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Researcher
Juliaan Leroy
Profile
Projects
Publications
Activities
Awards & Distinctions
109
Results
2013
Living related liver transplantation in an adult patient with hepatocellular adenoma and carcinoma 13 years after bone marrow transplantation for Fanconi anemia: a case report
Isabelle Colle
Genevieve Laureys
Sarah Raevens
Louis Libbrecht
Juliaan Leroy
KOEN REYNTJENS
Anja Geerts
Xavier Rogiers
Roberto Troisi
Holger Hoehn
et al.
A1
Journal Article
in
HEPATOLOGY RESEARCH
2013
Mutation of the iron-sulfur cluster assembly IBA57 gene causes lethal myopathy and encephalopathy
N Ajit Bolar
Arnaud Vanlander
C Wilbrecht
Nathalie Van der Aa
Joél Smet
Boel De Paepe
G Vandeweyer
F Kooy
François Eyskens
Elien De Latter
et al.
C3
Conference
2013
Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy
Nikhita Ajit Bolar
Arnaud Vanlander
Claudia Wilbrecht
Nathalie Van der Aa
Joél Smet
Boel De Paepe
Geert Vandeweyer
Frank Kooy
François Eyskens
Elien De Latter
et al.
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
2013
2010
Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients
Kristien Hoornaert
Inge Vereecke
Chantal Dewinter
Thomas Rosenberg
Frits A Beemer
Juliaan Leroy
Laila Bendix
Erik Björck
Maryse Bonduelle
Odile Boute
et al.
A1
Journal Article
in
EUROPEAN JOURNAL OF HUMAN GENETICS
2010
2009
Klinische genetica, cytogenetica en moleculaire genetica
Elfride De Baere
Juliaan Leroy
Anne De Paepe
Bookchapter
in
Codex medicus
2009
Mesomelic Dysplasia With Acral Synostoses Verloes-David-Pfeiffer Type: Follow-Up Study Documents Progressive Clinical Course
Bertrand Isidor
Antoine Hamel
Frank Plasschaert
Lieve Claus
Jacques-Marie Mercier
Geert Mortier
Juliaan Leroy
Alain Verloes
Albert David
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
2009
Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA
Joél Smet
Sara Seneca
Boel De Paepe
Ann Meulemans
Helene Verhelst
Juliaan Leroy
Linda De Meirleir
Willy Lissens
Rudy Van Coster
A1
Journal Article
in
ELECTROPHORESIS
2009
2007
Acanthosis nigricans in a child with mild osteochondrodysplasia and K650Q mutation in the FGFR3 gene
Juliaan Leroy
Lieve Nuytinck
Jo Lambert
Jean-Marie Naeyaert
Geert Mortier
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
2007
Congenital pontocerebellar atrophy and telencephalic defects in three siblings: a new subtype
Juliaan Leroy
G LYON
C FALLET
J AMIEL
Claudine De Praeter
Caroline Van den broecke
Piet Vanhaesebrouck
A1
Journal Article
in
ACTA NEUROPATHOLOGICA
2007
Czech dysplasia metatarsal type: another type II collagen disorder
Kristien Hoornaert
Ivo Marik
Kazimierz Kozlowski
Trevor Cole
Martine Le Merrer
Juliaan Leroy
Paul Coucke
David Sillence
Geert Mortier
A1
Journal Article
in
EUROPEAN JOURNAL OF HUMAN GENETICS
2007
2006
Diagnostic value of immunostaining in cultured skin fibroblasts from patients with oxidative phosphorylation defects
Boel De Paepe
Joél Smet
Juliaan Leroy
S Seneca
Edith George
Dirk Matthys
L Van Maldergem
E Scalais
W Lissens
L De Meirleir
et al.
A1
Journal Article
in
PEDIATRIC RESEARCH
2006
2005
Aminoacylase I deficiency: A novel inborn error of metabolism
Rudy Van Coster
EA GERLO
TG GIARDINA
UF ENGELKE
Joél Smet
Claudine De Praeter
VALERIE MEERSSCHAUT
LJ DE MEIRLEIR
SH SENECA
Bart Devreese
et al.
