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Journal Abstract Search

199 related items for PubMed ID: 1362414

  • 1. Cutaneous lesion associated with multiple endocrine neoplasia type 2A: lichen amyloidosis or notalgia paresthetica?
    Chabre O, Labat F, Pinel N, Berthod F, Tarel V, Bachelot I.
    Henry Ford Hosp Med J; 1992; 40(3-4):245-8. PubMed ID: 1362414
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  • 3. [Paresthetic notalgia and multiple endocrine neoplasia type 2a (Sipple's syndrome): 3 cases].
    Rivollier C, Emy P, Armingaud P, Buzacoux J, Chadenas D, Legoux A, Estève E.
    Ann Dermatol Venereol; 1999; 126(6-7):522-4. PubMed ID: 10495863
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  • 9. Multiple endocrine neoplasia type 2a associated with cutaneous lichen amyloidosis.
    Gagel RF, Levy ML, Donovan DT, Alford BR, Wheeler T, Tschen JA.
    Ann Intern Med; 1989 Nov 15; 111(10):802-6. PubMed ID: 2573304
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  • 10. Multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis: description of a new family.
    Pacini F, Fugazzola L, Bevilacqua G, Viacava P, Nardini V, Martino E.
    J Endocrinol Invest; 1993 Apr 15; 16(4):295-6. PubMed ID: 8099921
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  • 11. Multiple endocrine neoplasia 2 (MEN 2)/MEN 2A (Sipple syndrome).
    Kousseff BG.
    Dermatol Clin; 1995 Jan 15; 13(1):91-7. PubMed ID: 7712656
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  • 12. [The interdisciplinary aspects of notalgia paraesthetica].
    Wlotzke U, Stolz W, Hohenleutner U, Dorfmüller P, Korting HC, Landthaler M.
    Dtsch Med Wochenschr; 1994 Sep 30; 119(39):1307-11. PubMed ID: 7924928
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  • 13. Rare syndromes.
    Jabbour SA, Davidovici BB, Wolf R.
    Clin Dermatol; 2006 Sep 30; 24(4):299-316. PubMed ID: 16828412
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  • 14. Sipple syndrome with lichen amyloidosis as a paracrinopathy: pleiotropy, heterogeneity, or a contiguous gene?
    Kousseff BG, Espinoza C, Zamore GA.
    J Am Acad Dermatol; 1991 Oct 30; 25(4):651-7. PubMed ID: 1686438
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  • 15. Cutaneous macular amyloidosis associated with multiple endocrine neoplasia 2A.
    de Argila D, Ortiz-Romero PL, Ortiz-Frutos J, Rodriguez-Peralto JL, Iglesias L.
    Clin Exp Dermatol; 1996 Jul 30; 21(4):313-4. PubMed ID: 8959910
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  • 16. Familial poikylodermic cutaneous amyloidosis.
    Pardo Arranz L, Escalonilla García-Patos P, Román Curto C, Blanco Barrios S, Fernández López E, de Unamuno Pérez P.
    Eur J Dermatol; 2008 Jul 30; 18(3):289-91. PubMed ID: 18474457
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  • 17. RET mutation screening in familial cutaneous lichen amyloidosis and in skin amyloidosis associated with multiple endocrine neoplasia.
    Hofstra RM, Sijmons RH, Stelwagen T, Stulp RP, Kousseff BG, Lips CJ, Steijlen PM, Van Voorst Vader PC, Buys CH.
    J Invest Dermatol; 1996 Aug 30; 107(2):215-8. PubMed ID: 8757765
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