Showing 101 - 120 results of 421 for search '"dysplasia"', query time: 0.06s Refine Results
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    Radiographic Measurements and Diagnosis of Hip Dysplasia in Infants Using Computer Vision and a Rule-Based System by Ernesto Pérez Pérez, Roberto Díaz Amador, Karina Leonor Fernández Sánchez, José Julio Requeiro Molina, José Julio Requeiro Morejón

    Published 2022-10-01
    “…<p><strong>Background</strong>: the use of digital radiographs for the diagnosis of developmental dysplasia of the hip allows, in addition to early diagnosis and greater work efficiency, more precise measurements, patient monitoring and surgical planning.…”
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  6. 106

    Maxillonasal dysplasia (Binder's syndrome) and its treatment with costal cartilage graft: A follow-up study by Yogesh C. Bhatt, Kinnari A. Vyas, Mangesh S. Tandale, Nikhil S. Panse, Harpreet S. Bakshi, Rajat K. Srivastava

    Published 2008-04-01
    “…Maxillonasal dysplasia or Binder's syndrome is an uncommon congenital condition characterized by a retruded mid-face with an extremely flat nose. …”
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    The impact of an imperfect vaccine and pap cytologyscreening on the transmission of human papillomavirus and occurrenceof associated cervical dysplasia and cancer by Tufail Malik, Jody Reimer, Abba Gumel, Elamin H. Elbasha, Salaheddin Mahmud

    Published 2013-05-01
    “…., equilibrium in theabsence of HPV and associated dysplasia) is globally-asymptoticallystable if the associated reproduction number is less than unity. …”
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  9. 109

    Transgenerational associations between newborn metabolic profiles and bronchopulmonary dysplasia in neonates born to mothers with an obese phenotype by Jonathan D. Reiss, Wei Yang, Alan L. Chang, Jonathan Z. Long, Ivana Marić, Jochen Profit, Karl G. Sylvester, David K. Stevenson, Nima Aghaeepour, Gary M. Shaw

    Published 2025-01-01
    “…Abstract Maternal obesity increases risk for bronchopulmonary dysplasia (BPD) by up to 42%. Identifying metabolic features that may contribute to the association between maternal pre-pregnancy body mass index (BMI) and BPD is critical in defining the molecular relationship between these conditions. …”
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    Non-Operative Rehabilitation Principles for Use in Individuals with Acetabular Dysplasia: A North American Based Delphi Study by Ashley E. Disantis, RobRoy L. Martin, Keelan Enseki, Victoria Spaid, Michael McClincy

    Published 2023-12-01
    “…# Background Acetabular dysplasia (AD) is defined as a structurally deficient acetabulum and is a well-recognized cause of hip pain in young adults. …”
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    Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases by Virang Kumar, Natario L. Couser, Arti Pandya

    Published 2020-01-01
    “…Oculodentodigital dysplasia (ODDD) is a rare genetic disorder associated with a characteristic craniofacial profile with variable dental, limb, eye, and ocular adnexa abnormalities. …”
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    A Hybrid Oral Rehabilitation of Hypohidrotic Ectodermal Dysplasia: A Conservative Approach with Three-Year Follow-Up by Aryen Kaushik, HarshVardhan Sinha, M. N. Hombesh, Pooja Rani, Taranjeet Kaur

    Published 2021-01-01
    “…This case report presents a 19-year-old male patient with hypohidrotic ectodermal dysplasia, having a chief complaint of multiple missing teeth. …”
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    Prosthodontic Rehabilitation of Hereditary Ectodermal Dysplasia in an 11-Year-Old Patient with Flexible Denture: A Case Report by Neha Jain, Dinesh Naitam, Arti Wadkar, Anuradha Nemane, Shiva Katoch, Ashish Dewangan

    Published 2012-01-01
    “…Hereditary ectodermal dysplasia is a rare group of inherited disorders characterized by aplasia or dysplasia of two or more tissues of ectodermal origin such as hair, nails, teeth, and skin. …”
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    Clinical Diagnosis of X-Linked Spondyloepiphyseal Dysplasia Tarda and a Novel Missense Mutation in the Sedlin Gene (SEDL) by Lei Kong, Dongxu Wang, Shanshan Li, Chengsheng Zhang, Xiuyun Jiang, Qingbo Guan, Zhenlin Zhang, Fei Jing, Jin Xu

    Published 2018-01-01
    “…Objective. Spondyloepiphyseal dysplasia tarda (SEDT) is a rare hereditary bone disease characterized by spinal and epiphyseal anomalies. …”
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