-
1
-
-
0014348274
-
Fibromuscular dysplasia of the renal arteries: Arteriographic features, classification, and observations on natural history of the disease
-
Kincaid OW, Davis GD, Hallermann FJ, Hunt JC. Fibromuscular dysplasia of the renal arteries: arteriographic features, classification, and observations on natural history of the disease. Am J Roentgenol 1968; 104:271-282.
-
(1968)
Am J Roentgenol
, vol.104
, pp. 271-282
-
-
Kincaid, O.W.1
Davis, G.D.2
Hallermann, F.J.3
Hunt, J.C.4
-
2
-
-
0023499875
-
Arterial fibromuscular dysplasia
-
Luscher TF, Lie JT, Stanson AW, Houser OW, Hollier LH, Sheps SG. Arterial fibromuscular dysplasia. Mayo Clin Proc 1987; 62:931-952.
-
(1987)
Mayo Clin Proc
, vol.62
, pp. 931-952
-
-
Luscher, T.F.1
Lie, J.T.2
Stanson, A.W.3
Houser, O.W.4
Hollier, L.H.5
Sheps, S.G.6
-
3
-
-
0344976348
-
Renal artery fibrodysplasia
-
Novick A, Scoble J, Hamilton G, editors. London: Saunders
-
Stanley JC. Renal artery fibrodysplasia. In: Novick A, Scoble J, Hamilton G, editors. Renal vascular disease. London: Saunders; 1996, pp. 21-33.
-
(1996)
Renal Vascular Disease
, pp. 21-33
-
-
Stanley, J.C.1
-
4
-
-
0024433111
-
Etiologic factors in renovascular fibromuscular dysplasia
-
Sang CN, Whelton PK, Hamper UM, Connolly M, Kadir S, White RI, et al. Etiologic factors in renovascular fibromuscular dysplasia. Hypertension 1989; 14:472-479.
-
(1989)
Hypertension
, vol.14
, pp. 472-479
-
-
Sang, C.N.1
Whelton, P.K.2
Hamper, U.M.3
Connolly, M.4
Kadir, S.5
White, R.I.6
-
5
-
-
0032810131
-
Increased severity of multifocal renal arterial fibromuscular dysplasia in smokers
-
Bofinger A, Hawley C, Fisher P, Daunt N, Stowasser M, Gordon R. Increased severity of multifocal renal arterial fibromuscular dysplasia in smokers. J Hum Hypertens 1999; 13:517-520.
-
(1999)
J Hum Hypertens
, vol.13
, pp. 517-520
-
-
Bofinger, A.1
Hawley, C.2
Fisher, P.3
Daunt, N.4
Stowasser, M.5
Gordon, R.6
-
6
-
-
0031471641
-
Possible familial origin of multifocal renal artery fibromuscular dysplasia
-
Pannier-Moreau I, Grimbert P, Fiquet-Kempf B, Vuagnat A, Jeunemaitre X, Corvol P, et al. Possible familial origin of multifocal renal artery fibromuscular dysplasia. J Hypertens 1997; 15:1797-1801.
-
(1997)
J Hypertens
, vol.15
, pp. 1797-1801
-
-
Pannier-Moreau, I.1
Grimbert, P.2
Fiquet-Kempf, B.3
Vuagnat, A.4
Jeunemaitre, X.5
Corvol, P.6
-
7
-
-
0018906145
-
The genetics of fibromuscular dysplasia
-
Rushton AR. The genetics of fibromuscular dysplasia. Arch Intern Med 1980; 140:233-236.
-
(1980)
Arch Intern Med
, vol.140
, pp. 233-236
-
-
Rushton, A.R.1
-
8
-
-
0018862713
-
Penetrance estimates and recurrence risks for fibromuscular dysplasia
-
Gladstein K, Rushton AR, Kidd KK. Penetrance estimates and recurrence risks for fibromuscular dysplasia. Clin Genet 1980; 17:115-116.
-
(1980)
Clin Genet
, vol.17
, pp. 115-116
-
-
Gladstein, K.1
Rushton, A.R.2
Kidd, K.K.3
-
9
-
-
0026145888
-
The molecular genetics of α1-antitrypsin deficiency
-
Wu Y, Foreman. The molecular genetics of α1-antitrypsin deficiency. Bioessays 1991; 13:163-169.
