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Quoted phrase not found in phrase index: "Epiphyseal deformities of tubular bones"
Page 1
Hypophosphatemic rickets due to perturbations in renal tubular function.
Penido MG, Alon US. Penido MG, et al. Pediatr Nephrol. 2014 Mar;29(3):361-73. doi: 10.1007/s00467-013-2466-z. Epub 2013 May 1. Pediatr Nephrol. 2014. PMID: 23636577 Review.
The common denominator for all types of rickets is hypophosphatemia, leading to inadequate supply of the mineral to the growing bone. Hypophosphatemia can result from insufficient uptake of the mineral from the gut or its disproportionate losses in the kidney, the latter b …
The common denominator for all types of rickets is hypophosphatemia, leading to inadequate supply of the mineral to the growing bone. …
Three cases of Japanese acromicric/geleophysic dysplasia with FBN1 mutations: a comparison of clinical and radiological features.
Hasegawa K, Numakura C, Tanaka H, Furujo M, Kubo T, Higuchi Y, Yamashita M, Tsukahara H. Hasegawa K, et al. J Pediatr Endocrinol Metab. 2017 Jan 1;30(1):117-121. doi: 10.1515/jpem-2016-0258. J Pediatr Endocrinol Metab. 2017. PMID: 27935852
Compared with GD, AD presents with milder clinical and radiological features. Radiological findings of AD and GD consist of shortened tubular bones of the hands and feet, and deformed capital femoral epiphyses. ...Our patients, harboring FBN1 mutations …
Compared with GD, AD presents with milder clinical and radiological features. Radiological findings of AD and GD consist of shortened tub
Epiphyseal-metaphyseal enchondromatosis. A new clinical entity.
Gabos PG, Bowen JR. Gabos PG, et al. J Bone Joint Surg Am. 1998 Jun;80(6):782-92. doi: 10.2106/00004623-199806000-00002. J Bone Joint Surg Am. 1998. PMID: 9655096
We reviewed the cases of eight unrelated children who had an unusual form of enchondromatosis characterized by unilateral enchondromas arising within the epiphyseal and metaphyseal regions of the long tubular bones of the lower extremity. Unlike previously de …
We reviewed the cases of eight unrelated children who had an unusual form of enchondromatosis characterized by unilateral enchondromas arisi …
Preossified longitudinal epiphyseal bracket of the foot: treatment by partial bracket excision before ossification.
Shea KG, Mubarak SJ, Alamin T. Shea KG, et al. J Pediatr Orthop. 2001 May-Jun;21(3):360-5. J Pediatr Orthop. 2001. PMID: 11371821
The longitudinal epiphyseal bracket is a rare ossification defect of tubular bones in the hand and foot. This deformity contains an abnormal secondary ossification center, which may lead to progressive shortening and angular deformity of involve …
The longitudinal epiphyseal bracket is a rare ossification defect of tubular bones in the hand and foot. This deform
Correction of longitudinal epiphyseal bracket disease with external fixation: a case report with 6-year follow-up period.
Scott RT, Kissel C, Miller A. Scott RT, et al. J Foot Ankle Surg. 2011 Nov-Dec;50(6):714-7. doi: 10.1053/j.jfas.2011.04.038. Epub 2011 Jun 14. J Foot Ankle Surg. 2011. PMID: 21664835
Longitudinal epiphyseal bracket disease is a rare congenital abnormality of the tubular bones. This syndrome eventually leads to progressive shortening and angular deformity of the involved bone. When longitudinal epiphyseal bracke …
Longitudinal epiphyseal bracket disease is a rare congenital abnormality of the tubular bones. This syndrome eve …
Swedish metacarpophalangeal standards compared with previously published norms.
Laurencikas E, Rosenborg M. Laurencikas E, et al. Acta Radiol. 2000 Sep;41(5):498-502. doi: 10.1080/028418500127345785. Acta Radiol. 2000. PMID: 11016775
MATERIAL AND METHODS: A group of healthy Swedish children was followed longitudinally from the age of 1 month to 18 years. The length of the tubular bones of the hand was measured on radiographs. In addition to the conventional measurements including epiphyses
MATERIAL AND METHODS: A group of healthy Swedish children was followed longitudinally from the age of 1 month to 18 years. The length of the …
New form of platyspondylic lethal chondrodysplasia.
Akaba K, Nishimura G, Hashimoto M, Wakabayashi T, Kanasugi H, Hayasaka K. Akaba K, et al. Am J Med Genet. 1996 Dec 30;66(4):464-7. doi: 10.1002/(SICI)1096-8628(19961230)66:4<464::AID-AJMG16>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8989469
Laryngoscopy and neck CT disclosed laryngeal stenosis, and brain CT demonstrated hypoplasia of the corpus callosum. Skeletal survey demonstrated hypoplasia of facial bones and short skull base, extremely severe platyspondyly, hypoplastic ilia, and delayed epiphyseal
Laryngoscopy and neck CT disclosed laryngeal stenosis, and brain CT demonstrated hypoplasia of the corpus callosum. Skeletal survey demonstr …