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Severe hypoplasia of the abdominal aorta and its branches in a patient and his daughter.

Bibliographic reference Dejardin, A ; Goffette, Pierre ; Moulin, P. ; Verhelst, Robert ; Cornu, Guy ; et. al. Severe hypoplasia of the abdominal aorta and its branches in a patient and his daughter.. In: Journal of internal medicine, Vol. 255, no. 1, p. 130-6 (2004)
Permanent URL http://hdl.handle.net/2078.1/26711
  1. Giraud C, Arch Mal Coeur Vaiss, 78, 931 (1985)
  2. Suarez WA, Cardiol Young, 9, 323 (1999)
  3. Hata J, Arch Pathol Lab Med, 100, 652 (1976)
  4. Wright GB, Am J Cardiol, 52, 830 (1983)
  5. Vuong PN, Arch Pathol Lab Med, 113, 809 (1989)
  6. Bloor K, Br J Surg, 811
  7. Wessel A, Am J Med Genet, 52, 297 (1994)
  8. Rose Christof, Wessel Armin, Pankau Rainer, Partsch Carl-Joachim, Bürsch Joachim, Anomalies of the abdominal aorta in Williams-Beuren syndrome – another cause of arterial hypertension, 10.1007/s004310100835
  9. Connolly JE., J Cardiovasc Surg (Torino), 19, 563 (1978)
  10. Vuong PN, Vasa, 24, 194 (1995)
  11. Theodorides T., J Cardiovasc Surg (Torino), 20, 537 (1979)
  12. Durand I, Blaysat G, David N, Lacombe M, Tron P, Hypoplasie de l'aorte abdominale, cause rare d'hypertension artérielle du grand enfant, 10.1016/0929-693x(96)89918-0
  13. McElhinney D. B., Analysis of Cardiovascular Phenotype and Genotype-Phenotype Correlation in Individuals With a JAG1 Mutation and/or Alagille Syndrome, 10.1161/01.cir.0000037221.45902.69
  14. Sonel Birkan, Yalçın Peyman, Öztürk Erhan Arif, Bökesoy Işık, Butterfly vertebra: A case report, 10.1016/s0899-7071(01)00266-2
  15. Alagille D, J Pediatr, 86, 63 (1975)
  16. Li L, Nat Genet, 16, 243 (1997)
  17. Raas-Rothschild Annick, Shteyer Eyal, Lerer Israela, Nir Amiram, Granot Esther, Rein Azaria J.J.T., Jagged1 gene mutation for abdominal coarctation of the aorta in Alagille syndrome, 10.1002/ajmg.10652
  18. Letsch R, Thorac Cardiovasc Surg, 28, 206 (1980)
  19. Persu A, Presse Med, 26, 1429 (1997)
  20. Perez Errazquin F, Neurologia, 13, 247 (1998)
  21. Grange Dorothy K., Balfour Ian C., Chen Su-chiung, Wood Ellen G., Familial syndrome of progressive arterial occlusive disease consistent with fibromuscular dysplasia, hypertension, congenital cardiac defects, bone fragility, brachysyndactyly, and learning disabilities, 10.1002/(sici)1096-8628(19980217)75:5<469::aid-ajmg4>3.0.co;2-i
  22. Suzuki H, Daida H, Sakurai H, Yamaguchi H, Familial fibromuscular dysplasia of bilateral brachial arteries, 10.1136/hrt.82.2.251
  23. Pannier-Moreau Isabelle, Grimbert Philippe, Fiquet-Kempf Béatrice, Vuagnat Albert, Jeunemaitre Xavier, Corvol Pierre, Plouin Pierre-François, Possible familial origin of multifocal renal artery fibromuscular dysplasia : , 10.1097/00004872-199715120-00092
  24. Harrison EG, Mayo Clin Proc, 46, 161 (1971)
  25. Fiquet-Kempf B, Nephrologie, 20, 13 (1999)
  26. Dipple Katrina M., McCabe Edward R.B., Phenotypes of Patients with “Simple” Mendelian Disorders Are Complex Traits: Thresholds, Modifiers, and Systems Dynamics, 10.1086/302938
  27. Hamilton SJ, Friedman JM, Insights into the pathogenesis of neurofibromatosis 1 vasculopathy : Pathogenesis of NF1 vasculopathy, 10.1034/j.1399-0004.2000.580501.x
  28. Schievink W. I., Bjornsson J., Piepgras D. G., Coexistence of fibromuscular dysplasia and cystic medial necrosis in a patient with Marfan's syndrome and bilateral carotid artery dissections, 10.1161/01.str.25.12.2492
  29. Ewart Amanda K., Morris Colleen A., Atkinson Donald, Jin Weishan, Sternes Keith, Spallone Patricia, Stock A. Dean, Leppert Mark, Keating Mark T., Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome, 10.1038/ng0993-11
  30. Osborne Lucy R., Li Martin, Pober Barbara, Chitayat David, Bodurtha Joann, Mandel Ariane, Costa Teresa, Grebe Theresa, Cox Sarah, Tsui Lap-Chee, Scherer Stephen W., 10.1038/ng753
  31. Grimbert P, Arch Mal Coeur Vaiss, 91, 1069 (1998)
  32. Schievink WI, Neurosurgery, 43, 229 (1998)
  33. Bofinger A, Hawley C, Fisher P, Daunt N, Stowasser M, Gordon R, Polymorphisms of the renin-angiotensin system in patients with multifocal renal arterial fibromuscular dysplasia, 10.1038/sj.jhh.1001144
  34. Boutouyrie P, J Hypertens, 19, S8 (2001)