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Journal Abstract Search

146 related items for PubMed ID: 23347304

  • 1. Rabson-Mendenhall syndrome with recurrent cerebral infarcts caused by a novel INSR mutation.
    Mohanan S, Chandrashekar L, Semple RK, Thappa DM, Parameswaran N, Negi VS, Ramassamy S.
    Int J Dermatol; 2013 Feb; 52(2):182-5. PubMed ID: 23347304
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  • 3. Six cases with severe insulin resistance (SIR) associated with mutations of insulin receptor: Is a Bartter-like syndrome a feature of congenital SIR?
    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.
    Acta Diabetol; 2013 Dec; 50(6):951-7. PubMed ID: 23824322
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  • 10. Two novel insulin receptor gene mutations in a patient with Rabson-Mendenhall syndrome: the first Korean case confirmed by biochemical, and molecular evidence.
    Kim D, Cho SY, Yeau SH, Park SW, Sohn YB, Kwon MJ, Kim JY, Ki CS, Jin DK.
    J Korean Med Sci; 2012 May; 27(5):565-8. PubMed ID: 22563226
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  • 13. Use of a Sodium-Glucose Cotransporter 2 Inhibitor, Empagliflozin, in a Patient with Rabson-Mendenhall Syndrome.
    Dos Santos SS, Ramaldes LA, Gabbay MAL, Moises RCS, Dib SA.
    Horm Res Paediatr; 2021 May; 94(7-8):313-316. PubMed ID: 34551418
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  • 14. Clinical course of genetic diseases of the insulin receptor (type A and Rabson-Mendenhall syndromes): a 30-year prospective.
    Musso C, Cochran E, Moran SA, Skarulis MC, Oral EA, Taylor S, Gorden P.
    Medicine (Baltimore); 2004 Jul; 83(4):209-222. PubMed ID: 15232309
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  • 15. [Rabson-Mendenhall syndrome].
    Ando A.
    Nihon Rinsho; 1994 Oct; 52(10):2641-2. PubMed ID: 7983791
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  • 16. INSR novel mutations identified in a Chinese family with severe INSR-related insulin resistance syndromes: A case report.
    Yu L, Yu F, Ma Z, Lu H, Luo J, Sun T, Liu Q, Gan S.
    Medicine (Baltimore); 2022 Dec 09; 101(49):e32266. PubMed ID: 36626508
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  • 17. 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.
    Abe Y, Sato T, Takagi M, Watanabe T, Nagayama Y, Hasegawa T, Abe T.
    J Pediatr Endocrinol Metab; 2012 Dec 09; 25(5-6):587-90. PubMed ID: 22876563
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  • 19. Identification of a Novel Homozygous INSR Variant in a Patient with Rabson-Mendenhall Syndrome from the United Arab Emirates.
    Bastaki F, Nair P, Mohamed M, Khadora MM, Saif F, Tawfiq N, Al-Ali MT, Hamzeh AR.
    Horm Res Paediatr; 2017 Dec 09; 87(1):64-68. PubMed ID: 27326825
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  • 20. Clinical characteristics of insulin resistance syndromes: A nationwide survey in Japan.
    Takeuchi T, Ishigaki Y, Hirota Y, Hasegawa Y, Yorifuji T, Kadowaki H, Akamizu T, Ogawa W, Katagiri H.
    J Diabetes Investig; 2020 May 09; 11(3):603-616. PubMed ID: 31677333
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