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Jolanda Schieving

Showing results (1-10 of 13) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 13, 2026
Epilepsy in pediatric patients with PTEN hamartoma tumor syndrome: First step in recommendations for clinical managementRyan Jonker, Jolanda Schieving
Epileptic Disorders : International Epilepsy Journal with Videotape|May 13, 2011
Malignant migrating partial seizures in a 4-month-old boyH Jacobus Gilhuis, Jolanda Schieving, Machiel J Zwarts
Clinical Genetics|April 28, 2025
Deep Phenotyping of Pathology-Confirmed Benign Lesions in PTEN Hamartoma Tumor Syndrome PatientsAne J Schei-Andersen, Janneke H M Schuurs-Hoeijmakers, Rachel van der Post, et al.
International Dental Journal|May 2, 2024
Exploring the Prevalence of Oral Features for Early Detection of PTEN Hamartoma Tumour SyndromeAne J Schei-Andersen, Bart van Oirschot, Meggie M C M Drissen, et al.
Familial Cancer|March 18, 2025
Non-serous ovarian cancer in PTEN Hamartoma Tumor Syndrome: additional evidence for increased riskAne J Schei-Andersen, Vera M Witjes, Janet R Vos, et al.
International Journal of Cancer|June 11, 2024
Histopathological phenotyping of cancers in PTEN Hamartoma Tumor Syndrome for improved recognition: A single-center studyAne J Schei-Andersen, Linda A J Hendricks, Rachel S van der Post, et al.
Pediatric Hematology and Oncology|November 5, 2019
Social competence in newly diagnosed pediatric brain tumor patientsTessa B Kok, Janneke Koerts, Jurgen Lemiere, et al.
Cancer Discovery|January 11, 2013
Primary melanoma of the CNS in children is driven by congenital expression of oncogenic NRAS in melanocytesMalin Pedersen, Heidi V N Küsters-Vandevelde, Amaya Viros, et al.
Nature Genetics|July 12, 2016
Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrityJosefine S Witteveen, Marjolein H Willemsen, Thaís C D Dombroski, et al.
Journal of Medical Genetics|November 4, 2017
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literatureMargot R F Reijnders, Robert Janowski, Mohsan Alvi, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 13, 2026
Epilepsy in pediatric patients with PTEN hamartoma tumor syndrome: First step in recommendations for clinical managementRyan Jonker, Jolanda Schieving
Epileptic Disorders : International Epilepsy Journal with Videotape|May 13, 2011
Malignant migrating partial seizures in a 4-month-old boyH Jacobus Gilhuis, Jolanda Schieving, Machiel J Zwarts
Clinical Genetics|April 28, 2025
Deep Phenotyping of Pathology-Confirmed Benign Lesions in PTEN Hamartoma Tumor Syndrome PatientsAne J Schei-Andersen, Janneke H M Schuurs-Hoeijmakers, Rachel van der Post, et al.
International Dental Journal|May 2, 2024
Exploring the Prevalence of Oral Features for Early Detection of PTEN Hamartoma Tumour SyndromeAne J Schei-Andersen, Bart van Oirschot, Meggie M C M Drissen, et al.
Familial Cancer|March 18, 2025
Non-serous ovarian cancer in PTEN Hamartoma Tumor Syndrome: additional evidence for increased riskAne J Schei-Andersen, Vera M Witjes, Janet R Vos, et al.
International Journal of Cancer|June 11, 2024
Histopathological phenotyping of cancers in PTEN Hamartoma Tumor Syndrome for improved recognition: A single-center studyAne J Schei-Andersen, Linda A J Hendricks, Rachel S van der Post, et al.
Pediatric Hematology and Oncology|November 5, 2019
Social competence in newly diagnosed pediatric brain tumor patientsTessa B Kok, Janneke Koerts, Jurgen Lemiere, et al.
Cancer Discovery|January 11, 2013
Primary melanoma of the CNS in children is driven by congenital expression of oncogenic NRAS in melanocytesMalin Pedersen, Heidi V N Küsters-Vandevelde, Amaya Viros, et al.
Nature Genetics|July 12, 2016
Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrityJosefine S Witteveen, Marjolein H Willemsen, Thaís C D Dombroski, et al.
Journal of Medical Genetics|November 4, 2017
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literatureMargot R F Reijnders, Robert Janowski, Mohsan Alvi, et al.
Pageof 2