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Gallagher, James A ORCID: 0000-0002-0852-279X, Dillon, Jane P ORCID: 0000-0002-7055-5664, Sireau, Nicolas, Timmis, Oliver and Ranganath, Lakshminarayan R
(2016) Alkaptonuria: An example of a "fundamental disease"-A rare disease with important lessons for more common disorders. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 52. pp. 53-57.


Rudebeck, Mattias, Scott, Ciaran, Rhodes, Nicholas P ORCID: 0000-0002-5173-7032, van Kan, Christa, Olsson, Birgitta, Al-sbou, Mohammed, Hall, Anthony K, Sireau, Nicolas and Ranganath, Lakshminarayan R
(2021) Clinical development innovation in rare diseases: lessons learned and best practices from the DevelopAKUre consortium. ORPHANET JOURNAL OF RARE DISEASES, 16 (1). 510-.


Ranganath, Lakshminarayan R ORCID: 0000-0002-4205-2269, Milan, Anna M, Hughes, Andrew T, Khedr, Milad, Norman, Brendan P ORCID: 0000-0001-9293-4852, Alsbou, Mohammed, Imrich, Richard, Gornall, Matthew, Sireau, Nicolas, Gallagher, James A ORCID: 0000-0002-0852-279X
et al (show 1 more authors) (2022) Comparing nitisinone 2 mg and 10 mg in the treatment of alkaptonuria-An approach using statistical modelling. JIMD reports, 63 (1). pp. 80-92.


Ranganath, Lakshminarayan R, Psarelli, Eftychia Eirini ORCID: 0000-0002-3102-0288, Arnoux, Jean-Baptiste, Braconi, Daniela, Briggs, Michael, Broijersen, Anders, Loftus, Nadia, Bygott, Helen, Cox, Trevor F, Davison, Andrew S ORCID: 0000-0001-5501-4475
et al (show 39 more authors) (2020) Efficacy and safety of once-daily nitisinone for patients with alkaptonuria (SONIA 2): an international, multicentre, open-label, randomised controlled trial. The Lancet Diabetes and Endocrinology, 8 (9). pp. 762-772.


Ranganath, Lakshminarayan R, Milan, Anna M ORCID: 0000-0002-0452-2338, Hughes, Andrew T, Khedr, Milad ORCID: 0000-0002-4998-2397, Davison, Andrew S ORCID: 0000-0001-5501-4475, Shweihdi, Ella, Norman, Brendan P ORCID: 0000-0001-9293-4852, Hughes, Juliette H ORCID: 0000-0001-6155-4136, Bygott, Helen, Luangrath, Emily
et al (show 20 more authors) (2020) Homogentisic acid is not only eliminated by glomerular filtration and tubular secretion but also produced in the kidney in alkaptonuria. JOURNAL OF INHERITED METABOLIC DISEASE, 43 (4). pp. 737-747.

This list was generated on Sun Apr 7 11:41:11 2024 BST.