Literatuur over HME-MO | HME-MO vereniging Nederland(current)
Literatuur over HME-MO
Wetenschappelijke artikelen over HME-MO
Aaronson NK, et al. Translation, Validation and Norming of the Duth Language Version of the SF-36 Health Survey in Community and Cronic Disease Populations. J. Clin Epidemiol, 1998, 51: 1055-1068.
Akita S, Murase T, Yonenobu K, et al. Long term results of surgery for forearm deformities in patients with multiple cartilaginous exostoses. J Bone Joint Surg 2007; 89A:1993-1999.
Akker van den-Scheek, et al., Preoperative or postoperative self-efficacy: Which is a better predictor of outcome after total hip or knee arthroplasty? Patient Education and Counseling 2007; 66: 92-99.
Bernard, MA, et al. Diminished Levels of the Putative Tumor Suppressor Proteins EXT1 and EXT2 in Exostosis Chrondrocytes. Cell Motility and the Cytoskeleton 2001; 48: 149–162.
Bernard SA, Murphy MD, Flemming DJ, Kransdorf MJ. Improved differentiation of benign osteochondromas form secondary chondrosarcomas with standardized measurement of cartilage cap at CT and MR imaging. Rdiology 2010; 255:857-865.
Bess RS, et al. Spinal exostoses. Spine 2005; 30: 774-780.
Bottner F, et al. Surgical treatment of symptomatic osteochondroma. J Bone Joint Surg 2003; 85B: 1161-1165.
Bovée J. A molecular genetic characterisation of cartilaginous tumors.Proefschrift, Leiden, 2000.
Caroll KL, et al. Clinical Correlation to Genetic Variations of Hereditary Multiple Exostosis. J Pediatr Orthop 1999; 19: 785–791.
Centraal Bureau voor de Statistiek. ‘Vademecum Gezondheidsstatistiek Nederland’. Uitgave van CBS Voorburg, Heerlen, 2003.
Chin KR, et al. Osteochondromas of the distal aspect of the tibia or fibula. J Bone Joint Surg 2000; 82A: 1269-1278.
Darilek S, et al. Hereditary Multiple Exostosis and Pain. J. Pediatr Orthop 2005; 25: 369-376.
Ehrenfried A. Multiple cartilaginous exostoses – hereditary deforming chondrodysplasia. Brief report on a little known disease. J Am Med Assn 1915; 64: 1642-1646.
Geirnaerdt M. Gadolinium-enhanced MR imaging in the diagnosis of cartilaginous tumors. Proefschrift, Leiden, 1998.
Goud AL, Lange J de, Scholtes VAB, Bulstra SW, Ham SJ. Pain, physical and social functioning and quality of life in individuals with hereditary multiple exostoses in the Netherlands. A National cohort study. J Bone Joint Surg 2012; 94A:1013-1020.
Goud AL, Wuyts W, Bessems J, Bramer J, van der Woude HJ, Ham SJ. Intraossoeus atypical chondroid tumor or chondrosarcoma type 1 in patients with multiple osteochondromas. J Bone Joint Surg 2015; 97A:24-31.
Ham SJ, Maathuis P. Radiologisch onderzoek bij Hereditaire Multiple Exostosen in de Orthopaedische praktijk. In: HME-Newsflash nr. 4, oktober 2000: 6–8.
Ham SJ, Maathuis P. Chirurgische behandeling bij Hereditaire Multiple Exostosen (HME). In: HME-Newsflash nr. 4, oktober 2000: 9–11.
Ham SJ, et al. Drie patienten met herditaire multiple exostosen en maligne ontaarding van een bekkenosteochondroom. Ned. Tijdschr Geneesk 2004; 148: 1732-1738.
Ham SJ, de Lange J, van der Zwan AL, Schaap GR, van der Woude HJ, Heeg M.Klinische problemen bij multipele osteochondromen. Ned. Tijdschr Geneesk 2012; 156: 474-480.
Ham SJ. Multiple hereditary exostoses. Clinical problems and therapeutic options. Orthopaedics and Trauma. 2013: 27;118-125.
Harris, N.H.Postgraduate Textbook of Clinical Orthopaedics. Bristol/London/Boston, 1983, 613-614, 651-654.
Hennekam, R.C.M. Syndrome of the month: Heriditary Multiple Exostoses. J Med Genet 1991; 28, 262-266.
Het Multipel Exostose Syndroom. In: Folia Genetica. 1994; 4, 12-14.
Homan S, Scholtes VAS, Heeg M, van der Woude HJ, Ham SJ. Morphology and Developmental Dysplasia of the Hip in Patients with Multiple Hereditary Exostoses. Submitted.
Hosalkar H, et al. Abnormal scarring with keloid formation after osteochondroma excision in children with multiple hereditary exostoses. J Pediatr Orthop 2007; 27: 333-337.
Ishikawa J-I, Kato H, Fujioka F, et al. Tumor location affects the results of simple excision for multiple osteochondromas in the forearm. J Bone Joint Surg 2007; 89A:1238-1247.
