-
1
-
-
80655145234
-
Clinical review: Lipodystrophies: Genetic and acquired body fat disorders
-
Garg A. Clinical review: Lipodystrophies: Genetic and acquired body fat disorders. J Clin Endocrinol Metab. 2011;96(11):3313-3325.
-
(2011)
J Clin Endocrinol Metab
, vol.96
, Issue.11
, pp. 3313-3325
-
-
Garg, A.1
-
2
-
-
84867256114
-
Functional magnetic resonance imaging analysis of food-related brain activity in patients with lipodystrophy undergoing leptin replacement therapy
-
Aotani D, Ebihara K, Sawamoto N, Kusakabe T, Aizawa-Abe M, Kataoka S, Sakai T, Iogawa H, Ebihara C, Fujikura J, Hosoda K, Fukuyama H, Nakao K. Functional magnetic resonance imaging analysis of food-related brain activity in patients with lipodystrophy undergoing leptin replacement therapy. J Clin Endocrinol Metab. 2012;97(10):3663-3671.
-
(2012)
J Clin Endocrinol Metab
, vol.97
, Issue.10
, pp. 3663-3671
-
-
Aotani, D.1
Ebihara, K.2
Sawamoto, N.3
Kusakabe, T.4
Aizawa-Abe, M.5
Kataoka, S.6
Sakai, T.7
Iogawa, H.8
Ebihara, C.9
Fujikura, J.10
Hosoda, K.11
Fukuyama, H.12
Nakao, K.13
-
3
-
-
0037339129
-
Clinical features and metabolic derangements in acquired generalized lipodystrophy: Case reports and review of the literature
-
Misra A, Garg A. Clinical features and metabolic derangements in acquired generalized lipodystrophy: Case reports and review of the literature. Medicine (Baltimore). 2003;82(2):129-146.
-
(2003)
Medicine (Baltimore)
, vol.82
, Issue.2
, pp. 129-146
-
-
Misra, A.1
Garg, A.2
-
4
-
-
1542642958
-
Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: Report of 35 cases and review of the literature
-
Misra A, Peethambaram A, Garg A. Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: Report of 35 cases and review of the literature. Medicine (Baltimore). 2004;83(1):18-34.
-
(2004)
Medicine (Baltimore)
, vol.83
, Issue.1
, pp. 18-34
-
-
Misra, A.1
Peethambaram, A.2
Garg, A.3
-
5
-
-
12144288571
-
Changes in body composition in patients with severe lipodystrophy after leptin replacement therapy
-
Moran SA, Patten N, Young JR, Cochran E, Sebring N, Reynolds J, Premkumar A, Depaoli AM, Skarulis MC, Oral EA, Gorden P. Changes in body composition in patients with severe lipodystrophy after leptin replacement therapy. Metabolism. 2004;53(4):513-519.
-
(2004)
Metabolism
, vol.53
, Issue.4
, pp. 513-519
-
-
Moran, S.A.1
Patten, N.2
Young, J.R.3
Cochran, E.4
Sebring, N.5
Reynolds, J.6
Premkumar, A.7
DePaoli, A.M.8
Skarulis, M.C.9
Oral, E.A.10
Gorden, P.11
-
6
-
-
84897886068
-
Effects of leptin replacement therapy on pancreatic b-cell function in patients with lipodystrophy
-
Muniyappa R, Brown RJ, Mari A, Joseph J, Warren MA, Cochran EK, Skarulis MC, Gorden P. Effects of leptin replacement therapy on pancreatic b-cell function in patients with lipodystrophy. Diabetes Care. 2014;37(4):1101-1107.
-
(2014)
Diabetes Care
, vol.37
, Issue.4
, pp. 1101-1107
-
-
Muniyappa, R.1
Brown, R.J.2
Mari, A.3
Joseph, J.4
Ma, W.5
Cochran, E.K.6
Skarulis, M.C.7
Gorden, P.8
-
7
-
-
84858027751
-
Comparison of efficacy and safety of leptin replacement therapy in moderately and severely hypoleptinemic patients with familial partial lipodystrophy of the Dunnigan variety
-
Simha V, Subramanyam L, Szczepaniak L, Quittner C, Adams- Huet B, Snell P, Garg A. Comparison of efficacy and safety of leptin replacement therapy in moderately and severely hypoleptinemic patients with familial partial lipodystrophy of the Dunnigan variety. J Clin Endocrinol Metab. 2012;97(3):785-792.
-
(2012)
J Clin Endocrinol Metab
, vol.97
, Issue.3
, pp. 785-792
-
-
Simha, V.1
Subramanyam, L.2
Szczepaniak, L.3
Quittner, C.4
Adams-Huet, B.5
Snell, P.6
Garg, A.7
-
8
-
-
0036556445
-
Cardiomyopathy in congenital complete lipodystrophy
-
Bhayana S, Siu VM, Joubert GI, Clarson CL, Cao H, Hegele RA. Cardiomyopathy in congenital complete lipodystrophy. Clin Genet. 2002;61(4):283-287.
-
(2002)
Clin Genet
, vol.61
, Issue.4
, pp. 283-287
-
-
Bhayana, S.1
Siu, V.M.2
Joubert, G.I.3
Clarson, C.L.4
Cao, H.5
Hegele, R.A.6
-
9
-
-
77951643226
-
LMNA mutations, skeletal muscle lipid metabolism, and insulin resistance
-
Boschmann M, Engeli S, Moro C, Luedtke A, Adams F, Gorzelniak K, Rahn G,Mähler A, Dobberstein K, Krüger A, Schmidt S, Spuler S, Luft FC, Smith SR, Schmidt HH, Jordan J. LMNA mutations, skeletal muscle lipid metabolism, and insulin resistance. J Clin Endocrinol Metab. 2010;95(4):1634-1643.
