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Anusha Uttarilli
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Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI
PN Kantaputra, H Kayserili, Y Güven, W Kantaputra, MC Balci, ...
Journal of inherited metabolic disease 37, 263-268, 2014
552014
Super-rapid race for saving lives by developing COVID-19 vaccines
A Uttarilli, S Amalakanti, PR Kommoju, S Sharma, P Goyal, GK Manjunath, ...
Journal of Integrative Bioinformatics 18 (1), 27-43, 2021
342021
Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations
PN Kantaputra, H Kayserili, Y Guven, W Kantaputra, MC Balci, ...
American Journal of Medical Genetics Part A 164 (6), 1443-1453, 2014
312014
Identification and characterization of 20 novel pathogenic variants in 60 unrelated Indian patients with mucopolysaccharidoses type I and type II
A Uttarilli, P Ranganath, D Matta, J Md Nurul Jain, K Prasad, AS Babu, ...
Clinical genetics 90 (6), 496-508, 2016
292016
Phenotyping and genotyping of skeletal dysplasias: Evolution of a center and a decade of experience in India
A Uttarilli, H Shah, GSL Bhavani, P Upadhyai, A Shukla, KM Girisha
Bone 120, 204-211, 2019
212019
Novel mutations of the arylsulphatase B (ARSB) gene in Indian patients with mucopolysaccharidosis type VI
A Uttarilli, P Ranganath, SJN Jain, PC Krishna, A Sinha, IC Verma, ...
Indian Journal of Medical Research 142 (4), 414-425, 2015
92015
Functional characterization of arylsulfatase B mutations in Indian patients with Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI)
A Uttarilli, D Pasumarthi, P Ranganath, AB Dalal
Gene 599, 19-27, 2017
72017
Hunter syndrome with late age of presentation: clinical description of a case and review of the literature
A Gupta, A Uttarilli, A Dalal, KM Girisha
Case Reports 2015, bcr2015209305, 2015
62015
GAPO syndrome with deafness: new feature or incidental finding?
S Aggarwal, A Uttarilli, AB Dalal
Clinical Dysmorphology 22 (4), 161-163, 2013
62013
A review of skeletal dysplasia research in India
A Uttarilli, H Shah, A Shukla, KM Girisha
Journal of Postgraduate Medicine 64 (2), 98-103, 2018
42018
Mongolian spots in GM1 gangliosidosis: a pictorial report
S Mishra, P Pai, A Uttarilli, KM Girisha
Clinical Dysmorphology 30 (1), 6-9, 2021
32021
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A Uttarilli, D Pasumarthi, P Ranganath, AB Dalal
2016
Molecular analysis of mucopolysaccharidoses: identification and characterization of pathogenic mutations in Indian population
A Uttarilli, SJMN Jain, AB Dalal, P Ranganath, SR Phadke, G Kumar, ...
Molecular Cytogenetics 7, 1-1, 2014
2014
Molecular analysis of mucopolysaccharidoses in indian population
A Uttarilli
Manipal, 0
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Articles 1–14