about
Autism-like socio-communicative deficits and stereotypies in mice lacking heparan sulfateUnsuspected osteochondroma-like outgrowths in the cranial base of Hereditary Multiple Exostoses patients and modeling and treatment with a BMP antagonist in mice.Enigmatic cranial superstructures among Chamorro ancestors from the Mariana Islands: gross anatomy and microanatomy.A mouse model of chondrocyte-specific somatic mutation reveals a role for Ext1 loss of heterozygosity in multiple hereditary exostoses.Molecular, phenotypic aspects and therapeutic horizons of rare genetic bone disorders.Solitary thoracic osteochondroma presenting as Brown-Séquard syndrome.The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in Hereditary Multiple Exostoses: insights into pathogenesis.Subacromial impingement syndrome in a patient with hereditary multiple exostosis: a case report.Glycobiology and the growth plate: current concepts in multiple hereditary exostosesDevelopmental pattern of the hip in patients with hereditary multiple exostoses.Osteochondroma: ignore or investigate?Identification of a rare case of intra-articular osteochondroma manifesting as three loose bodies in a patient with hereditary multiple osteochondromas: A case report.Multiple osteochondroma of the hand: initial and long-term follow-up study.Eccentric Training as an Adjunct to Rehabilitation Program for Hereditary Multiple Exostoses: A Case Report.NFAT restricts osteochondroma formation from entheseal progenitorsFactors affecting outcomes in patients treated surgically for upper extremity tumors and tumor-like lesions.Identification of a novel mutation in the EXT1 gene from a patient with multiple osteochondromas by exome sequencing.Autologous Fat Grafting as a Last Resort for Unsustainable Pain in a Woman with Multiple OsteochondromasMultimodality imaging features of hereditary multiple exostosesAn Osteological Study on the Prevalence of Osteochondromas.Hereditary Multiple Exostoses: New Insights into Pathogenesis, Clinical Complications, and Potential Treatments.Aberrant perichondrial BMP signaling mediates multiple osteochondromagenesis in miceCervical osteochondroma presenting as brown-sequard syndrome in a child with hereditary multiple exostosisMultiple hereditary exostoses and stroke due to vertebral artery dissection.Secondary Chondrosarcoma of the Lumbosacral Region: Are any Bones Spared in the Multiple Hereditary Exostoses?Bilateral total hip arthroplasty in a young man with hereditary multiple exostoses.A genotype-phenotype study of hereditary multiple exostoses in forty-six Chinese patients.The pathogenic roles of heparan sulfate deficiency in hereditary multiple exostoses.Palovarotene Inhibits Osteochondroma Formation in a Mouse Model of Multiple Hereditary Exostoses.Osteoblastic heparan sulfate regulates osteoprotegerin function and bone mass.Novel exostosin-2 mutation identified in a Chinese family with hereditary multiple osteochondroma.Total knee arthroplasty in patients with multiple hereditary exostoses
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մարտին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Manifestations of hereditary multiple exostoses.
@ast
Manifestations of hereditary multiple exostoses.
@en
Manifestations of hereditary multiple exostoses.
@nl
type
label
Manifestations of hereditary multiple exostoses.
@ast
Manifestations of hereditary multiple exostoses.
@en
Manifestations of hereditary multiple exostoses.
@nl
prefLabel
Manifestations of hereditary multiple exostoses.
@ast
Manifestations of hereditary multiple exostoses.
@en
Manifestations of hereditary multiple exostoses.
@nl
P1476
Manifestations of hereditary multiple exostoses.
@en
P2093
John P Dormans
Jonathan R Stieber
P304
P577
2005-03-01T00:00:00Z