Published in J Coll Physicians Surg Pak on November 01, 2010
Natural history and treatment of fibrous dysplasia of bone: a multicenter clinicopathologic study promoted by the European Pediatric Orthopaedic Society. J Pediatr Orthop B (2003) 1.78
Screening for developmental hip dysplasia (DDH)-clinically or sonographically? Comments to the current discussion and proposals. Pediatr Radiol (2012) 1.40
Radiographic evaluation of idiopathic clubfeet undergoing Ponseti treatment. J Bone Joint Surg Am (2007) 1.17
Accuracy of complex lower-limb deformity correction with external fixation: a comparison of the Taylor Spatial Frame with the Ilizarov ring fixator. J Child Orthop (2006) 1.16
Dysplasia of the cruciate ligaments: radiographic assessment and classification. J Bone Joint Surg Am (2006) 1.15
Does open reduction of the developmental dislocated hip increase the risk of osteonecrosis? Clin Orthop Relat Res (2011) 1.07
Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome. J Neurol Sci (2007) 1.04
Correction of post-traumatic lower limb deformities using the Taylor spatial frame. Int Orthop (2009) 1.00
Persistent torticollis, facial asymmetry, grooved tongue, and dolicho-odontoid process in connection with atlas malformation complex in three family subjects. Eur Spine J (2007) 0.98
External fixation in clubfoot treatment - a review of the literature. J Pediatr Orthop B (2012) 0.93
Hypohidrotic ectodermal dysplasia with tibial aplasia. Clin Dysmorphol (2002) 0.93
Spinal and pelvic corrections in a patient with spondylocostal dysplasia syndrome and hemimyelomeningocele. Afr J Paediatr Surg (2014) 0.92
Atlanto-axial segmentation defects and os odontoideum in two male siblings with opsismodysplasia. Skeletal Radiol (2008) 0.91
Deformity correction in children with hereditary hypophosphatemic rickets. Clin Orthop Relat Res (2008) 0.91
Asymmetrical skull, ptosis, hypertelorism, high nasal bridge, clefting, umbilical anomalies, and skeletal anomalies in sibs: is Carnevale syndrome a separate entity? Am J Med Genet A (2007) 0.90
A novel form of ischio-vertebral syndrome. Skeletal Radiol (2006) 0.90
Torsional profile versus gait analysis: consistency between the anatomic torsion and the resulting gait pattern in patients with rotational malalignment of the lower extremity. Gait Posture (2010) 0.89
Magnetic resonance evaluation of acetabular residual dysplasia in developmental dysplasia of the hip: a preliminary study of 27 patients. J Pediatr Orthop (2009) 0.89
Early results of the Ponseti method using the Steenbek foot abduction brace: a prospective study of 95 feet. J Pediatr Orthop B (2008) 0.89
Osteochondritis dissecans and Osgood Schlatter disease in a family with Stickler syndrome. Pediatr Rheumatol Online J (2009) 0.88
Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndrome. Orphanet J Rare Dis (2007) 0.88
Caudal regression syndrome and popliteal webbing in connection with maternal diabetes mellitus: a case report and literature review. Cases J (2008) 0.87
Windswept lower limb deformities in patients with hypophosphataemic rickets. Swiss Med Wkly (2013) 0.87
Treatment options for developmental dislocation of the hip after walking age. J Pediatr Orthop B (2005) 0.85
Treatment of varus deformities of the lower limbs in patients with achondroplasia and hypochondroplasia. Open Orthop J (2013) 0.85
Craniovertebral malformation complex in a child with Weismann-Netter-Stuhl syndrome. J Pediatr (Rio J) (2006) 0.83
The management of knee dislocation in a child with Larsen syndrome. Clinics (Sao Paulo) (2011) 0.83
Mutations at Ser331 in the HSN type I gene SPTLC1 are associated with a distinct syndromic phenotype. Eur J Med Genet (2013) 0.83
Pharmacological management of aseptic osteonecrosis in children. Expert Opin Pharmacother (2004) 0.82
Significant ophthalmoarthropathy associated with ectodermal dysplasia in a child with Marshall-Stickler overlap: a case report. Cases J (2008) 0.82
