FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Philippe Debeer

Research Profile

Anatomy

Disorders

Concepts & Ideas

Physiology

Mutation

Chemicals & Drugs

Procedures

Devices

Joint Prosthesis

Genes & Molecular Sequences

Dominant Genes

Co-author Network

Publications

TOP 3
Pieter Slagmolen; Paul Suetens; Philippe Debeer; Jan D'Hooge; KH Peers; Lennart Scheys; Johan Bellemans
In regard to: "In vivo strain analysis of the intact supraspinatus tendon by ultrasound speckles tracking imaging" (Journal of Orthopaedic Research, Vol. 29, No. 12, pp. 1931-1937, May 2011).
Ilse Degreef; Philippe Debeer
Post-vaccination frozen shoulder syndrome. Report of 3 cases.
Lieven De Wilde; Saartje Defoort; Wendy Speeckaert; Tom R G M Verstraeten; Philippe Debeer
A 3D-CT scan study of the humeral and glenoid planes in 150 normal shoulders.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Philippe Debeer (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Pieter Slagmolen; Paul Suetens; Philippe Debeer; Jan D'Hooge; KH Peers; Lennart Scheys; Johan Bellemans
In regard to: "In vivo strain analysis of the intact supraspinatus tendon by ultrasound speckles tracking imaging" (Journal of Orthopaedic Research, Vol. 29, No. 12, pp. 1931-1937, May 2011).
Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2012;30(12):2054-6; author reply 2056-7.
2012: Ilse Degreef; Philippe Debeer
Post-vaccination frozen shoulder syndrome. Report of 3 cases.
Acta chirurgica Belgica 2012;112(6):447-9.
2012: Lieven De Wilde; Saartje Defoort; Wendy Speeckaert; Tom R G M Verstraeten; Philippe Debeer
A 3D-CT scan study of the humeral and glenoid planes in 150 normal shoulders.
Surgical and radiologic anatomy : SRA 2012;34(8):743-50.
2012: Sofie Goeminne; Philippe Debeer
The natural evolution of neglected lesser tuberosity fractures in skeletally immature patients.
Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2012;21(8):e6-e11.
2012: Filip Verhaegen; Ide Smets; Marc Bosquet; Peter Brys; Philippe Debeer
Chronic anterior shoulder dislocation: aspects of current management and potential complications.
Acta orthopaedica Belgica 2012;78(3):291-5.
2012: Nathalie Brison; Philippe Debeer; Sebastian Fantini; Frank P Luyten; Christine Oley; Vincenzo Zappavigna; Przemko Tylzanowski
An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning.
Human molecular genetics 2012;21(11):2464-75.
2012: Nathalie Brison; Przemko Tylzanowski; Philippe Debeer
Limb skeletal malformations - what the HOX is going on?
European journal of medical genetics 2012;55(1):1-7.
2011: Lucas Luyckx; Thomas Luyckx; Peter Donceel; Philippe Debeer
Return to work after arthroscopic subacromial decompression.
Acta orthopaedica Belgica 2011;77(6):737-42.
2011: Luk Verhelst; José Stuyck; Johan Bellemans; Philippe Debeer
Resection arthroplasty of the shoulder as a salvage procedure for deep shoulder infection: does the use of a cement spacer improve outcome?
Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2011;20(8):1224-33.
2011: Nathalie Van Meir; Inge Fourneau; Philippe Debeer
Varicose veins at the spinoglenoidal notch: an unusual cause of suprascapular nerve compression.
Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2011;20(7):e21-4.
2011: Boyan Dimitrov; Irina Balikova; T J L de Ravel; Hilde Van Esch; Maryse De Smedt; Emiel Baten; Joris R Vermeesch; Irena Bradinova; Emil Simeonov; Koen Devriendt; Jean-Pierre Fryns; Philippe Debeer
2q31.1 microdeletion syndrome: redefining the associated clinical phenotype.
Journal of medical genetics 2011;48(2):98-104.
2010: Sofie Goeminne; Philippe Debeer
Delayed migration of a metal suture anchor into the glenohumeral joint.
Acta orthopaedica Belgica 2010;76(6):834-7.
2010: Alexander Van Tongel; Michael Schreurs; Frans Bruyninckx; Philippe Debeer
Bilateral Parsonage-Turner syndrome with unilateral brachialis muscle wasting: a case report.
Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2010;19(8):e14-6.
2010: Philippe Debeer; Luc De Smet
Outcome of latissimus dorsi transfer for irreparable rotator cuff tears.
Acta orthopaedica Belgica 2010;76(4):449-55.
2010: Boyan Ivanov Dimitrov; Thierry Voet; Luc De Smet; Joris Robert Vermeesch; Koen Devriendt; Jean-Pierre Fryns; Philippe Debeer
Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactyly.
Journal of medical genetics 2010;47(8):569-74.
2010: Laurence Ceulemans; Philippe Debeer; Ilse Degreef; Luc De Smet
Outcome of index finger pollicisation.
Journal of hand and microsurgery 2010;2(1):13-7.
2010: Nouchka Spapens; Ilse Degreef; Philippe Debeer
Posttraumatic pseudarthrosis of the clavicle in an 8-year-old girl.
Journal of pediatric orthopedics. Part B 2010;19(2):188-90.
2010: Thomas Luyckx; Philippe Debeer
Management of full thickness rotator cuff tears. A survey amongst members of the Flemish Elbow and Shoulder Surgeons Society (FLESSS).
Acta orthopaedica Belgica 2010;76(1):14-21.
2010: B I Dimitrov; T J L de Ravel; J Van Driessche; C de Die-Smulders; A Toutain; Joris R Vermeesch; Jean-Pierre Fryns; koenraad devriendt; Philippe Debeer
Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements.
Journal of medical genetics 2010;47(2):103-11.
2009: Laurens Ceulemans; Ilse Degreef; Philippe Debeer; Luc De Smet
Outcome of index finger pollicisation for the congenital absent or severely hypoplastic thumb.
Acta orthopaedica Belgica 2009;75(2):175-80.
2008: Bart Middernacht; Lieven De Wilde; Daniel Molé; Luc Favard; Philippe Debeer
Glenosphere disengagement: a potentially serious default in reverse shoulder surgery.
Clinical orthopaedics and related research 2008;466(4):892-8.
2007: Alexander Ryckaert; Guy Nelen; Jos Stuyck; Philippe Debeer
Superior instability of a shoulder hemiarthroplasty with skin perforation.
Orthopedics 2007;30(11):968-9.
2007: Philippe Debeer; Valerie Race; Marc Gewillig; koenraad devriendt; Jean-Pierre Frijns
Novel TBX5 mutations in patients with Holt-Oram syndrome.
Clinical orthopaedics and related research 2007;462():20-6.
2007: Peter Ruette; Jos Stuyck; Philippe Debeer
Neuropathic arthropathy of the shoulder and elbow associated with syringomyelia: a report of 3 cases.
Acta orthopaedica Belgica 2007;73(4):525-9.
2007: Philippe Debeer; Bart Van de Meulebroucke; Jos Stuyck; Raf Sciot; Ignace Samson
Postradiation soft tissue sarcoma of the shoulder: a case report.
Acta orthopaedica Belgica 2007;73(4):521-4.
2007: Philippe Debeer; E Van Den Eede; P Moens
Scapular winging: an unusual complication of bracing in idiopathic scoliosis.
Clinical orthopaedics and related research 2007;461():258-61.
2007: Luc De Smet; R De Kesel; Ilse Degreef; Philippe Debeer
Responsiveness of the Dutch version of the DASH as an outcome measure for carpal tunnel syndrome.
The Journal of hand surgery, European volume 2007;32(1):74-6.
2006: Katherine Horsnell; Manir Ali; Saghira Malik; Louise Wilson; Christine Hall; Philippe Debeer; Yanick J Crow
Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansion.
European journal of medical genetics 2006;49(5):396-401.
2006: Ruben Jacobs; Philippe Debeer
Calcifying tendinitis of the rotator cuff: functional outcome after arthroscopic treatment.
Acta orthopaedica Belgica 2006;72(3):276-81.
2006: Philippe Debeer; Herbert Plasschaert; Jos Stuyck
Resection arthroplasty of the infected shoulder: a salvage procedure for the elderly patient.
Acta orthopaedica Belgica 2006;72(2):126-30.
2006: Jan Hellemans; Philippe Debeer; Michael Wright; Andreas R Janecke; Klaus W Kjaer; Peter C M Verdonk; Ravi Savarirayan; Lina Basel; Celia Moss; Johannes Roth; Albert David; Anne De Paepe; Paul Coucke; Geert R Mortier
Germline LEMD3 mutations are rare in sporadic patients with isolated melorheostosis.
Human mutation 2006;27(3):290.
2006: Ilse Degreef; Philippe Debeer
Heterotopic ossification of the supraspinatus tendon after rotator cuff repair: case report.
