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Journal Abstract Search
128 related items for PubMed ID: 12811651
21. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family. Meinecke P. Genet Couns; 1993; 4(2):147-51. PubMed ID: 8395190 [Abstract] [Full Text] [Related]
22. [Exploration of renal arteries by angio-MRI]. Grenier N, Brichaux JC, Degreze P, Douws C, Palussière J, Trillaud H. Ann Radiol (Paris); 1995; 38(1-2):69-78. PubMed ID: 7632017 [Abstract] [Full Text] [Related]
23. Blepharophimosis, ptosis, polythelia and brachydactyly (BPPB): a new autosomal dominant syndrome? Wittebol-Post D, Hennekam RC. Clin Dysmorphol; 1993 Oct; 2(4):346-50. PubMed ID: 8305965 [Abstract] [Full Text] [Related]
24. Renovascular hypertension due to bilateral renal artery stenosis treated with stent implantation in a 12-year old girl. Niimura F, Matsuda S, Okamoto S, Suganuma E, Takakura H, Sugiyama Y, Shimizu T, Morimoto T, Oh Y, Koizumi J. Tokai J Exp Clin Med; 2008 Jul 20; 33(2):78-83. PubMed ID: 21318972 [Abstract] [Full Text] [Related]
25. Brachydactyly type A1 with short humerus and associated skeletal features. Lacombe D, Delrue MA, Rooryck C, Morice-Picard F, Arveiler B, Maugey-Laulom B, Mundlos S, Toutain A, Chateil JF. Am J Med Genet A; 2010 Dec 20; 152A(12):3016-21. PubMed ID: 21077205 [Abstract] [Full Text] [Related]
29. The evolution of acute hypertensive arterial disease. Byrom FB. Prog Cardiovasc Dis; 1974 Dec 20; 17(1):31-7. PubMed ID: 4600580 [No Abstract] [Full Text] [Related]
30. A distinctive autosomal recessive syndrome of severe disproportionate short stature with short long bones, brachydactyly, and hypotrichosis in two consanguineous Arab families. Shalev SA, Spiegel R, Borochowitz ZU. Eur J Med Genet; 2012 Apr 20; 55(4):256-64. PubMed ID: 22440536 [Abstract] [Full Text] [Related]
31. [Arterial hypertension due to compression of the renal artery, revealing ovarian cancer]. Jan F, Roussel L, Lassailly R, Chopin D, Rahmouni A, Levy E, Cachin JC. Presse Med; 1999 Apr 24; 28(16):841-4. PubMed ID: 10337336 [Abstract] [Full Text] [Related]
32. Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension. Toka HR, Bähring S, Chitayat D, Melby JC, Whitehead R, Jeschke E, Wienker TF, Toka O, Schuster H, Luft FC. Ann Intern Med; 1998 Aug 01; 129(3):204-8. PubMed ID: 9696728 [Abstract] [Full Text] [Related]
33. Small intrarenal arterial malformation as a cause of hypertension in a child. White AA, Palubinskas AJ. Radiology; 1970 Apr 01; 95(1):139-40. PubMed ID: 5417034 [No Abstract] [Full Text] [Related]
34. [Familial reno-vascular hypertension (author's transl)]. Plagnol P, Gillet JM, Cambuzat JM, Broussin J. J Radiol Electrol Med Nucl; 1975 Feb 01; 56(2):173-4. PubMed ID: 1151915 [Abstract] [Full Text] [Related]
36. Renal volume, renin-angiotensin-aldosterone system, hypertension, and left ventricular hypertrophy in patients with autosomal dominant polycystic kidney disease. Schrier RW. J Am Soc Nephrol; 2009 Sep 01; 20(9):1888-93. PubMed ID: 19696226 [Abstract] [Full Text] [Related]
37. [Moyamoya disease associated with stenosis of extracranial arteries: a case report and review of the literature]. Kaczorowska M, Jóźwiak S, Litwin M, Kmieć T, Kuczyński D, Jurkiewicz E, Kościerza I. Neurol Neurochir Pol; 2005 Sep 01; 39(3):242-6. PubMed ID: 15981166 [Abstract] [Full Text] [Related]