Items where authors include "Parekh, S."

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Number of items: 7.

Article

Bukavina, L. orcid.org/0000-0001-7129-6230, Isali, I., Parekh, S. et al. (16 more authors) (2025) Genetic susceptibility and environmental risk factors in bladder cancer: evidence from the UK biobank. Bladder Cancer, 11 (3). ISSN 2352-3727

Humphreys, J. orcid.org/0000-0002-3252-0962, Graham, A., Rodd, H.D. orcid.org/0000-0003-2973-2558 et al. (5 more authors) (2024) Molar incisor hypomineralisation: Teaching and assessment across the undergraduate dental curricula in the UK. International Journal of Paediatric Dentistry, 34 (5). pp. 576-583. ISSN 0960-7439

Monteiro, J., Balmer, R., Lafferty, F. et al. (4 more authors) (2024) Establishment of a clinical network for children with amelogenesis imperfecta and dentinogenesis imperfecta in the UK: 4-year experience. EUROPEAN ARCHIVES OF PAEDIATRIC DENTISTRY, 25 (1). pp. 85-91. ISSN 1818-6300

Monteiro, J. orcid.org/0000-0001-9676-1995, Balmer, R. orcid.org/0009-0004-5314-2157, Lafferty, F. orcid.org/0000-0002-4879-7915 et al. (4 more authors) (2024) Establishment of a clinical network for children with amelogenesis imperfecta and dentinogenesis imperfecta in the UK: 4-year experience. European Archives of Paediatric Dentistry, 25. pp. 85-91. ISSN 1818-6300

Rodd, H.D. orcid.org/0000-0003-2973-2558, Nazzal, H., Bonifacio, C.C. orcid.org/0000-0001-6515-2927 et al. (17 more authors) (2023) An international investigation of Molar Incisor Hypomineralisation (iMIH) and Its association with dental anomalies: development of a protocol. Dentistry Journal, 11 (5). 117. ISSN 2304-6767

Lafferty, F., Al Siyabi, H., Sinadinos, A. et al. (6 more authors) (2021) The burden of dental care in Amelogenesis Imperfecta paediatric patients in the UK NHS: a retrospective, multi-centred analysis. European Archives of Paediatric Dentistry, 22 (5). pp. 929-936. ISSN 1818-6300

Durkin, A., DeVile, C., Arundel, P. et al. (11 more authors) (2021) Expanding the phenotype of SPARC-related osteogenesis imperfecta : clinical findings in two patients with pathogenic variants in SPARC and literature review. Journal of Medical Genetics, 59 (8). pp. 810-816. ISSN 0022-2593

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