Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia-Reference-Cited by-同舟云学术

Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia

Published:2024-02-04 Issue:2 Volume:42 Page:155-165
ISSN:0914-8779
Container-title:Journal of Bone and Mineral Metabolism
language:en
Short-container-title:J Bone Miner Metab

Author:

Ragate Divya C.^ORCID,Memon Saba Samad^ORCID,Karlekar Manjiri^ORCID,Lila Anurag Ranjan^ORCID,Sarathi Vijaya^ORCID,Jamale Tukaram,Thakare Sayali,Patil Virendra A.,Shah Nalini S.,Bandgar Tushar R.^ORCID

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s00774-023-01490-3.pdf

Reference37 articles.

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2. Albuquerque ALB, dos Santos Borges R, Conegundes AF, Dos Santos EE, Fu FMM, Araujo CT, Vaz de Castro PAS, Simões e Silva AC (2023) Inherited Fanconi syndrome. World J Pediatr 19:619–634. https://doi.org/10.1007/s12519-023-00685-y

3. Reichold M, Klootwijk ED, Reinders J, Otto EA, Milani M, Broeker C, Laing C, Wiesner J, Devi S, Zhou W, Schmitt R (2018) Glycine amidinotransferase (GATM), renal Fanconi syndrome, and kidney failure. J Am Soc Nephrol 29:1849–1858. https://doi.org/10.1681/ASN.2017111179

4. Klootwijk ED, Reichold M, Helip-Wooley A, Tolaymat A, Broeker C, Robinette SL, Reinders J, Peindl D, Renner K, Eberhart K, Assmann N (2014) Mistargeting of peroxisomal EHHADH and inherited renal Fanconi’s syndrome. N Engl J Med 370:129–138. https://doi.org/10.1056/NEJMoa1307581

5. Magen D, Berger L, Coady MJ, Ilivitzki A, Militianu D, Tieder M, Selig S, Lapointe JY, Zelikovic I, Skorecki K (2010) A loss-of-function mutation in NaPi-IIa and renal Fanconi’s syndrome. N Engl J Med 362:1102–1109. https://doi.org/10.1056/NEJMoa0905647

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