A1
Journal Article
in
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
2005
Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome
Stefan Vermeulen
Franki Speleman
L VANRANSBEECK
Jasmine Verspeet
Björn Menten
MR VERSCHRAEGEN-SPAE
Philippe De Wilde
Ludwine Messiaen
RC MICHAELIS
Juliaan Leroy
A1
Journal Article
in
EUROPEAN JOURNAL OF HUMAN GENETICS
2005
Immunocytochemical staining of cultured fibroblasts is a valuable first line screening test for oxidative phosphorylation defects.
Boel De Paepe
Joél Smet
Juliaan Leroy
S SENECA
Edith George
Dirk Matthys
L VAN MALDERGEM
E SCALAIS
W LISSENS
L DE MEIRLEIR
et al.
C3
Conference
2005
Immunocytochemiscal staining of cultured fibroblasts is available first line screening test for oxidative phosphorylation.
Boel De Paepe
Joél Smet
Juliaan Leroy
S SENECA
Edith George
Dirk Matthys
L VAN MALDERGEM
E SCALAIS
W LISSENS
L DE MEIRLEIR
et al.
C3
Conference
2005
Klinische genetica, cytogenetica en moleculaire genetica
Elfride De Baere
Anne De Paepe
Juliaan Leroy
Bookchapter
in
Codex medicus
2005
2004
A new type of autosomal recessive spondyloepiphyseal dysplasia tarda
Juliaan Leroy
Bart Leroy
LV Emmery
Ludwine Messiaen
JW Spranger
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
2004
Ataxia oculomotor apraxia I
Juliaan Leroy
F ROELENS
M DE RAMMELAERE
Rudy Van Coster
Jan De Bleecker
C3
Conference
2004
Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux
CF BARTELS
H BUKULMEZ
P PADAYATTI
DK RHEE
C VAN RAVENSWAAIJ-ARTS
RM PAULI
S MUNDLOS
D CHITAYAT
LY SHIH
LI AL-GAZALI
et al.
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2004
2003
Unfortunate oversight
Juliaan Leroy
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
2003
2002
A patient severely affected by spinal neurofibromas carries a recurrent splice site mutation in the NF1 gene.
K WIMMER
M MUHLBAUER
M ECKART
T CALLENS
H REHDER
T BIRKNER
Juliaan Leroy
C FONATSCH
Ludwine Messiaen
A1
Journal Article
in
EUROPEAN JOURNAL OF HUMAN GENETICS
2002
Disorders of lysosomal enzymes: clinical phenotypes.
Juliaan Leroy
Bookchapter
in
Connective tissue and its heritable disorders: molecular, genetic, and medical aspects / Royce PM, Steinmann B (eds), New York, Wiley-Liss Inc, 2nd Ed. - ISBN 0471251852
2002
Expression of the multidrug transporter P-glycoprotein is highly correlated with clinical outcome in childhood acute lymphoblastic leukemia: Results of a long-term prospective study.
Catharina Dhooge
Barbara De Moerloose
Genevieve Laureys
A FERSTER
Dirk De Bacquer
Jan Philippé
Juliaan Leroy
Yves Benoit
A1
Journal Article
in
LEUKEMIA & LYMPHOMA
2002
Oligosaccharidoses and allied disorders
Juliaan Leroy
Bookchapter
in
Emery and Rimoin's principles and practice of medical genetics / Rimoin DL, Connor JM, Pyeritz RE, Korf BR (eds), Churchill Livingstone, London, 4th Ed., Chapter 99, p. 2677-2711. -
2002
2001
Clinical and radiographic features of multiple epiphyseal dysplasia not linked to the COMP or type IX collagen genes.
Geert Mortier
K CHAPMAN
Juliaan Leroy
MD BRIGGS
A1
Journal Article
in
EUROPEAN JOURNAL OF HUMAN GENETICS
2001
Dominant inheritance of sialuria, an inborn error of feedback inhibition.
