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R. Zeevaert · SciRah

Researcher profile · Semantic Scholar

R. Zeevaert

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R. Zeevaert — researcher profile on SciRah

h-index: 15
Works: 36
Citations: 1,029

Most-cited papers

TMEM165 deficiency causes a congenital disorder of glycosylation.
F. Foulquier, Mustapha Amyere, J. Jaeken, R. Zeevaert +16 more
2012American Journal of Human Genetics190 citations Open access
Semantic Scholar
A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation.
F. Foulquier, D. Ungar, E. Reynders, R. Zeevaert +8 more
2007Human Molecular Genetics125 citations Open access
Semantic Scholar
International clinical guidelines for the management of phosphomannomutase 2‐congenital disorders of glycosylation: Diagnosis, treatment and follow up
R. Altassan, Romain Péanne, J. Jaeken, R. Barone +50 more
2019Journal of Inherited Metabolic Disease124 citations Open access
Semantic Scholar
Deficiencies in subunits of the Conserved Oligomeric Golgi (COG) complex define a novel group of Congenital Disorders of Glycosylation.
R. Zeevaert, F. Foulquier, J. Jaeken, G. Matthijs
2008Molecular Genetics and Metabolism119 citations
Semantic Scholar
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia
E. Morava, R. Zeevaert, E. Korsch, K. Huijben +6 more
2007European Journal of Human Genetics68 citations Open access
Semantic Scholar
Evaluation of the FreeStyle® Libre Flash Glucose Monitoring System in Children and Adolescents with Type 1 Diabetes
G. Massa, Inge Gys, Anniek Op 't Eyndt, Esmiralda Bevilacqua +3 more
2018Hormone Research in Paediatrics63 citations
Semantic Scholar
Bone Dysplasia as a Key Feature in Three Patients with a Novel Congenital Disorder of Glycosylation (CDG) Type II Due to a Deep Intronic Splice Mutation in TMEM165.
R. Zeevaert, F. de Zegher, L. Sturiale, D. Garozzo +4 more
2013JIMD Reports51 citations Open access
Semantic Scholar
Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1.
R. Zeevaert, F. Foulquier, B. Dimitrov, E. Reynders +5 more
2008Human Molecular Genetics51 citations
Semantic Scholar
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia
E. Morava, R. Zeevaert, E. Korsch, K. Huijben +6 more
2007European Journal of Human Genetics50 citations
Semantic Scholar
A new mutation in COG7 extends the spectrum of COG subunit deficiencies.
R. Zeevaert, F. Foulquier, D. Cheillan, Isabelle Cloix +5 more
2009European Journal of Medical Genetics39 citations
Semantic Scholar
A novel mutation causing mild, atypical fumarylacetoacetase deficiency (Tyrosinemia type I): a case report
D. Cassiman, R. Zeevaert, E. Holme, E. Kvittingen +1 more
2009Orphanet Journal of Rare Diseases31 citations Open access
Semantic Scholar
Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern.
M. Mohamed, M. Guillard, S. Wortmann, S. Çırak +15 more
2011Biochimica et Biophysica Acta30 citations Open access
Semantic Scholar
Identification of a novel PEX14 mutation in Zellweger syndrome
S. Huybrechts, P. V. Van Veldhoven, I. Hoffman, R. Zeevaert +6 more
2008Journal of Medical Genetics24 citations
Semantic Scholar
PGM1 deficiency diagnosed during an endocrine work-up of low IGF-1 mediated growth failure
R. Zeevaert, E. Scalais, Laura Muiño Mosquera, L. D. De Meirleir +4 more
2016Acta Clinica Belgica19 citations Open access
Semantic Scholar
Comparison of flash glucose monitoring with real time continuous glucose monitoring in children and adolescents with type 1 diabetes treated with continuous subcutaneous insulin infusion.
G. Massa, Inge Gys, Esmiralda Bevilacqua, A. Wijnands +1 more
2019Diabetes Research and Clinical Practice18 citations
Semantic Scholar
Chronotropic incompetence is more frequent in obese adolescents and relates to systemic inflammation and exercise intolerance.
W. Franssen, C. Keytsman, N. Marinus, K. Verboven +6 more
