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Journal Abstract Search

126 related items for PubMed ID: 12472537

  • 1. Type 1 segmental cutaneous leiomyomatosis.
    Lang K, Reifenberger J, Ruzicka T, Megahed M.
    Clin Exp Dermatol; 2002 Nov; 27(8):649-50. PubMed ID: 12472537
    [Abstract] [Full Text] [Related]

  • 2. [Familial occurrence of a type 2 segmental manifestation of cutaneous leiomyomatosis].
    Renner R, Sticherling M.
    J Dtsch Dermatol Ges; 2005 Sep; 3(9):695-9. PubMed ID: 16173977
    [Abstract] [Full Text] [Related]

  • 3. Two cases of type 2 segmental manifestation in a family with cutaneous leiomyomatosis.
    König A, Happle R.
    Eur J Dermatol; 2000 Dec; 10(8):590-2. PubMed ID: 11125318
    [Abstract] [Full Text] [Related]

  • 4. Cutaneous leiomyomatosis with type 2 segmental involvement.
    Tsoitis G, Kanitakis J, Papadimitriou C, Hatzibougias Y, Asvesti K, Happle R.
    J Dermatol; 2001 May; 28(5):251-5. PubMed ID: 11436362
    [Abstract] [Full Text] [Related]

  • 5. Multiple cutaneous and uterine leiomyomatosis or reed syndrome: a retrospective study of 13 cases.
    Collgros H, Iglesias-Sancho M, Tribó-Boixareu MJ, Creus-Vila L, Umbert-Millet P, Salleras-Redonnet M.
    Actas Dermosifiliogr; 2015 Mar; 106(2):117-25. PubMed ID: 25439147
    [Abstract] [Full Text] [Related]

  • 6. A novel missense mutation in fumarate hydratase in an Italian patient with a diffuse variant of cutaneous leiomyomatosis (Reed's syndrome).
    Rongioletti F, Fausti V, Ferrando B, Parodi A, Mandich P, Pasini B.
    Dermatology; 2010 Mar; 221(4):378-80. PubMed ID: 21051878
    [Abstract] [Full Text] [Related]

  • 7. Novel FH mutation in a patient with cutaneous leiomyomatosis associated with cutis verticis gyrata, eruptive collagenoma and Charcot-Marie-Tooth disease.
    Marque M, Gardie B, Bressac de Paillerets B, Rustin P, Guillot B, Richard S, Bessis D.
    Br J Dermatol; 2010 Dec; 163(6):1337-9. PubMed ID: 20560959
    [Abstract] [Full Text] [Related]

  • 8. [Atypical leiomyoma in a patient with cutaneous leiomyomatosis and mutation of the enzyme fumarate hydratase].
    Calderón-Komáromy A, Arias-Palomo D, Tardío JC, Freites-Martínez A, Borbujo J.
    Invest Clin; 2016 Mar; 57(1):59-65. PubMed ID: 27382802
    [Abstract] [Full Text] [Related]

  • 9. Atypical pilar leiomyomatosis: an unusual presentation of multiple atypical cutaneous leiomyomas.
    Cook DL, Pugliano-Mauro MA, Schultz ZL.
    J Cutan Pathol; 2013 Jun; 40(6):564-8. PubMed ID: 23550704
    [Abstract] [Full Text] [Related]

  • 10. Single base mutation in the fumarate hydratase gene leading to segmental cutaneous leiomyomatosis.
    Huter E, Wortham NC, Hartschuh W, Enk A, Jappe U.
    Acta Derm Venereol; 2008 Jun; 88(1):63-5. PubMed ID: 18176756
    [No Abstract] [Full Text] [Related]

  • 11. [Segmental type 2 manifestation of autosome dominant skin diseases. Development of a new formal genetic concept].
    Happle R.
    Hautarzt; 2001 Apr; 52(4):283-7. PubMed ID: 11382117
    [Abstract] [Full Text] [Related]

  • 12. Evidence for a new fumarate hydratase gene mutation in a unilateral type 2 segmental leiomyomatosis.
    Parmentier L, Tomlinson I, Happle R, Borradori L.
    Dermatology; 2010 Apr; 221(2):149-53. PubMed ID: 20628236
    [Abstract] [Full Text] [Related]

  • 13. Type 2 segmental manifestation of cutaneous leiomyomatosis in four unrelated women with additional uterine leiomyomas (Reed's Syndrome).
    Ritzmann S, Hanneken S, Neumann NJ, Ruzicka T, Kruse R.
    Dermatology; 2006 Apr; 212(1):84-7. PubMed ID: 16319483
    [No Abstract] [Full Text] [Related]

  • 14. The syndrome of hereditary leiomyomatosis and renal cell cancer (HLRCC): The clinical features of an individual with a fumarate hydratase gene mutation.
    Varol A, Stapleton K, Roscioli T.
    Australas J Dermatol; 2006 Nov; 47(4):274-6. PubMed ID: 17034471
    [Abstract] [Full Text] [Related]

  • 15. Familial multiple cutaneous leiomyomas.
    Fernández-Pugnaire MA, Delgado-Florencio V.
    Dermatology; 1995 Nov; 191(4):295-8. PubMed ID: 8573925
    [Abstract] [Full Text] [Related]

  • 16. Clinical and molecular genetic aspects of hereditary multiple cutaneous leiomyomatosis.
    Badeloe S, Frank J.
    Eur J Dermatol; 2009 Nov; 19(6):545-51. PubMed ID: 19939761
    [Abstract] [Full Text] [Related]

  • 17. Familial leiomyomatosis cutis affecting nine family members in two successive generations including four cases of Reed's syndrome.
    Mandal RK, Koley S, Banerjee S, Kabiraj SP, Ghosh SK, Kumar P.
    Indian J Dermatol Venereol Leprol; 2013 Nov; 79(1):83-7. PubMed ID: 23254734
    [Abstract] [Full Text] [Related]

  • 18. Two sisters with Reed's syndrome: treatment with pregabalin.
    Yaldiz M, Metin M, Erdem MT, Dikicier BS, Kahyaoglu Z.
    Dermatol Online J; 2015 Sep 17; 21(9):. PubMed ID: 26437289
    [Abstract] [Full Text] [Related]

  • 19. A retrospective review of 48 individuals, including 12 families, molecularly diagnosed with hereditary leiomyomatosis and renal cell cancer (HLRCC).
    Bhola PT, Gilpin C, Smith A, Graham GE.
    Fam Cancer; 2018 Oct 17; 17(4):615-620. PubMed ID: 29423582
    [Abstract] [Full Text] [Related]

  • 20. Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology.
    Kiuru M, Launonen V, Hietala M, Aittomäki K, Vierimaa O, Salovaara R, Arola J, Pukkala E, Sistonen P, Herva R, Aaltonen LA.
    Am J Pathol; 2001 Sep 17; 159(3):825-9. PubMed ID: 11549574
    [Abstract] [Full Text] [Related]

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