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Journal of Neuropathology and Experimental Neurology
|
July 11, 2007
A comparative morphologic analysis of adult onset leukodystrophy with neuroaxonal spheroids and pigmented glia--a role for oxidative damage
Zarina S Ali, J Patrick Van Der Voorn, James M Powers
Journal of Pediatric Surgery
|
June 19, 2012
Eosinophilic esophagitis after esophageal atresia: is there an association? Case presentation and literature review
Ramon R Gorter, Hugo A Heij, J Patrick van der Voorn, et al.
Acta Neuropathologica
|
March 26, 2004
The leukoencephalopathy of infantile GM1 gangliosidosis: oligodendrocytic loss and axonal dysfunction
J Patrick van der Voorn, Wout Kamphorst, Marjo S van der Knaap, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
March 20, 2014
[A boy with cervical focal myositis]
Serge Prop, Dannis van Vuurden, Martijn van der Kuip, et al.
Journal of Neuropathology and Experimental Neurology
|
June 26, 2004
The life and death of oligodendrocytes in vanishing white matter disease
Keith Van Haren, J Patrick van der Voorn, Derick R Peterson, et al.
Pediatric Research
|
March 18, 2021
Exposure to intrauterine inflammation and late-onset sepsis in very preterm infants
Marle B van Doorn, J Patrick van der Voorn, Helen L Tanger, et al.
Neuroradiology
|
June 2, 2009
Unraveling pathology in juvenile Alexander disease: serial quantitative MR imaging and spectroscopy of white matter
J Patrick van der Voorn, Petra J W Pouwels, Gajja S Salomons, et al.
Children (Basel, Switzerland)
|
September 28, 2023
The Prevalence and Clinical Impact of Transition Zone Anastomosis in Hirschsprung Disease: A Systematic Review and Meta-Analysis
Hosnieya Labib, Daniëlle Roorda, J Patrick van der Voorn, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
January 27, 2012
[Dysphagia after introduction of solid food: typical presentation of congenital oesophageal stenosis]
Esther Kockelkoren, Christien Sleeboom, J Patrick van der Voorn, et al.
Hormone Research in Paediatrics
|
January 24, 2015
WT1 deletion leading to severe 46,XY gonadal dysgenesis, Wilms tumor and gonadoblastoma: case report
Martijn J J Finken, Yvonne M C Hendriks, J Patrick van der Voorn, et al.
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of 3
Search research articles
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Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Journal of Neuropathology and Experimental Neurology
|
July 11, 2007
A comparative morphologic analysis of adult onset leukodystrophy with neuroaxonal spheroids and pigmented glia--a role for oxidative damage
Zarina S Ali, J Patrick Van Der Voorn, James M Powers
Journal of Pediatric Surgery
|
June 19, 2012
Eosinophilic esophagitis after esophageal atresia: is there an association? Case presentation and literature review
Ramon R Gorter, Hugo A Heij, J Patrick van der Voorn, et al.
Acta Neuropathologica
|
March 26, 2004
The leukoencephalopathy of infantile GM1 gangliosidosis: oligodendrocytic loss and axonal dysfunction
J Patrick van der Voorn, Wout Kamphorst, Marjo S van der Knaap, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
March 20, 2014
[A boy with cervical focal myositis]
Serge Prop, Dannis van Vuurden, Martijn van der Kuip, et al.
Journal of Neuropathology and Experimental Neurology
|
June 26, 2004
The life and death of oligodendrocytes in vanishing white matter disease
Keith Van Haren, J Patrick van der Voorn, Derick R Peterson, et al.
Pediatric Research
|
March 18, 2021
Exposure to intrauterine inflammation and late-onset sepsis in very preterm infants
Marle B van Doorn, J Patrick van der Voorn, Helen L Tanger, et al.
Neuroradiology
|
June 2, 2009
Unraveling pathology in juvenile Alexander disease: serial quantitative MR imaging and spectroscopy of white matter
J Patrick van der Voorn, Petra J W Pouwels, Gajja S Salomons, et al.
Children (Basel, Switzerland)
|
September 28, 2023
The Prevalence and Clinical Impact of Transition Zone Anastomosis in Hirschsprung Disease: A Systematic Review and Meta-Analysis
Hosnieya Labib, Daniëlle Roorda, J Patrick van der Voorn, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
January 27, 2012
[Dysphagia after introduction of solid food: typical presentation of congenital oesophageal stenosis]
Esther Kockelkoren, Christien Sleeboom, J Patrick van der Voorn, et al.
Hormone Research in Paediatrics
|
January 24, 2015
WT1 deletion leading to severe 46,XY gonadal dysgenesis, Wilms tumor and gonadoblastoma: case report
Martijn J J Finken, Yvonne M C Hendriks, J Patrick van der Voorn, et al.
Page
of 3