127 related articles for article (PubMed ID: 25616299)
21. Intestinal lymphangiectasia in an adolescent. A case study of edema.
Gallo-Van Ess DM; Strasburger VC; Turetsky RA
J Adolesc Health Care; 1986 Jul; 7(4):259-64. PubMed ID: 3721949
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis.
Connell FC; Kalidas K; Ostergaard P; Brice G; Murday V; Mortimer PS; Jeffrey I; Jeffery S; Mansour S
Clin Genet; 2012 Feb; 81(2):191-7. PubMed ID: 22239599
[No Abstract] [Full Text] [Related]
24. 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]
25. Intestinal Lymphangiestasia With Hennekam Syndrome.
Viswanathan P; Novak I
J Pediatr Gastroenterol Nutr; 2017 Dec; 65(6):e133. PubMed ID: 26863383
[No Abstract] [Full Text] [Related]
26. 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]
27. [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]
28. 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]
29. 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]
30. 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]
31. 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]
32. 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]
33. A primary intestinal lymphangiectasia hiding the diagnosis of pleural and pericardial tuberculosis: a clinical observation.
Hammi S; Berrani H; Benouchen T; Lamlami N; Elkhiyat I; Bourkadi JE
Pan Afr Med J; 2017; 26():89. PubMed ID: 28491220
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. [Variant analysis of CCBE1 gene in a case of Hennekam lymphangiectasia-lymphedema syndrome type 1].
Ren Y; Liu Y; Lyu Y; Gao M; Wang D; Wan Y; Ma J; Shen N; Gai Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jun; 37(6):669-672. PubMed ID: 32472549
[TBL] [Abstract][Full Text] [Related]
36. Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis.
Shinwari K; Guojun L; Deryabina SS; Bolkov MA; Tuzankina IA; Chereshnev VA
ScientificWorldJournal; 2021; 2021():6642626. PubMed ID: 34234628
[TBL] [Abstract][Full Text] [Related]
37. Disorders of the intestinal mesenteric lymphatic system.
Fox U; Lucani G
Lymphology; 1993 Jun; 26(2):61-6. PubMed ID: 8355519
[TBL] [Abstract][Full Text] [Related]
38. Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations.
Alders M; Mendola A; Adès L; Al Gazali L; Bellini C; Dallapiccola B; Edery P; Frank U; Hornshuh F; Huisman SA; Jagadeesh S; Kayserili H; Keng WT; Lev D; Prada CE; Sampson JR; Schmidtke J; Shashi V; van Bever Y; Van der Aa N; Verhagen JM; Verheij JB; Vikkula M; Hennekam RC
Mol Syndromol; 2013 Mar; 4(3):107-13. PubMed ID: 23653581
[TBL] [Abstract][Full Text] [Related]
39. A child with diarrhea and recurrent otitis.
Mönkemüller K; Fry LC; Heiduk M
Gastroenterology; 2012 Mar; 142(3):432, 677. PubMed ID: 22281272
[No Abstract] [Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