-
(2010)
J Clin Endocrinol Metab
, vol.95
, Issue.4
, pp. 1634-1643
-
-
Boschmann, M.1
Engeli, S.2
Moro, C.3
Luedtke, A.4
Adams, F.5
Gorzelniak, K.6
Rahn, G.7
Mähler, A.8
Dobberstein, K.9
Krüger, A.10
Schmidt, S.11
Spuler, S.12
Luft, F.C.13
Smith, S.R.14
Schmidt, H.H.15
Jordan, J.16
-
10
-
-
84929347106
-
Partial and generalized lipodystrophy: Comparison of baseline characteristics and response to metreleptin
-
Diker-Cohen T, Cochran E, Gorden P, Brown RJ. Partial and generalized lipodystrophy: Comparison of baseline characteristics and response to metreleptin. J Clin Endocrinol Metab. 2015; 100(5):1802-1810.
-
(2015)
J Clin Endocrinol Metab
, vol.100
, Issue.5
, pp. 1802-1810
-
-
Diker-Cohen, T.1
Cochran, E.2
Gorden, P.3
Brown, R.J.4
-
11
-
-
33846950833
-
Efficacy and safety of leptin-replacement therapy and possible mechanisms of leptin actions in patients with generalized lipodystrophy
-
Ebihara K, Kusakabe T, Hirata M, Masuzaki H, Miyanaga F, Kobayashi N, Tanaka T, Chusho H, Miyazawa T, Hayashi T, Hosoda K, Ogawa Y, DePaoli AM, Fukushima M, Nakao K. Efficacy and safety of leptin-replacement therapy and possible mechanisms of leptin actions in patients with generalized lipodystrophy. J Clin Endocrinol Metab. 2007;92(2):532-541.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, Issue.2
, pp. 532-541
-
-
Ebihara, K.1
Kusakabe, T.2
Hirata, M.3
Masuzaki, H.4
Miyanaga, F.5
Kobayashi, N.6
Tanaka, T.7
Chusho, H.8
Miyazawa, T.9
Hayashi, T.10
Hosoda, K.11
Ogawa, Y.12
DePaoli, A.M.13
Fukushima, M.14
Nakao, K.15
-
12
-
-
77954754209
-
Cardiomyopathy in congenital and acquired generalized lipodystrophy: A clinical assessment
-
Lupsa BC, Sachdev V, Lungu AO, Rosing DR, Gorden P. Cardiomyopathy in congenital and acquired generalized lipodystrophy: A clinical assessment. Medicine (Baltimore). 2010;89(4): 245-250.
-
(2010)
Medicine (Baltimore)
, vol.89
, Issue.4
, pp. 245-250
-
-
Lupsa, B.C.1
Sachdev, V.2
Lungu, A.O.3
Rosing, D.R.4
Gorden, P.5
-
13
-
-
84885977479
-
Novel forms of lipodystrophy: Why should we care?
-
Rother KI, Brown RJ. Novel forms of lipodystrophy: why should we care?. Diabetes Care. 2013;36(8):2142-2145.
-
(2013)
Diabetes Care
, vol.36
, Issue.8
, pp. 2142-2145
-
-
Rother, K.I.1
Brown, R.J.2
-
14
-
-
84939987109
-
Recombinant human leptin treatment in genetic lipodystrophic syndromes: The longterm Spanish experience
-
Araujo-VilarD, Sánchez-Iglesias S, Guillín-Amarelle C, Castro A, Lage M, PazosM, Rial JM, Blasco J,Guillén-Navarro E, Domingo-Jiménez R, del CampoMR,González-Mendez B, Casanueva FF. Recombinant human leptin treatment in genetic lipodystrophic syndromes: The longterm Spanish experience. Endocrine. 2015;49(1):139-147.
-
(2015)
Endocrine
, vol.49
, Issue.1
, pp. 139-147
-
-
Araujo-Vilar, D.1
Sánchez-Iglesias, S.2
Guillín-Amarelle, C.3
Castro, A.4
Lage, M.5
Pazos, M.6
Rial, J.M.7
Blasco, J.8
Guillén-Navarro, E.9
Domingo-Jiménez, R.10
Del Campo, M.R.11
González-Méndez, B.12
Casanueva, F.F.13
-
15
-
-
84901626063
-
Berardinelli-Seip syndrome type 1 in an Egyptian child
-
Metwalley KA, Farghaly HS. Berardinelli-Seip syndrome type 1 in an Egyptian child. Indian J Hum Genet. 2014;20(1):75-78.
-
(2014)
Indian J Hum Genet
, vol.20
, Issue.1
, pp. 75-78
-
-
Metwalley, K.A.1
Farghaly, H.S.2
-
16
-
-
84880316181
-
Mutations in PIK3R1 cause SHORT syndrome
-
Innes AM; FORGE Canada Consortium
-
Dyment DA, Smith AC, Alcantara D, Schwartzentruber JA, Basel- Vanagaite L, Curry CJ, Temple IK, Reardon W, Mansour S, Haq MR, Gilbert R, Lehmann OJ, Vanstone MR, Beaulieu CL, Majewski J, Bulman DE, O'Driscoll M, Boycott KM, Innes AM; FORGE Canada Consortium. Mutations in PIK3R1 cause SHORT syndrome. Am J Hum Genet. 2013;93(1):158-166.
-
(2013)
Am J Hum Genet
, vol.93
, Issue.1
, pp. 158-166
-
-
Dyment, D.A.1
Smith, A.C.2
Alcantara, D.3
Schwartzentruber, J.A.4
Basel-Vanagaite, L.5
Curry, C.J.6
Temple, I.K.7
Reardon, W.8
Mansour, S.9
Haq, M.R.10
Gilbert, R.11
Lehmann, O.J.12
Vanstone, M.R.13
Beaulieu, C.L.14
Majewski, J.15
De, B.16
O'Driscoll, M.17
Boycott, K.M.18
-
17
-
-
77956097576
-
Congenital generalized lipodystrophy, type 4 (CGL4) associated with myopathy due to novel PTRF mutations
-
Shastry S, Delgado MR, Dirik E, Turkmen M, Agarwal AK, Garg A. Congenital generalized lipodystrophy, type 4 (CGL4) associated with myopathy due to novel PTRF mutations. Am J Med Genet A. 2010;152A(9):2245-2253.
