-
1
-
-
0031726017
-
Lymphedema: Classification, diagnosis and therapy
-
Szuba A., Rockson SG Lymphedema: classification, diagnosis and therapy. Vasc Med. 1998 ; 3: 145-156.
-
(1998)
Vasc Med.
, vol.3
, pp. 145-156
-
-
Szuba, A.1
Rockson, S.G.2
-
2
-
-
0021799963
-
Primary lymphedema in children and adolescents: A follow-up study and review
-
Smeltzer DM, Stickler GB, Schirger A. Primary lymphedema in children and adolescents: a follow-up study and review. Pediatrics. 1985 ; 76: 206-218.
-
(1985)
Pediatrics
, vol.76
, pp. 206-218
-
-
Smeltzer, D.M.1
Stickler, G.B.2
Schirger, A.3
-
3
-
-
0037229314
-
The third circulation: Radionuclide lymphoscintigraphy in the evaluation of lymphedema
-
Szuba A., Shin WS, Strauss HW, Rockson S. The third circulation: radionuclide lymphoscintigraphy in the evaluation of lymphedema. J Nucl Med. 2003 ; 44: 43-57.
-
(2003)
J Nucl Med.
, vol.44
, pp. 43-57
-
-
Szuba, A.1
Shin, W.S.2
Strauss, H.W.3
Rockson, S.4
-
4
-
-
0034076410
-
Radionuclide lymphangioscintigraphy in the evaluation of peripheral lymphedema
-
Williams WH, Witte CL, Witte MH, McNeill GC Radionuclide lymphangioscintigraphy in the evaluation of peripheral lymphedema. Clin Nucl Med. 2000 ; 25: 451-464.
-
(2000)
Clin Nucl Med.
, vol.25
, pp. 451-464
-
-
Williams, W.H.1
Witte, C.L.2
Witte, M.H.3
McNeill, G.C.4
-
5
-
-
0034329969
-
Advances in imaging of lymph flow disorders
-
Witte CL, Witte MH, Unger EC, et al. Advances in imaging of lymph flow disorders. Radiographics. 2000 ; 20: 1697-1719.
-
(2000)
Radiographics
, vol.20
, pp. 1697-1719
-
-
Witte, C.L.1
Witte, M.H.2
Unger, E.C.3
-
6
-
-
0037323287
-
Differential diagnosis, investigation, and current treatment of lower limb lymphedema
-
Tiwari A., Cheng KS, Button M., Myint F., Hamilton G. Differential diagnosis, investigation, and current treatment of lower limb lymphedema. Arch Surg. 2003 ; 138: 152-161.
-
(2003)
Arch Surg.
, vol.138
, pp. 152-161
-
-
Tiwari, A.1
Cheng, K.S.2
Button, M.3
Myint, F.4
Hamilton, G.5
-
7
-
-
0742266633
-
Syndromic classification of hereditary lymphedema
-
Northup KA, Witte MH, Witte CL Syndromic classification of hereditary lymphedema. Lymphology. 2003 ; 36: 162-189.
-
(2003)
Lymphology
, vol.36
, pp. 162-189
-
-
Northup, K.A.1
Witte, M.H.2
Witte, C.L.3
-
8
-
-
13644255777
-
The potential for molecular treatment strategies in lymphatic disease
-
An A., Rockson SG The potential for molecular treatment strategies in lymphatic disease. Lymphat Res Biol. 2004 ; 2: 173-181.
-
(2004)
Lymphat Res Biol.
, vol.2
, pp. 173-181
-
-
An, A.1
Rockson, S.G.2
-
9
-
-
33748771724
-
New insights into the molecular control of the lymphatic vascular system and its role in disease
-
Cueni LN, Detmar M. New insights into the molecular control of the lymphatic vascular system and its role in disease. J Invest Dermatol. 2006 ; 12: 2167-2177.
-
(2006)
J Invest Dermatol.
, vol.12
, pp. 2167-2177
-
-
Cueni, L.N.1
Detmar, M.2
-
10
-
-
0346458751
-
Lymphatic vasculature development
-
Oliver G. Lymphatic vasculature development. Nat Rev Immunol. 2004 ; 4: 35-45.
-
(2004)
Nat Rev Immunol
, vol.4
, pp. 35-45
-
-
Oliver, G.1
-
11
-
-
0035886703
-
Lymphangiogenesis and lymphangiodysplasia: From molecular to clinical lymphology
-
Witte MH, Bernas MJ, Martin CP, Witte CL Lymphangiogenesis and lymphangiodysplasia: from molecular to clinical lymphology. Microsc Res Tech. 2001 ; 55: 122-145.
-
(2001)
Microsc Res Tech
, vol.55
, pp. 122-145
-
-
Witte, M.H.1
Bernas, M.J.2
Martin, C.P.3
Witte, C.L.4
-
12
-
-
13444254036
-
Milroy disease and the VEGFR-3 mutation phenotype
-
Brice G., Child AH, Evans A., et al. Milroy disease and the VEGFR-3 mutation phenotype. J Med Genet. 2005 ; 42: 98-102.
-
(2005)
J Med Genet.
