-
1
-
-
0000107920
-
Monoclonal gammopathies: Multiple myeloma, amyloidosis, and related disorders
-
In Schrier RW Ed; Lippincot: Williams & Wilkins
-
Ronco PM, Aucouturier P, Mougenot B. Monoclonal gammopathies: Multiple myeloma, amyloidosis, and related disorders. In Schrier RW Ed. Diseases of the Kidney and Urinary Tract. Lippincot: Williams & Wilkins 2001; 2205-53.
-
(2001)
Diseases of the Kidney and Urinary Tract
, pp. 2205-2253
-
-
Ronco, P.M.1
Aucouturier, P.2
Mougenot, B.3
-
3
-
-
0034759636
-
Les fièvres récurrentes héréditaires à l'ère de la biologie moléculaire
-
Mery JP, Dodé C, Grateau G. Les fièvres récurrentes héréditaires à l'ère de la biologie moléculaire. Médecine/Sciences 2001; 17: 1008-16.
-
(2001)
Médecine/Sciences
, vol.17
, pp. 1008-1016
-
-
Mery, J.P.1
Dodé, C.2
Grateau, G.3
-
4
-
-
0026653798
-
Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16
-
Pras E, Aksentijevich I, Gruberg L. Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16. N Engl J Med 1992; 23: 1509-13.
-
(1992)
N Engl J Med
, vol.23
, pp. 1509-1513
-
-
Pras, E.1
Aksentijevich, I.2
Gruberg, L.3
-
5
-
-
0034031649
-
The genetic basis of autosomal dominant familial Mediterranean fever
-
Booth DR, Gillmore JD, Lachmann HJ. The genetic basis of autosomal dominant familial Mediterranean fever. Q J Med 2000; 93: 217-21.
-
(2000)
Q J Med
, vol.93
, pp. 217-221
-
-
Booth, D.R.1
Gillmore, J.D.2
Lachmann, H.J.3
-
6
-
-
0032574208
-
Family Mediterranean fever
-
Ben-Chetrit E, Levy M. Family Mediterranean fever. Lancet 1998; 351: 659-64.
-
(1998)
Lancet
, vol.351
, pp. 659-664
-
-
Ben-Chetrit, E.1
Levy, M.2
-
7
-
-
0038192476
-
Clonage du gène de la fièvre Méditerranéenne familiale: Quels espoirs pour la compréhension de l'amylose AA?
-
Actualités Néphrol Hôp Necker, Paris, Flammarion Médecine-Sciences, Paris
-
Pras E. Clonage du gène de la fièvre Méditerranéenne familiale: Quels espoirs pour la compréhension de l'amylose AA? Actualités Néphrol Hôp Necker, Paris, Flammarion Médecine-Sciences, Paris 1998: 271-9.
-
(1998)
, pp. 271-279
-
-
Pras, E.1
-
8
-
-
0033754004
-
Identification of MEFV-independent modifying genetic factors for familial Mediterranean fever
-
Cazeneuve C, Ajrapetyan H, Papin S. Identification of MEFV-independent modifying genetic factors for familial Mediterranean fever. Am J Hum Genet 2000; 67: 1136-43.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1136-1143
-
-
Cazeneuve, C.1
Ajrapetyan, H.2
Papin, S.3
-
9
-
-
0033515520
-
Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes
-
McDermott MF, Aksentijevich I, Galon J. Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell 1999; 97: 133-44.
-
(1999)
Cell
, vol.97
, pp. 133-144
-
-
McDermott, M.F.1
Aksentijevich, I.2
Galon, J.3
-
11
-
-
0033919244
-
A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French family
-
Dodé C, Papo T, Fieschi C. A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French family. Arthritis Rheum 2000; 43: 1535-42.
-
(2000)
Arthritis Rheum
, vol.43
, pp. 1535-1542
-
-
Dodé, C.1
Papo, T.2
Fieschi, C.3
-
12
-
-
0035046357
-
Autosomal dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene
-
Jadoul M, Dodé C, Cosyns JP. Autosomal dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene. Kindey Int 2001; 59: 1677-82.
-
(2001)
Kindey Int
, vol.59
, pp. 1677-1682
-
-
Jadoul, M.1
Dodé, C.2
Cosyns, J.P.3
-
13
-
-
0034926933
-
The tumor-necrosis-factor receptor-associated periodic syndrome: New mutations in TNFRSF1A, ancestral origins, genotype-phenotype studies, and evidence for further genetic heterogeneity of periodic fevers
-
Aksentijevich I, Galon J, Soares M. The tumor-necrosis-factor receptor-associated periodic syndrome: New mutations in TNFRSF1A, ancestral origins, genotype-phenotype studies, and evidence for further genetic heterogeneity of periodic fevers. Am J Hum Genet 2001; 69: 301-14.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 301-314
-
-
Aksentijevich, I.1
Galon, J.2
Soares, M.3
-
14
-
-
0035189451
-
A fever gene comes in from the cold
-
Kastner DL, O'Shea J. A fever gene comes in from the cold. Nat Genet 2001; 29: 241-2.
