorders

30%

Rare Disease

20%

Birth Defect

20%

Herbal Medicine

20%

Medical Science

20%

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Articles9

Effects of Turmeric and Rosemary Extract on Oxidative Stress Markers in Goats

Article Link

Year:

2025

A Rare De Novo Mutation in the TRIM8 Gene in a 17-Year-Old Boy with Steroid-Resistant Nephrotic Syndrome: Case Report

Article Link

Year:

2024

Leukodystrophy with Macrocephaly, Refractory Epilepsy, and Severe Hyponatremia—The Neonatal Type of Alexander Disease

Article Link

Year:

2024

The Expression of Selected Cytokine Genes in the Livers of Young Castrated Bucks after Supplementation with a Mixture of Dry Curcuma longa and Rosmarinus officinalis Extracts

Article Link

Year:

2023

Effect of Supplementation with Curcuma longa and Rosmarinus officinalis Extract Mixture on Acute Phase Protein, Cathelicidin, Defensin and Cytolytic Protein Gene Expression in the Livers of Young Castrated Polish White Improved Bucks

Article Link

Year:

2023

<scp>FINCA syndrome—Defining neurobehavioral phenotype in survivors into late childhood</scp>

Article Link

Year:

2022

Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the ANKRD11 Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3

Article Link

Year:

2021

Case Report: Blepharophimosis and Ptosis as Leading Dysmorphic Features of Rare Congenital Malformation Syndrome With Developmental Delay – New Cases With TRAF7 Variants

Article Link

Year:

2021

Evidence of the milder phenotypic spectrum of c.1582G>A PIGT variant: Delineation based on seven novel Polish patients

Article Link

Year:

2020

Collaborators14

Aleksandra Landowska

Instytut Matki i Dziecka

POLAND

Jarosław Kaba

Warsaw University of Life Sciences

POLAND

Krzysztof Szczałuba

assistant professor

Medical University of Warsaw

POLAND

Elżbieta Szczepanik

Instytut Matki i Dziecka

POLAND

Katarzyna Niepokój

Institute of Mother and Child

POLAND

Marta Smyk

Institute of Mother and Child

POLAND

Magdalena Machnikowska-Sokołowska

MD, PhD, ass., Head of Magnetic Resonance Department

Medical University of Silesia

POLAND

Anna Kutkowska-Kaźmierczak

Instytut Matki i Dziecka

POLAND

Mateusz Dawidziuk

Instytut Matki i Dziecka

POLAND

Malgorzata Pac

Head od department of immunology

Instytut Pomnik -Centrum Zdrowia Dziecka

POLAND

Michał Czopowicz

Scientist and lecturer

Warsaw University of Life Sciences-SGGW, Faculty of Veterinary Medicine

POLAND

Ploski R

POLAND

Maria Szczepanska

Prof.

Medical University of Silesia Faculty of Medical Sciences in Zabrze

POLAND

Marcin Mickiewicz

assistant professor

Warsaw University of Life Sciences

POLAND

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Karolina Rutkowska

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Articles9

Effects of Turmeric and Rosemary Extract on Oxidative Stress Markers in Goats

A Rare De Novo Mutation in the <i>TRIM8</i> Gene in a 17-Year-Old Boy with Steroid-Resistant Nephrotic Syndrome: Case Report

Leukodystrophy with Macrocephaly, Refractory Epilepsy, and Severe Hyponatremia—The Neonatal Type of Alexander Disease

The Expression of Selected Cytokine Genes in the Livers of Young Castrated Bucks after Supplementation with a Mixture of Dry <i>Curcuma longa</i> and <i>Rosmarinus officinalis</i> Extracts

Effect of Supplementation with <i>Curcuma longa</i> and <i>Rosmarinus officinalis</i> Extract Mixture on Acute Phase Protein, Cathelicidin, Defensin and Cytolytic Protein Gene Expression in the Livers of Young Castrated Polish White Improved Bucks

<scp>FINCA syndrome—Defining neurobehavioral phenotype in survivors into late childhood</scp>

Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the <i>ANKRD11</i> Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3

Case Report: Blepharophimosis and Ptosis as Leading Dysmorphic Features of Rare Congenital Malformation Syndrome With Developmental Delay – New Cases With TRAF7 Variants

Evidence of the milder phenotypic spectrum of c.1582G>A PIGT variant: Delineation based on seven novel Polish patients

Collaborators14

Aleksandra Landowska

Jarosław Kaba

Krzysztof Szczałuba

Elżbieta Szczepanik

Katarzyna Niepokój

Marta Smyk

Magdalena Machnikowska-Sokołowska

Anna Kutkowska-Kaźmierczak

Mateusz Dawidziuk

Malgorzata Pac

Michał Czopowicz

Ploski R

Maria Szczepanska

Marcin Mickiewicz

How do I reach out?

Karolina Rutkowska

How do I reach out?

Contact this professor

Research Interests

Ask ApplyKite AI

Articles9

Effects of Turmeric and Rosemary Extract on Oxidative Stress Markers in Goats

A Rare De Novo Mutation in the <i>TRIM8</i> Gene in a 17-Year-Old Boy with Steroid-Resistant Nephrotic Syndrome: Case Report

Leukodystrophy with Macrocephaly, Refractory Epilepsy, and Severe Hyponatremia—The Neonatal Type of Alexander Disease

The Expression of Selected Cytokine Genes in the Livers of Young Castrated Bucks after Supplementation with a Mixture of Dry <i>Curcuma longa</i> and <i>Rosmarinus officinalis</i> Extracts

Effect of Supplementation with <i>Curcuma longa</i> and <i>Rosmarinus officinalis</i> Extract Mixture on Acute Phase Protein, Cathelicidin, Defensin and Cytolytic Protein Gene Expression in the Livers of Young Castrated Polish White Improved Bucks

<scp>FINCA syndrome—Defining neurobehavioral phenotype in survivors into late childhood</scp>

Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the <i>ANKRD11</i> Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3

Case Report: Blepharophimosis and Ptosis as Leading Dysmorphic Features of Rare Congenital Malformation Syndrome With Developmental Delay – New Cases With TRAF7 Variants

Evidence of the milder phenotypic spectrum of c.1582G&gt;A PIGT variant: Delineation based on seven novel Polish patients

Collaborators14

Aleksandra Landowska

Jarosław Kaba

Krzysztof Szczałuba

Elżbieta Szczepanik

Katarzyna Niepokój

Marta Smyk

Magdalena Machnikowska-Sokołowska

Anna Kutkowska-Kaźmierczak

Mateusz Dawidziuk

Malgorzata Pac

Michał Czopowicz

Ploski R

Maria Szczepanska

Marcin Mickiewicz

How do I reach out?

Evidence of the milder phenotypic spectrum of c.1582G>A PIGT variant: Delineation based on seven novel Polish patients