BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 10649792)

  • 1. Two brothers with Hennekam syndrome and cerebral abnormalities.
    Huppke P; Christen HJ; Sattler B; Hanefeld F
    Clin Dysmorphol; 2000 Jan; 9(1):21-4. PubMed ID: 10649792
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Intestinal lymphangiectasia, lymphedema, mental retardation, and typical face: confirmation of the Hennekam syndrome.
    Gabrielli O; Catassi C; Carlucci A; Coppa GV; Giorgi P
    Am J Med Genet; 1991 Aug; 40(2):244-7. PubMed ID: 1897580
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Further delineation of Hennekam syndrome.
    Al-Gazali LI; Hertecant J; Ahmed R; Khan NA; Padmanabhan R
    Clin Dysmorphol; 2003 Oct; 12(4):227-32. PubMed ID: 14564208
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Hennekam syndrome].
    Erkan T; Kutlu T; Cullu F; Celik M; Demir T; Tüysüz B; Tümay GT
    Arch Pediatr; 1998 Dec; 5(12):1344-6. PubMed ID: 9885742
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: further case of Hennekam syndrome with a severe phenotype.
    Forzano F; Faravelli F; Loy A; Di Rocco M
    Am J Med Genet; 2002 Jul; 111(1):68-70. PubMed ID: 12124738
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.
    Hennekam RC; Geerdink RA; Hamel BC; Hennekam FA; Kraus P; Rammeloo JA; Tillemans AA
    Am J Med Genet; 1989 Dec; 34(4):593-600. PubMed ID: 2624276
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lymphoscintigraphic manifestations of Hennekam syndrome--a case report.
    Rockson SG; de los Santos M; Szuba A
    Angiology; 1999 Dec; 50(12):1017-20. PubMed ID: 10609768
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review.
    Van Balkom ID; Alders M; Allanson J; Bellini C; Frank U; De Jong G; Kolbe I; Lacombe D; Rockson S; Rowe P; Wijburg F; Hennekam RC
    Am J Med Genet; 2002 Nov; 112(4):412-21. PubMed ID: 12376947
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.
    Angle B; Hersh JH
    Am J Med Genet; 1997 Aug; 71(2):211-4. PubMed ID: 9217224
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Persistence of Müllerian derivatives and intestinal lymphangiectasis in two newborn brothers: confirmation of the Urioste syndrome.
    Bellini C; Bonioli E; Josso N; Belville C; Mazzella M; Costabel S; Sementa AR; Marino CE; Tomà P; Hennekam RC; Serra G
    Am J Med Genet; 2001 Nov; 104(1):69-74. PubMed ID: 11746031
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Aplasia cutis congenita, skull defect, brain heterotopia, and intestinal lymphangiectasia.
    Bonioli E; Hennekam RC; Spena G; Morcaldi G; Di Stefano A; Serra G; Bellini C
    Am J Med Genet A; 2005 Jan; 132A(2):202-5. PubMed ID: 15578573
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cutaneous manifestations and massive genital involvement in Hennekam syndrome.
    Musumeci ML; Nasca MR; De Pasquale R; Schwartz RA; Micali G
    Pediatr Dermatol; 2006; 23(3):239-42. PubMed ID: 16780470
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Hennekam syndrome: a case report and review of literature].
    Zhang N; Shen WB; Cai HC; Yan XM; Liu SL; Wu D; Sun G; Qian JM; Dun ZN; Zhao YQ
    Zhonghua Nei Ke Za Zhi; 2013 Mar; 52(3):192-6. PubMed ID: 23856108
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Craniosynostosis and kidney malformation in a case of Hennekam syndrome.
    Cormier-Daire V; Lyonnet S; Lehnert A; Martin D; Salomon R; Patey N; Broyer M; Ricour C; Munnich A
    Am J Med Genet; 1995 May; 57(1):66-8. PubMed ID: 7645602
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A case of Hennekam syndrome presenting with massive pericardial effusion].
    Nişli K; Oner N; Kayserili H; Ertuğrul T
    Turk Kardiyol Dern Ars; 2008 Jul; 36(5):325-8. PubMed ID: 18984984
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lymphangiectasia with persistent Müllerian derivatives: confirmation of autosomal recessive Urioste syndrome.
    van Haelst MM; Hoogeboom J; Galjaard RJ; Kleijer WJ; den Hollander NS; de Krijger RR; Hennekam RC; Niermeijer MF
    Am J Med Genet; 2001 Nov; 104(1):65-8. PubMed ID: 11746030
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intestinal lymphangiectasia-A novel finding in Van Maldergem syndrome challenging the role of lymphedema for the distinction from Hennekam syndrome.
    de Meij TGJ; Zwijnenburg PJG; Broers CJM; Bökenkamp A
    Am J Med Genet A; 2019 Jul; 179(7):1398-1399. PubMed ID: 31063239
    [No Abstract]   [Full Text] [Related]  

  • 18. Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome.
    Boone PM; Paterson S; Mohajeri K; Zhu W; Genetti CA; Tai DJC; Nori N; Agrawal PB; Bacino CA; Bi W; Talkowski ME; Hogan BM; Rodan LH
    Am J Med Genet A; 2020 Jan; 182(1):189-194. PubMed ID: 31633297
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A complicated case study: Hennekam syndrome].
    Deng XL; Yin F; Zhang GY; Duan YD
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 Jan; 17(1):77-80. PubMed ID: 25616299
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hennekam syndrome: a rare cause of primary lymphedema.
    Elmansour I; Chiheb S; Benchikhi H
    Dermatol Online J; 2014 Aug; 20(8):. PubMed ID: 25148287
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.