Juliaan Leroy
R SEPPALA
M HUIZING
Georges Dacremont
H DE SIMPEL
Rudy Van Coster
E ORVISKY
DM KRASNEWICH
WA GAHL
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2001
Het chronisch longlijden van de preterme pasgeborene
Koenraad Smets
Piet Vanhaesebrouck
Juliaan Leroy
Dissertation
2001
Imaging studies in the diagnostic workup of neonatal nasal obstruction.
Bart Vanzieleghem
Marc Lemmerling
Hubert Vermeersch
P GOVAERT
Ingeborg Dhooge
Françoise Meire
Geert Mortier
Juliaan Leroy
Marc Kunnen
A1
Journal Article
in
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY
2001
2000
Articulation in Beckwith-Wiedemann syndrome: Two case studies.
John Van Borsel
B MORLION
K VAN SNICK
Juliaan Leroy
A1
Journal Article
in
AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY
2000
Clinical and radiographic features of a family with hypochondroplasia owing to a novel Asn540Ser mutation in the fibroblast growth factor receptor 3 gene
Geert Mortier
Lieve Nuytinck
Margarita Craen
Jean-Pierre Renard
Juliaan Leroy
Anne De Paepe
A1
Journal Article
in
JOURNAL OF MEDICAL GENETICS
2000
Lip en/of gehemeltespleet: componenten in een vloeidiagram van multidisciplinaire aanpak
M Van Vlierberghe
M Moerman
Geert Mortier
C De Clercq
S Monstrey
Juliaan Leroy
A2
Journal Article
in
TIJDSCHRIFT VAN DE BELGISCHE KINDERARTS = JOURNAL DU PEDIATRE BELGE
2000
1999
Discrepant flow cytometric expression and function of P-glycoprotein in neuroblastic tumors
Barbara De Moerloose
Catharina Dhooge
Genevieve Laureys
Yves Benoit
M DEMARCHE
C DEVALCK
D PLANTAZ
Juliaan Leroy
Jan Philippé
A1
Journal Article
in
CYTOMETRY
1999
Fungal intracranial aneurysm in a child with familial chronic mucocutaneous candidiasis.
Bart Loeys
Rudy Van Coster
Luc Defreyne
Juliaan Leroy
A1
Journal Article
in
EUROPEAN JOURNAL OF PEDIATRICS
1999
Macroglossia and speech in Beckwith-Wiedemann syndrome: a sample survey study.
John Van Borsel
K VAN SNICK
Juliaan Leroy
A1
Journal Article
in
INTERNATIONAL JOURNAL OF LANGUAGE & COMMUNICATION DISORDERS
1999
P-Glycoproteine in de aanpak van chemotherapieresistentie.
Barbara De Moerloose
Catharina Dhooge
J PHILIPPE
Yves Benoit
Jozef Kint
Juliaan Leroy
A2
Journal Article
in
TIJDSCHRIFT VOOR GENEESKUNDE
1999
Pediatrische aanpak bij Groep B streptococcen infecties
Piet Vanhaesebrouck
Claudine De Praeter
P Govaert
Koenraad Smets
Paul Defoort
Gerda Verschraegen
Juliaan Leroy
A2
Journal Article
in
TIJDSCHRIFT VAN DE BELGISCHE KINDERARTS = JOURNAL DU PEDIATRE BELGE
1999
The Meier-Gorlin syndrome, or ear patella short stature syndrome, in sibs.
Bart Loeys
Marc Lemmerling
CE VAN MOL
Juliaan Leroy
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
1999
1998
Bruck syndrome: neonatal presentation and natural course in three patients.
Juliaan Leroy
Lieve Nuytinck
Anne De Paepe
M DE RAMMELAERE
Y GILLEROT
A VERLOES
Bart Loeys
W DE GROOTE
A1
Journal Article
in
PEDIATRIC RADIOLOGY
1998
De genetica in het jaar 2000
Juliaan Leroy
A4
Journal Article
in
ACTA MEDICA CATHOLICA
1998
Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia multiple epiphyseal dysplasia disease spectrum
Michael D Briggs
Geert Mortier
Willam G Cole
Lily M King
Steven S Golik
Jacky Bonaventure
Lieve Nuytinck
Anne De Paepe
Juliaan Leroy
Leslie Biesecker
et al.