-
(2010)
Am J Med Genet A
, vol.152 A
, Issue.9
, pp. 2245-2253
-
-
Shastry, S.1
Delgado, M.R.2
Dirik, E.3
Turkmen, M.4
Agarwal, A.K.5
Garg, A.6
-
18
-
-
41549146084
-
Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy
-
Kim CA, Delépine M, Boutet E, El Mourabit H, Le Lay S, Meier M, Nemani M, Bridel E, Leite CC, Bertola DR, Semple RK, O'Rahilly S, Dugail I, Capeau J, Lathrop M, Magré J. Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy. J Clin Endocrinol Metab. 2008;93(4): 1129-1134.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, Issue.4
, pp. 1129-1134
-
-
Kim, C.A.1
Delépine, M.2
Boutet, E.3
El Mourabit, H.4
Le Lay, S.5
Meier, M.6
Nemani, M.7
Bridel, E.8
Leite, C.C.9
Bertola, D.R.10
Semple, R.K.11
O'Rahilly, S.12
Dugail, I.13
Capeau, J.14
Lathrop, M.15
Magré, J.16
-
19
-
-
84908058862
-
Mandibuloacral dysplasia type A-associated progeria caused by homozygous LMNA mutation in a family from Southern China
-
Luo DQ, Wang XZ, Meng Y, He DY, Chen YM, Ke ZY, Yan M, Huang Y, Chen DF. Mandibuloacral dysplasia type A-associated progeria caused by homozygous LMNA mutation in a family from Southern China. BMC Pediatr. 2014;14:256.
-
(2014)
BMC Pediatr
, vol.14
, pp. 256
-
-
Luo, D.Q.1
Wang, X.Z.2
Meng, Y.3
He, D.Y.4
Chen, Y.M.5
Ke, Z.Y.6
Yan, M.7
Huang, Y.8
Chen, D.F.9
-
20
-
-
2542528670
-
A family with severe insulin resistance and diabetes due to a mutation in AKT2
-
George S, Rochford JJ, Wolfrum C, Gray SL, Schinner S, Wilson JC, Soos MA, Murgatroyd PR, Williams RM, Acerini CL, Dunger DB, Barford D, Umpleby AM, Wareham NJ, Davies HA, Schafer AJ, Stoffel M, O'Rahilly S, Barroso I. A family with severe insulin resistance and diabetes due to a mutation in AKT2. Science. 2004; 304(5675):1325-1328.
-
(2004)
Science
, vol.304
, Issue.5675
, pp. 1325-1328
-
-
George, S.1
Rochford, J.J.2
Wolfrum, C.3
Gray, S.L.4
Schinner, S.5
Wilson, J.C.6
Ma, S.7
Murgatroyd, P.R.8
Williams, R.M.9
Acerini, C.L.10
Dunger, D.B.11
Barford, D.12
Umpleby, A.M.13
Wareham, N.J.14
Davies, H.A.15
Schafer, A.J.16
Stoffel, M.17
O'Rahilly, S.18
Barroso, I.19
-
21
-
-
84920019338
-
Clinical and molecular characterization of a novel PLIN1 frameshift mutation identified in patients with familial partial lipodystrophy
-
Kozusko K, Tsang VH, Bottomley W, Cho YH, Gandotra S, Mimmack M, Lim K, Isaac I, Patel S, Saudek V, O'Rahilly S, Srinivasan S, Greenfield JR, Barroso I, Campbell LV, Savage DB. Clinical and molecular characterization of a novel PLIN1 frameshift mutation identified in patients with familial partial lipodystrophy. Diabetes. 2015;64(1):299-310.
-
(2015)
Diabetes
, vol.64
, Issue.1
, pp. 299-310
-
-
Kozusko, K.1
Tsang, V.H.2
Bottomley, W.3
Cho, Y.H.4
Gandotra, S.5
Mimmack, M.6
Lim, K.7
Isaac, I.8
Patel, S.9
Saudek, V.10
O'Rahilly, S.11
Srinivasan, S.12
Greenfield, J.R.13
Barroso, I.14
Campbell, L.V.15
Savage, D.B.16
-
22
-
-
43449130399
-
Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblings
-
Miyoshi Y, Akagi M, Agarwal AK, Namba N, Kato-Nishimura K, Mohri I, Yamagata M, Nakajima S, Mushiake S, Shima M, Auchus RJ, Taniike M, Garg A, Ozono K. Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblings. Clin Genet. 2008;73(6):535-544.
-
(2008)
Clin Genet
, vol.73
, Issue.6
, pp. 535-544
-
-
Miyoshi, Y.1
Akagi, M.2
Agarwal, A.K.3
Namba, N.4
Kato-Nishimura, K.5
Mohri, I.6
Yamagata, M.7
Nakajima, S.8
Mushiake, S.9
Shima, M.10
Auchus, R.J.11
Taniike, M.12
Garg, A.13
Ozono, K.14
-
23
-
-
79952185823
-
Difficult to manage diabetes mellitus associated with generalized congenital lipodystrophy. Report of two cases
-
Cardona-Hernández R, Suárez-Ortega L, Torres M. [Difficult to manage diabetes mellitus associated with generalized congenital lipodystrophy. Report of two cases]. An Pediatr (Barc). 2011;74(2): 126-130.
-
(2011)
An Pediatr (Barc)
, vol.74
, Issue.2
, pp. 126-130
-
-
Cardona-Hernández, R.1
Suárez-Ortega, L.2
Torres, M.3
-
24
-
-
38949105879
-
Phenotype and course of Hutchinson-Gilford progeria syndrome
-
Merideth MA, Gordon LB, Clauss S, Sachdev V, Smith AC, Perry MB, Brewer CC, Zalewski C, Kim HJ, Solomon B, Brooks BP, Gerber LH, Turner ML, Domingo DL, Hart TC, Graf J, Reynolds JC, Gropman A, Yanovski JA, Gerhard-Herman M, Collins FS, Nabel EG, Cannon RO III, Gahl WA, Introne WJ. Phenotype and course of Hutchinson-Gilford progeria syndrome. N Engl J Med. 2008;358(6):592-604.