Sonographic classification of idiopathic clubfoot according to severity. J Pediatr Orthop B (2006) 0.82
The diagnosis and management of patients with idiopathic osteolysis. Pediatr Rheumatol Online J (2011) 0.81
Occipitoatlantoaxial junction malformation and early onset senile ankylosing vertebral hyperostosis in a girl with MURCS association. Am J Med Genet A (2009) 0.81
Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report. J Med Case Rep (2008) 0.80
Outward bulging of the right parietal bone in connection with fibrous dysplasia in an infant: a case report. Cases J (2008) 0.80
Recurrence of axial malalignment after surgical correction in congenital femoral deficiency and fibular hemimelia. Int Orthop (2011) 0.80
Ischiopubic and odontoid synchondrosis in a boy with progressive pseudorheumatoid chondrodysplasia. Pediatr Rheumatol Online J (2007) 0.80
Prevalence of osteoarthritis and clinical results after the Elmslie-Trillat procedure: a retrospective long-term follow-up. Int Orthop (2013) 0.79
Distinctive spine abnormalities in patients with Goldenhar syndrome: tomographic assessment. Eur Spine J (2014) 0.79
A hypoplastic atlas and long odontoid process in a girl manifesting phenotypic features resembling spondyloepimetaphyseal dysplasia joint laxity syndrome. Skeletal Radiol (2008) 0.79
Femoral-tibial-synostosis in a child with Roberts syndrome (Pseudothalidomide): a case report. Cases J (2008) 0.79
Familial vertebral segmentation defects, Sprengel anomaly, and omovertebral bone with variable expressivity. Am J Med Genet A (2005) 0.79
Windswept deformity in a patient with Schwartz-Jampel syndrome. Swiss Med Wkly (2012) 0.79
Radiographic and tomographic analysis in patients with stickler syndrome type I. Int J Med Sci (2013) 0.79
Long-term results of a nationwide general ultrasound screening system for developmental disorders of the hip: the Austrian hip screening program. J Child Orthop (2014) 0.79
Siblings with glaucoma, mental retardation and short stature. Clin Dysmorphol (2003) 0.78
Cervico-thoracic kyphosis in a girl with Pierre Robin sequence. Ger Med Sci (2011) 0.78
Neurogenic hip dislocation in cerebral palsy: quality of life and results after hip reconstruction. J Child Orthop (2008) 0.78
Interobserver reliability of radiographic measurements of contralateral feet of pediatric patients with unilateral clubfoot. J Bone Joint Surg Am (2010) 0.78
Progressive non-infectious anterior vertebral fusion, split cord malformation and situs inversus visceralis. BMC Musculoskelet Disord (2006) 0.78
Progressive noninfectious anterior vertebral fusion in a girl with axial mesodermal dysplasia spectrum. Clin Dysmorphol (2008) 0.78
Distinctive tomographic abnormalities of the craniocervical region in a patient with osteogenesis imperfecta type IV B. Clinics (Sao Paulo) (2010) 0.77
Spinal exostosis in a boy with multiple hereditary exostoses. Case Rep Orthop (2013) 0.77
Musculo-skeletal abnormalities in patients with Marfan syndrome. Clin Med Insights Arthritis Musculoskelet Disord (2013) 0.77
Diffuse skull base/cervical fusion syndromes in two siblings with spondylocostal dysostosis syndrome: analysis via three dimensional computed tomography scanning. Spine (Phila Pa 1976) (2008) 0.77
Progressive acetabular dysplasia in a boy with mucopolysaccharoidosis type IV A (Morquio syndrome): a case report. Cases J (2008) 0.76
A child with split-hand/foot associated with tibial hemimelia (SHFLD syndrome) and thrombocytopenia maps to chromosome region 17p13.3. Am J Med Genet A (2014) 0.76
Wrist arthroscopy in children and adolescents: a single surgeon experience of thirty-four cases. Int Orthop (2011) 0.75
Pathomorphologic findings of wrist arthroscopy in children and adolescents with chronic wrist pain. Arthroscopy (2012) 0.75