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
1998
MRI findings in a neonate with cerebellar agenesis.
Rudy Van Coster
Claudine De Praeter
Piet Vanhaesebrouck
Juliaan Leroy
A1
Journal Article
in
PEDIATRIC NEUROLOGY
1998
Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples.
Rudy Van Coster
Sandra Janssens
JP MISSON
A VERLOES
Juliaan Leroy
A1
Journal Article
in
PRENATAL DIAGNOSIS
1998
1997
Autopsy diagnosis of the Smith-Lemli-Opitz syndrome
Franny Faes
ELI Vercruysse
Georges Dacremont
Anne De Paepe
Juliaan Leroy
C3
Conference
1997
Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: Lack of genotype/phenotype correlations.
J MEYER
P SUDBECK
M HELD
T WAGNER
ML SCHMITZ
FD BRICARELLI
E EGGERMONT
U FRIEDRICH
OA HAAS
A KOBELT
et al.
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
1997
1996
Blomstrand lethal osteochondrodysplasia.
Juliaan Leroy
G KEERSMAECKERS
M COPPENS
JE DUMON
Hendrik Roels
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
1996
Consensus en controverse rondom groep B streptococcus infectie in de zwangerschap
Piet Vanhaesebrouck
Claudine De Praeter
P Govaert
Koenraad Smets
Paul Defoort
Gerda Verschraegen
Juliaan Leroy
A4
Journal Article
in
TIJDSCHRIFT VAN DE BELGISCHE KINDERARTS
1996
Diamanten jubileum: gelegenheid tot nadenken
Juliaan Leroy
A2
Journal Article
in
TIJDSCHRIFT VOOR GENEESKUNDE
1996
Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: A new example of the Chitty syndrome.
SG VANDAELE
Rudy Van Coster
Françoise Meire
AM SMETS
Juliaan Leroy
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
1996
Gastro-intestinale problemen bij meervoudig gehandicapte kinderen.
Myriam Van Winckel
Eddy Robberecht
Juliaan Leroy
A2
Journal Article
in
TIJDSCHRIFT VOOR GENEESKUNDE
1996
Genetic counseling as we enter the 21st Century. 8th internat, clinical genetics seminar, Greece (1996)
Juliaan Leroy
C1
Conference
1996
Is de (kinder)arts hersteld van zijn vigintifobie.
Piet Vanhaesebrouck
Claudine De Praeter
P GOVAERT
Koenraad Smets
Myriam Van Winckel
Juliaan Leroy
A2
Journal Article
in
TIJDSCHRIFT VOOR GENEESKUNDE
1996
Neonatally fatal microcephaly in three sibs
Juliaan Leroy
G LYON
P GOVAERT
Piet Vanhaesebrouck
Paul Defoort
C1
Conference
1996
Organisation of Medium Level Neonatal Care in Belgium
P JEANNIN
Piet Vanhaesebrouck
R VAN HECKE
Koenraad Smets
Juliaan Leroy
C1
Conference
1996
1995
CONSTITUTIONAL TRANSLOCATION T(1-17)(P36.31-P36.13-Q11.2Q12.1) IN A NEUROBLASTOMA PATIENT. ESTABLISHMENT OF SOMATIC-CELL HYBRIDS AND IDENTIFICATION OF PND/A12M2 ON CHROMOSOME-1 AND NF1/SCYA7 ON CHROMOSOME-17 AS BREAKPOINT FLANKING SINGLE-COPY MARKERS.