-
(2008)
N Engl J Med
, vol.358
, Issue.6
, pp. 592-604
-
-
Ma, M.1
Gordon, L.B.2
Clauss, S.3
Sachdev, V.4
Smith, A.C.5
Perry, M.B.6
Brewer, C.C.7
Zalewski, C.8
Kim, H.J.9
Solomon, B.10
Brooks, B.P.11
Gerber, L.H.12
Turner, M.L.13
Domingo, D.L.14
Hart, T.C.15
Graf, J.16
Reynolds, J.C.17
Gropman, A.18
Yanovski, J.A.19
Gerhard-Herman, M.20
Collins, F.S.21
Nabel, E.G.22
Cannon, R.O.23
Gahl, W.A.24
Introne, W.J.25
more..
-
25
-
-
0041919374
-
Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia
-
Agarwal AK, Fryns JP, Auchus RJ, Garg A. Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia. Hum Mol Genet. 2003;12(16):1995-2001.
-
(2003)
Hum Mol Genet
, vol.12
, Issue.16
, pp. 1995-2001
-
-
Agarwal, A.K.1
Fryns, J.P.2
Auchus, R.J.3
Garg, A.4
-
26
-
-
0001259675
-
Leprechaunism: A euphemism for a rare familial disorder
-
Donohue WL, Uchida I. Leprechaunism: A euphemism for a rare familial disorder. J Pediatr. 1954;45(5):505-519.
-
(1954)
J Pediatr
, vol.45
, Issue.5
, pp. 505-519
-
-
Donohue, W.L.1
Uchida, I.2
-
27
-
-
84944517417
-
Leptin therapy in patients with lipodystrophy and syndromic insulin resistance
-
In: Dagogo-Jack S, ed., Cham, Switzerland: Springer International Publishing
-
Brown RJ, Gorden P. Leptin therapy in patients with lipodystrophy and syndromic insulin resistance. In: Dagogo-Jack S, ed. Leptin: Regulation and Clinical Applications. Cham, Switzerland: Springer International Publishing; 2015:225-236.
-
(2015)
Leptin: Regulation and Clinical Applications
, pp. 225-236
-
-
Brown, R.J.1
Gorden, P.2
-
28
-
-
84859420793
-
Thiazolidinedione response in familial lipodystrophy patients with LMNA mutations: A case series
-
Luedtke A, BoschmannM, Colpe C, Engeli S, Adams F, Birkenfeld AL, Haufe S, Rahn G, Luft FC, Schmidt HH, Jordan J. Thiazolidinedione response in familial lipodystrophy patients with LMNA mutations: A case series. Horm Metab Res 2012;44: 306-311.
-
(2012)
Horm Metab Res
, vol.44
, pp. 306-311
-
-
Luedtke, A.1
Boschmann, M.2
Colpe, C.3
Engeli, S.4
Adams, F.5
Birkenfeld, A.L.6
Haufe, S.7
Rahn, G.8
Luft, F.C.9
Schmidt, H.H.10
Jordan, J.11
-
29
-
-
85012039696
-
-
U.S. Food and Drug Administration, [New release], Accessed 15 April 2016.
-
U.S. Food and Drug Administration. FDA approves Myalept to treat rare metabolic disease. [New release]. 2014. Available at: Http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ ucm387060.htm. Accessed 15 April 2016.
-
(2014)
FDA Approves Myalept to Treat Rare Metabolic Disease
-
-
-
30
-
-
21344447493
-
Long-term efficacy of leptin replacement in patients with generalized lipodystrophy
-
Javor ED, Cochran EK, Musso C, Young JR, Depaoli AM, Gorden P. Long-term efficacy of leptin replacement in patients with generalized lipodystrophy. Diabetes. 2005;54(7):1994-2002.
-
(2005)
Diabetes
, vol.54
, Issue.7
, pp. 1994-2002
-
-
Javor, E.D.1
Cochran, E.K.2
Musso, C.3
Young, J.R.4
DePaoli, A.M.5
Gorden, P.6
-
31
-
-
0043172530
-
Effect of leptin replacement on intrahepatic and intramyocellular lipid content in patients with generalized lipodystrophy
-
Simha V, Szczepaniak LS, Wagner AJ, DePaoli AM, Garg A. Effect of leptin replacement on intrahepatic and intramyocellular lipid content in patients with generalized lipodystrophy. Diabetes Care. 2003;26(1):30-35.
-
(2003)
Diabetes Care
, vol.26
, Issue.1
, pp. 30-35
-
-
Simha, V.1
Szczepaniak, L.S.2
Wagner, A.J.3
DePaoli, A.M.4
Garg, A.5
-
32
-
-
0037148928
-
Leptin-replacement therapy for lipodystrophy
-
Oral EA, Simha V, Ruiz E, Andewelt A, Premkumar A, Snell P, Wagner AJ, DePaoli AM, Reitman ML, Taylor SI, Gorden P, Garg A. Leptin-replacement therapy for lipodystrophy. N Engl J Med. 2002;346(8):570-578.
-
(2002)
N Engl J Med
, vol.346
, Issue.8
, pp. 570-578
-
-
Oral, E.A.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
-
33
-
-
4544286790
-
Effects of exogenous leptin on satiety and satiation in patients with lipodystrophy and leptin insufficiency
-
McDuffie JR, Riggs PA, Calis KA, Freedman RJ, Oral EA, DePaoli AM, Yanovski JA. Effects of exogenous leptin on satiety and satiation in patients with lipodystrophy and leptin insufficiency. J Clin Endocrinol Metab. 2004;89(9):4258-4263.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, Issue.9
, pp. 4258-4263
-
-
McDuffie, J.R.1
Riggs, P.A.2
Calis, K.A.3
Freedman, R.J.4
Oral, E.A.5
DePaoli, A.M.6
Yanovski, J.A.7
-
34
-
-
84878656502
-
Leptin's role in lipodystrophic and nonlipodystrophic insulin-resistant and diabetic individuals
-
Moon HS, Dalamaga M, Kim SY, Polyzos SA, Hamnvik OP, Magkos F, Paruthi J, Mantzoros CS. Leptin's role in lipodystrophic and nonlipodystrophic insulin-resistant and diabetic individuals. Endocr Rev. 2013;34(3):377-412.
