121 related articles for article (PubMed ID: 23856108)
1. [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]
2. [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]
3. 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]
4. 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]
5. A novel CCBE1 mutation leading to a mild form of hennekam syndrome: case report and review of the literature.
Frosk P; Chodirker B; Simard L; El-Matary W; Hanlon-Dearman A; Schwartzentruber J; Majewski J; ; Rockman-Greenberg C
BMC Med Genet; 2015 Apr; 16():28. PubMed ID: 25925991
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
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. 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]
10. 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]
11. Hennekam syndrome: a rare and often ignored cause of intestinal lymphangiectasia.
Kapoor S
Endoscopy; 2014 Jun; 46(6):542. PubMed ID: 24870712
[No 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. 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]
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. 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. Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.
Brouillard P; Dupont L; Helaers R; Coulie R; Tiller GE; Peeden J; Colige A; Vikkula M
Hum Mol Genet; 2017 Nov; 26(21):4095-4104. PubMed ID: 28985353
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. Intestinal lymphangiectasia in a 3-month-old girl: A case report of Hennekam syndrome caused by CCBE1 mutation.
Fattorusso A; Pieri ES; Dell'Isola GB; Prontera P; Mencaroni E; Stangoni G; Esposito S
Medicine (Baltimore); 2020 Jul; 99(27):e20995. PubMed ID: 32629717
[TBL] [Abstract][Full Text] [Related]
19. Functional Dissection of the CCBE1 Protein: A Crucial Requirement for the Collagen Repeat Domain.
Roukens MG; Peterson-Maduro J; Padberg Y; Jeltsch M; Leppänen VM; Bos FL; Alitalo K; Schulte-Merker S; Schulte D
Circ Res; 2015 May; 116(10):1660-9. PubMed ID: 25814692
[TBL] [Abstract][Full Text] [Related]
20. A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression.
Jackson CC; Best L; Lorenzo L; Casanova JL; Wacker J; Bertz S; Agaimy A; Harrer T
J Clin Immunol; 2016 Jan; 36(1):19-27. PubMed ID: 26686525
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