Genevieve Laureys
Franki Speleman
R VERSTEEG
P VANDERDRIFT
A CHAN
Juliaan Leroy
U FRANCKE
G OPDENAKKER
Nadine Van Roy
A1
Journal Article
in
ONCOGENE
1995
Gastro esophageal reflux in severely neurologically impaired children
Myriam Van Winckel
Eddy Robberecht
S CADRANEL
Martine De Vos
Juliaan Leroy
A4
Journal Article
in
PEDIATRICS
1995
PSEUDOACHONDROPLASIA AND MULTIPLE EPIPHYSEAL DYSPLASIA DUE TO MUTATIONS IN THE CARTILAGE OLIGOMERIC MATRIX PROTEIN GENE.
MD BRIGGS
SMG HOFFMAN
LM KING
AS OLSEN
H MOHRENWEISER
Juliaan Leroy
Geert Mortier
DL RIMOIN
RS LACHMAN
ES GAINES
et al.
A1
Journal Article
in
NATURE GENETICS
1995
Valor diagnostico de los anticuerpos (IgG e IgA) frente a las proteinas de la lèche de vaca en pacientes intolerantes
JM GAMIZ JIMENEZ
Eddy Robberecht
Myriam Van Winckel
Georges Dacremont
Georges Van Maele
Juliaan Leroy
A2
Journal Article
in
Acta Pediatrica Espanola
1995
1994
AMINOTERMINAL PROPEPTIDE OF TYPE-III PROCOLLAGEN IN CORD-BLOOD AND AMNIOTIC-FLUID OF APPROPRIATE-FOR-GESTATIONAL-AGE INFANTS - A PREDICTOR OF AGE-RELATED FETAL GROWTH-RATE.
Piet Vanhaesebrouck
Jozef Kint
Marc Dhont
C DEPRAETER
Juliaan Leroy
A1
Journal Article
in
PEDIATRIC RESEARCH
1994
AMINOTERMINAL PROPEPTIDE OF TYPE-III PROCOLLAGEN IN CORD-BLOOD AND AMNIOTIC-FLUID OF HIGH-RISK PREGNANCIES - A BIOCHEMICAL APPROACH TO THE DYNAMIC ASSESSMENT OF DEVIANT FETAL GROWTH.
Piet Vanhaesebrouck
Jozef Kint
H VANKETS
P GOVAERT
K SMETS
Paul Defoort
Juliaan Leroy
A1
Journal Article
in
PEDIATRIC RESEARCH
1994
Mutations in the gene for collagen type III: phenotypic spectrum and genotype-phenotype correlation
Anne De Paepe
L NUYTINCK
Juliaan Leroy
[0-9]{2}
1994
Single-strand conformation polymorphism (SSCP) analysis of the COL3A1 gene detects a mutation that results in the substitution of glycine-1009 to valine and causes severe Ehlers-Danlos syndrome type-IV
Lieve Nuytinck
Anne De Paepe
Jean-Pierre Renard
Filip Adriaens
Juliaan Leroy
A1
Journal Article
in
HUMAN MUTATION
1994
Thoracic deformity, presenting sign in congenital myopathy' with gradually improving clinical course'
Juliaan Leroy
Piet Vanhaesebrouck
P GOVAERT
Paul Defoort
C1
Conference
1994
1993
Deficient Expression of Decorin in Infantile Progeroid Patients
LA BEAVAN
E QUENTIN-HOFFMAN
E SCHONHERR
F SNIGULA
Juliaan Leroy
H KRESSE
A2
Journal Article
in
J. Biol. Chem.
1993
Identificatie en karakterisatie van het gen voor neurofibromatose type 1 (NF1): recente ontwikkelingen
Ludwine Messiaen
Juliaan Leroy
A2
Journal Article
in
TIJDSCHRIFT VOOR GENEESKUNDE
1993
Klinische genetica
Juliaan Leroy
HG Brunner
Bookchapter
in
Kindergeneeskunde
1993
Klinische genetica
Juliaan Leroy
MF Niermeyer
Bookchapter
in
Kindergeneeskunde
1993
LACK OF INDEPENDENCE BETWEEN 5 DNA POLYMORPHISMS IN THE NF1 GENE.
Ludwine Messiaen
S DEBIE
T MOENS
A VANDENENDEN
Juliaan Leroy
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
1993
MOLECULAR CYTOGENETIC ANALYSIS OF A FAMILIAL PERICENTRIC-INVERSION OF CHROMOSOME-12.