-
(2013)
Endocr Rev
, vol.34
, Issue.3
, pp. 377-412
-
-
Moon, H.S.1
Dalamaga, M.2
Kim, S.Y.3
Polyzos, S.A.4
Hamnvik, O.P.5
Magkos, F.6
Paruthi, J.7
Mantzoros, C.S.8
-
35
-
-
84881513620
-
The clinical approach to the detection of lipodystrophy-an AACE consensus statement
-
American Association of Clinical Endocrinologists
-
Handelsman Y, Oral EA, Bloomgarden ZT, Brown RJ, Chan JL, Einhorn D, Garber AJ, Garg A, Garvey WT, Grunberger G, Henry RR, Lavin N, Tapiador CD, Weyer C; American Association of Clinical Endocrinologists. The clinical approach to the detection of lipodystrophy-an AACE consensus statement. Endocr Pract. 2013;19(1):107-116.
-
(2013)
Endocr Pract
, vol.19
, Issue.1
, pp. 107-116
-
-
Handelsman, Y.1
Oral, E.A.2
Bloomgarden, Z.T.3
Brown, R.J.4
Chan, J.L.5
Einhorn, D.6
Garber, A.J.7
Garg, A.8
Garvey, W.T.9
Grunberger, G.10
Henry, R.R.11
Lavin, N.12
Tapiador, C.D.13
Weyer, C.14
-
36
-
-
84856529263
-
-
Institute of Medicine of the National Academies, Accessed 29 June 2016.
-
Institute of Medicine of the National Academies. Clinical Practice Guidelines We Can Trust: Standards for Developing Trustworthy Clinical Practice Guidelines (CPGs). 2011. Available at: Http:// www.nationalacademies.org/hmd//media/Files/Report%20Files/ 2011/Clinical-Practice-Guidelines-We-Can-Trust/Clinical%20Practice% 20Guidelines%202011%20Insert.pdf. Accessed 29 June 2016.
-
(2011)
Clinical Practice Guidelines We Can Trust: Standards for Developing Trustworthy Clinical Practice Guidelines (CPGs)
-
-
-
37
-
-
85012055257
-
-
National Guideline Clearinghouse, Accessed 29 June 2016.
-
National Guideline Clearinghouse. Criteria for Inclusion of Clinical Practice Guidelines in NGC. 2016. Available at: Http://www. guideline.gov/about/inclusion-criteria.aspx. Accessed 29 June 2016.
-
(2016)
Criteria for Inclusion of Clinical Practice Guidelines in NGC
-
-
-
38
-
-
84859304384
-
Guidelines International Network: Toward international standards for clinical practice guidelines
-
Board of Trustees of the Guidelines International Network
-
Qaseem A, Forland F, Macbeth F, Ollenschläger G, Phillips S, van der Wees P; Board of Trustees of the Guidelines International Network. Guidelines International Network: Toward international standards for clinical practice guidelines. Ann Intern Med. 2012; 156(7):525-531.
-
(2012)
Ann Intern Med
, vol.156
, Issue.7
, pp. 525-531
-
-
Qaseem, A.1
Forland, F.2
Macbeth, F.3
Ollenschläger, G.4
Phillips, S.5
Van Der Wees, P.6
-
39
-
-
44649107013
-
Patient-important outcomes in registered diabetes trials
-
Gandhi GY, Murad MH, Fujiyoshi A, Mullan RJ, Flynn DN, Elamin MB, Swiglo BA, Isley WL, Guyatt GH, Montori VM. Patient-important outcomes in registered diabetes trials. JAMA. 2008;299(21):2543-2549.
-
(2008)
JAMA
, vol.299
, Issue.21
, pp. 2543-2549
-
-
Gandhi, G.Y.1
Murad, M.H.2
Fujiyoshi, A.3
Mullan, R.J.4
Flynn, D.N.5
Elamin, M.B.6
Swiglo, B.A.7
Isley, W.L.8
Guyatt, G.H.9
Montori, V.M.10
-
40
-
-
78649718251
-
A Taiwanese boy with congenital generalized lipodystrophy caused by homozygous Ile262fs mutation in the BSCL2 gene
-
Huang HH, Chen TH, Hsiao HP, Huang CT, Wang CC, Shiau YH, Chao MC. A Taiwanese boy with congenital generalized lipodystrophy caused by homozygous Ile262fs mutation in the BSCL2 gene. Kaohsiung J Med Sci. 2010;26(11):615-620.
-
(2010)
Kaohsiung J Med Sci
, vol.26
, Issue.11
, pp. 615-620
-
-
Huang, H.H.1
Chen, T.H.2
Hsiao, H.P.3
Huang, C.T.4
Wang, C.C.5
Shiau, Y.H.6
Chao, M.C.7
-
41
-
-
0033305362
-
A gene for congenital generalized lipodystrophy maps to human chromosome 9q34
-
Garg A, Wilson R, Barnes R, Arioglu E, Zaidi Z, Gurakan F, Kocak N, O'Rahilly S, Taylor SI, Patel SB, Bowcock AM. A gene for congenital generalized lipodystrophy maps to human chromosome 9q34. J Clin Endocrinol Metab. 1999;84(9):3390-3394.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, Issue.9
, pp. 3390-3394
-
-
Garg, A.1
Wilson, R.2
Barnes, R.3
Arioglu, E.4
Zaidi, Z.5
Gurakan, F.6
Kocak, N.7
O'Rahilly, S.8
Taylor, S.I.9
Patel, S.B.10
Bowcock, A.M.11
-
42
-
-
0034941121
-
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13
-
BSCL WorkingGroup
-
Magré J,DelépineM, Khallouf E, Gedde-Dahl T Jr, VanMaldergem L, Sobel E, Papp J, Meier M, Mégarbané A, Bachy A, Verloes A, d'Abronzo FH, Seemanova E, Assan R, Baudic N, Bourut C, Czernichow P, Huet F, Grigorescu F, de Kerdanet M, Lacombe D, Labrune P, Lanza M, Loret H, Matsuda F, Navarro J, Nivelon- ChevalierA, Polak M,Robert JJ, Tric P, Tubiana-RufiN,Vigouroux C, Weissenbach J, Savasta S,Maassen JA, Trygstad O, Bogalho P, Freitas P, Medina JL, Bonnicci F, Joffe BI, Loyson G, Panz VR, Raal FJ, O'Rahilly S, Stephenson T, Kahn CR, Lathrop M, Capeau J; BSCL WorkingGroup. Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. Nat Genet. 2001;28(4):365-370.
