Results 161 to 170 of about 16,131 (205)

Distinction Between Dysplasia, Malformation, and Deformity-Towards the Proper Diagnosis and Treatment of Hip Development Disorders. [PDF]

Diagnostics (Basel)
Dygut J, Piwowar M.
europepmc   +1 more source

Universal Hip Ultrasound Screening in Newborns: A 21-Month Prospective Observational Study in a Spoke Center. [PDF]

Med Sci (Basel)
Ragusa N, Gianotto NR, Deut V, Mattivi C, Compagno F, Cherubini Scarafoni M, Dominici S, Berger M.   +7 more
europepmc   +1 more source

Impact of hip dislocation on the development of the hip joint and femoral trochlear in rats: an in vivo study. [PDF]

Am J Transl Res
Wang S, Li M, Liu B, Liu Z, Zhang N, Dong G.   +5 more
europepmc   +1 more source

Super-resolution ultrasound imaging reveals microvascular alterations in joint capsule of dysplastic hip: a rabbit model study. [PDF]

BMC Musculoskelet Disord
Wan J, Qiao Y, Lv P, Hong K, Ye L, Wang J, Zhang C.   +6 more
europepmc   +1 more source

Indications and Outcomes of Total Hip Arthroplasty in Patients Aged 15 to 45 years. [PDF]

J Am Acad Orthop Surg Glob Res Rev
Ratnasamy PP, Gouzoulis MJ, Kaszuba SV, Rudisill KE, Vasudevan RS, Grauer JN, Rubin LE.   +6 more
europepmc   +1 more source

Congenital dislocation of the hip

Journal of British Surgery, 1939
openaire   +1 more source

Multilevel congenital lumbar facet joint aplasia presenting with L5-S1 spondylolisthesis in a patient with connective tissue disease. [PDF]

Surg Neurol Int
Lam VH, Lozano CS, Kassay AD, He Y, Ginsberg HJ.   +4 more
europepmc   +1 more source

Current Trends and Future Directions in the Diagnosis and Management of Pediatric Orthopedic Disorders. [PDF]

Cureus
Al-Rumaih MH, Al-Otaibi AF, Almukhlafi TS.   +2 more
europepmc   +1 more source

Anatomical alignment of the acetabular component using transverse acetabular ligament in total hip replacement: a prospective cohort study. [PDF]

Sci Rep
Nguyen DH, Nguyen TT, Dang VH, Nguyen BH, Le KT, Pham ST, Bui NH, Le VN, Vu DN, Tran TD, Vo HL.   +10 more
europepmc   +1 more source

c.7156C > T p.(Gln2386*) variant causes loss-of-function of the USP9X gene in a female-restricted X-linked syndromic intellectual disability: a case report. [PDF]

J Med Case Rep
da Silva Campos TA, Bernardes AH, Pinto IP, da Silva Teixeira HA, da Silva JF, do Prado Santos VC, Zatarin R, da Cruz AD.   +7 more
europepmc   +1 more source