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Journal of Pediatric Orthopaedics B, ISSN 1060-152X, 09/2019, Volume 28, Issue 5, pp. 505 - 508
Osteogenesis imperfecta (OI) is a genetic disorder characterized by fragile bones. It is our aim to illustrate variability in clinical presentation of severe... 
Case studies | Osteogenesis imperfecta | Care and treatment | Pediatric research | Osteotomy | Methods
Journal Article
Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 09/2017, Volume 50, Issue S1, pp. 182 - 182
Journal Article
BDJ open, ISSN 2056-807X, 2017, Volume 3, Issue 1, p. 17021
Osteogenesis imperfecta type III (OMIM 259420) is a severe autosomal recessive disorder. Affected individuals have multiple fractures, develop limb deformities... 
Hypoplasia | Mandible | Swallowing | Hereditary diseases | Literature reviews | Radiography | Fractures | Computed tomography | Sinus | Osteogenesis imperfecta | Skull | Palate | Bone matrix | Bone (cortical) | Osteogenesis
Journal Article
South African Medical Journal, ISSN 0256-9574, 06/2016, Volume 106, Issue 6, pp. S90 - S93
Individuals with osteogenesis imperfecta type III (OI III) are severely physically disabled due to frequent fracturing. Their disability poses numerous... 
MEDICINE, GENERAL & INTERNAL | Fractures, Bone - etiology | Social Behavior | Humans | Osteogenesis Imperfecta - epidemiology | South Africa - epidemiology | Fractures, Bone - epidemiology | Osteogenesis Imperfecta - physiopathology
Journal Article
Journal of Pediatric Orthopaedics B, ISSN 1060-152X, 03/2019, Volume 28, Issue 2, pp. 179 - 185
Osteogenesis imperfecta (OI) is a rare congenital osteodystrophy. Patients with OI present with osteoporosis, extreme bone fragility and severe deformities of... 
MANAGEMENT | treatment of deformities | ROD | LOWER-LIMBS | osteotomies | minimally invasive | osteogenesis imperfecta | CHILDREN | Sofield-Millar technique | ADOLESCENTS | SOFIELD-MILLAR OPERATION | PEDIATRICS | Fassier-Duval nail | EXPERIENCE | BONE | ORTHOPEDICS | surgery
Journal Article
Egyptian Journal of Medical Human Genetics, ISSN 1110-8630, 04/2016, Volume 17, Issue 2, pp. 197 - 200
Osteogenesis imperfecta is a genetic disorder of bones, which has different types. Type III is characterized by recurrent fractures, progressive bone... 
Osteogenesis imperfecta | Ventricular function | ECHO | Cardiac function | Osteogenesis imperfecta type III | Extra skeletal abnormalities | Genetic aspects
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2001, Volume 69, Issue 5, pp. 989 - 1001
Journal Article
Journal of Biomedical Materials Research Part A, ISSN 1549-3296, 10/2006, Volume 79A, Issue 1, pp. 71 - 77
Journal Article
A & A case reports, ISSN 2325-7237, 07/2017, Volume 9, Issue 2, pp. 60 - 63
Osteogenesis imperfecta (OI) is a rare disabling genetic connective tissue disorder. General anesthesia in these patients is associated with increased risks.... 
Conscious Sedation - methods | Anesthesia, Epidural - methods | Osteotomy | Anesthesia, Spinal - methods | Humans | Dexmedetomidine | Female | Hypnotics and Sedatives | Child | Osteogenesis Imperfecta - surgery
Journal Article
Journal Article