Franki Speleman
Nadine Van Roy
E DEVOS
C HILLIKER
RFS SUIJKERBUIJK
Juliaan Leroy
A1
Journal Article
in
CLINICAL GENETICS
1993
Neurofibromatose: beter verkend landschap en bredere horizon
Juliaan Leroy
A2
Journal Article
in
TIJDSCHRIFT VOOR GENEESKUNDE
1993
Neurofïbromatose type 2
A Van den Enden
Juliaan Leroy
A2
Journal Article
in
TIJDSCHRIFT VOOR GENEESKUNDE
1993
On the variability of the Brachmann-De Lange Syndrome in seven patients.
Juliaan Leroy
J PERSIJN
V VANDEWEGHE
R VANHECKE
Ann Oostra
S DEBIE
Margarita Craen
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
1993
Osteoporosis-pseudoglioma syndrome
Anne De Paepe
Juliaan Leroy
Lieve Nuytinck
Françoise Meire
Jan Capoen
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
1993
The Lujan syndrome or mental retardation with marfanoid habitus: the challenge of adequate nosological definition
Juliaan Leroy
Geert Mortier
CA De Brandt
KA Logghe
Anne De Paepe
C3
Conference
1993
Tricho-rhino-phalangeal syndrome type I (TRP I) due to an apparently balanced translocation involving 8q24
Fabienne E Marchau
Bernadette C Van Roy
Paul M Parizel
Julien R Lambert
Ilse De Canck
Juliaan Leroy
Carine M Gevaert
Patrick J Willems
Jan E Dumon
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
1993
1992
Acute suppurative thyroiditis complicating second allogeneic transplant for juvenile CMML
M Poelman
Yves Benoit
Genevieve Laureys
Margarita Craen
Juliaan Leroy
A1
Journal Article
in
BONE MARROW TRANSPLANTATION
1992
BECKER-TYPE MUSCULAR-DYSTROPHY - REPORT OF A FAMILY WITH ONE POSTMORTEM STUDY.
JJ MARTIN
Juliaan Leroy
C CEUTERICK
U LUBKE
E VANBUGGENHOUT
J VANVUCHELEN
C VANBROECKHOVEN
A1
Journal Article
in
CLINICAL NEUROLOGY AND NEUROSURGERY
1992
Detection of subtle reciprocal translocations by fluorescence in situ hibridization.
Franki Speleman
Nadine Van Roy
J WIEGANT
MR VERSCHRAEGEN-SPAE
Yves Benoit
P GOVAERT
L GOOSSENS
Juliaan Leroy
A1
Journal Article
in
CLINICAL GENETICS
1992
Fluorescentie in situ hybridisatie. Nieuwe mogelijkheden voor het chromosomenonderzoek.
Franki Speleman
Nadine Van Roy
Juliaan Leroy
A2
Journal Article
in
TIJDSCHRIFT VOOR GENEESKUNDE
1992
IgG subclass deficiency in children with recurrent bronchitis.
Frans De Baets
Jozef Kint
Romain Pauwels
Juliaan Leroy
A1
Journal Article
in
EUROPEAN JOURNAL OF PEDIATRICS
1992
Malignant melanoma of soft parts : further cytogenetic characterization
Franki Speleman
Cecile Colpaert
Gerda Goovaerts
Juliaan Leroy
Eric Van Marck
A1
Journal Article
in
CANCER GENETICS AND CYTOGENETICS
1992
Molecular cytogenetic analysis of a complex t(10;20;ll) translocation in Ewing's Sarcoma.
Franki Speleman
Nadine Van Roy
J WIEGANT
AM DIERICK
Dirk Uyttendaele
Juliaan Leroy
A1
Journal Article
in
GENES CHROMOSOMES & CANCER
1992
PERINATAL MANIFESTATIONS OF MATERNAL YELLOW NAIL SYNDROME.