-
(2001)
Nat Genet
, vol.28
, Issue.4
, pp. 365-370
-
-
Magré, J.1
Delépine, M.2
Khallouf, E.3
Gedde-Dahl, T.4
Van Maldergem, L.5
Sobel, E.6
Papp, J.7
Meier, M.8
Mégarbané, 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..
-
43
-
-
0037982806
-
Prevalence of mutations in AGPAT2 among human lipodystrophies
-
Magré J, Delépine M, Van Maldergem L, Robert JJ, Maassen JA, Meier M, Panz VR, Kim CA, Tubiana-Rufi N, Czernichow P, Seemanova E, Buchanan CR, Lacombe D, Vigouroux C, Lascols O, Kahn CR, Capeau J, Lathrop M. Prevalence of mutations in AGPAT2 among human lipodystrophies. Diabetes. 2003;52(6): 1573-1578.
-
(2003)
Diabetes
, vol.52
, Issue.6
, pp. 1573-1578
-
-
Magré, J.1
Delépine, M.2
Van Maldergem, L.3
Robert, J.J.4
Maassen, J.A.5
Meier, M.6
Panz, V.R.7
Kim, C.A.8
Tubiana-Rufi, N.9
Czernichow, P.10
Seemanova, E.11
Buchanan, C.R.12
Lacombe, D.13
Vigouroux, C.14
Lascols, O.15
Kahn, C.R.16
Capeau, J.17
Lathrop, M.18
-
44
-
-
0010044876
-
The structure and functions of human lysophosphatidic acid acyltransferases
-
Leung DW. The structure and functions of human lysophosphatidic acid acyltransferases. Front Biosci. 2001;6:D944-D953.
-
(2001)
Front Biosci
, vol.6
, pp. D944-D953
-
-
Leung, D.W.1
-
45
-
-
84898017031
-
BSCL2/seipin regulates adipogenesis through actin cytoskeleton remodelling
-
Yang W, Thein S, Wang X, Bi X, Ericksen RE, Xu F, Han W. BSCL2/seipin regulates adipogenesis through actin cytoskeleton remodelling. Hum Mol Genet. 2014;23(2):502-513.
-
(2014)
Hum Mol Genet
, vol.23
, Issue.2
, pp. 502-513
-
-
Yang, W.1
Thein, S.2
Wang, X.3
Bi, X.4
Ericksen, R.E.5
Xu, F.6
Han, W.7
-
46
-
-
0038607416
-
Congenital generalized lipodystrophy: Significance of triglyceride biosynthetic pathways
-
Agarwal AK, Garg A. Congenital generalized lipodystrophy: Significance of triglyceride biosynthetic pathways. Trends Endocrinol Metab. 2003;14(5):214-221.
-
(2003)
Trends Endocrinol Metab
, vol.14
, Issue.5
, pp. 214-221
-
-
Agarwal, A.K.1
Garg, A.2
-
47
-
-
31644447235
-
Phenotypic heterogeneity in biochemical parameters correlates with mutations in AGPAT2 or Seipin genes among Berardinelli-Seip congenital lipodystrophy patients
-
Gomes KB, Pardini VC, Ferreira AC, Fernandes AP. Phenotypic heterogeneity in biochemical parameters correlates with mutations in AGPAT2 or Seipin genes among Berardinelli-Seip congenital lipodystrophy patients. J Inherit Metab Dis. 2005;28(6):1123-1131.
-
(2005)
J Inherit Metab Dis
, vol.28
, Issue.6
, pp. 1123-1131
-
-
Gomes, K.B.1
Pardini, V.C.2
Ferreira, A.C.3
Fernandes, A.P.4
-
48
-
-
0012447846
-
Generalized lipodystrophy, infectious mononucleosis, mild infantile hemiplegia
-
Davis J. Generalized lipodystrophy, infectious mononucleosis, mild infantile hemiplegia. Proc R Soc Med. 1954;47(2):128-129.
-
(1954)
Proc R Soc Med
, vol.47
, Issue.2
, pp. 128-129
-
-
Davis, J.1
-
49
-
-
73049137505
-
Lipohistiodiaresis: A syndrome of lipodystrophy universalis, accelerated growth, lipemia, hepatic cirrhosis, and insulin-resistant diabetes without ketosis
-
Hansen AE, McQuarrie I, Ziegler MR. Lipohistiodiaresis: A syndrome of lipodystrophy universalis, accelerated growth, lipemia, hepatic cirrhosis, and insulin-resistant diabetes without ketosis. J Lancet. 1961;81:533-541.
-
(1961)
J Lancet
, vol.81
, pp. 533-541
-
-
Hansen, A.E.1
McQuarrie, I.2
Ziegler, M.R.3
-
50
-
-
0023507413
-
Lipoatrophic panniculitis: A possible autoimmune inflammatory disease of fat. Report of three cases
-
Billings JK, Milgraum SS, Gupta AK, Headington JT, Rasmussen JE. Lipoatrophic panniculitis: A possible autoimmune inflammatory disease of fat. Report of three cases. Arch Dermatol. 1987;123(12): 1662-1666.
-
(1987)
Arch Dermatol
, vol.123
, Issue.12
, pp. 1662-1666
-
-
Billings, J.K.1
Milgraum, S.S.2
Gupta, A.K.3
Headington, J.T.4
Rasmussen, J.E.5
-
52
-
-
77953395291
-
Acquired generalized lipodystrophy associated with autoimmune hepatitis and low serum C4 level
-
Eren E, Özkan TB, Çakir ED, Saǧlam H, TarimÖ. Acquired generalized lipodystrophy associated with autoimmune hepatitis and low serum C4 level. J Clin Res Pediatr Endocrinol. 2010;2(1):39-42.
