-
6
-
-
4243667178
-
Hepatocellular carcinoma, liver failure and liver mortality in obesity-related cryptogenic cirrhosis
-
(2001)
Hepatology
, vol.34
-
-
Ratziu, V.D.1
Bonyhay, L.2
Cavallaro, L.3
Di Martino, V.4
Giral, P.5
Charlotte, F.6
Opolon, P.7
Poynard, T.8
-
8
-
-
0034978317
-
Insulin resistance in non-alcoholic steatohepatitis
-
(2001)
Dig Liver Dis
, vol.33
, pp. 353-358
-
-
Comert, B.1
Mas, M.R.2
Erdem, H.3
Dinc, A.4
Saglamkaya, U.5
Cigerim, M.6
Kuzhan, O.7
Unal, T.8
Kocabalkan, F.9
-
9
-
-
0035084699
-
Nonalcoholic steatohepatitis: Association of insulin resistance and mitochondrial abnormalities
-
(2001)
Gastroenterology
, vol.120
, pp. 1183-1192
-
-
Sanyal, A.J.1
Campbell-Sargent, C.2
Mirshahi, F.3
Rizzo, W.B.4
Contos, M.J.5
Sterling, R.K.6
Luketic, V.A.7
Shiffman, M.L.8
Clore, J.N.9
-
10
-
-
0035431018
-
Nonalcoholic fatty liver disease: A feature of the metabolic syndrome
-
(2001)
Diabetes
, vol.50
, pp. 1844-1850
-
-
Marchesini, G.1
Brizi, M.2
Bianchi, G.3
Tomassetti, S.4
Bugianesi, E.5
Lenzi, M.6
McCullough, A.J.7
Natale, S.8
Forlani, G.9
Melchionda, N.10
-
11
-
-
18244364864
-
NASH and insulin resistance: Insulin hypersecretion and specific association with the insulin resistance syndrome
-
(2002)
Hepatology
, vol.35
, pp. 373-379
-
-
Chitturi, S.1
Abeygunasekera, S.2
Farrell, G.C.3
Holmes-Walker, J.4
Hui, J.M.5
Fung, C.6
Karim, R.7
Lin, R.8
Samarasinghe, D.9
Liddle, C.10
Weltman, M.11
George, J.12
-
12
-
-
0031992167
-
Role of hyperinsulinemia and glucose intolerance in the pathogenesis of nonalcoholic fatty liver in patients with normal body weight
-
(1998)
Korean J Intern Med
, vol.13
, pp. 12-14
-
-
Lee, J.H.1
Rhee, P.L.2
Lee, J.K.3
Lee, K.T.4
Kim, J.J.5
Koh, K.C.6
Paik, S.W.7
Rhee, J.C.8
Choi, K.W.9
-
13
-
-
18244385511
-
Nonalcoholic steatohepatitis, insulin resistance, and metabolic syndrome: Further evidence for an etiologic association
-
(2002)
Hepatology
, vol.35
, pp. 367-372
-
-
Pagano, G.1
Pacini, G.2
Musso, G.3
Gambino, R.4
Mecca, F.5
Depetris, N.6
Cassader, M.7
David, E.8
Cavallo-Perin, P.9
Rizzetto, M.10
-
15
-
-
0025299388
-
"Portal" adipose tissue as a generator of risk factors for cardiovascular disease and diabetes
-
(1990)
Arteriosclerosis
, vol.10
, pp. 493-498
-
-
Bjorntorp, P.1
-
21
-
-
0027585532
-
1H localized magnetic resonance spectroscopy and comparison with computed tomography
-
(1993)
Invest Radiol
, vol.28
, pp. 297-302
-
-
Longo, R.1
Ricci, C.2
Masutti, F.3
Vidimari, R.4
Croce, L.S.5
Bercich, L.6
Tiribelli, C.7
Dalla Palma, L.8
-
22
-
-
18544403656
-
Noninvasive in vivo quantitative assessment of fat content in human liver
-
(1997)
J Hepatol
, vol.27
, pp. 108-113
-
-
Ricci, C.1
Longo, R.2
Gioulis, E.3
Bosco, M.4
Pollesello, P.5
Masutti, F.6
Croce, L.S.7
Paoletti, S.8
De Bernard, B.9
Tiribelli, C.10
Dalla Palma, L.11
-
23
-
-
0036312905
-
Fat accumulation in the liver is associated with defects in insulin suppression of glucose production and serum free fatty acids independent of obesity in normal men
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 3023-3028
-
-
Seppälä-Lindroos, A.1
Vehkavaara, S.2
Häkkinen, A.-M.3
Goto, T.4
Westerbacka, J.5
Sovijärvi, A.6
Halavaara, J.7
Yki-Järvinen, H.8
-
29
-
-
0017313468
-
Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 30-1976
-
(1976)
N Engl J Med
, vol.295
, pp. 214-218
-
-
-
32
-
-
0035870558
-
Lipoatrophic diabetes and end-stage liver disease secondary to nonalcoholic steatohepatitis with recurrence after liver transplantation
-
(2001)
Transplantation
, vol.71
, pp. 892-895
-
-
Cauble, M.S.1
Gilroy, R.2
Sorrell, M.F.3
Mailliard, M.E.4
Sudan, D.L.5
Anderson, J.C.6
Wisecarver, J.L.7
Balakrishnan, S.8
Larsen, J.L.9
-
33
-
-
0036578783
-
AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34
-
(2002)
Nat Genet
, vol.31
, pp. 21-23
-
-
Agarwal, A.K.1
Arioglu, E.2
De Almeida, S.3
Akkoc, N.4
Taylor, S.I.5
Bowcock, A.M.6
Barnes, R.I.7
Garg, A.8
-
34
-
-
0034941121
-
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13
-
(2001)
Nat Genet
, vol.28
, pp. 365-370
-
-
Magre, J.1
Delepine, M.2
Khallouf, E.3
Gedde-Dahl T., Jr.4
Van Maldergem, L.5
Sobel, E.6
Papp, J.7
Meier, M.8
Megarbane, A.9
Bachy, A.10
Verloes, A.11
D'Abronzo, F.H.12
Seemanova, E.13
Assan, R.14
Baudic, N.15
Bourut, C.16
Czernichow, P.17
Huet, F.18
Grigorescu, F.19
De Kerdanet, M.20
Lacombe, D.21
Labrune, P.22
Lanza, M.23
Loret, H.24
Matsuda, F.25
Navarro, J.26
Nivelon-Chevalier, A.27
Polak, M.28
Robert, J.J.29
Tric, P.30
Tubiana-Rufi, N.31
Vigouroux, C.32
Weissenbach, J.33
Savasta, S.34
Maassen, J.A.35
Trygstad, O.36
Bogalho, P.37
Freitas, P.38
Medina, J.L.39
Bonnicci, F.40
Joffe, B.I.41
Loyson, G.42
Panz, V.R.43
Raal, F.J.44
O'Rahilly, S.45
Stephenson, T.46
Kahn, C.R.47
Lathrop, M.48
Capeau, J.49
more..