P GOVAERT
Juliaan Leroy
Romain Pauwels
Piet Vanhaesebrouck
C DEPRAETER
H VANKETS
M GOETEYN
A1
Journal Article
in
PEDIATRICS
1992
PUTATIVE MONOSOMY-21 IN 2 PATIENTS - CLINICAL FINDINGS AND INVESTIGATION USING FLUORESCENCE INSITU HYBRIDIZATION.
DL VILJOEN
Franki Speleman
R SMART
Nadine Van Roy
J DUTOIT
Juliaan Leroy
A1
Journal Article
in
CLINICAL GENETICS
1992
Radiological case of the month : extensive neonatal subarachnoid hematoma
P Govaert
Juliaan Leroy
Jacques Caemaert
BP Wood
A1
Journal Article
in
AMERICAN JOURNAL OF DISEASES OF CHILDREN
1992
The prognostic value of serum lactate dehydrogenase in children with acute lymphoblastic leukemia (ALL)
D Bullens
Yves Benoit
G Laureys
K Dhooge
Jean Plum
Geert Leroux-Roels
Juliaan Leroy
C3
Conference
1992
1991
Analysis of whole-arm translocations in malignant blood cells by nonisotopic in situ hybridization
Franki Speleman
K Mangelschots
M Vercruyssen
P Dal Cin
A Aventin
Fritz Offner
Genevieve Laureys
H Van den Berghe
Juliaan Leroy
A1
Journal Article
in
CYTOGENETICS AND CELL GENETICS
1991
Characterization of a de novo duplication of 11p14→p13, using fluorescent in situ hybridization and Southern hybridization
Franki Speleman
M Mannens
B Redeker
M Vercruyssen
Patric Van Oostveldt
Juliaan Leroy
R Slater
A1
Journal Article
in
CYTOGENETICS AND CELL GENETICS
1991
Chromosome analysis in human oocytes unfertilized in vitro : a mathematical model for the estimation of the first meiotic non-disjunction frequency
Petra De Sutter
Marc Dhont
MR Verschraegen-Spae
H Steyaert
W Corijn
Juliaan Leroy
Dirk Vandekerckhove
A1
Journal Article
in
HUMAN REPRODUCTION
1991
Creatine kinase isoenzyme BB concentrations in the cerebrospinal fluid of newborns : relationship to short-term outcome
C Depraeter
Piet Vanhaesebrouck
P Govaert
Joris Delanghe
Juliaan Leroy
A1
Journal Article
in
PEDIATRICS
1991
EPISIOTOMY AND NEONATAL LIDOCAINE INTOXICATION
C DEPRAETER
Piet Vanhaesebrouck
N DEPRAETER
P GOVAERT
Marcus Bogaert
Juliaan Leroy
A1
Journal Article
in
EUROPEAN JOURNAL OF PEDIATRICS
1991
HOW IDIOPATHIC IS IDIOPATHIC EXTERNAL HYDROCEPHALUS
P GOVAERT
Ann Oostra
Dirk Matthys
Piet Vanhaesebrouck
Juliaan Leroy
A1
Journal Article
in
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
1991
IGG SUBCLASS SPECIFIC ANTIBODY-RESPONSE IN RECURRENT BRONCHITIS.
