Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Reggie Hamdy"'
Autor:
David T. Bertrand, Ruisen Fu, Kyle Kavaseri, Isabelle Villemure, Frank Rauch, Reggie Hamdy, Haisheng Yang, Bettina M. Willie
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract Distraction osteogenesis (DO) is a valuable surgical method for limb lengthening and bone defect correction, but its lengthy consolidation phase presents challenges. The accordion technique (AT), involving compression and distraction of bone
Externí odkaz:
https://doaj.org/article/ba98f96f2d7a4bb8bed0b4a9ef05a84f
Ophthalmological screening guidelines for individuals with Osteogenesis Imperfecta: a scoping review
Autor:
Sarah Moussa, Jasmine Rocci, Reggie Hamdy, Jakob Grauslund, Marie-Louise Lyster, Argerie Tsimicalis
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Osteogenesis imperfecta (OI) is a connective tissue disorder in which the Type 1 collagen is defective. The eye is a structure rich in collagen Type 1 and is heavily impacted by the disease. Many vision-threatening eye diseases ha
Externí odkaz:
https://doaj.org/article/eb79491e127b4c4c97c6f093663c185d
Autor:
Argerie Tsimicalis, Jennifer Stinson, Kelly Thorstad, Frank Rauch, Reggie Hamdy, Khadidja Chougui, Sofia Addab, Telma Palomo, Mitchell Bernstein, Noemi Dahan-Oliel, Louis-Nicolas Veilleux, Laura Massochin Nunes Pinto, Raissa Passos dos Santos
Publikováno v:
JMIR Research Protocols, Vol 12, p e47524 (2023)
BackgroundInnovative approaches are needed to address the self-management needs of youths with osteogenesis imperfecta (OI) transitioning into adult-oriented health care systems. Using a sequentially phased research approach, the goal is to design, d
Externí odkaz:
https://doaj.org/article/4b66ad13bc4148f18a211fa9904c04c5
Autor:
Josephine T. Tauer, Hadil Al-Jallad, Mayumi Umebayashi, Dena Bakhsh, Damian Rauch, Simon D. Tran, Frank Rauch, Reggie Hamdy
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract Pediatric patients with Osteogenesis Imperfecta (OI), a heritable connective tissue disorder, frequently suffer from long bone deformations. Surgical correction often results in bone non-unions, necessitating revision surgery with autogenous
Externí odkaz:
https://doaj.org/article/7e7d0b830fd74be392b333996d84d02c
Autor:
Sofia Addab, Stephanie Thierry, Marie-Elaine Lafrance, Sunny Jeong, Jennifer Brown, Carter Brown, Sylvie-Anne Plourde, Angela Gugliotti, Kelly Thorstad, Reggie Hamdy, Frank Rauch, Argerie Tsimicalis
Publikováno v:
McGill Journal of Medicine, Vol 20, Iss 1 (2022)
Background: Children with osteogenesis imperfecta (OI) live in fear of fracturing a bone. As fractures are unpredictable, there is a need for tools and knowledge to immobilize a fracture during emergencies. Inspired by a patient recognized in their l
Externí odkaz:
https://doaj.org/article/0ecc061a46d147e7b1f38c5332499ec5
Autor:
Marianne Gagnon, Gabriela Marino Merlo, Rita Yap, Jessica Collins, Caroline Elfassy, Bonita Sawatzky, Jacquelyn Marsh, Reggie Hamdy, Louis-Nicolas Veilleux, Noémi Dahan-Oliel
Publikováno v:
Journal of Medical Internet Research, Vol 23, Iss 7, p e27064 (2021)
BackgroundArthrogryposis multiplex congenita (AMC) is characterized by joint contractures and muscle weakness, which limit daily activities. Youths with AMC require frequent physical therapeutic follow-ups to limit the recurrence of contractures and
Externí odkaz:
https://doaj.org/article/ae8de5931b764562ab3b11967ea37b3d
Autor:
Hemant Sharma, Kim Cocks, Joel Gagnier, Paul Harwood, David Ferguson, Reggie Hamdy, Nando Ferriera
Publikováno v:
BMJ Open, Vol 10, Iss 12 (2020)
Introduction Lower limb conditions requiring reconstructive surgery can be either congenital or acquired from trauma, infection or other medical conditions. Patient-reported outcome measures (PROMs) are often used by healthcare professionals to asses
Externí odkaz:
https://doaj.org/article/6eaa1f96edaf4371a4032a5bbd11fab0
Autor:
Yasir Alabdulkarim, Bayan Ghalimah, Mohammad Al-Otaibi, Hadil F Al-Jallad, Mina Mekhael, Bettina Willie, Reggie Hamdy
Publikováno v:
Journal of Limb Lengthening & Reconstruction, Vol 3, Iss 1, Pp 4-18 (2017)
The management of large bone defects, atrophic nonunions, and other conditions with poor bone formation presents a formidable challenge to the treating physician, as all available techniques of bone reconstruction have drawbacks. Recent advances in s
Externí odkaz:
https://doaj.org/article/ac742b0db59b41a790341a72f4fc3c3e
Slipped capital femoral epiphysis in a healthy 5-year-old child: A case report and literature review
Publikováno v:
Saudi Journal of Medicine and Medical Sciences, Vol 2, Iss 2, Pp 117-119 (2014)
Slipped capital femoral epiphysis (SCFE) is an adolescent hip disorder of increasing prevalence, particularly within patients aged younger than 10 years. When present in these younger patients, SCFE is usually associated with metabolic abnormality or
Externí odkaz:
https://doaj.org/article/648503cd53f5480c839c056c80120892
Publikováno v:
International Journal of Pediatrics, Vol 2012 (2012)
Children with musculoskeletal conditions experience muscle weakness, difficulty walking and limitations in physical activities. Standard treatment includes physiotherapy, casting, and surgery. The use of botulinum toxins appears as a promising treatm
Externí odkaz:
https://doaj.org/article/d1dbccf42d014757a77a637599194f1a