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Results 1 to 16 of 16

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Deep Venous Thrombosis of the Axillary and Subclavian Vein After Osteosynthesis of a Midshaft Clavicular Fracture: A Case ReportCLAES, Tom; DEBEER, Philippe; BELLEMANS, Johan et al.American journal of sports medicine. 2010, Vol 38, Num 6, pp 1255-1258, issn 0363-5465, 4 p.Article

Resection arthroplasty of the shoulder as a salvage procedure for deep shoulder infection: does the use of a cement spacer improve outcome?VERHELST, Luk; STUYCK, Jose; BELLEMANS, Johan et al.Journal of shoulder and elbow surgery. 2011, Vol 20, Num 8, pp 1224-1233, issn 1058-2746, 10 p.Article

Superior instability of a shoulder hemiarthroplasty with skin perforationRYCKAERT, Alexander; NELEN, Guy; STUYCK, Jos et al.Orthopedics (Thorofare). 2007, Vol 30, Num 11, pp 968-969, issn 0147-7447, 2 p.Article

Scapular winging after vaginal deliveryDEBEER, Philippe; DEVLIEGER, Roland; BRYS, Peter et al.BJOG (Oxford. Print). 2004, Vol 111, Num 7, pp 758-759, issn 1470-0328, 2 p.Article

Glenosphere Disengagement : A Potentially Serious Default in Reverse Shoulder SurgeryMIDDERNACHT, Bart; DE WILDE, Lieven; MOLE, Daniel et al.Clinical orthopaedics and related research. 2008, Vol 466, Num 4, pp 892-898, issn 0009-921X, 7 p.Article

An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with GIi3R function during limb pyre-patterningBRISON, Nathalie; DEBEER, Philippe; FANTINI, Sebastian et al.Human molecular genetics (Print). 2012, Vol 21, Num 11, pp 2464-2475, issn 0964-6906, 12 p.Article

A 3D-CT scan study of the humeral and glenoid planes in 150 normal shouldersDE WILDE, Lieven; DEFOORT, Saartje; VERSTRAETEN, Tom R. G. M et al.Surgical and radiologic anatomy (Print). 2012, Vol 34, Num 8, pp 743-750, issn 0930-1038, 8 p.Article

2q31.1 microdeletion syndrome: redefining the associated clinical phenotypeDIMITROV, Boyan; BALIKOVA, Irina; FRYNS, Jean-Pierre et al.Journal of medical genetics. 2011, Vol 48, Num 2, pp 98-104, issn 0022-2593, 7 p.Article

A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid featuresVAN ESCH, Hilde; AGARWAL, Anil K; DEBEER, Philippe et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 2, pp 517-521, issn 0021-972X, 5 p.Article

Melorheostosis in a family with autosomal dominant osteopoikilosis: Report of a third familyDEBEER, Philippe; PYKELS, E; LAMMENS, J et al.American journal of medical genetics. 2003, Vol 119A, Num 2, pp 188-193, issn 0148-7299, 6 p.Article

Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosisHELLEMANS, Jan; PREOBRAZHENSKA, Olena; SAVARIRAYAN, Ravi et al.Nature genetics. 2004, Vol 36, Num 11, pp 1213-1218, issn 1061-4036, 6 p.Article

Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutationsDEBEER, Philippe; PEETERS, H; KALFF-SUSKE, M et al.American journal of medical genetics. 2003, Vol 120A, Num 1, pp 49-58, issn 0148-7299, 10 p.Article

Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani-Lenz-like non-syndromic oligosyndactylyDIMITROV, Boyan Ivanov; VOET, Thierry; DE SMET, Luc et al.Journal of medical genetics. 2010, Vol 47, Num 8, pp 569-574, issn 0022-2593, 6 p.Article

A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotypeFANTINI, Sebastian; VACCARI, Giulia; BRISON, Nathalie et al.Human molecular genetics (Print). 2009, Vol 18, Num 5, pp 847-860, issn 0964-6906, 14 p.Article

Novel TBX5 mutations in patients with holt-oram syndrome : Genetics in OrthopaedicsDEBEER, Philippe; RACE, Valerie; GEWILLIG, Marc et al.Clinical orthopaedics and related research. 2007, Num 462, pp 20-26, issn 0009-921X, 7 p.Article

Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansionHORSNELL, Katherine; ALI, Manir; MALIK, Saghira et al.European journal of medical genetics. 2006, Vol 49, Num 5, pp 396-401, issn 1769-7212, 6 p.Article

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