Frans De Baets
Romain Pauwels
I SCHRAMME
Juliaan Leroy
A1
Journal Article
in
ARCHIVES OF DISEASE IN CHILDHOOD
1991
Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridization
Franki Speleman
Juliaan Leroy
Nadine Van Roy
Anne De Paepe
R Suukerbuuk
J Brunner
L Looijenga
M Verschraegen-Spae
E Orye
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
1991
1990
CONSTITUTIONAL TRANSLOCATION T(1-17)(P36-Q12-21) IN A PATIENT WITH NEUROBLASTOMA
Genevieve Laureys
Franki Speleman
G OPDENAKKER
Yves Benoit
Juliaan Leroy
A1
Journal Article
in
GENES CHROMOSOMES & CANCER
1990
Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, Southern hybridization and non-isotopic in situ hybridization
Franki Speleman
Bart Van der Auwera
Kathelijne Mangelschots
Miet Vercruyssen
Ton Raap
Joop Wiegant
Margarita Craen
Juliaan Leroy
A1
Journal Article
in
HUMAN GENETICS
1990
1989
Cytogenetic investigation of a case of congenital fibrosarcoma
Franki Speleman
Paola Dal Cin
Kristiaan De Potter
Genevieve Laureys
Hendrik Roels
Juliaan Leroy
Herman Van Den Berghe
A1
Journal Article
in
CANCER GENETICS AND CYTOGENETICS
1989
De novo terminal deletion 7P22.1-pter in a child without craniosynostosis
Franki Speleman
Margarita Craen
Juliaan Leroy
A1
Journal Article
in
JOURNAL OF MEDICAL GENETICS
1989
1988
Dermatomyositis with paracrystalline inclusions and polymicrogyria in two sisters
Jan De Bleecker
Jacques De Reuck
J MARTIN
C CEUTERICK
Dietbrand Carton
Juliaan Leroy
C1
Conference
1988
1987
Polymicrogyria and dermatomyositis in two sisters
Jacques De Reuck
Dietbrand Carton
J MARTIN
C CEUTERICK
Jan De Bleecker
Juliaan Leroy
C1
Conference
1987
Aminoterminal Propeptide of Type III Procollagen in Cord Blood and Amniotic Fluid of Appropriate-for-Gestaüonal-Age Infants: A Predictor of Age-Related Fetal Growth Rate. Pediatrie Research, 1994,36, pp. 64-70.
Piet Vanhaesebrouck
J KDMT
M DHONT
Claudine De Praeter
Juliaan Leroy
[0-9]{2}
Chapter 97 in 'Emery and Rimoin's Principles and Practice of Medical Genetics'. D.L. Rimoin, J.M. Connor, R.E. Pyeritz, eds., 3rd Edit., Churchill Livingstone, New York, pp. 2O81-2103, 1996.
Juliaan Leroy
Bookchapter
Deficient decorin biosynthesis in the neonatal progeroid syndrome'. Chapter 24 in 'Dysmorphology and Genetics of Cardiovascular Disorders', Bartsocas CS, Beighton P., Eds., HTA Medical Publications, Athens, 1994, pp 166-176.
Juliaan Leroy
L BEAVAN
E QUENTIN-HOFFMAN
H KRESSE
Bookchapter
Disorders of lysosomal enzymes. Chapter 23 in 'Connective tissue and its heritable Disorders'. Royce P.M. and Steinmann B., eds., Wiley-Liss, New York, 1992, pp. 613-639.
Juliaan Leroy
U WIESMANN
Bookchapter
Heredity, development and behavior. Chapter 22 in: Developmental-Behavioral Pediatrics. Edit. M.D. Levine, W.B. Carey, A.C. Crocker, 2e edit., 1992, pp. 195-212, W.B. Saunders Comp.
Juliaan Leroy
Bookchapter
Hoofdstuk 22 in Codex Medicus, E. Eyskens, L. Feenstra, A.E. Meinders en J.P. Vandenbroucke, Eds., 10e druk, Elsevier, Arnhem, pp. 799-817.
Juliaan Leroy
[0-9]{2}
Medische Genetica en moleculaire Biologie. (1996).
Juliaan Leroy
[0-9]{2}
Oligosaccharidoses.
Juliaan Leroy
[0-9]{2}
Substitution of Gly 769 by serine in collagen type III in a three generation family showing variable expressivity of EDS type IV. Proceed. 5th Internat. Conference on osteogenesis imperfecta, 1993, pp. 114-115.
Anne De Paepe
L NUYTINCK
K WETTINCK
Juliaan Leroy
C1
Conference
The mucolipidoses (including I-cell disease). Chapter 19 in Handbook of Clinical Neurology. Vol. 66, Revised Series 22, Neurodystrophies and Neurolipidoses, P.J. Vinken, G.W. Bruyn, H.W. Moser, Eds., Elsevier, Amsterdam, pp. 377-387, 1996.
Juliaan Leroy
Bookchapter