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Case Reports in Endocrinology
|
April 30, 2021
An Adolescent with Transient Hyperthyroxinemia after Blunt Trauma to Head and Neck
Michelle Romijn, Leo M G Geeraedts, Jonathan I M L Verbeke, et al.
Global Pediatric Health
|
July 14, 2016
Prevesical Calcification and Hydronephrosis in a Girl Treated for Vesicoureteral Reflux
Sarah Kuipers, Eric H J R van der Horst, Jonathan I M L Verbeke, et al.
Pediatric Neurology
|
March 25, 2008
Cushing's triad in pneumococcal meningitis due to brainstem ischemia: early detection by diffusion-weighted MRI
Eric G Haarman, R Jeroen Vermeulen, A Marceline van Furth, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 4, 2005
Carbonic anhydrase type II deficiency
Roel J Bolt, Janneke M B Wennink, Jonathan I M L Verbeke, et al.
Journal of Neurosurgery. Pediatrics
|
April 2, 2008
Postoperative hemicerebellar inflammation mimicking recurrent tumor after resection of a medulloblastoma. Case report
Saskia E Luijnenburg, Patrick W Hanlo, K Sen Han, et al.
Journal of Perinatal Medicine
|
October 15, 2017
Fetal MRI, lower acceptance by women in research vs. clinical setting
Bloeme J van der Knoop, Roland J Vermeulen, Jonathan I M L Verbeke, et al.
American Journal of Medical Genetics. Part A
|
June 27, 2024
Leukoencephalopathy with calcifications, developmental brain abnormalities and skeletal dysplasia due to homozygosity for a hypomorphic CSF1R variant: A report of three siblings
Shanice Beerepoot, Jonathan I M L Verbeke, Maud Plantinga, et al.
European Journal of Pediatrics
|
November 12, 2013
Anuria in a solitary kidney with Candida bezoars managed conservatively
Jaap V Schilperoort, Liesbeth L de Wall, Henricus J R van der Horst, et al.
Clinical Genetics
|
November 24, 2025
FAM20B Related Skeletal Dysplasia: Expanding the Prenatal Phenotype
Arda Arduç, Linda C Zuurbier, Merel C van Maarle, et al.
Neuropediatrics
|
May 22, 2012
A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?
Cengiz Yalcinkaya, Ozdem Erturk, Beyhan Tuysuz, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Case Reports in Endocrinology
|
April 30, 2021
An Adolescent with Transient Hyperthyroxinemia after Blunt Trauma to Head and Neck
Michelle Romijn, Leo M G Geeraedts, Jonathan I M L Verbeke, et al.
Global Pediatric Health
|
July 14, 2016
Prevesical Calcification and Hydronephrosis in a Girl Treated for Vesicoureteral Reflux
Sarah Kuipers, Eric H J R van der Horst, Jonathan I M L Verbeke, et al.
Pediatric Neurology
|
March 25, 2008
Cushing's triad in pneumococcal meningitis due to brainstem ischemia: early detection by diffusion-weighted MRI
Eric G Haarman, R Jeroen Vermeulen, A Marceline van Furth, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 4, 2005
Carbonic anhydrase type II deficiency
Roel J Bolt, Janneke M B Wennink, Jonathan I M L Verbeke, et al.
Journal of Neurosurgery. Pediatrics
|
April 2, 2008
Postoperative hemicerebellar inflammation mimicking recurrent tumor after resection of a medulloblastoma. Case report
Saskia E Luijnenburg, Patrick W Hanlo, K Sen Han, et al.
Journal of Perinatal Medicine
|
October 15, 2017
Fetal MRI, lower acceptance by women in research vs. clinical setting
Bloeme J van der Knoop, Roland J Vermeulen, Jonathan I M L Verbeke, et al.
American Journal of Medical Genetics. Part A
|
June 27, 2024
Leukoencephalopathy with calcifications, developmental brain abnormalities and skeletal dysplasia due to homozygosity for a hypomorphic CSF1R variant: A report of three siblings
Shanice Beerepoot, Jonathan I M L Verbeke, Maud Plantinga, et al.
European Journal of Pediatrics
|
November 12, 2013
Anuria in a solitary kidney with Candida bezoars managed conservatively
Jaap V Schilperoort, Liesbeth L de Wall, Henricus J R van der Horst, et al.
Clinical Genetics
|
November 24, 2025
FAM20B Related Skeletal Dysplasia: Expanding the Prenatal Phenotype
Arda Arduç, Linda C Zuurbier, Merel C van Maarle, et al.
Neuropediatrics
|
May 22, 2012
A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?
Cengiz Yalcinkaya, Ozdem Erturk, Beyhan Tuysuz, et al.
Page
of 2