Keith A. Studies on the anatomical changes which accompany certain growth-disorders of the human body. 1. The nature of the structural alterations in the disorder known as multiple exostoses. J Anat 1920; 54: 101-115.
Kivioja K, et al. Chondrosarcoma in a family with multiple hereditary exostoses. J Bone Joint Surg 2000; 82B: 261-266.
Lange J de. Multiple Exostosen, in kort bestek. Overzichtartikel. Uitgave van de HME-MO Vereniging Nederland. 2001, 1-9.
Lange J de, Ham J. Hereditary multiple exostoses/multiple osteochondromen en de gevolgen hiervan in Nederland. Onderzoeksrapport HME-MO Vereniging Nederland.
Legeai-Mallet L, et al. Complete penetrance and expressivity skewing in Hereditary multiple exostoses. Clin Genet 1997; 52: 12-16.
Mader K, et al. Shortening and deformity of radius and ulna in children: correction of axis and length by callus distraction. J Pediatr Orthop 2003; 12B: 183-191.
Masada K, et al. Operations for forearm deformity caused by multiple osteochondromas. J Bone Joint Surg 1989; 71B: 24-29.
McCormick C, et al. New perspectives on the molecular basis of hereditary bone tumours. Molecular Medicine Today1999; 5: 481–486.
Menchetti G, Pompella A. Hereditary Multiple Exostosis: Pediatric Aspects and Differential Diagnosis. Pediatric Rec. Commun1989; 3: 261 – 270.
Mikawa Y, et al. Cervical spinal cord compression in hereditary multiple exostoses. Arch Orthop Trauma Surg 1997; 116: 112-115.
Murphy MD, Choi JJ, Kransdorf MJ, Flemming DJ, Gannon FH. Imging of osteochondroma: variants and complications with radiologic-pathologic correlation. Radiographics 2000; 20:1407-1434.
Noonan KJ, et al. Natural history of multiple hereditary osteochondromatosis of the lower extremity and ankle. J Pediatr Orthop 2002; 22: 120-124.
NVOG (Nederlandse Vereniging voor Obstetrie en Gynaecologie). ‘De kwaliteit van verloskundige zorg en het aantal keizersneden in uw ziekenhuis’. In: Leeswijzer NVOG-indicatoren Keizersneden. 2004: 1-5.
Oosterbos M, van der Zwan A, van der Woude HJ, Ham SJ. Correction of ankle valgus in multiple hereditary exostoses by temporal medial hemiepiphyseodesis of the distal tibia using 8-plate. Geaccepteerd J Ped Orthop.
Pedrini E, Jennes I, Tremosini M, et al. Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of “protective” and “risk” factors. J Bone Joint Surg 2011; 93A:2294-2302.
Philippe C, et al. Mutation Screening of the EXT1 and EXT2 Genes in Patients with Hereditary Multiple Exostoses. Am J Human Genet 1997; 61: 520-528.
Porter DE, et al. Clinical and Radiographic Analysis of Osteochondromas and Growth Disturbance in Hereditary Multiple Exostoses. J Pediatr Orthop 2000; 20 ; 246–250.
Porter DE, et al. Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype study. J Bone Joint Surg 2004; 86B: 1041-1046.
Roach JW, Klatt JWB, Faulkner ND. Involvement of the spine in patients with multiple hereditary exostoses. J Bone Joint Surg 2009; 91A:1942-1948.
Rupprecht M, Spiro AS, Rueger JM, Stucker R. Temporary screw epiphysiodesis of the distal tibia: a therapeutic option for ankle valgus in patients with hereditary multiple exostosis. J Pediatr Orthop 2011; 31:89-94.
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Takikawa K, et al. Characteristic factors of ankle valgus with multiple cartilaginous exostoses. J Pediatr Orthop 2008; 28: 761-765.
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Wu Y, et al. Assignment of a second locus for multiple exostoses to the pericentromenic region of chromosome 11. Human Molec Genet 1994; 3: 167-171.
Wuyts W. et al. Het Multiple Exostose Syndroom, genetische aspecten Tijdschr Geneesk 1995; 51: 191-195.
Wuyts W, et al. Positional cloning of a gene involved in Hereditary Multiple Exostoses. Human Molec Genet 1996; 5: 1547-1557.
Wuyts W, et al. Indentification and Characterization of a Novel Member of the EXT Gene Family, EXT2. Eur J Genet 1997; 5: 382-389.
Wuyts W. Identification of a new family of EXT genes /Identificatie van een nieuwe familie van EXT genen. Proefschrift, Antwerpen 1997-1998.
Wuyts W, et al. Mutations in EXT1 and EXT2 genes in Hereditary Multiple Exostoses. Am J Genet 1998; 62: 346-354.
Wuyts W. Genetische aspecten van Multiple Exostoses. In: HME-Newsflash nr. 2, december 1999, 4–5.
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Zee KI van der, Sanderman R.Het meten van de algemene gezondheidstoestand met de RAND-36, Een Handleiding. Uitgave: Noordelijk Centrum voor Gezondheidsvraagstukken, Rijksuniversiteit Groningen,1993.
