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OC.04.10: IMPACT OF ANNUAL CASE VOLUME ON COLORECTAL ENDOSCOPIC SUBMUCOSAL DISSECTION PROCEDURAL OUTCOMES AND SAFETY IN A LARGE MULTICENTRIC PROSPECTIVE COHORT STUDY

Digestive and liver disease, 2024-04, Vol.56, p.S146-S147

2024

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Liver abscess : case report and literature review

Revue médicale de Liège, 2020-11, Vol.75 (11), p.731

2020

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Effect of an Integrated, Multidisciplinary Nationwide Approach to Type 1 Diabetes Care on Metabolic Outcomes: An Observational Real-World Study

Diabetes technology & therapeutics, 2021-08, Vol.23 (8), p.565-576

2021

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Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1

Human molecular genetics, 2009-02, Vol.18 (3), p.517-524

2009

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Identification of a novel PEX14 mutation in Zellweger syndrome

Journal of medical genetics, 2008-06, Vol.45 (6), p.376-383

2008

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Low serum FT4 and cortisol concentrations in early onset hyperphagic obesity: a clue to SIM1 deficiency

Acta clinica belgica (English ed. Online), 2016-03, Vol.71 (S2), p.11

2016

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Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern

Biochimica et biophysica acta, 2011-06, Vol.1812 (6), p.691-698

2011

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A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia

European journal of human genetics : EJHG, 2007-06, Vol.15 (6), p.638-645

2007

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Poor growth response during the first year of growth hormone treatment in short prepubertal children with growth hormone deficiency and born small for gestational age: a comparison of different criteria

International journal of pediatric endocrinology, 2018-10, Vol.2018 (1), p.9-9, Article 9

2018

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Validation of Prediction Models for Near Adult Height in Children with Idiopathic Growth Hormone Deficiency Treated with Growth Hormone: A Belgian Registry Study

Hormone research in paediatrics, 2016-01, Vol.86 (3), p.161-168

2016

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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

JIMD Reports - Case and Research Reports, 2012/5, 2013, Vol.8, p.145-152

2013

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Laattijdige neonatale hypocalciëmie:belang van correcte diagnostiek en behandeling

Tijdschrift voor geneeskunde, 2015 (16), p.1042-1046

2015

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MLP023 CDG phenotype characterized by failure to thrive, hypotonia, microcephaly and hyperthermia in two infants of North African origin

European journal of paediatric neurology, 2007, Vol.11, p.106-106

2007

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Identification of a novel PEX14 mutation in Zellweger syndrome

BMJ case reports, 2009, Vol.2009 (jan21 1), p.bcr0720080503-bcr0720080503

2009

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Erratum: A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia

European journal of human genetics : EJHG, 2007-06, Vol.15 (7), p.819-819

2007

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A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia

European journal of human genetics : EJHG, 2007-07, Vol.15 (7), p.819-819

2007

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Application of a generic biosphere model for dose assessments to five European sites

Journal of radiological protection, 2006-06, Vol.26 (2), p.161-187

2006

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Complementary studies: biosphere modelling for dose assessments of radioactive waste repositories

Journal of environmental radioactivity, 1999-01, Vol.42 (2-3), p.237-254

1999

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Poetologische Transformationen ? Die beiden Fassungen von Ilse Aichingers Roman. Die größere Hoffnung unter besonderer Berücksichtigung des Magischen Realismus

Études germaniques, 2006-06, Vol.242 (2), p.219-242

2006

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Environmental modelling of NORM

Radioprotection, 2009, Vol.44 (5), p.23-28

2009

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Slow channel syndrome due to an autosomal translocation at 2q31-9p27

Revue neurologique, 2002-05, Vol.158 (5 Pt 1), p.605-608

2002

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Osteoarticular hemochromatosis

Revue médicale de Liège, 1999-03, Vol.54 (3), p.169

1999

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Fibromyalgie et affections voisines : analyse du comportement électromyographique au cours d’un effort musculaire isométrique

Revue du rhumatisme (Ed. française : 1993), 2010-05, Vol.77 (3), p.296-300

2010

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Effects of model complexity on uncertainty estimates

Journal of environmental radioactivity, 1999-01, Vol.42 (2-3), p.255-270

1999

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Syndrome du canal lent associé à une translocation autosomique 2q31-9p27

Revue neurologique, 2002, Vol.158 (5), p.605-608

2002

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OC.04.10: IMPACT OF ANNUAL CASE VOLUME ON COLORECTAL ENDOSCOPIC SUBMUCOSAL DISSECTION PROCEDURAL OUTCOMES AND SAFETY IN A LARGE MULTICENTRIC PROSPECTIVE COHORT STUDY

Liver abscess : case report and literature review

Effect of an Integrated, Multidisciplinary Nationwide Approach to Type 1 Diabetes Care on Metabolic Outcomes: An Observational Real-World Study

Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1

Identification of a novel PEX14 mutation in Zellweger syndrome

Low serum FT4 and cortisol concentrations in early onset hyperphagic obesity: a clue to SIM1 deficiency

Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern

A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia

Poor growth response during the first year of growth hormone treatment in short prepubertal children with growth hormone deficiency and born small for gestational age: a comparison of different criteria

Validation of Prediction Models for Near Adult Height in Children with Idiopathic Growth Hormone Deficiency Treated with Growth Hormone: A Belgian Registry Study

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

Laattijdige neonatale hypocalciëmie:belang van correcte diagnostiek en behandeling

MLP023 CDG phenotype characterized by failure to thrive, hypotonia, microcephaly and hyperthermia in two infants of North African origin

Identification of a novel PEX14 mutation in Zellweger syndrome

Erratum: A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia

A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia

Application of a generic biosphere model for dose assessments to five European sites

Complementary studies: biosphere modelling for dose assessments of radioactive waste repositories

Poetologische Transformationen ? Die beiden Fassungen von Ilse Aichingers Roman. Die größere Hoffnung unter besonderer Berücksichtigung des Magischen Realismus

Environmental modelling of NORM

Slow channel syndrome due to an autosomal translocation at 2q31-9p27

Osteoarticular hemochromatosis

Fibromyalgie et affections voisines : analyse du comportement électromyographique au cours d’un effort musculaire isométrique

Effects of model complexity on uncertainty estimates

Syndrome du canal lent associé à une translocation autosomique 2q31-9p27

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