-
(2010)
J Clin Res Pediatr Endocrinol
, vol.2
, Issue.1
, pp. 39-42
-
-
Eren, E.1
Özkan, T.B.2
Çakir, E.D.3
Saǧlam, H.4
Tarim, Ö.5
-
53
-
-
74549143737
-
Long-term outcome and prognostic factors of juvenile dermatomyositis: A multinational, multicenter study of 490 patients
-
Ravelli A, Trail L, Ferrari C, Ruperto N, Pistorio A, Pilkington C, Maillard S, Oliveira SK, Sztajnbok F, Cuttica R, Beltramelli M, Corona F, Katsicas MM, Russo R, Ferriani V, Burgos-Vargas R, Magni-Manzoni S, Solis-Valleoj E, Bandeira M, Zulian F, Baca V, Cortis E, Falcini F, Alessio M, Alpigiani MG, Gerloni V, Saad- Magalhaes C, Podda R, Silva CA, Lepore L, Felici E, Rossi F, Sala E, Martini A. Long-term outcome and prognostic factors of juvenile dermatomyositis: A multinational, multicenter study of 490 patients. Arthritis Care Res (Hoboken). 2010;62(1):63-72.
-
(2010)
Arthritis Care Res (Hoboken)
, vol.62
, Issue.1
, pp. 63-72
-
-
Ravelli, A.1
Trail, L.2
Ferrari, C.3
Ruperto, N.4
Pistorio, A.5
Pilkington, C.6
Maillard, S.7
Oliveira, S.K.8
Sztajnbok, F.9
Cuttica, R.10
Beltramelli, M.11
Corona, F.12
Katsicas, M.M.13
Russo, R.14
Ferriani, V.15
Burgos-Vargas, R.16
Magni-Manzoni, S.17
Solis-Valleoj, E.18
Bandeira, M.19
Zulian, F.20
Baca, V.21
Cortis, E.22
Falcini, F.23
Alessio, M.24
Alpigiani, M.G.25
Gerloni, V.26
Saad-Magalhaes, C.27
Podda, R.28
Silva, C.A.29
Lepore, L.30
Felici, E.31
Rossi, F.32
Sala, E.33
Martini, A.34
more..
-
54
-
-
0344442411
-
Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or seipin genes
-
Simha V, Garg A. Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or seipin genes. J Clin EndocrinolMetab. 2003;88(11):5433-5437.
-
(2003)
J Clin EndocrinolMetab
, vol.88
, Issue.11
, pp. 5433-5437
-
-
Simha, V.1
Garg, A.2
-
55
-
-
0026767508
-
Peculiar distribution of adipose tissue in patients with congenital generalized lipodystrophy
-
Garg A, Fleckenstein JL, Peshock RM, Grundy SM. Peculiar distribution of adipose tissue in patients with congenital generalized lipodystrophy. J Clin Endocrinol Metab. 1992;75(2):358-361.
-
(1992)
J Clin Endocrinol Metab
, vol.75
, Issue.2
, pp. 358-361
-
-
Garg, A.1
Fleckenstein, J.L.2
Peshock, R.M.3
Grundy, S.M.4
-
56
-
-
33144478823
-
Peroxisomal proliferator activated receptor-gamma deficiency in a Canadian kindred with familial partial lipodystrophy type 3 (FPLD3)
-
Francis GA, Li G, Casey R, Wang J, Cao H, Leff T, Hegele RA. Peroxisomal proliferator activated receptor-gamma deficiency in a Canadian kindred with familial partial lipodystrophy type 3 (FPLD3). BMC Med Genet. 2006;7:3.
-
(2006)
BMC Med Genet
, vol.7
, pp. 3
-
-
Francis, G.A.1
Li, G.2
Casey, R.3
Wang, J.4
Cao, H.5
Leff, T.6
Hegele, R.A.7
-
57
-
-
67949115766
-
Comparison of phenotypes in male and female individuals of a new family with Dunnigan type of familial partial lipodystrophy due to a lamin A/C R482W mutation
-
Laudes M, Oberhauser F,Walgenbach K, Schubert M, Schulte DM, Faust M, Krone W. Comparison of phenotypes in male and female individuals of a new family with Dunnigan type of familial partial lipodystrophy due to a lamin A/C R482W mutation. Horm Metab Res 2009; 41:414-417.
-
(2009)
Horm Metab Res
, vol.41
, pp. 414-417
-
-
Laudes, M.1
Oberhauser, F.2
Walgenbach, K.3
Schubert, M.4
Schulte, D.M.5
Faust, M.6
Krone, W.7
-
58
-
-
84890746974
-
Biochemical, hormonal and genetic evaluation of the families of two Brazilian patients with type 2 familial partial lipodystrophy
-
Caldas D, Silva Júnior WS, Simonetti JP, Costa EV, Farias ML. [Biochemical, hormonal and genetic evaluation of the families of two Brazilian patients with type 2 familial partial lipodystrophy]. Arq Bras Endocrinol Metabol. 2013;57(8):583-593.
-
(2013)
Arq Bras Endocrinol Metabol
, vol.57
, Issue.8
, pp. 583-593
-
-
Caldas, D.1
Silva Júnior, W.S.2
Simonetti, J.P.3
Costa, E.V.4
Farias, M.L.5
-
59
-
-
0037253150
-
Phenotypic gender differences in subjects with familial partial lipodystrophy (Dunnigan variety) due to a nuclear lamin A/C R482Wmutation
-
Araujo-VilarD, Loidi L,Dominguez F,Cabezas-Cerrato J. Phenotypic gender differences in subjects with familial partial lipodystrophy (Dunnigan variety) due to a nuclear lamin A/C R482Wmutation. Horm Metab Res 2003;35:29-35.
