W. Hop

Publications843
h-index111
Citations48,858
Highly Influential Citations1,399
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Long-term Follow-up of a Randomized Controlled Trial of Suture Versus Mesh Repair of Incisional Hernia
TLDR
Mesh repair results in a lower recurrence rate and less abdominal pain and does not result in more complications than suture repair, and should be abandoned.
View on Wolters Kluwer
Laparoscopic surgery versus open surgery for colon cancer: short-term outcomes of a randomised trial.
View on PubMed
Hybrid genotypes in the pathogenic yeast Cryptococcus neoformans.
TLDR
The authors propose the existence of two species, C. neoformans (Sanfelice) Vuillemin and C. bacillisporus Kwon-Chung, which differ in geographical distribution, serotypes and ecological origin, and within each species three AFLP genotypes occur.
View on PubMed
Dutch national survey to test the STRONGkids nutritional risk screening tool in hospitalized children.
View on PubMed
Laparoscopic versus open surgery for rectal cancer (COLOR II): short-term outcomes of a randomised, phase 3 trial.
View on PubMed
Prognostic value of minimal residual disease in acute lymphoblastic leukaemia in childhood
View on Elsevier
Immunophenotyping of blood lymphocytes in childhood. Reference values for lymphocyte subpopulations.
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An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis.
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A randomized trial investigating an exercise program to prevent reduction of bone mineral density and impairment of motor performance during treatment for childhood acute lymphoblastic leukemia
TLDR
A randomized study investigating whether an exercise program could prevent side effects of acute lymphoblastic leukemia treatment found it possible to reduce bone mineral density, altered body composition, impaired motor performance and passive ankle dorsiflexion.
View on Wiley
The natural course of non–classic Pompe’s disease; a review of 225 published cases
TLDR
The natural course of cases not fitting the definition of classic infantile Pompe’s disease, a review of 109 reports including 225 cases shows a continuous spectrum of phenotypes, with patients with a later onset of symptoms seemed to have a better prognosis.
View on Springer
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