For: | Manak I, Gurney AM, Mccloskey KD, Woolf AS, Roberts NA. Dysfunctional bladder neurophysiology in urofacial syndrome Hpse2 mutant mice. Neurourology and Urodynamics 2020;39:1930-8. [DOI: 10.1002/nau.24450] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis] |
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Number | Citing Articles |
1 | Grenier C, Lopes FM, Cueto-gonzález AM, Rovira-moreno E, Gander R, Jarvis BW, Mccloskey KD, Gurney AM, Beaman GM, Newman WG, Woolf AS, Roberts NA. Neurogenic defects underlie functional bladder outflow tract obstruction associated with biallelic variants inLRIG2.. [DOI: 10.1101/2022.12.06.22283097] [Reference Citation Analysis] |
2 | Beaman GM, Lopes FM, Hofmann A, Roesch W, Promm M, Bijlsma EK, Patel C, Akinci A, Burgu B, Knijnenburg J, Ho G, Aufschlaeger C, Dathe S, Voelckel MA, Cohen M, Yue WW, Stuart HM, Mckenzie EA, Elvin M, Roberts NA, Woolf AS, Newman WG. Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder. Front Genet 2022;13:896125. [DOI: 10.3389/fgene.2022.896125] [Reference Citation Analysis] |
3 | Lopes FM, Woolf AS, Roberts NA. Envisioning treating genetically-defined urinary tract malformations with viral vector-mediated gene therapy. J Pediatr Urol 2021;17:610-20. [PMID: 34312114 DOI: 10.1016/j.jpurol.2021.07.002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis] |
4 | Osorio S, Rivillas ND, Martinez JA. Urofacial (ochoa) syndrome: A literature review. J Pediatr Urol 2021;17:246-54. [PMID: 33558177 DOI: 10.1016/j.jpurol.2021.01.017] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis] |