Clinical rheumatology 2006;25(2):251-3.
2006: Hilde Van Esch; Anil Agarwal; Philippe Debeer; Jean-Pierre Fryns; Abhimanyu Garg
A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features.
The Journal of clinical endocrinology and metabolism 2006;91(2):517-21.
2005: Ilse Degreef; Philippe Debeer; Bert Van Herck; Els Van Den Eeden; Koen Peers; Luc De Smet
Treatment of irreparable rotator cuff tears by latissimus dorsi muscle transfer.
Acta orthopaedica Belgica 2005;71(6):667-71.
2005: Ilse Degreef; J Verduyckt; Philippe Debeer; Luc De Smet
An unusual cause of shoulder pain: osteoid osteoma of the acromion--a case report.
Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2005;14(6):643-4.
2005: Philippe Debeer; Hilde Van Esch; Christel Huysmans; E Pijkels; Luc De Smet; Wim Van de Ven; koenraad devriendt; Jean-Pierre Fryns
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD).
European journal of medical genetics 2005;48(4):377-87.
2005: Philippe Debeer; Filip Robyns
Fracture of the scapular spine in a patient with a Delta III prosthesis.
Acta orthopaedica Belgica 2005;71(5):612-4.
2005: Luc De Smet; Philippe Debeer; Ilse Degreef
Fixation of a periprosthetic humeral fracture with CCG-cable system.
Acta chirurgica Belgica 2005;105(5):543-4.
2005: Philippe Debeer; Peter Brys
Osteochondritis dissecans of the humeral head: clinical and radiological findings.
Acta orthopaedica Belgica 2005;71(4):484-8.
2005: Philippe Debeer; Christel Huysmans; Wim J M Van De Ven; Jean-Pierre Fryns; koenraad devriendt
Carpal and tarsal synostoses and transverse reduction defects of the toes in two brothers heterozygous for a double de novo NOGGIN mutation.
American journal of medical genetics. Part A 2005;134(3):318-20.
2005: Philippe Debeer; koenraad devriendt
Early recognition of basal cell naevus syndrome.
European journal of pediatrics 2005;164(3):123-5.
2004: Jan Hellemans; Olena Preobrazhenska; Andy Willaert; Philippe Debeer; Peter C M Verdonk; Teresa Costa; Koen Janssens; Björn Menten; Nadine Van Roy; Stefan Vermeulen; Ravi Savarirayan; Wim Van Hul; Filip Vanhoenacker; Danny Huylebroeck; Anne De Paepe; Jean-Marie Naeyaert; Jo Vandesompele; Frank Speleman; Kristin Verschueren; Paul J Coucke; Geert R Mortier
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.
Nature genetics 2004;36(11):1213-8.
2004: Philippe Debeer; Jean-Pierre Fryns; koenraad devriendt; E Baten; Christel Huysmans; Wim J M Van De Ven
A novel NOG mutation Pro37Arg in a family with tarsal and carpal synostoses.
American journal of medical genetics. Part A 2004;128A(4):439-40.
2004: Philippe Debeer; Roland Devlieger; Peter Brys; Bernard Spitz
Scapular winging after vaginal delivery.
BJOG : an international journal of obstetrics and gynaecology 2004;111(7):758-9.
2004: Philippe Debeer; L Vandenbossche; T J L de Ravel; C Desloovere; Luc De Smet; Christel Huysmans; Reinhilde Thoelen; Joris R Vermeesch; Wim J M Van De Ven; Jean-Pierre Fryns
Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1.
Clinical genetics 2004;65(2):153-5.
2004: Philippe Debeer; Luc De Smet; Jean-Pierre Fryns
Bilateral aplasia of the thumb, proximal radioulnar synostosis and unilateral synostosis of metacarpals 4 and 5.
Genetic counseling (Geneva, Switzerland) 2004;15(1):67-71.
2003: Philippe Debeer; Hilde Peeters; S Driess; L De Smet; K Freese; G Matthijs; Dorothea Bornholdt; koenraad devriendt; Karl-Heinz Grzeschik; Jean-Pierre Fryns; M Kalff-Suske
Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations.
American journal of medical genetics. Part A 2003;120A(1):49-58.
2003: Philippe Debeer; E Pykels; J Lammens; koenraad devriendt; Jean-Pierre Fryns
Melorheostosis in a family with autosomal dominant osteopoikilosis: report of a third family.
American journal of medical genetics. Part A 2003;119A(2):188-93.
2003: Hilde Peeters; Philippe Debeer; Amos Bairoch; Valérie Wilquet; Christel Huysmans; E Parthoens; Jean-Pierre Fryns; Marc Gewillig; Y Nakamura; N Niikawa; Wim Van de Ven; koenraad devriendt
