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Bartter-like syndrome in patients with molecular defects of the insulin receptor gene

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References

  1. Grasso V, Colombo C, Favalli V, Galderisi A, Rabbone I, Gombos S, Bonora E, Massa O, Meschi F, Cerutti F, Iafusco D, Bonfanti R, Monciotti C, Barbetti F (2013) Six cases with severe insulin resistance (SIR) associated with mutations of insulin receptor: Is a Bartter-like syndrome a feature of congenital SIR? Acta Diabetol 50:951–957

    Article  PubMed  Google Scholar 

  2. Nozu K, Fu XJ, Kaito H, Kanda K, Yokoyama N, Przybyslaw Krol R, Nakajima T, Kajiyama M, Iijima K, Matsuo M (2007) A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism. Pediatr Nephrol 22:1219–1223

    Article  PubMed  Google Scholar 

  3. Abe Y, Sato T, Takagi M, Watanabe T, Nagayama Y, Hasegawa T, Abe T (2012) A case of Rabson-Mendenhall syndrome with a novel mutation in the tyrosine kinase domain of the insulin receptor gene complicated by medullary sponge kidney. J Pediatr Endocrinol Metab 25:587–590

    Article  PubMed  CAS  Google Scholar 

  4. Cheng CJ, Huang CL (2011) Activation of PI3-kinase stimulates endocytosis of ROMK via Akt1/SGK1-dependent phosphorylation of WNK1. J Am Soc Nephrol 22:460–471

    Article  PubMed  CAS  PubMed Central  Google Scholar 

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Conflict of interest

Toru Watanabe and Yuki Abe declare that we have no conflict of interest.

Human rights disclosure

All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation of the Niigata City General Hospital and with the Helsinki Declaration of 1975, as revised in 2008.

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Informed consent was obtained from parents of the patient for being included in the study.

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Correspondence to Toru Watanabe.

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Watanabe, T., Abe, Y. Bartter-like syndrome in patients with molecular defects of the insulin receptor gene. Acta Diabetol 51, 891–892 (2014). https://doi.org/10.1007/s00592-014-0606-y

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  • DOI: https://doi.org/10.1007/s00592-014-0606-y

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