hitesh Shah
hitesh Shah
Department of Orthopaedics, KMC, Manipal University, Manipal
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Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion
E Klopocki, S Lohan, SC Doelken, S Stricker, CW Ockeloen, ...
Journal of medical genetics 49 (2), 119-125, 2012
Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia
A Dalal, SL Bhavani G, PP Togarrati, T Bierhals, MR Nandineni, S Danda, ...
American Journal of Medical Genetics Part A 158 (11), 2820-2828, 2012
Congenital pseudarthrosis of the tibia: Management and complications
H Shah, M Rousset, F Canavese
Indian journal of orthopaedics 46, 616-626, 2012
Management of severe crouch gait in children and adolescents with cerebral palsy
B Joseph, K Reddy, RA Varghese, H Shah, SN Doddabasappa
Journal of Pediatric Orthopaedics 30 (8), 832-839, 2010
Perthes disease: evaluation and management
H Shah
Orthopedic Clinics 45 (1), 87-97, 2014
Congenital pseudarthrosis of the tibia treated with intramedullary rodding and cortical bone grafting: a follow-up study at skeletal maturity
H Shah, SN Doddabasappa, B Joseph
Journal of Pediatric Orthopaedics 31 (1), 79-88, 2011
Effect of prophylactic trochanteric epiphyseodesis in older children with Perthes' disease
H Shah, ND Siddesh, B Joseph, SN Nair
Journal of Pediatric Orthopaedics 29 (8), 889-895, 2009
Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly
E Klopocki, C Kähler, N Foulds, H Shah, B Joseph, H Vogel, S Lüttgen, ...
European journal of human genetics 20 (6), 705-708, 2012
Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta
J Mrosk, GSL Bhavani, H Shah, J Hecht, U Krüger, A Shukla, U Kornak, ...
Bone 110, 368-377, 2018
Clinical utility of fetal autopsy and its impact on genetic counseling
SS Nayak, A Shukla, L Lewis, R Kadavigere, M Mathew, PK Adiga, ...
Prenatal Diagnosis 35 (7), 685-691, 2015
Mutations in patients with osteogenesis imperfecta from consanguineous Indian families
J Stephen, KM Girisha, A Dalal, A Shukla, H Shah, P Srivastava, U Kornak, ...
European journal of medical genetics 58 (1), 21-27, 2015
GALNS mutations in Indian patients with mucopolysaccharidosis IVA
AM Bidchol, A Dalal, H Shah, S Nampoothiri, M Kabra, N Gupta, S Danda, ...
American Journal of Medical Genetics Part A 164 (11), 2793-2801, 2014
Congenital posteromedial bowing of the tibia: a retrospective analysis of growth abnormalities in the leg
HH Shah, SN Doddabasappa, B Joseph
Journal of Pediatric Orthopaedics B 18 (3), 120-128, 2009
Pre-axial mirror polydactyly associated with tibial deficiency: a study of the patterns of skeletal anomalies of the foot and leg
R Verghese, H Shah, G Rebello, B Joseph
Journal of children's orthopaedics 1 (1), 49-54, 2007
Quantitative measures for evaluating the radiographic outcome of Legg-Calvé-Perthes disease
H Shah, ND Siddesh, H Pai, S Tercier, B Joseph
JBJS 95 (4), 354-361, 2013
Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy
GSL Bhavani, H Shah, A Shukla, N Gupta, K Gowrishankar, AP Rao, ...
American journal of medical genetics Part A 170 (2), 410-417, 2016
Environmental tobacco and wood smoke increase the risk of Legg-Calvé-Perthes disease
AB Daniel, H Shah, A Kamath, V Guddettu, B Joseph
Clinical Orthopaedics and Related Research® 470, 2369-2375, 2012
What factors influence union and refracture of congenital pseudarthrosis of the tibia? A multicenter long-term study
H Shah, B Joseph, BVS Nair, DB Kotian, IH Choi, BS Richards, ...
Journal of Pediatric Orthopaedics 38 (6), e332-e337, 2018
Mutation spectrum of COL1A1 and COL1A2 genes in Indian patients with osteogenesis imperfecta
J Stephen, A Shukla, A Dalal, KM Girisha, H Shah, N Gupta, M Kabra, ...
American journal of medical genetics Part A 164 (6), 1482-1489, 2014
Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia
L Guo, KM Girisha, A Iida, M Hebbar, A Shukla, H Shah, G Nishimura, ...
Journal of human genetics 62 (3), 437-441, 2017
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