Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Christine M. Alvarez"'
Autor:
Tim Bhatnagar, Lise Leveille, Christine M. Alvarez, Diane Wickenheiser, Kishore Mulpuri, Alec Black, Frances Scheepers, Karen R. Davies
Publikováno v:
Abstracts of the 26th Annual Meeting of the GCMAS.
Publikováno v:
The Journal of bone and joint surgery. American volume. 100(18)
Background Congenital idiopathic clubfoot is a condition that affects, on average, approximately 1 in 1,000 infants. One broadly adopted method of management, described by Ponseti, is the performance of a percutaneous complete tenotomy when hindfoot
Publikováno v:
Journal of Children's Orthopaedics
Background The manipulations, casts, and Botox® method for treating idiopathic clubfoot is an alternative non-surgical treatment method. Botox®-induced reversible muscle paralysis of the gastrocsoleus enables a physician to manipulate and cast the
Publikováno v:
European Journal of Paediatric Neurology. 18:171-175
Background Pediatric indications for Onabotulinumtoxin A ® extend beyond treatment of skeletal muscle conditions. Each of the indications for Onabotulinumtoxin A ® use have adverse events reported in the past. The aim of this study was to review dv
Publikováno v:
Handbook of Human Motion ISBN: 9783319308081
Handbook of Human Motion
Handbook of Human Motion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::245e67cebd548465583bdd631d95f380
https://doi.org/10.1007/978-3-319-30808-1_60-1
https://doi.org/10.1007/978-3-319-30808-1_60-1
Autor:
B. S. Richards, Maya Vella, Nadav Ahituv, Frederick R. Dietz, Carlos A. Bacino, W. Lu, Susan H. Blanton, Christine M. Alvarez, Jacqueline T. Hecht, N. Sikka, Julia E. VanderMeer
Publikováno v:
American Journal of Medical Genetics Part A. :1620-1627
Clubfoot is a common birth defect characterized by inward posturing and rigid downward displacement of one or both feet. The etiology of syndromic forms of clubfoot is varied and the causes of isolated clubfoot are not well understood. A microduplica
Publikováno v:
Journal of Pediatric Orthopaedics. 32:210-214
Hereditary multiple exostoses (HME) is a rare genetic disorder, which can be associated with severe complications that may significantly affect the health-related quality of life (HRQL). Our primary objective was to describe the baseline HRQL in HME
Autor:
Michael J. Bamshad, Douglas Barnes, Christine M. Alvarez, Jacqueline T. Hecht, Katelyn S. Weymouth, Matthew B. Dobbs, Anita E. Beck, Susan H. Blanton, Laura E. Mitchell, Christina A. Gurnett, Steve Richards
Publikováno v:
American Journal of Medical Genetics Part A. 155:2170-2179
Isolated clubfoot is a relatively common birth defect that affects approximately 4,000 newborns in the US each year. Calf muscles in the affected leg(s) are underdeveloped and remain small even after corrective treatment. This observation suggests th
Autor:
Christine M. Alvarez, Jacqueline T. Hecht, B. Stephen Richards, Katelyn S. Weymouth, Susan H. Blanton, Douglas Barnes, Amy Sommer
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 91:20-28
Isolated clubfoot is a common orthopedic birth defect that affects approximately 135,000 newborns worldwide. It is characterized by ankle equinus, hindfoot varus, and forefoot adductus. Although numerous studies suggest a multifactorial etiology, the
Publikováno v:
Clinical Orthopaedics & Related Research. 462:73-79
Hereditary multiple exostosis (HME) is an autosomal dominant condition resulting predominantly from mutations in the exostosin 1 (EXT1) and exostosin 2 (EXT2) genes. We asked two questions in our study: first, what is the anatomic burden of subjects