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse.
Human genetics 2003;112(5-6):573-80.
2003: Philippe Debeer; L De Borre; Luc De Smet; Jean-Pierre Fryns
Asymmetrical Larsen syndrome in a young girl: a second example of somatic mosaicism in this syndrome.
Genetic counseling (Geneva, Switzerland) 2003;14(1):95-100.
2002: Philippe Debeer; R Mols; Christel Huysmans; koenraad devriendt; Wim J M Van De Ven; Jean-Pierre Fryns
Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11).
Clinical genetics 2002;62(5):410-4.
2002: Philippe Debeer; Chiara Bacchelli; Peter J Scambler; L De Smet; J-P Fryns; Frances R Goodman
Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13.
Journal of medical genetics 2002;39(11):852-6.
2002: Philippe Debeer; T J L de Ravel; koenraad devriendt; Jean-Pierre Fryns; Christel Huysmans; Wim J M Van De Ven
Human homologues of Osr1 and Osr2 are not involved in a syndrome with distal limb deficiencies, oral abnormalities, and renal defects.
American journal of medical genetics 2002;111(4):455-6.
2002: Philippe Debeer; Luc De Smet; Wim J M Van De Ven; G Fabry; J P Fryns
Genes and orthopedics: from gene to clinic and vice versa.
Acta orthopaedica Belgica 2002;68(3):203-14.
2002: Philippe Debeer; Eric F P M Schoenmakers; Waleed O Twal; Scott Argraves; L De Smet; Jean-Pierre Fryns; Wim J M Van De Ven
The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly.
Journal of medical genetics 2002;39(2):98-104.
2002: Philippe Debeer; Peter Brys; L De Smet; J P Fryns
Unilateral absence of the trapezius and pectoralis major muscle: a variant of Poland syndrome.
Genetic counseling (Geneva, Switzerland) 2002;13(4):449-53.
2002: Luc De Smet; Philippe Debeer
Fetal hydantoin syndrome with unilateral atypical cleft hand: additional evidence for vascular disruption.
Genetic counseling (Geneva, Switzerland) 2002;13(2):157-61.
2001: R Jacobs; Philippe Debeer; Luc De Smet
Treatment of rotator cuff arthropathy with a reversed Delta shoulder prosthesis.
Acta orthopaedica Belgica 2001;67(4):344-7.
2001: Hilde Peeters; Philippe Debeer; Peter Groenen; Hilde Van Esch; G Vanderlinden; Benedicte Eyskens; Luc Mertens; Marc Gewillig; Wim Van de Ven; Jean-Pierre Fryns; koenraad devriendt
Recurrent involvement of chromosomal region 6q21 in heterotaxy.
American journal of medical genetics 2001;103(1):44-7.
2001: Philippe Debeer; Luc De Smet; Jean-Pierre Fryns
Intrafamilial clinical variability in type C brachydactyly.
Genetic counseling (Geneva, Switzerland) 2001;12(4):353-8.
2000: Philippe Debeer; Eric F P M Schoenmakers; Reinhilde Thoelen; Maureen Holvoet; T Kuittinen; Guy Fabry; Jean-Pierre Fryns; Frances R Goodman; Wim J M Van De Ven
Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint.
European journal of human genetics : EJHG 2000;8(8):561-70.
2000: Philippe Debeer; R Decorte; S Delvaux; Johan Bellemans
DNA analysis of a transplanted cryopreserved meniscal allograft.
Arthroscopy : the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association 2000;16(1):71-5.
1999: koenraad devriendt; J Jaeken; G Matthijs; Hilde Van Esch; Philippe Debeer; M Gewillig; J P Fryns
Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent Ductus botalli.
American journal of human genetics 1999;65(1):249-51.
1998: Philippe Debeer; Eric F P M Schoenmakers; L De Smet; Wim J M Van De Ven; J P Fryns
Co-segregation of an apparently balanced reciprocal t(12;22)(p11.2;q13.3) with a complex type of 3/3'/4 synpolydactyly associated with metacarpal, metatarsal and tarsal synostoses in three family members.
Clinical dysmorphology 1998;7(3):225-8.
1998: Philippe Debeer; Eric F P M Schoenmakers; Reinhilde Thoelen; Jean-Pierre Fryns; Wim J M Van De Ven
Physical mapping of the t(12;22) translocation breakpoints in a family with a complex type of 3/3'/4 synpolydactyly.
Cytogenetics and cell genetics 1998;81(3-4):229-34.