-
(2003)
Horm Metab Res
, vol.35
, pp. 29-35
-
-
Araujo-Vilar, D.1
Loidi, L.2
Dominguez, F.3
Cabezas-Cerrato, J.4
-
60
-
-
17744363062
-
Dyslipemia in familial partial lipodystrophy caused by an R482W mutation in theLMNAgene
-
Schmidt HHJ, Genschel J, Baier P, Schmidt M, Ockenga J, Tietge UJF, Pröpsting M, Büttner C, Manns MP, Lochs H, Brabant G. Dyslipemia in familial partial lipodystrophy caused by an R482W mutation in theLMNAgene. J Clin Endocrinol Metab. 2001;86(5): 2289-2295.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, Issue.5
, pp. 2289-2295
-
-
Schmidt, H.H.J.1
Genschel, J.2
Baier, P.3
Schmidt, M.4
Ockenga, J.5
Tietge, U.J.F.6
Pröpsting, M.7
Büttner, C.8
Manns, M.P.9
Lochs, H.10
Brabant, G.11
-
61
-
-
34447528982
-
Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronism
-
Vantyghem MC, Faivre-Defrance F, Marcelli-Tourvieille S, Fermon C, Evrard A, Bourdelle-Hego MF, Vigouroux C, Defebvre L, Delemer B, Wemeau JL. Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronism. Clin Endocrinol (Oxf). 2007;67(2):247-249.
-
(2007)
Clin Endocrinol (Oxf)
, vol.67
, Issue.2
, pp. 247-249
-
-
Vantyghem, M.C.1
Faivre-Defrance, F.2
Marcelli-Tourvieille, S.3
Fermon, C.4
Evrard, A.5
Bourdelle-Hego, M.F.6
Vigouroux, C.7
Defebvre, L.8
Delemer, B.9
Wemeau, J.L.10
-
63
-
-
85063658445
-
Recurrent stroke as a presenting feature of acquired partial lipodystrophy
-
Prasad NR,Reddy PA,Menon B, KarthikTS, Ahmed F,Chakravarthy M. Recurrent stroke as a presenting feature of acquired partial lipodystrophy. Indian J Endocrinol Metab. 2012;16(Suppl 2): S455-S457.
-
(2012)
Indian J Endocrinol Metab
, vol.16
, pp. S455-S457
-
-
Prasad, N.R.1
Reddy, P.A.2
Menon, B.3
Karthik, T.S.4
Ahmed, F.5
Chakravarthy, M.6
-
64
-
-
84903897703
-
How to read a systematic review and meta-analysis and apply the results to patient care: Users' guides to the medical literature
-
Murad MH, Montori VM, Ioannidis JP, Jaeschke R, Devereaux PJ, Prasad K, Neumann I, Carrasco-Labra A, Agoritsas T, Hatala R, Meade MO,Wyer P, Cook DJ, Guyatt G. How to read a systematic review and meta-analysis and apply the results to patient care: Users' guides to the medical literature. JAMA. 2014;312(2):171-179.
-
(2014)
JAMA
, vol.312
, Issue.2
, pp. 171-179
-
-
Murad, M.H.1
Montori, V.M.2
Ioannidis, J.P.3
Jaeschke, R.4
Devereaux, P.J.5
Prasad, K.6
Neumann, I.7
Carrasco-Labra, A.8
Agoritsas, T.9
Hatala, R.10
Meade, M.O.11
Wyer, P.12
Cook, D.J.13
Guyatt, G.14
-
65
-
-
84965184994
-
Plasma leptin concentrations are highly correlated to emotional states throughout the day
-
Licinio J, Negrao AB, Wong ML. Plasma leptin concentrations are highly correlated to emotional states throughout the day. Transl Psychiatry. 2014;4:e475.
-
(2014)
Transl Psychiatry
, vol.4
, pp. e475
-
-
Licinio, J.1
Negrao, A.B.2
Wong, M.L.3
-
66
-
-
74949143243
-
Narrative review: The role of leptin in human physiology: Emerging clinical applications
-
Kelesidis T, Kelesidis I, Chou S, Mantzoros CS. Narrative review: The role of leptin in human physiology: Emerging clinical applications. Ann Intern Med. 2010;152(2):93-100.
-
(2010)
Ann Intern Med
, vol.152
, Issue.2
, pp. 93-100
-
-
Kelesidis, T.1
Kelesidis, I.2
Chou, S.3
Mantzoros, C.S.4
-
67
-
-
84873876984
-
Serum leptin values in the healthy obese and non-obese subjects of Rawalpindi
-
Kazmi A, Sattar A, Hashim R, Khan SP, Younus M, Khan FA. Serum leptin values in the healthy obese and non-obese subjects of Rawalpindi. J Pak Med Assoc. 2013;63(2):245-248.
-
(2013)
J Pak Med Assoc
, vol.63
, Issue.2
, pp. 245-248
-
-
Kazmi, A.1
Sattar, A.2
Hashim, R.3
Khan, S.P.4
Younus, M.5
Khan, F.A.6
-
68
-
-
84930800726
-
Reference values for leptin and adiponectin in children below the age of 10 based on the IDEFICS cohort
-
IDEFICS Consortium
-
Erhardt E, Foraita R, Pigeot I, Barba G, Veidebaum T, Tornaritis M, Michels N, Eiben G, Ahrens W, Moreno LA, Kovács E, Molnár D; IDEFICS Consortium. Reference values for leptin and adiponectin in children below the age of 10 based on the IDEFICS cohort. Int J Obes. 2014;38(Suppl 2):S32-S38.
-
(2014)
Int J Obes
, vol.38
, pp. S32-S38
-
-
Erhardt, E.1
Foraita, R.2
Pigeot, I.3
Barba, G.4
Veidebaum, T.5
Tornaritis, M.6
Michels, N.7
Eiben, G.8
Ahrens, W.9
Moreno, L.A.10
Kovács, E.11
Molnár, D.12
-
69
-
-
84883334505
-
A meta-analysis of reference values of leptin concentration in healthy postmenopausal women
-
Zhou X, Chai Y, Chen K, Yang Y, Liu Z. A meta-analysis of reference values of leptin concentration in healthy postmenopausal women. PLoS One. 2013;8(8):e72734.
-
(2013)
PLoS One
, vol.8
, Issue.8
, pp. e72734
-
-
Zhou, X.1
Chai, Y.2
Chen, K.3
Yang, Y.4
Liu, Z.5
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