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Page 1
Nipple Pain in Breastfeeding Mothers: Incidence, Causes and Treatments.
Kent JC, Ashton E, Hardwick CM, Rowan MK, Chia ES, Fairclough KA, Menon LL, Scott C, Mather-McCaw G, Navarro K, Geddes DT. Kent JC, et al. Among authors: ashton e. Int J Environ Res Public Health. 2015 Sep 29;12(10):12247-63. doi: 10.3390/ijerph121012247. Int J Environ Res Public Health. 2015. PMID: 26426034 Free PMC article.
Two Brothers from Macedonia with Gitelman Syndrome.
Janchevska A, Tasic V, Jordanova O, Gucev Z, Jenkins L, Jovanovska N, Plaseska-Karanfilska D, Ashton E, Bockenhauer D. Janchevska A, et al. Among authors: ashton e. Balkan J Med Genet. 2023 Jul 31;26(1):69-74. doi: 10.2478/bjmg-2023-0009. eCollection 2023 Jul. Balkan J Med Genet. 2023. PMID: 37576796 Free PMC article.
Impact of sarcopenia indexes on survival and severe immune acute toxicity in metastatic non-small cell lung cancer patients treated with PD-1 immune checkpoint inhibitors.
Ashton E, Arrondeau J, Jouinot A, Boudou-Rouquette P, Hirsch L, Huillard O, Ulmann G, Lupo-Mansuet A, Damotte D, Wislez M, Alifano M, Alexandre J, Goldwasser F. Ashton E, et al. Clin Nutr. 2023 Jun;42(6):944-953. doi: 10.1016/j.clnu.2023.03.023. Epub 2023 Apr 14. Clin Nutr. 2023. PMID: 37099986
Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria.
Savige J, Storey H, Watson E, Hertz JM, Deltas C, Renieri A, Mari F, Hilbert P, Plevova P, Byers P, Cerkauskaite A, Gregory M, Cerkauskiene R, Ljubanovic DG, Becherucci F, Errichiello C, Massella L, Aiello V, Lennon R, Hopkinson L, Koziell A, Lungu A, Rothe HM, Hoefele J, Zacchia M, Martic TN, Gupta A, van Eerde A, Gear S, Landini S, Palazzo V, Al-Rabadi L, Claes K, Corveleyn A, Van Hoof E, van Geel M, Williams M, Ashton E, Belge H, Ars E, Bierzynska A, Gangemi C, Lipska-Ziętkiewicz BS. Savige J, et al. Among authors: ashton e. Eur J Hum Genet. 2024 Jan;32(1):132. doi: 10.1038/s41431-023-01288-x. Eur J Hum Genet. 2024. PMID: 36721056 Free PMC article. No abstract available.
Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study.
Sinha R, Pradhan S, Banerjee S, Jahan A, Akhtar S, Pahari A, Raut S, Parakh P, Basu S, Srivastava P, Nayak S, Thenral SG, Ramprasad V, Ashton E, Bockenhauer D, Mandal K. Sinha R, et al. Among authors: ashton e. Pediatr Nephrol. 2022 Aug;37(8):1811-1836. doi: 10.1007/s00467-021-05388-y. Epub 2022 Jan 10. Pediatr Nephrol. 2022. PMID: 35006361
120 results