-
35
-
-
0034059075
-
Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy
-
(2000)
Hum Mol Genet
, vol.9
, pp. 109-112
-
-
Cao, H.1
Hegele, R.A.2
-
36
-
-
0033912260
-
Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1192-1198
-
-
Speckman, R.A.1
Garg, A.2
Du, F.3
Bennett, L.4
Veile, R.5
Arioglu, E.6
Taylor, S.I.7
Lovett, M.8
Bowcock, A.M.9
-
37
-
-
0033951216
-
LMNA, encoding lamin A/C, is mutated in partial lipodystrophy
-
(2000)
Nat Genet
, vol.24
, pp. 153-156
-
-
Shackleton, S.1
Lloyd, D.J.2
Jackson, S.N.3
Evans, R.4
Niermeijer, M.F.5
Singh, B.M.6
Schmidt, H.7
Brabant, G.8
Kumar, S.9
Durrington, P.N.10
Gregory, S.11
O'Rahilly, S.12
Trembath, R.C.13
-
40
-
-
0033636915
-
Serum leptin levels in patients with nonalcoholic steatohepatitis
-
(2000)
Am J Gastroenterol
, vol.95
, pp. 3584-3589
-
-
Uygun, A.1
Kadayifci, A.2
Yesilova, Z.3
Erdil, A.4
Yaman, H.5
Saka, M.6
Deveci, M.S.7
Bagci, S.8
Gulsen, M.9
Karaeren, N.10
Dagalp, K.11
-
41
-
-
0032747483
-
Relationship between serum leptin and fatty liver in Japanese male adolescent university students
-
(1999)
Am J Gastroenterol
, vol.94
, pp. 3328-3335
-
-
Tobe, K.1
Ogura, T.2
Tsukamoto, C.3
Imai, A.4
Matsuura, K.5
Iwasaki, Y.6
Shimomura, H.7
Higashi, T.8
Tsuji, T.9
-
42
-
-
0033304576
-
Human leptin deficiency caused by a missense mutation: Multiple endocrine defects, decreased sympathetic tone, and immune system dysfunction indicate new targets for leptin action, greater central than peripheral resistance to the effects of leptin, and spontaneous correction of leptin-mediated defects
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 3686-3695
-
-
Ozata, M.1
Ozdemir, I.C.2
Licinio, J.3
-
43
-
-
0344450708
-
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
-
(1998)
Nature
, vol.392
, pp. 398-401
-
-
Clement, K.1
Vaisse, C.2
Lahlou, N.3
Cabrol, S.4
Pelloux, V.5
Cassuto, D.6
Gourmelen, M.7
Dina, C.8
Chambaz, J.9
Lacorte, J.M.10
Basdevant, A.11
Bougneres, P.12
Lebouc, Y.13
Froguel, P.14
Guy-Grand, B.15
-
44
-
-
0030878110
-
Congenital leptin deficiency is associated with severe early-onset obesity in humans
-
(1997)
Nature
, vol.387
, pp. 903-908
-
-
Montague, C.T.1
Farooqi, I.S.2
Whitehead, J.P.3
Soos, M.A.4
Rau, H.5
Wareham, N.J.6
Sewter, C.P.7
Digby, J.E.8
Mohammed, S.N.9
Hurst, J.A.10
Cheetham, C.H.11
Earley, A.R.12
Barnett, A.H.13
Prins, J.B.14
O'Rahilly, S.15
-
46
-
-
0037148928
-
Leptin-replacement therapy for lipodystrophy
-
(2002)
N Engl J Med
, vol.346
, pp. 570-578
-
-
Arioglu Oral, E.1
Simha, V.2
Ruiz, E.3
Andewelt, A.4
Premkumar, A.5
Snell, P.6
Wagner, A.J.7
DePaoli, A.M.8
Reitman, M.L.9
Taylor, S.I.10
Gorden, P.11
Garg, A.12
-
48
-
-
26144441304
-
Leptin reverses insulin resistance and hepatic steatosis in patients with severe lipodystrophy
-
(2002)
J Investig Med
, vol.50
-
-
Peterson, K.F.1
Arioglu Oral, E.2
Dufour, S.3
Befroy, D.4
Ariyan, C.5
Yu, C.6
Taylor, S.I.7
Gorden, P.8
Shulman, G.I.9
|