List of bibliographic references
Number of relevant bibliographic references: 37.
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Ident. | Authors (with country if any) | Title |
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002E29 (2014) |
R M Digiovanni ; R P Erickson ; E C Ohlson ; M. Bernas ; M H Witte | A novel FLT4 mutation identified in a patient with Milroy disease. |
004F04 (2011) |
C. Campisi [Italie] ; M H Witte ; E. Fulcheri ; C. Campisi ; C. Bellini ; G. Villa ; C. Campisi ; P L Santi ; A. Parodi ; G. Murdaca ; F. Puppo ; F. Boccardo | General surgery, translational lymphology and lymphatic surgery. |
005717 (2010) |
S K Daley [États-Unis] ; M J Bernas ; B D Stea ; F. Bracamonte ; M. Mckenna ; A. Stejskal ; E D Hirleman ; M H Witte | Radioprotection from radiation-induced lymphedema without tumor protection. |
006256 (2009) |
M H Witte [États-Unis] ; R P Erickson ; M. Khalil ; M. Dellinger ; M. Bernas ; T. Grogan ; H. Nitta ; J. Feng ; D. Duggan ; C L Witte | Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2. |
006417 (2009) |
C. Bellini [Italie] ; M H Witte ; C. Campisi ; E. Bonioli ; F. Boccardo | Congenital lymphatic dysplasias: genetics review and resources for the lymphologist. |
006B00 (2008) |
M T Dellinger [États-Unis] ; K. Thome ; M J Bernas ; R P Erickson ; M H Witte | Novel FOXC2 missense mutation identified in patient with lymphedema-distichiasis syndrome and review. |
007231 (2007) |
M H Witte ; M. Bernas | Silver bullets and shotguns in lymphedema therapy. |
007A91 (2006) |
V. Jensen [États-Unis] ; M H Witte ; R. Latifi | Massive localized lipolymphedema pseudotumor in a morbidly obese patient. |
007C07 (2006) |
A. Noon [États-Unis] ; R J Hunter ; M H Witte ; B. Kriederman ; M. Bernas ; M. Rennels ; D. Percy ; S. Enerb Ck ; R P Erickson | Comparative lymphatic, ocular, and metabolic phenotypes of Foxc2 haploinsufficient and aP2-FOXC2 transgenic mice. |
008B29 (2004) |
M. Bernas ; M H Witte | Alternative/complementary treatment in lymphology: trying the untried and testing the untested. |
009061 (2003) |
K A Northup [États-Unis] ; M H Witte ; C L Witte | Syndromic classification of hereditary lymphedema. |
009D68 (2001) |
M J Bernas ; C L Witte ; M H Witte | 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. |
009D78 (2001) |
C J Holberg [États-Unis] ; R P Erickson ; M J Bernas ; M H Witte ; K E Fultz ; M. Andrade ; C L Witte | Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families. |
00A695 (2000) |
W H Williams [États-Unis] ; C L Witte ; M H Witte ; G C Mcneill | Radionuclide lymphangioscintigraphy in the evaluation of peripheral lymphedema. |
00AF42 (1999) |
L. Lee-Donaldson [États-Unis] ; M H Witte ; M. Bernas ; C L Witte ; D. Way ; B. Stea | Refinement of a rodent model of peripheral lymphedema. |
00B023 (1999) |
C L Witte [États-Unis] ; M H Witte | Diagnostic and interventional imaging of lymphatic disorders. |
00B735 (1998) |
M H Witte [États-Unis] ; R. Erickson ; M. Bernas ; M. Andrade ; F. Reiser ; W. Conlon ; H E Hoyme ; C L Witte | Phenotypic and genotypic heterogeneity in familial Milroy lymphedema. |
00B786 (1998) |
A M Stazzone ; P. Borgs ; C L Witte ; M H Witte | Lymphangitis and refractory lymphedema after treatment with topical cantharidin. |
00B798 (1998) |
M H Witte [États-Unis] ; C L Witte ; M. Bernas | ISL Consensus Document revisited: suggested modifications (summarized from discussions at the 16th ICL, Madrid, Spain, September 1997 and the Interim ISL Executive Committee meeting). |
00B831 (1998) |
C L Witte ; M H Witte | Consensus and dogma. |
00BF30 (1997) |
M H Witte [États-Unis] ; D L Way ; C L Witte ; M. Bernas | Lymphangiogenesis: mechanisms, significance and clinical implications. |
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