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Journal Abstract Search

124 related items for PubMed ID: 37940834

  • 1.
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  • 2. Pediatric cervical kyphosis in the MRI era (1984-2008) with long-term follow up: literature review.
    Menezes AH, Traynelis VC.
    Childs Nerv Syst; 2022 Feb; 38(2):361-377. PubMed ID: 34806157
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  • 3. Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures".
    Costantini A, Valta H, Baratang NV, Yap P, Bertola DR, Yamamoto GL, Kim CA, Chen J, Wierenga KJ, Fanning EA, Escobar L, McWalter K, McLaughlin H, Willaert R, Begtrup A, Alm JJ, Reinhardt DP, Mäkitie O, Campeau PM.
    Bone; 2019 Apr; 121():163-171. PubMed ID: 30599297
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  • 5. Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies.
    Machol K, Jain M, Almannai M, Orand T, Lu JT, Tran A, Chen Y, Schlesinger A, Gibbs R, Bonafe L, Campos-Xavier AB, Unger S, Superti-Furga A, Lee BH, Campeau PM, Burrage LC.
    Am J Med Genet A; 2017 Mar; 173(3):733-739. PubMed ID: 27888646
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  • 8. The Managment of cervical spine abnormalities in children with spondyloepiphyseal dysplasia congenita: Observational study.
    Al Kaissi A, Ryabykh S, Pavlova OM, Ochirova P, Kenis V, Chehida FB, Ganger R, Grill F, Kircher SG.
    Medicine (Baltimore); 2019 Jan; 98(1):e13780. PubMed ID: 30608389
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  • 9. Automated reanalysis, a novel way to diagnose an ultra-rare condition: Fibronectin-1-related spondylometaphyseal dysplasia (SMD-FN1).
    Sabir AH, Singhal J, Man J, Mensah NE, Ahn JW, Cheung MS, Irving M.
    Clin Dysmorphol; 2021 Jul 01; 30(3):154-158. PubMed ID: 33605604
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  • 12. Mechanistic insights into the cellular effects of a novel FN1 variant associated with a spondylometaphyseal dysplasia.
    Cadoff EB, Sheffer R, Wientroub S, Ovadia D, Meiner V, Schwarzbauer JE.
    Clin Genet; 2018 Nov 01; 94(5):429-437. PubMed ID: 30051459
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  • 13. Cervical myelopathy involving os odontoideum and retro-odontoid cyst treated with Harms C1-C2 arthrodesis.
    Le Pape S, Gauthé R, Latrobe C, Leroux J, Roussignol X, Ould-Slimane M.
    Orthop Traumatol Surg Res; 2016 Oct 01; 102(6):817-20. PubMed ID: 27475720
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  • 15. Balloon kyphoplasty and additional anterior odontoid screw fixation for treatment of unstable osteolytic lesions of the vertebral body C2: a case series.
    Voelker A, von der Hoeh NH, Heyde CE.
    BMC Musculoskelet Disord; 2018 Jul 27; 19(1):259. PubMed ID: 30049274
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  • 16. Spondylometaphyseal dysplasia, Sutcliffe type: a rediscovered entity.
    Kozlowski K, Napiontek M, Beim ER.
    Can Assoc Radiol J; 1992 Oct 27; 43(5):364-8. PubMed ID: 1393702
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  • 18. Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: a case report.
    Chen J, Ma X, Zhou Y, Li G, Guo Q.
    BMC Pediatr; 2017 Jul 24; 17(1):175. PubMed ID: 28738883
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  • 19. Spondylometaphyseal dysplasia, corner fracture type: a heritable condition associated with coxa vara.
    Langer LO, Brill PW, Ozonoff MB, Pauli RM, Wilson WG, Alford BA, Pavlov H, Drake DG.
    Radiology; 1990 Jun 24; 175(3):761-6. PubMed ID: 2343127
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  • 20. Cervical Instability and Quadriparesis Requiring Stabilization in Pediatric Patient Caused by a Mutation in COL2A1.
    Pandey A, Giantini-Larsen A, Greenfield JP.
    World Neurosurg; 2023 Aug 24; 176():159-160. PubMed ID: 37141942
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