Results 41 to 50 of about 43,622 (268)

Hip Joint Osteochondroma: Systematic Review of the Literature and Report of Three Further Cases

open access: yesAdvances in Orthopedics, 2014
The aim of this study is to systematically review the literature with regards to surgical treatment of patients with hip joint osteochondromas, and to report our surgical management of three paediatric patients who had femoral neck or acetabular ...
Asim M. Makhdom   +5 more
doaj   +1 more source

Hip Ultrasonography in the Diagnosis of Developmental Dysplasia of the Hip: Bakırköy Experience

open access: yesHaseki Tıp Bülteni, 2014
Aim: The purpose of the study was to determine the prevalence, incidence, and etiology as well as the risk factors for developmental dysplasia of the hip in newborns in whom we performed ultrasonography for screening using Graff’s method in our clinic ...
Altuğ Duramaz   +5 more
doaj   +1 more source

Birmingham Royal Orthopaedic Hospital (BROH) Femoral Offset—An Ancillary Measure of Adult Dysplasia of the Hip

open access: yesIndian Journal of Radiology and Imaging, 2023
Introduction Adult dysplasia of the hip (ADH) is a disorder of abnormal development of the hip joint resulting in a shallow acetabulum and uncovering of the femoral head.
Karthikeyan P. Iyengar   +7 more
doaj   +1 more source

Triple pelvic osteotomy as treatment for osteoarthritis secondary to developmental dysplasia of the hip [PDF]

open access: yes, 2018
Joint-preserving osteotomies are an established treatment for adult hip pain secondary to developmental dysplasia of the hip. However, their value for advanced osteoarthritis is unclear. Therefore this study addresses the question of long-term results of
Janssen, Dirk   +2 more
core  

Return to Sport and Athletic Function in an Active Population After Primary Arthroscopic Labral Reconstruction of the Hip [PDF]

open access: yes, 2020
Background: Labral reconstruction has been advocated as an alternative to debridement for the treatment of irreparable labral tears, showing favorable short-term results.
Chen, Sarah L.   +7 more
core   +1 more source

Approaches to canine health surveillance [PDF]

open access: yes, 2014
Effective canine health surveillance systems can be used to monitor disease in the general population, prioritise disorders for strategic control and focus clinical research, and to evaluate the success of these measures.
Brodbelt, D C   +5 more
core   +2 more sources

The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley   +1 more source

Total hip arthroplasty for developmental hip dysplasia [PDF]

open access: yesInternational Orthopaedics, 2005
We reviewed 38 hip replacements in 33 female patients (mean age 55.3 years) with developmental hip dysplasia. One patient had died and the remaining 32 patients (36 hips) had a mean follow-up of 12.2 years (range 8-19 years). All hips were replaced using the Müller cemented implant, and in 32 hips bulk femoral head autograft was used.
Papachristou, G   +6 more
openaire   +3 more sources

Outerbridge grade IV cartilage lesions in the hip identified at arthroscopy [PDF]

open access: yes, 2017
No abstract ...
McLean, Michael   +2 more
core   +1 more source

KDM2B‐Related Neurodevelopmental Disorder A Case‐Series Supporting the CxxC Domain Phenotype With Emphasis on Ocular and Dermatologic Features

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes   +3 more
wiley   +1 more source

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