- Bizarre Parosteal Osteochondromatous Proliferation (Nora's lesion) of the Big Toe. (A Report of Two Cases and Review)
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Kim SW, Suh JH, Shin SM, Cho BK
- KMID: 1428848
- J Korean Foot Ankle Soc.
- 2013 Mar;17(1):68-73.
Bizarre parosteal osteochondromatous proliferation (BPOP) is an rare benign tumor which involve mostly tubular bones of feet and hand. BPOP has clinical, radiographic, and histologic similarities with osteochondroma.Radiologically, BPOP has... -
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- A prospective longitudinal study of normal reference ranges for the length of fetal limb bones by ultrasound examination
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Kang WS, Park KH, Hong JS, Shin DM, Park HS
- KMID: 2273313
- Korean J Obstet Gynecol.
- 2008 Mar;51(3):297-304.
OBJECTIVE: To establish the reference ranges for the length of fetal limb bones (femur, tibia, fibula, humerus, ulna, radius, foot) at 12 to 38 weeks' gestation. METHODS: The candidates of this... -
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- Pyogenic Osteomyelitis with Multiple Lesions
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Lee HK, Kim YM, Bae DK, Chung MS
- KMID: 2471464
- J Korean Orthop Assoc.
- 1974 Dec;9(4):411-417.
- doi: 10.4055/jkoa.1974.9.4.411
Sixteen cases of pyogenic osteomyelitis with multiple lesions were observed in the Department of Orthopedic Surgery, Seoul National University Hospital during the last 9 years. Multiple osteomyelitis occured in male... -
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- 99mTc-HDP Pinhole SPECT Findings of Foot Reflex Sympathetic Dystrophy: Radiographic and MRI Correlation and a Speculation about Subperiosteal Bone Resorption
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Kim SH, Chung SK, Bahk YW, Chung YA, Song KS
- KMID: 1130043
- J Korean Med Sci.
- 2003 Oct;18(5):707-714.
- doi: 10.3346/jkms.2003.18.5.707
Reflex sympathetic dystrophy (RSD) is a common rheumatic disorder manifesting painful swelling, discoloration, stiffening and atrophy of the skin. Radiographic alterations include small, spotty subperiosteal bone resorption (SBR) and diffuse... -
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- First Korean Family with a Mutation in TPM2 Associated with Sheldon-Hall Syndrome
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Ko JM, Choi IH, Baek GH, Kim KW
- KMID: 1777569
- J Korean Med Sci.
- 2013 May;28(5):780-783.
- doi: 10.3346/jkms.2013.28.5.780
Sheldon-Hall syndrome (SHS) is a rare autosomal dominant, inherited arthrogryposis syndrome characterized by multiple congenital contractures of the distal limbs. To date, four genes that encode the skeletal muscle fiber... -
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