Fractures in connection with an atypical form of craniodiaphyseal dysplasia: case report of a boy and his mother. Clinics (Sao Paulo) (2012) 0.75
Craniosynostosis, Scheuermann's disease, and intellectual disability resembling Shprintzen-Goldberg syndrome: a report on a family over 4 generations: Case report. Medicine (Baltimore) (2017) 0.75
Synophyrs, curly eyelashes and Ptyrigium colli in a girl with Desbuquois dysplasia: a case report and review of the literature. Cases J (2009) 0.75
The aetiology behind torticollis and variable spine defects in patients with Müllerian duct/renal aplasia-cervicothoracic somite dysplasia syndrome: 3D CT scan analysis. Eur Spine J (2011) 0.75
Broad spectrum of skeletal malformation complex in patients with cleidocranial dysplasia syndrome: radiographic and tomographic study. Clin Med Insights Arthritis Musculoskelet Disord (2013) 0.75
A patient with melorheostosis manifesting with features similar to tricho-dento-osseous syndrome: a case report. J Med Case Rep (2008) 0.75
Management of progressive genu varum in a patient with Dyggve-Melchior-Clausen syndrome. Ger Med Sci (2011) 0.75
Mid-diaphyseal Endosteal Thickening With Subsequent Medullary Narrowing in a Patient With Hallermann-Streiff Syndrome. J Clin Med Res (2011) 0.75
Distinctive spinal changes in two patients with unusual forms of autosomal dominant endosteal hyperostosis: a case series. J Med Case Rep (2007) 0.75
Congenital contractures and distinctive phenotypic features consistent with Stuve-Wiedmann syndrome in a male infant. Cases J (2008) 0.75
Atlanto-axial rotatory fixation in a girl with Spondylocarpotarsal synostosis syndrome. Scoliosis (2006) 0.75
Subtotal amelia in a child with autosomal recessive hypohidrotic ectodermal dysplasia. Afr Health Sci (2005) 0.75
Severe skew foot deformity in a patient with freeman-sheldon syndrome. J Clin Med Res (2011) 0.75
Occipito-vertebral dissociation in connection with extensive cervical spine malsegmentation in a boy with Möbius syndrome. Clinics (Sao Paulo) (2009) 0.75
Tomographic assessment of the spine in children with spondylocostal dysotosis syndrome. Clinics (Sao Paulo) (2010) 0.75
Correction of the axial and appendicular deformities in a patient with Silver-Russel syndrome. Afr J Paediatr Surg (2015) 0.75
Spine malformation complex in 3 diverse syndromic entities: Case reports. Medicine (Baltimore) (2016) 0.75
Ball and socket ankle joint in connection with bilateral tarsal synostosis in a boy with congenital absence of the portal vain: a novel malformation complex. Cases J (2008) 0.75
Vertebral hyperostosis, ankylosed vertebral fracture and atlantoaxial rotatory subluxation in an elderly patient with a history of infantile idiopathic scoliosis; a case report. J Med Case Rep (2007) 0.75
Progressive joint limitations as the first alarming signs in a boy with short - limbed dwarfism: A case report. Cases J (2008) 0.75
The constellation of skeletal deformities in a family with mixed types of mucopolysaccharidoses: Case report. Medicine (Baltimore) (2016) 0.75
Dysmorphic facies and diffuse posterior spine ankylosis in a patient with unusual form of spondyloenchondrodysplasia (Spranger type IV). Eur Spine J (2012) 0.75
Spinal and extraspinal deformities in a patient with dysspondyloenchondromatosis. Ger Med Sci (2013) 0.75
Extra phenotypic features in a girl with Miller syndrome. Clin Dysmorphol (2011) 0.75
Progressive anterior knee pain associated with patellar instability in a 57-year-old father and his daughter. Skeletal Radiol (2010) 0.75
Facial dysmorphism associated with distinctive spine abnormalities in a girl and her mother: novel syndromic association. Clin Dysmorphol (2011) 0.75
Clinicoradiographic presentation of a girl with progressive pseudorheumatoid arthropathy. J Coll Physicians Surg Pak (2010) 0.75
Distinctive tomographic features of atlantoaxial dislocation in a boy with acromesomelic dysplasia du Pan syndrome. Clin Dysmorphol (2009) 0.75