-
(2001)
Nat Genet
, vol.29
, pp. 241-242
-
-
Kastner, D.L.1
O'Shea, J.2
-
15
-
-
0035179970
-
Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome
-
Hoffman HM, Mueller JL, Broide DH. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome. Nat Genet 2001; 29: 301-5.
-
(2001)
Nat Genet
, vol.29
, pp. 301-305
-
-
Hoffman, H.M.1
Mueller, J.L.2
Broide, D.H.3
-
16
-
-
0031802371
-
Familial amyloid polyneuropathy type I (Portuguese): Distribution and characterization of renal amyloid deposits
-
Lobato L, Beirao I, Guimaraes SM. Familial amyloid polyneuropathy type I (Portuguese): Distribution and characterization of renal amyloid deposits. Am J Kidney Dis 1998; 31: 940-6.
-
(1998)
Am J Kidney Dis
, vol.31
, pp. 940-946
-
-
Lobato, L.1
Beirao, I.2
Guimaraes, S.M.3
-
17
-
-
0031907376
-
Hereditary nephropathic system amyloidosis caused by a novel variant apolipoprotein A-I
-
Persey MR, Booth DR, Booth SE. Hereditary nephropathic system amyloidosis caused by a novel variant apolipoprotein A-I. Kidney Int 1998; 53: 276-81.
-
(1998)
Kidney Int
, vol.53
, pp. 276-281
-
-
Persey, M.R.1
Booth, D.R.2
Booth, S.E.3
-
18
-
-
0034783502
-
Renal amyloidosis caused by a novel stop-codon mutation in the apolipoprotein A-II gene
-
Yazaki M, Liepnieks JJ, Yamashita T. Renal amyloidosis caused by a novel stop-codon mutation in the apolipoprotein A-II gene. Kidney Int 2001; 60: 1658-65.
-
(2001)
Kidney Int
, vol.60
, pp. 1658-1665
-
-
Yazaki, M.1
Liepnieks, J.J.2
Yamashita, T.3
-
19
-
-
0031468862
-
Renal amyloidosis with a frame shift mutation in fibrinogen Aα-chain producing a novel amyloid protein
-
Hamidi Asl L, Liepnieks JJ, Uemichi T. Renal amyloidosis with a frame shift mutation in fibrinogen Aα-chain producing a novel amyloid protein. Blood 1997; 90: 4799.
-
(1997)
Blood
, vol.90
, pp. 4799
-
-
Hamidi Asl, L.1
Liepnieks, J.J.2
Uemichi, T.3
-
20
-
-
0036189848
-
Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family
-
Valleix S, Drunat S, Philit JB. Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family. Kidney Int 2002; 61: 907-12.
-
(2002)
Kidney Int
, vol.61
, pp. 907-912
-
-
Valleix, S.1
Drunat, S.2
Philit, J.B.3
-
21
-
-
0034126224
-
Liver transplantation for hereditary transthyretin amyloidosis
-
Suhr OB, Herlenius G, Friman S. Liver transplantation for hereditary transthyretin amyloidosis. Liver Transplant 2000; 6: 263-76.
-
(2000)
Liver Transplant
, vol.6
, pp. 263-276
-
-
Suhr, O.B.1
Herlenius, G.2
Friman, S.3
-
22
-
-
0034020609
-
Curative hepatorenal transplantation in systemic amyloidosis caused by the Glu625Val fibrinogen alpha-chain variant in an English family
-
Gillmore JD, Booth DR, Rela M. Curative hepatorenal transplantation in systemic amyloidosis caused by the Glu625Val fibrinogen alpha-chain variant in an English family. Q J Med 2000; 93: 269-75.
-
(2000)
Q J Med
, vol.93
, pp. 269-275
-
-
Gillmore, J.D.1
Booth, D.R.2
Rela, M.3
-
23
-
-
0035870770
-
Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26Arg
-
Gillmore JD, Stangou AJ, Tennent GA. Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26Arg. Transplantation 2001; 71: 986-92.
-
(2001)
Transplantation
, vol.71
, pp. 986-992
-
-
Gillmore, J.D.1
Stangou, A.J.2
Tennent, G.A.3
-
24
-
-
0031989127
-
Apolipoprotein AI and amyloidosis: A genetic model for aging
-
Benson MD. Apolipoprotein AI and amyloidosis: A genetic model for aging. Kidney Int 1998; 53: 508-9.
-
(1998)
Kidney Int
, vol.53
, pp. 508-509
-
-
Benson, M.D.1
|