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Journal Abstract Search

138 related items for PubMed ID: 32843252

  • 1.
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  • 2. A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans.
    Tuhan H, Ceylaner S, Nalbantoğlu Ö, Acar S, Abacı A, Böber E, Demir K.
    J Clin Res Pediatr Endocrinol; 2017 Dec 15; 9(4):371-374. PubMed ID: 28663160
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  • 5. 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 15; 50(6):951-7. PubMed ID: 23824322
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  • 6. A Novel Mutation in the INSR Gene Causes Severe Insulin Resistance and Rabson-Mendenhall Syndrome in a Paraguayan Patient.
    Rojas Velazquez MN, Blanco F, Ayala-Lugo A, Franco L, Jolly V, Di Tore D, Martínez de Lapiscina I, Janner M, Flück CE, Pandey AV.
    Int J Mol Sci; 2024 Mar 08; 25(6):. PubMed ID: 38542117
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  • 10. [A case of Rabson-Mendenhall syndrome].
    Ma L, Wang J, Fang YX.
    Zhonghua Er Ke Za Zhi; 2013 Jul 08; 51(7):545-7. PubMed ID: 24267141
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  • 11. 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 08; 83(4):209-222. PubMed ID: 15232309
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  • 13. A novel homozygous missense mutation in the insulin receptor gene results in an atypical presentation of Rabson-Mendenhall syndrome.
    Ben Abdelaziz R, Ben Chehida A, Azzouz H, Boudabbous H, Lascols O, Ben Turkia H, Tebib N.
    Eur J Med Genet; 2016 Jan 08; 59(1):16-9. PubMed ID: 26691667
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  • 15. Fibroepithelial papillomatosis ("skin tags") in Rabson-Mendenhall syndrome.
    Kirby EJ, Beals DA.
    J Pediatr Surg; 2008 Apr 08; 43(4):e21-6. PubMed ID: 18405695
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  • 17. 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 08; 27(5):565-8. PubMed ID: 22563226
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  • 18. [Rabson-Mendenhall syndrome].
    Ando A.
    Nihon Rinsho; 1994 Oct 08; 52(10):2641-2. PubMed ID: 7983791
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  • 19. 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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  • 20. Syndrome of Congenital Insulin Resistance Caused by a Novel INSR Gene Mutation.
    Rojek A, Wikiera B, Noczynska A, Niedziela M.
    J Clin Res Pediatr Endocrinol; 2023 Aug 23; 15(3):312-317. PubMed ID: 34965699
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