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Journal Abstract Search

137 related items for PubMed ID: 12047650

  • 1. What syndrome is this? Rabson-Mendenhall syndrome.
    Hardaway CA, Gibbs NF.
    Pediatr Dermatol; 2002; 19(3):267-70. PubMed ID: 12047650
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  • 4. Rabson-Mendenhall syndrome.
    Parveen BA, Sindhuja R.
    Int J Dermatol; 2008 Aug; 47(8):839-41. PubMed ID: 18717867
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  • 6. Fibroepithelial papillomatosis ("skin tags") in Rabson-Mendenhall syndrome.
    Kirby EJ, Beals DA.
    J Pediatr Surg; 2008 Apr; 43(4):e21-6. PubMed ID: 18405695
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  • 11. Rabson-Mendenhall Syndrome in a brother-sister pair in Kuwait: Diagnosis and 5 year follow up.
    Al-Kandari H, Al-Abdulrazzaq D, Al-Jaser F, Al-Mulla F, Davidsson L.
    Prim Care Diabetes; 2021 Feb; 15(1):175-177. PubMed ID: 32843252
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  • 12. 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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  • 13. 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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  • 14. Rabson Mendenhall Syndrome caused by a novel missense mutation.
    Sinnarajah K, Dayasiri MB, Dissanayake ND, Kudagammana ST, Jayaweera AH.
    Int J Pediatr Endocrinol; 2016 Dec 15; 2016():21. PubMed ID: 27891155
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  • 18. Mutations in the insulin receptor gene in patients with genetic syndromes of insulin resistance and acanthosis nigricans.
    Accili D, Barbetti F, Cama A, Kadowaki H, Kadowaki T, Imano E, Levy-Toledano R, Taylor SI.
    J Invest Dermatol; 1992 Jun 15; 98(6 Suppl):77S-81S. PubMed ID: 1588128
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