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Journal Abstract Search

128 related items for PubMed ID: 24345188

  • 1. Glomuvenous malformations with smooth muscle and eccrine glands: unusual histopathologic features in a familial setting.
    Borroni RG, Grassi S, Concardi M, Puccio I, Giordano C, Agozzino M, Caspani C, Grasso M, Diegoli M, Arbustini E.
    J Cutan Pathol; 2014 Mar; 41(3):308-15. PubMed ID: 24345188
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  • 2. Incomplete penetrance of GLMN gene c.395-1G>C mutation in a family with glomuvenous malformations.
    Borroni RG, Grassi S, Diegoli M, Grasso M, Arbustini E.
    Int J Dermatol; 2014 Nov; 53(11):1362-4. PubMed ID: 24961656
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  • 3. Type 2 segmental glomangiomas.
    Hoekzema R, Zonneveld IM, van der Wal AC.
    Dermatol Online J; 2010 Jan 15; 16(1):8. PubMed ID: 20137750
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  • 4. Multiple disseminated glomuvenous malformations: do we know enough?
    Solovan C, Chiticariu E, Beinsan D, Zurac S, Baderca F.
    Rom J Morphol Embryol; 2012 Jan 15; 53(4):1077-80. PubMed ID: 23303036
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  • 5. A novel mutation of the glomulin gene in an Italian family with autosomal dominant cutaneous glomuvenous malformations.
    Borroni RG, Narula N, Diegoli M, Grasso M, Concardi M, Rosso R, Cerica A, Brazzelli V, Arbustini E.
    Exp Dermatol; 2011 Dec 15; 20(12):1032-4. PubMed ID: 22092580
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  • 6. Mutation analysis in Irish families with glomuvenous malformations.
    O'Hagan AH, Moloney FJ, Buckley C, Bingham EA, Walsh MY, McKenna KE, McGibbon D, Hughes AE.
    Br J Dermatol; 2006 Mar 15; 154(3):450-2. PubMed ID: 16445774
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  • 7. Glomuvenous malformation (glomangioma) and venous malformation: distinct clinicopathologic and genetic entities.
    Boon LM, Mulliken JB, Enjolras O, Vikkula M.
    Arch Dermatol; 2004 Aug 15; 140(8):971-6. PubMed ID: 15313813
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  • 8. Genetic analysis of a family with hereditary glomuvenous malformations.
    Ostberg A, Moreno G, Su T, Trisnowati N, Marchuk D, Murrell DF.
    Australas J Dermatol; 2007 Aug 15; 48(3):170-3. PubMed ID: 17680968
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  • 12. Congenital plaque-type glomuvenous malformations presenting in childhood.
    Mallory SB, Enjolras O, Boon LM, Rogers E, Berk DR, Blei F, Baselga E, Ros AM, Vikkula M.
    Arch Dermatol; 2006 Jul 15; 142(7):892-6. PubMed ID: 16847206
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  • 13. Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect.
    Brouillard P, Ghassibé M, Penington A, Boon LM, Dompmartin A, Temple IK, Cordisco M, Adams D, Piette F, Harper JI, Syed S, Boralevi F, Taïeb A, Danda S, Baselga E, Enjolras O, Mulliken JB, Vikkula M.
    J Med Genet; 2005 Feb 15; 42(2):e13. PubMed ID: 15689436
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  • 14. Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation.
    Jiang X, Yang C, Wang Z, Liang L, Gong Z, Huang S, Xu Z, Zhang B, Pei X, Cai L, Wang H, Lin Z.
    Br J Dermatol; 2024 Jun 20; 191(1):107-116. PubMed ID: 38489583
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  • 17. [Multiple familial glomangioma].
    Troschke A, Weyers W, Schill WB.
    Hautarzt; 1993 Nov 20; 44(11):731-4. PubMed ID: 8276593
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  • 18. Congenital plaque-type glomuvenous malformation associated with chylous ascites.
    Tejedor M, Martín-Santiago A, Gómez C, Fiol M, Benítez-Segura I.
    Pediatr Dermatol; 2010 Nov 20; 27(6):673-5. PubMed ID: 21510024
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  • 20. Loss of heterozygosity in a case of glomuvenous malformations.
    Ohata C, Matsuda M, Hamada T, Shintani T, Muto I, Nagata H, Furumura M, Nakama T.
    J Dermatol; 2015 Jun 20; 42(6):646-7. PubMed ID: 25809388
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