-
(1991)
Bioessays
, vol.13
, pp. 163-169
-
-
Wu, Y.1
Foreman2
-
10
-
-
0000713561
-
1-antitrypsin deficiency
-
Scriver CR, Beaudet AL, Sly WS, Valle D, editors. New York: McGraw Hill
-
1-antitrypsin deficiency. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic & molecular bases of inherited disease. 7th ed. vol. 3. New York: McGraw Hill; 1995. pp. 4125-4158.
-
(1995)
The Metabolic & Molecular Bases of Inherited Disease. 7th Ed.
, vol.3
, pp. 4125-4158
-
-
Cox, D.W.1
-
15
-
-
0031449035
-
Fibromuscular dysplasia of the internal carotid artery in a child with alpha-1-antitrypsin deficiency
-
Solder B, Streif W, Ellmunter H, Mayr U, Jaschke W. Fibromuscular dysplasia of the internal carotid artery in a child with alpha-1-antitrypsin deficiency. Dev Med Child Neurol 1997; 39:827-829.
-
(1997)
Dev Med Child Neurol
, vol.39
, pp. 827-829
-
-
Solder, B.1
Streif, W.2
Ellmunter, H.3
Mayr, U.4
Jaschke, W.5
-
16
-
-
0031696058
-
Atraumatic loss of a kidney in a patient with alpha1-antitrypsin deficiency
-
Randers E, Jonler M, Lund AM, Danielsen H. Atraumatic loss of a kidney in a patient with alpha1-antitrypsin deficiency. Nephron 1998; 80:71-75.
-
(1998)
Nephron
, vol.80
, pp. 71-75
-
-
Randers, E.1
Jonler, M.2
Lund, A.M.3
Danielsen, H.4
-
17
-
-
1442323629
-
Evidence for carotid and radial artery wall subclinical lesions in renal fibromuscular dysplasia
-
Boutouyrie P, Gimenez-Roqueplo AP, Fine E, Laloux B, Fiquet-Kempf B, Plouin PF, et al. Evidence for carotid and radial artery wall subclinical lesions in renal fibromuscular dysplasia. J Hypertens 2003; 21:2287-2295.
-
(2003)
J Hypertens
, vol.21
, pp. 2287-2295
-
-
Boutouyrie, P.1
Gimenez-Roqueplo, A.P.2
Fine, E.3
Laloux, B.4
Fiquet-Kempf, B.5
Plouin, P.F.6
-
18
-
-
0027933569
-
Short report: HYPERGENE: A clinical and genetic database for genetic analysis of human hypertension
-
Charru A, Jeunemaitre X, Soubrier F, Corvol P, Chatellier G. Short report: HYPERGENE: a clinical and genetic database for genetic analysis of human hypertension. J Hypertens 1994; 12:981-998.
-
(1994)
J Hypertens
, vol.12
, pp. 981-998
-
-
Charru, A.1
Jeunemaitre, X.2
Soubrier, F.3
Corvol, P.4
Chatellier, G.5
-
19
-
-
0346365089
-
P2Y12 H2 haplotype is associated with peripheral arterial disease: A case-control study
-
Fontana P, Gaussem P, Aiach M, Fiessinger JN, Emmerich J, Reny JL P2Y12 H2 haplotype is associated with peripheral arterial disease: a case-control study. Circulation 2003; 24:2971-2973.
-
(2003)
Circulation
, vol.24
, pp. 2971-2973
-
-
Fontana, P.1
Gaussem, P.2
Aiach, M.3
Fiessinger, J.N.4
Emmerich, J.5
Reny, J.L.6
-
20
-
-
16944365257
-
Haplotypes of angiotensinogen in essential hypertension
-
Jeunemaitre X, Inoue I, Williams C, Charru A, Tichet J, Powers M, et al. Haplotypes of angiotensinogen in essential hypertension. Am J Hum Genet 1997; 60:1448-1460.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1448-1460
-
-
Jeunemaitre, X.1
Inoue, I.2
Williams, C.3
Charru, A.4
Tichet, J.5
Powers, M.6
-
21
-
-
1642313766
-
A new algorithm for haplotype-based association analysis: The Stochastic-EM algorithm
-
Tregouet DA, Escolano S, Tiret L, Mallet A, Golmard JL. A new algorithm for haplotype-based association analysis: the Stochastic-EM algorithm. Ann Hum Genet 2004; 68:165-177.
-
(2004)
Ann Hum Genet
, vol.68
, pp. 165-177
-
-
Tregouet, D.A.1
Escolano, S.2
Tiret, L.3
Mallet, A.4
Golmard, J.L.5
-
22
-
-
0037011795
-
1-anti-trypsin deficiency - A model of conformational diseases
-
1-anti-trypsin deficiency - a model of conformational diseases. N Engl J Med 2002; 346:45-53.
