Nouri A, Cheng JS, Davies B, Kotter M, Schaller K, Tessitore E (2020) Degenerative cervical myelopathy: A brief review of past perspectives, present developments, and future directions. J Clin Med 9(2):535
Article PubMed PubMed Central Google Scholar
Tetreault L, Goldstein CL, Arnold P, Harrop J, Hilibrand A, Nouri A et al (2015) Degenerative cervical myelopathy: A spectrum of related disorders affecting the aging spine. Neurosurgery 77(Suppl 4):S51–67
Davies BM, Mowforth OD, Smith EK, Kotter MR (2018) Degenerative cervical myelopathy. BMJ 360:k186
Article PubMed PubMed Central Google Scholar
Kalsi-Ryan S, Karadimas SK, Fehlings MG (2013) Cervical spondylotic myelopathy: the clinical phenomenon and the current pathobiology of an increasingly prevalent and devastating disorder. Neurosci Rev J Bringing Neurobiol Neurol Psychiatry 19(4):409–421
Ogut E (2025) Anatomical variability, morphofunctional characteristics, and clinical relevance of accessory ossicles of the back: implications for spinal pathophysiology and differential diagnosis. J Orthop Surg 20:240
Öğüt E, Şekerci R, Şen H, Çakın H, Gediz T, Keles-Celik N (2020) Anatomo-radiological importance and the incidence of Os odontoideum in Turkish subjects: a retrospective study. Surg Radiol Anat SRA 42(6):701–710
Patel AA, Spiker WR, Daubs M, Brodke DS, Cannon-Albright LA (2012) Evidence of an inherited predisposition for cervical spondylotic myelopathy. Spine 37(1):26–29
Article PubMed PubMed Central Google Scholar
Pope DH, Davies BM, Mowforth OD, Bowden AR, Kotter MRN (2020) Genetics of degenerative cervical myelopathy: A systematic review and Meta-Analysis of candidate gene studies. J Clin Med 9(1):282
Article PubMed PubMed Central CAS Google Scholar
Shlykov MA, Giles EM, Kelly MP, Lin SJ, Pham VT, Saccone NL et al (2023) Evaluation of genetic and nongenetic risk factors for degenerative cervical myelopathy. Spine 48(16):1117–1126
Article PubMed PubMed Central Google Scholar
Eskola PJ, Lemmelä S, Kjaer P, Solovieva S, Männikkö M, Tommerup N et al (2012) Genetic association studies in lumbar disc degeneration: a systematic review. PLoS ONE 7(11):e49995
Article PubMed PubMed Central CAS Google Scholar
Yang H, Hu Z, Zhuang C, Liu R, Zhang Y (2018) Association between the polymorphisms of CALM1 gene and osteoarthritis risk: a meta-analysis based on observational studies. Biosci Rep 38(5):BSR20181128
Article PubMed PubMed Central Google Scholar
Hussey JW, Limpitikul WB, Dick IE (2023) Calmodulin mutations in human disease. Channels Austin Tex 17(1):2165278
Ryan JA, Eisner EA, DuRaine G, You Z, Reddi AH (2009) Mechanical compression of articular cartilage induces chondrocyte proliferation and inhibits proteoglycan synthesis by activating the ERK pathway: implications for tissue engineering and regenerative medicine. J Tissue Eng Regen Med 3(2):107–116
Article PubMed CAS Google Scholar
Mototani H, Mabuchi A, Saito S, Fujioka M, Iida A, Takatori Y et al (2005) A functional single-nucleotide polymorphism in the core promoter region of CALM1 is associated with hip osteoarthritis in Japanese. Hum Mol Genet 14(8):1009–1017
Article PubMed CAS Google Scholar
Nouri A, Tetreault L, Singh A, Karadimas SK, Fehlings MG (2015) Degenerative cervical myelopathy: epidemiology, genetics, and pathogenesis. Spine 40(12):E675–693
Suzuki A, Daubs MD, Hayashi T, Ruangchainikom M, Xiong C, Phan K et al (2017) Magnetic resonance classification system of cervical intervertebral disk degeneration: its validity and meaning. Clin Spine Surg 30(5):E547–E553
Kaur G, Bhadada SK, Santra M, Pal R, Sarma P, Sachdeva N et al (2022) Multilevel annotation of germline MEN1 variants of synonymous, nonsynonymous, and uncertain significance in Indian patients with sporadic primary hyperparathyroidism. J Bone Min Res Off J Am Soc Bone Min Res 37(10):1860–1875
Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J et al (2015) Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American college of medical genetics and genomics and the association for molecular pathology. Genet Med Off J Am Coll Med Genet 17(5):405–424
Association of calmodulin 1 gene polymorphisms with susceptibility to adolescent idiopathic scoliosis| Request PDF. ResearchGate. [cited 2025 Jun 4]; Available from: https://www.researchgate.net/publication/51727536_Association_of_calmodulin1_gene_polymorphisms_with_susceptibility_to_adolescent_idiopathic_scoliosis
Zhang L, Feng X, McDonald JM (2003) The role of calmodulin in the regulation of osteoclastogenesis. Endocrinology 144(10):4536–4543
Article PubMed CAS Google Scholar
Loughlin J, Sinsheimer JS, Carr A, Chapman K (2006) The CALM1 core promoter polymorphism is not associated with hip osteoarthritis in a united Kingdom Caucasian population. Osteoarthritis Cartilage 14(3):295–298
Article PubMed CAS Google Scholar
Rajasekaran S, Kanna RM, Senthil N, Raveendran M, Ranjani V, Cheung KMC et al (2015) Genetic susceptibility of lumbar degenerative disc disease in young Indian adults. Eur Spine J Off Publ Eur Spine Soc Eur Spinal Deform Soc Eur Sect Cerv Spine Res Soc 24(9):1969–1975
Le HV, Wick JB, Van BW, Klineberg EO (2022) Ossification of the posterior longitudinal ligament: pathophysiology, diagnosis, and management. J Am Acad Orthop Surg 30(17):820–830
Comments (0)