2021Journal of Sport and Health Science12 citations Open access
Semantic Scholar
International clinical guidelines for the management of phosphomannomutase 2‐congenital disorders of glycosylation: Diagnosis, treatment and follow up
R. Altassan, Romain Péanne, J. Jaeken, R. Barone +50 more
2019Journal of Inherited Metabolic Disease10 citations Open access
Semantic Scholar
Identification of a novel PEX14 mutation in Zellweger syndrome
S. Huybrechts, P. Van Veldhoven, I. Hoffman, R. Zeevaert +6 more
2009BMJ Case Reports4 citations Open access
Semantic Scholar
Congenital Disorders of Glycosylation (CDG): Update and Perspectives
R. Zeevaert, E. Schollen, H. Carchon, G. Matthijs +1 more
20064 citations
Semantic Scholar
The organisation of paediatric hospital-at-home care: a multi-country comparative study
M. Lefèvre, Jens Detollenaere, R. Zeevaert, C. Van de Voorde
2023Journal of Integrated Care3 citations
Semantic Scholar
A novel mutation in cog7 expands the spectrum of cog deficiencies
R. Zeevaert, D. Cheillan, F. Foulquier, G. Matthijs +1 more
20091 citations
Semantic Scholar
E-book: Endocrinologie 2021
F. V. van Gool, T. Maes, B. Decallonne, G. Massa +14 more
2022Tijdschrift voor Geneeskunde0 citations
Semantic Scholar
Insulin Resistance and Impaired Glucose Tolerance in Overweight/Obese Adolescents Attending an Obesity Clinic in Belgium
R. Zeevaert, Kelly L. Faust, T. Otte, Sigrid Vanhaesebrouck +1 more
20190 citations
Semantic Scholar
Clinical characteristics of children with a congenital non-syndromatic combined growth hormone deficiency in Belgium
V. Beauloye, R. Zeevaert
20150 citations
Semantic Scholar
Late neonatal hypocalcemia: Importance of correct diagnosis and treatment
N. Boelsma, F. Cools, K. De Waele, M. den Brinker +4 more
20150 citations
Semantic Scholar
The Triglyceride-to-HDL Cholesterol Ratio is Associated with Insulin Resistance in Obese Boys But Not in Obese Girls
G. Massa, L. Bervoets, Jonas Massa, R. Zeevaert
20150 citations
Semantic Scholar
Clinical Characteristics of Children with Congenital Combined GH Deficiency without Associated Syndrome in Belgium
R. Zeevaert, F. Verlinde, Muriel Thomas, Z. F. De +5 more
20150 citations
Semantic Scholar
Mutations in TMEM165 cause a new Congenital Disorder of Glycosylation type II and affect pH homeostasis
Riet Bammens, Foulquier François, Mustapha Amyere, R. Zeevaert +6 more
20110 citations
Semantic Scholar
TPARL-towards understanding of its physiological role in pH homeostasis
F. Foulquier, J. Jaeken, Mustapha Amyere, R. Zeevaert +4 more
20110 citations
Semantic Scholar
Dysostin, a new gene involved in CDG and affecting pH homeostasis
F. Foulquier, J. Jaeken, Mustapha Amyere, R. Zeevaert +4 more
20100 citations
Semantic Scholar
Advances in Congenital Disorders of Glycosylation type II
R. Zeevaert
20080 citations
Semantic Scholar
A possible role for the conserved oligomeric Golgi complex subunit I (COGI) in autosomal recessive cerebrocostomandibular syndrome
R. Zeevaert, F. Foulquier, E. Reynders, W. Annaert +2 more
20080 citations
Semantic Scholar
MLP023 CDG phenotype characterized by failure to thrive, hypotonia, microcephaly and hyperthermia in two infants of North African origin
A. Jansen, K. Keymolen, R. Zeevaert, G. Matthijs +3 more
20070 citations
Semantic Scholar
Isolated increase of trisialotransferrin in the serum of CDG patients with evidence for a defect in demannosylation
R. Zeevaert, H. Carchon, P. Mills, B. Winchester +1 more
20060 citations
Semantic Scholar
A deficiency in cog1 causes a novel congenital disorder of glycosylation type ii
G. Matthijs, F. Foulquier, R. Zeevaert, J. Jaeken +5 more
20050 citations
Semantic Scholar
A New, Unusually Mild Type Ii Congenital Disorder of Glycosylation
R. Zeevaert, E. Schollen, P. Mills, L. Lagae +4 more
20050 citations
Semantic Scholar

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