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Petra Konecna

Showing results (1-10 of 9) with videos related to

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Journal of Clinical Research in Pediatric Endocrinology|May 25, 2016
A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case ReportDagmar Prochazkova, Zuzana Hruba, Petra Konecna, et al.
Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|March 12, 2020
Comparative immunohistochemical study of deep infiltrating endometriosis, lymph node endometriosis and atypical ovarian endometriosis including description of a perineural invasionJiri Lenz, Radek Chvatal, Ludek Fiala, et al.
Andrologia|May 1, 2021
Premature ejaculation and stressLudek Fiala, Jiri Lenz, Petra Konecna, et al.
Veterinary Medicine and Science|May 13, 2022
Unique expression patterns of the embryonal stem cell marker SOX2 and hormone receptors suggest the existence of a subpopulation of epithelial stem/progenitor cells in porcine and bovine endometriumJiri Lenz, Petra Konecna, Frantisek Tichy, et al.
The American Journal of Dermatopathology|December 28, 2019
Novel EIF5A-USP6 Gene Fusion in Nodular Fasciitis Associated With Unusual Pathologic Features: A Report of a Case and Review of the LiteratureJiri Lenz, Michael Michal, Marian Svajdler, et al.
Nutrients|November 27, 2021
Low-Carbohydrate Diet among Children with Type 1 Diabetes: A Multi-Center StudyVit Neuman, Lukas Plachy, Stepanka Pruhova, et al.
Frontiers in Endocrinology|November 1, 2023
Are all HCL systems the same? long term outcomes of three HCL systems in children with type 1 diabetes: real-life registry-based studyAlzbeta Santova, Lukas Plachy, Vit Neuman, et al.
Diabetes Technology & Therapeutics|January 6, 2025
The Longer, the Better: Continuous Glucose Monitoring Use for ≥90% Is Superior to 70%-89% in Achieving Tighter Glycemic Outcomes in Children with Type 1 DiabetesAlzbeta Santova, Vit Neuman, Lukas Plachy, et al.
Scientific Reports|November 20, 2024
Diagnostic efficacy and clinical utility of whole-exome sequencing in Czech pediatric patients with rare and undiagnosed diseasesKaterina Slaba, Petra Pokorna, Robin Jugas, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Journal of Clinical Research in Pediatric Endocrinology|May 25, 2016
A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case ReportDagmar Prochazkova, Zuzana Hruba, Petra Konecna, et al.
Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|March 12, 2020
Comparative immunohistochemical study of deep infiltrating endometriosis, lymph node endometriosis and atypical ovarian endometriosis including description of a perineural invasionJiri Lenz, Radek Chvatal, Ludek Fiala, et al.
Andrologia|May 1, 2021
Premature ejaculation and stressLudek Fiala, Jiri Lenz, Petra Konecna, et al.
Veterinary Medicine and Science|May 13, 2022
Unique expression patterns of the embryonal stem cell marker SOX2 and hormone receptors suggest the existence of a subpopulation of epithelial stem/progenitor cells in porcine and bovine endometriumJiri Lenz, Petra Konecna, Frantisek Tichy, et al.
The American Journal of Dermatopathology|December 28, 2019
Novel EIF5A-USP6 Gene Fusion in Nodular Fasciitis Associated With Unusual Pathologic Features: A Report of a Case and Review of the LiteratureJiri Lenz, Michael Michal, Marian Svajdler, et al.
Nutrients|November 27, 2021
Low-Carbohydrate Diet among Children with Type 1 Diabetes: A Multi-Center StudyVit Neuman, Lukas Plachy, Stepanka Pruhova, et al.
Frontiers in Endocrinology|November 1, 2023
Are all HCL systems the same? long term outcomes of three HCL systems in children with type 1 diabetes: real-life registry-based studyAlzbeta Santova, Lukas Plachy, Vit Neuman, et al.
Diabetes Technology & Therapeutics|January 6, 2025
The Longer, the Better: Continuous Glucose Monitoring Use for ≥90% Is Superior to 70%-89% in Achieving Tighter Glycemic Outcomes in Children with Type 1 DiabetesAlzbeta Santova, Vit Neuman, Lukas Plachy, et al.
Scientific Reports|November 20, 2024
Diagnostic efficacy and clinical utility of whole-exome sequencing in Czech pediatric patients with rare and undiagnosed diseasesKaterina Slaba, Petra Pokorna, Robin Jugas, et al.
Pageof 1