, vol.42
, pp. 98-102
-
-
Brice, G.1
Child, A.H.2
Evans, A.3
-
13
-
-
0034041161
-
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema
-
Karkkainen MJ, Ferrell RE, Lawrence EC, et al. Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema. Nat Genet. 2000 ; 25: 153-159.
-
(2000)
Nat Genet.
, vol.25
, pp. 153-159
-
-
Karkkainen, M.J.1
Ferrell, R.E.2
Lawrence, E.C.3
-
14
-
-
0033646615
-
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome
-
Fang J., Dagenais SL, Erickson RP, et al. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome. Am J Hum Genet. 2000 ; 67: 1382-1388.
-
(2000)
Am J Hum Genet.
, vol.67
, pp. 1382-1388
-
-
Fang, J.1
Dagenais, S.L.2
Erickson, R.P.3
-
15
-
-
34247168398
-
Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb
-
Mellor RH, Brice G., Stanton AW, et al. Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb. Circulation. 2007 ; 115: 1912-1920.
-
(1912)
Circulation
, vol.115
-
-
Mellor, R.H.1
Brice, G.2
Stanton, A.W.3
-
16
-
-
0037794552
-
Age of onset in hereditary lymphedema
-
Levinson KL, Feingold E., Ferrell RE, Glover TW, Traboulsi EI, Finegold DN Age of onset in hereditary lymphedema. J Pediatr. 2003 ; 142: 704-708.
-
(2003)
J Pediatr.
, vol.142
, pp. 704-708
-
-
Levinson, K.L.1
Feingold, E.2
Ferrell, R.E.3
Glover, T.W.4
Traboulsi, E.I.5
Finegold, D.N.6
-
17
-
-
0038353732
-
Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedematelangiectasia
-
Irrthum A., Devriendt K., Chitayat D., et al. Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedematelangiectasia. Am J Hum Genet. 2003 ; 72: 1470-1478.
-
(2003)
Am J Hum Genet.
, vol.72
, pp. 1470-1478
-
-
Irrthum, A.1
Devriendt, K.2
Chitayat, D.3
-
19
-
-
0036657496
-
Lymphedema: An immunologically vulnerable site for development of neoplasms
-
Ruocco V., Schwartz RA, Ruocco E. Lymphedema: an immunologically vulnerable site for development of neoplasms. J Am Acad Dermatol. 2002 ; 47: 124-127.
-
(2002)
J Am Acad Dermatol.
, vol.47
, pp. 124-127
-
-
Ruocco, V.1
Schwartz, R.A.2
Ruocco, E.3
-
20
-
-
0031695871
-
Lymphangiosarcoma of the pubic region: A rare complication arising in congenital non-hereditary lymphedema
-
Cerri A., Gianni C., Corbellino M., Pizzuto M., Moneghini L., Crosti C. Lymphangiosarcoma of the pubic region: a rare complication arising in congenital non-hereditary lymphedema. Eur J Dermatol. 1998 ; 8: 511-514.
-
(1998)
Eur J Dermatol.
, vol.8
, pp. 511-514
-
-
Cerri, A.1
Gianni, C.2
Corbellino, M.3
Pizzuto, M.4
Moneghini, L.5
Crosti, C.6
-
21
-
-
0035122850
-
Lymphedema
-
Rockson SG Lymphedema. Am J Med. 2001 ; 110: 288-295.
-
(2001)
Am J Med.
, vol.110
, pp. 288-295
-
-
Rockson, S.G.1
-
22
-
-
0032980935
-
Benzo-pyrones in the treatment of lymphoedema
-
Casley-Smith JR Benzo-pyrones in the treatment of lymphoedema. Int Angiol. 1999 ; 18: 31-41.
-
(1999)
Int Angiol.
, vol.18
, pp. 31-41
-
-
Casley-Smith, J.R.1
-
23
-
-
0034743384
-
-
International Society of Lymphology Executive Committee.
-
Bernas MJ, Witte CL, Witte MH ; International Society of Lymphology Executive Committee. The diagnosis and treatment of peripheral lymphedema: draft revision of the 1995 Consensus Document of the International Society of Lymphology Executive Committee for discussion at the September 3-7, 2001, XVIII International Congress of Lymphology in Genoa, Italy. Lymphology. 2001 ;34: 84-91.
-
The Diagnosis and Treatment of Peripheral Lymphedema: Draft Revision of the 1995 Consensus Document of the International Society of Lymphology Executive Committee for Discussion at the September 3-7, 2001, XVIII International Congress of Lymphology in Genoa, Italy
-
-
Bernas, M.J.1
Witte, C.L.2
Witte, M.H.3
-
24
-
-
0037373489
-
VEGF-C gene therapy augments postnatal lymphangiogenesis and ameliorates secondary lymphedema
-
Yoon YS, Murayama T., Gravereaux E., et al. VEGF-C gene therapy augments postnatal lymphangiogenesis and ameliorates secondary lymphedema. J Clin Invest. 2003, 11: 717-725.
-
(2003)
J Clin Invest.
, vol.11
, pp. 717-725
-
-
Yoon, Y.S.1
Murayama, T.2
Gravereaux, E.3
|