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Dariusz Patkowski

Biographic Data

ID7900574
NAMEDariusz Patkowski
GIVEN NAMESDariusz
FAMILY NAMEPatkowski
SIGNATUREPATKOWSKI D
AFFILIATIONSWroclaw Medical University
ORCID0000-0002-4583-5517
VERIFIEDYes
TOTAL WORKS3
TOTAL CITATIONS0
WORKS AS AUTHOR3
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2022
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Mind the Missing Gap

    Open Access•Marco Di Mitri, Riccardo Coletta et al.•ARTICLE•Children•2025

    Background: Esophageal atresia (EA) type A, characterized by the absence of a tracheoesophageal fistula and typically presenting with a long esophageal gap, usually requires staged repair. Methods: We report a rare case of a newborn with type A EA in which both the proximal and distal esophageal pouches were unexpectedly close and located in the cervical region. This anatomical variant allowed for a successful primary anastomosis through a cervic…

  • Preserved Voluntary Micturition Control despite Early Urinary Diversion in Infancy—A Clue to a New Strategy

    Open Access•Dominika Borselle, Dariusz Patkowski et al.•ARTICLE•Children•2022

    Micturition is an involuntary process based on spinal arcs in infants and children until a defined age. The awareness and voluntary control of voiding depends on specific areas in the central nervous system, especially cortical regions. The cells and connections between these areas develop over time and regulate the voiding process. The ability to maintain continence and to adjust physiological needs to appropriate environmental conditions is con…

  • Reliability and Validity of the Polish Version of the Esophageal-Atresia-Quality-of-Life Questionnaires to Assess Condition-Specific Quality of Life in Children and Adolescents Born with Esophageal At…

    Open Access•Anna Rozensztrauch, Robert Śmigiel et al.•ARTICLE•International Journal of…•2022

    Aim: This study reports the reliability and validity of the Polish version of the Esophageal Atresia Quality of Life (EA-QOL) questionnaires, which were originally developed in Sweden and Germany. Methods: A total of 50 families of children (23 aged 2 to 7, and 27 aged 8 to 17) with EA/TEF (esophageal atresia/tracheoesophageal fistula) participated in the study. The development and validation of the Polish version of the EA-QOL involved forward-b…

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  • Preserved Voluntary Micturition Control despite Early Urinary Diversion in Infancy—A Clue to a New Strategy

    Open Access•Dominika Borselle, Dariusz Patkowski et al.•ARTICLE•Children•2022

    Micturition is an involuntary process based on spinal arcs in infants and children until a defined age. The awareness and voluntary control of voiding depends on specific areas in the central nervous system, especially cortical regions. The cells and connections between these areas develop over time and regulate the voiding process. The ability to maintain continence and to adjust physiological needs to appropriate environmental conditions is con…

  • Reliability and Validity of the Polish Version of the Esophageal-Atresia-Quality-of-Life Questionnaires to Assess Condition-Specific Quality of Life in Children and Adolescents Born with Esophageal At…

    Open Access•Anna Rozensztrauch, Robert Śmigiel et al.•ARTICLE•International Journal of…•2022

    Aim: This study reports the reliability and validity of the Polish version of the Esophageal Atresia Quality of Life (EA-QOL) questionnaires, which were originally developed in Sweden and Germany. Methods: A total of 50 families of children (23 aged 2 to 7, and 27 aged 8 to 17) with EA/TEF (esophageal atresia/tracheoesophageal fistula) participated in the study. The development and validation of the Polish version of the EA-QOL involved forward-b…

  • Mind the Missing Gap

    Open Access•Marco Di Mitri, Riccardo Coletta et al.•ARTICLE•Children•2025

    Background: Esophageal atresia (EA) type A, characterized by the absence of a tracheoesophageal fistula and typically presenting with a long esophageal gap, usually requires staged repair. Methods: We report a rare case of a newborn with type A EA in which both the proximal and distal esophageal pouches were unexpectedly close and located in the cervical region. This anatomical variant allowed for a successful primary anastomosis through a cervic…

Medicine (3 works) · Esophageal and GI Pathology (2 works) · Tracheal and airway disorders (2 works) · Anastomosis (1 work) · Anatomy (1 work) · Atresia (1 work) · Clinical Psychology (1 work) · Clinical Psychology (1 work) · Congenital Diaphragmatic Hernia Studies (1 work) · Construct validity (1 work)

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