These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 8727164)

  • 1. Genetic heterogeneity of inherited cerebral cavernous malformation.
    Günel M; Awad IA; Finberg K; Steinberg GK; Craig HD; Cepeda O; Nelson-Williams C; Lifton RP
    Neurosurgery; 1996 Jun; 38(6):1265-71. PubMed ID: 8727164
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in KRIT1 in familial cerebral cavernous malformations.
    Zhang J; Clatterbuck RE; Rigamonti D; Dietz HC
    Neurosurgery; 2000 May; 46(5):1272-7; discussion 1277-9. PubMed ID: 10807272
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig.
    Johnson EW; Iyer LM; Rich SS; Orr HT; Gil-Nagel A; Kurth JH; Zabramski JM; Marchuk DA; Weissenbach J; Clericuzio CL; Davis LE; Hart BL; Gusella JF; Kosofsky BE; Louis DN; Morrison LA; Green ED; Weber JL
    Genome Res; 1995 Nov; 5(4):368-80. PubMed ID: 8750196
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Linkage of the locus for cerebral cavernous hemangiomas to human chromosome 7q in four families of Mexican-American descent.
    Polymeropoulos MH; Hurko O; Hsu F; Rubenstein J; Basnet S; Lane K; Dietz H; Spetzler RF; Rigamonti D
    Neurology; 1997 Mar; 48(3):752-7. PubMed ID: 9065560
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A founder mutation as a cause of cerebral cavernous malformation in Hispanic Americans.
    Gunel M; Awad IA; Finberg K; Anson JA; Steinberg GK; Batjer HH; Kopitnik TA; Morrison L; Giannotta SL; Nelson-Williams C; Lifton RP
    N Engl J Med; 1996 Apr; 334(15):946-51. PubMed ID: 8596595
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutational analysis of 206 families with cavernous malformations.
    Laurans MS; DiLuna ML; Shin D; Niazi F; Voorhees JR; Nelson-Williams C; Johnson EW; Siegel AM; Steinberg GK; Berg MJ; Scott RM; Tedeschi G; Enevoldson TP; Anson J; Rouleau GA; Ogilvy C; Awad IA; Lifton RP; Gunel M
    J Neurosurg; 2003 Jul; 99(1):38-43. PubMed ID: 12854741
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.
    Craig HD; Günel M; Cepeda O; Johnson EW; Ptacek L; Steinberg GK; Ogilvy CS; Berg MJ; Crawford SC; Scott RM; Steichen-Gersdorf E; Sabroe R; Kennedy CT; Mettler G; Beis MJ; Fryer A; Awad IA; Lifton RP
    Hum Mol Genet; 1998 Nov; 7(12):1851-8. PubMed ID: 9811928
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial cerebral cavernous angioma: a gene localized to a 15-cM interval on chromosome 7q.
    Gil-Nagel A; Dubovsky J; Wilcox KJ; Stewart JM; Anderson VE; Leppik IE; Orr HT; Johnson EW; Weber JL; Rich SS
    Ann Neurol; 1996 Jun; 39(6):807-10. PubMed ID: 8651655
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A locus for cerebral cavernous malformations maps to chromosome 7q in two families.
    Marchuk DA; Gallione CJ; Morrison LA; Clericuzio CL; Hart BL; Kosofsky BE; Louis DN; Gusella JF; Davis LE; Prenger VL
    Genomics; 1995 Jul; 28(2):311-4. PubMed ID: 8530042
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation.
    Dupré N; Verlaan DJ; Hand CK; Laurent SB; Turecki G; Davenport WJ; Acciarri N; Dichgans J; Ohkuma A; Siegel AM; Rouleau GA
    Can J Neurol Sci; 2003 May; 30(2):122-8. PubMed ID: 12774951
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families.
    Laberge S; Labauge P; Maréchal E; Maciazek J; Tournier-Lasserve E
    Eur J Hum Genet; 1999; 7(4):499-504. PubMed ID: 10352941
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial presumed cerebral cavernous angiomas diagnosed by MRI: three generations.
    Mori T; Fujimoto M; Sakae K; Shimada K; Shin H; Sakakibara T; Yamaki T; Ueda S
    Neuroradiology; 1996 Oct; 38(7):641-5. PubMed ID: 8912319
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21.
    Günel M; Awad IA; Anson J; Lifton RP
    Proc Natl Acad Sci U S A; 1995 Jul; 92(14):6620-4. PubMed ID: 7604043
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A gene responsible for cavernous malformations of the brain maps to chromosome 7q.
    Dubovsky J; Zabramski JM; Kurth J; Spetzler RF; Rich SS; Orr HT; Weber JL
    Hum Mol Genet; 1995 Mar; 4(3):453-8. PubMed ID: 7795602
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An association between autosomal dominant cerebral cavernomas and a distinctive hyperkeratotic cutaneous vascular malformation in 4 families.
    Labauge P; Enjolras O; Bonerandi JJ; Laberge S; Dandurand M; Joujoux JM; Tournier-Lasserve E
    Ann Neurol; 1999 Feb; 45(2):250-4. PubMed ID: 9989629
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spanish families with cavernous angiomas do not share the Hispano-American CCM1 haplotype.
    Jung HH; Labauge P; Laberge S; Maréchal E; Tournier-Lasserve E; Lucas M; Garcia-Moreno JM; Gamero MA; Izquierdo G; Touriner-Lasserve E
    J Neurol Neurosurg Psychiatry; 1999 Oct; 67(4):551-2. PubMed ID: 10610389
    [No Abstract]   [Full Text] [Related]  

  • 17. Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.
    Battistini S; Rocchi R; Cerase A; Citterio A; Tassi L; Lando G; Patrosso MC; Galli R; Brunori P; Sgrò DL; Pitillo G; Lo Russo G; Marocchi A; Penco S
    Arch Neurol; 2007 Jun; 64(6):843-8. PubMed ID: 17562932
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds.
    Spadaro M; Giunti P; Lulli P; Frontali M; Jodice C; Cappellacci S; Morellini M; Persichetti F; Trabace S; Anastasi R
    Acta Neurol Scand; 1992 Apr; 85(4):257-65. PubMed ID: 1585797
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Linkage of a medium sized Scottish autosomal dominant retinitis pigmentosa family to chromosome 7q.
    Mohamed Z; Bell C; Hammer HM; Converse CA; Esakowitz L; Haites NE
    J Med Genet; 1996 Aug; 33(8):714-5. PubMed ID: 8863169
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de Neurochirurgie.
    Labauge P; Laberge S; Brunereau L; Levy C; Tournier-Lasserve E
    Lancet; 1998 Dec; 352(9144):1892-7. PubMed ID: 9863787
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.