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Number of items: 6.

Article

Wharton, S.B., Verber, N.S., Wagner, B.E. et al. (6 more authors) (2019) Combined FUS+ basophilic inclusion body disease and atypical tauopathy presenting with an ALS/MND-plus phenotype. Neuropathology and Applied Neurobiology. ISSN 0305-1846

Balasubramanian, M. orcid.org/0000-0003-1488-3695, Padidela, R., Pollitt, R.C. orcid.org/0000-0002-8864-397X et al. (6 more authors) (2017) P4HB recurrent missense mutation causing Cole-Carpenter syndrome. Journal of Medical Genetics. ISSN 0022-2593

Zis, P., Rao, D.G., Wagner, B.E. et al. (3 more authors) (2017) Cerebellar ataxia and sensory ganglionopathy associated with light-chain myeloma. Cerebellum Ataxias, 4. 1. ISSN 2053-8871

Parkash, V., Mudhar, H.S., Wagner, B.E. et al. (6 more authors) (2016) Bilateral Ocular Myositis Associated with Whipple's Disease. Ocular Oncology and Pathology, 3. pp. 17-21. ISSN 2296-4681

Balasubramanian, M. orcid.org/0000-0003-1488-3695, Sobey, G.J., Wagner, B.E. et al. (6 more authors) (2016) Osteogenesis imperfecta: Ultrastructural and histological findings on examination of skin revealing novel insights into genotype-phenotype correlation. Ultrastructural Pathology, 40 (2). pp. 71-76. ISSN 0191-3123

Streets, A.J., Wagner, B.E., Harris, P.C. et al. (2 more authors) (2009) Homophilic and heterophilic polycystin 1 interactions regulate E-cadherin recruitment and junction assembly in MDCK cells. Journal of Cell Science, 122 (9). pp. 1410-1417. ISSN 0021-9533

This list was generated on Mon Oct 14 02:04:33 2019 BST.