-
(2002)
N Engl J Med
, vol.346
, pp. 45-53
-
-
Carell, R.W.1
Lomas, D.A.2
-
23
-
-
2942638034
-
α1-antitrypsin deficiency: Molecular pathophysiology
-
Lomas DA, Parfrey H. α1-antitrypsin deficiency: molecular pathophysiology. Thorax 2004; 59:529-535.
-
(2004)
Thorax
, vol.59
, pp. 529-535
-
-
Lomas, D.A.1
Parfrey, H.2
-
24
-
-
0036433482
-
1-anti- tryspin deficiency. Summary of an analysis of published genetic epidemiologic surveys
-
1-anti-tryspin deficiency. Summary of an analysis of published genetic epidemiologic surveys. Chest 2002; 122:1818-1829.
-
(2002)
Chest
, vol.122
, pp. 1818-1829
-
-
De Serres, F.J.1
-
25
-
-
0031964132
-
Alpha-1-antitrypsin deficiency in spontaneous intracranial arterial dissections
-
Schievink WI, Katzmann JA, Piepgras DG. Alpha-1-antitrypsin deficiency in spontaneous intracranial arterial dissections. Cerebrovasc Dis 1998; 8:42-44.
-
(1998)
Cerebrovasc Dis
, vol.8
, pp. 42-44
-
-
Schievink, W.I.1
Katzmann, J.A.2
Piepgras, D.G.3
-
27
-
-
0033951435
-
Alpha-1-antitrypsin phenotypes in patients with renal arterial fibromuscular dysplasia
-
Bofinger A, Hawley C, Fisher P, Daunt N, Stowasser M, Gordon R. Alpha-1-antitrypsin phenotypes in patients with renal arterial fibromuscular dysplasia. J Hum Hypertens 2000; 14:91-94.
-
(2000)
J Hum Hypertens
, vol.14
, pp. 91-94
-
-
Bofinger, A.1
Hawley, C.2
Fisher, P.3
Daunt, N.4
Stowasser, M.5
Gordon, R.6
-
28
-
-
17444440733
-
Levels of alpha1-antitrypsin in plasma and risk of spontaneous cervical artery dissections: A case-control study
-
Vila N, Millan M, Ferrer X, Riutort N, Escudero D. Levels of alpha1-antitrypsin in plasma and risk of spontaneous cervical artery dissections: a case-control study. Stroke 2003; 34:E168-E169.
-
(2003)
Stroke
, vol.34
-
-
Vila, N.1
Millan, M.2
Ferrer, X.3
Riutort, N.4
Escudero, D.5
-
29
-
-
1842475913
-
Alpha-1-antitrypsin deficiency alleles are not associated with cervical artery dissections
-
Grond-Ginsbach C, Engelter S, Werner I, Hausser I, Muller US, Brandt T, et al. Alpha-1-antitrypsin deficiency alleles are not associated with cervical artery dissections. Neurology 2004; 62:1190-1192.
-
(2004)
Neurology
, vol.62
, pp. 1190-1192
-
-
Grond-Ginsbach, C.1
Engelter, S.2
Werner, I.3
Hausser, I.4
Muller, U.S.5
Brandt, T.6
-
30
-
-
19944427458
-
Protease inhibitors in spontaneous cervical artery dissections
-
Konrad C, Langer C, Muller GA, Berger K, Dziewas R, Stogbauer F, et al. Protease inhibitors in spontaneous cervical artery dissections. Stroke 2005; 36:9-13.
-
(2005)
Stroke
, vol.36
, pp. 9-13
-
-
Konrad, C.1
Langer, C.2
Muller, G.A.3
Berger, K.4
Dziewas, R.5
Stogbauer, F.6
-
31
-
-
0024413797
-
Incidental fibromuscular dysplasia in potential renal donors: Long-term clinical follow-up
-
Cragg AH, Smith TP, Thompson BH, Maroney TP, Stanson AW, Shaw GT, et al. Incidental fibromuscular dysplasia in potential renal donors: long-term clinical follow-up. Radiology 1989; 172:145-147.
-
(1989)
Radiology
, vol.172
, pp. 145-147
-
-
Cragg, A.H.1
Smith, T.P.2
Thompson, B.H.3
Maroney, T.P.4
Stanson, A.W.5
Shaw, G.T.6
|