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European Journal of Medical Genetics
|
October 12, 2021
Red flags for early recognition of adult patients with PTEN Hamartoma Tumour Syndrome
Meggie M C M Drissen, Jolanda H Schieving, Janneke H M Schuurs-Hoeijmakers, et al.
Pediatric Neurology
|
April 20, 2016
The Genetic Homogeneity of CAPOS Syndrome: Four New Patients With the c.2452G>A (p.Glu818Lys) Mutation in the ATP1A3 Gene
Roderick P P W M Maas, Jolanda H Schieving, Meyke Schouten, et al.
BMC Medical Education
|
February 11, 2023
Interprofessional simulation of acute care for nursing and medical students: interprofessional competencies and transfer to the workplace
Pepijn Krielen, Malon Meeuwsen, Edward C T H Tan, et al.
European Journal of Medical Genetics
|
July 18, 2024
Increased frequency of infections and autoimmune disease in adults with PTEN Hamartoma Tumour Syndrome
Meggie M C M Drissen, Janet R Vos, Estel Collado Camps, et al.
Radiation Oncology (London, England)
|
November 25, 2015
Acute toxicity profile of craniospinal irradiation with intensity-modulated radiation therapy in children with medulloblastoma: A prospective analysis
Maurice C Cox, Johannes M Kusters, Corrie E Gidding, et al.
Archives of Neurology
|
January 11, 2012
Novel hypomyelinating leukoencephalopathy affecting early myelinating structures
Marjan E Steenweg, Nicole I Wolf, Jolanda H Schieving, et al.
Developmental Medicine and Child Neurology
|
February 14, 2026
Consensus-based follow-up and treatment registry for GNAO1-associated disorder
Larissa R Heideman, Nicole I Wolf, Moritz Thiel, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
August 8, 2024
Experience in a PTEN Hamartoma Tumor Syndrome Expertise Centre: Yield of Thyroid Ultrasound Surveillance in Children with PTEN Hamartoma Tumor Syndrome
Esther M G Bormans, Janneke H M Schuurs-Hoeijmakers, Petra van Setten, et al.
Annals of Neurology
|
April 30, 2014
Mutations in RARS cause hypomyelination
Nicole I Wolf, Gajja S Salomons, Richard J Rodenburg, et al.
Brain : a Journal of Neurology
|
June 4, 2019
De novo SPAST mutations may cause a complex SPG4 phenotype
Jolanda H Schieving, Susanne T de Bot, Laura A van de Pol, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 27) with videos related to
Sort By:
Page
of 3
European Journal of Medical Genetics
|
October 12, 2021
Red flags for early recognition of adult patients with PTEN Hamartoma Tumour Syndrome
Meggie M C M Drissen, Jolanda H Schieving, Janneke H M Schuurs-Hoeijmakers, et al.
Pediatric Neurology
|
April 20, 2016
The Genetic Homogeneity of CAPOS Syndrome: Four New Patients With the c.2452G>A (p.Glu818Lys) Mutation in the ATP1A3 Gene
Roderick P P W M Maas, Jolanda H Schieving, Meyke Schouten, et al.
BMC Medical Education
|
February 11, 2023
Interprofessional simulation of acute care for nursing and medical students: interprofessional competencies and transfer to the workplace
Pepijn Krielen, Malon Meeuwsen, Edward C T H Tan, et al.
European Journal of Medical Genetics
|
July 18, 2024
Increased frequency of infections and autoimmune disease in adults with PTEN Hamartoma Tumour Syndrome
Meggie M C M Drissen, Janet R Vos, Estel Collado Camps, et al.
Radiation Oncology (London, England)
|
November 25, 2015
Acute toxicity profile of craniospinal irradiation with intensity-modulated radiation therapy in children with medulloblastoma: A prospective analysis
Maurice C Cox, Johannes M Kusters, Corrie E Gidding, et al.
Archives of Neurology
|
January 11, 2012
Novel hypomyelinating leukoencephalopathy affecting early myelinating structures
Marjan E Steenweg, Nicole I Wolf, Jolanda H Schieving, et al.
Developmental Medicine and Child Neurology
|
February 14, 2026
Consensus-based follow-up and treatment registry for GNAO1-associated disorder
Larissa R Heideman, Nicole I Wolf, Moritz Thiel, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
August 8, 2024
Experience in a PTEN Hamartoma Tumor Syndrome Expertise Centre: Yield of Thyroid Ultrasound Surveillance in Children with PTEN Hamartoma Tumor Syndrome
Esther M G Bormans, Janneke H M Schuurs-Hoeijmakers, Petra van Setten, et al.
Annals of Neurology
|
April 30, 2014
Mutations in RARS cause hypomyelination
Nicole I Wolf, Gajja S Salomons, Richard J Rodenburg, et al.
Brain : a Journal of Neurology
|
June 4, 2019
De novo SPAST mutations may cause a complex SPG4 phenotype
Jolanda H Schieving, Susanne T de Bot, Laura A van de Pol, et al.
Page
of 3