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 *

134 related articles for article (PubMed ID: 1897580)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Protein-losing gastroenteropathy with facial anomaly and growth retardation: a mild case of Hennekam syndrome.
    Yasunaga M; Yamanaka C; Mayumi M; Momoi T; Mikawa H
    Am J Med Genet; 1993 Feb; 45(4):477-80. PubMed ID: 8465855
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Familial congenital pulmonary lymphangectasia, non-immune hydrops fetalis, facial and lower limb lymphedema: confirmation of Njolstad's report.
    Jacquemont S; Barbarot S; Bocéno M; Stalder JF; David A
    Am J Med Genet; 2000 Aug; 93(4):264-8. PubMed ID: 10946350
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. [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]  

  • 13. 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]  

  • 14. [Hennekam syndrome].
    Kato R
    Ryoikibetsu Shokogun Shirizu; 2001; (33):805-6. PubMed ID: 11462695
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Costello syndrome: further clinical delineation, natural history, genetic definition, and nosology.
    Zampino G; Mastroiacovo P; Ricci R; Zollino M; Segni G; Martini-Neri ME; Neri G
    Am J Med Genet; 1993 Aug; 47(2):176-83. PubMed ID: 8213903
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome.
    Schrander-Stumpel C; de Die-Smulders C; Fryns JP; da Costa J; Bouckaert P
    Am J Med Genet; 1990 Sep; 37(1):133-5. PubMed ID: 2240030
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The Costello syndrome.
    Say B; Güçsavaş M; Morgan H; York C
    Am J Med Genet; 1993 Aug; 47(2):163-5. PubMed ID: 8213897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Confirmation of Kapur-Toriello syndrome in an Italian patient.
    Zelante L; Candela MA; Savoia A; Gasparini P
    Clin Dysmorphol; 1999 Apr; 8(2):151-3. PubMed ID: 10319207
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.