Serveur d'exploration sur le lymphœdème - Analysis (UK)

Index « Auteurs » - entrée « Kevin G. Burnand »
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Kevin D. Hall < Kevin G. Burnand < Kevin Goode  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 5.
Ident.Authors (with country if any)Title
000621 (2011) Russell H. Mellor [Royaume-Uni] ; Naomi Tate ; Anthony W B. Stanton ; Charlotte Hubert ; Taija M Kinen ; Alberto Smith ; Kevin G. Burnand ; Steve Jeffery ; J Rodney Levick ; Peter S. MortimerMutations in FOXC2 in humans (lymphoedema distichiasis syndrome) cause lymphatic dysfunction on dependency.
000701 (2011) Russell H. Mellor [Royaume-Uni] ; Naomi Tate [Royaume-Uni] ; Anthony W. B. Stanton [Royaume-Uni] ; Charlotte Hubert [Royaume-Uni] ; Taija M Kinen [Royaume-Uni] ; Alberto Smith [Royaume-Uni] ; Kevin G. Burnand [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; J. Rodney Levick [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni]Mutations in FOXC2 in Humans (Lymphoedema Distichiasis Syndrome) Cause Lymphatic Dysfunction on Dependency
000769 (2010) Russell H. Mellor [Royaume-Uni] ; Charlotte E. Hubert [Royaume-Uni] ; Anthony W. B. Stanton [Royaume-Uni] ; Naomi Tate [Royaume-Uni] ; Victoria Akhras [Royaume-Uni] ; Alberto Smith [Royaume-Uni] ; Kevin G. Burnand [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; Taija M Kinen [Royaume-Uni] ; J. Rodney Levick [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni]Lymphatic Dysfunction, Not Aplasia, Underlies Milroy Disease
000969 (2007) Russell H. Mellor [Royaume-Uni] ; Glen Brice ; Anthony W B. Stanton ; Jane French ; Alberto Smith ; Steve Jeffery ; J Rodney Levick ; Kevin G. Burnand ; Peter S. MortimerMutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb.
000A37 (2007) Russell H. Mellor [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Anthony W. B. Stanton [Royaume-Uni] ; Jane French [Royaume-Uni] ; Alberto Smith [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; J. Rodney Levick [Royaume-Uni] ; Kevin G. Burnand [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni]Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb

List of associated KwdEn.i

Nombre de
documents
Descripteur
3Adult
3Female
3Humans
3Lymphedema (genetics)
3Male
3Middle Aged
3Mutation
2Aged
2Foot
2Forearm
2Forkhead Transcription Factors (genetics)
2Human
2Lymphatic System (pathology)
2Lymphedema
2Lymphedema (diagnostic imaging)
2Lymphedema (pathology)
2Lymphedema (physiopathology)
2Ultrasonography, Doppler, Color
2Young Adult
1Biopsy
1Cardiovascular disease
1Case-Control Studies
1Chromosomes, Human, Pair 16 (genetics)
1Circulatory system
1Dextrans
1Distichiasis
1Dysfunction
1Eyelashes (abnormalities)
1Eyelashes (diagnostic imaging)
1Eyelashes (pathology)
1Fluorescein-5-isothiocyanate (analogs & derivatives)
1Fluorescence
1Fluorescent Dyes
1Genes, Dominant
1Germ-Line Mutation
1Gravitation
1Immunohistochemistry
1Leg (blood supply)
1Leg (diagnostic imaging)
1Lower limb
1Lymphatic
1Lymphatic Abnormalities (diagnostic imaging)
1Lymphatic Abnormalities (genetics)
1Lymphatic Abnormalities (physiopathology)
1Lymphatic System (diagnostic imaging)
1Lymphatic System (physiology)
1Lymphatic System (physiopathology)
1Lymphatic Vessels (diagnostic imaging)
1Lymphatic Vessels (embryology)
1Lymphatic Vessels (pathology)
1Lymphedema (etiology)
1Lymphography
1Lymphography (methods)
1Mammalia
1Microlymphography
1Mutagenesis, Insertional
1Mutation, Missense
1Saphenous Vein (diagnostic imaging)
1Saphenous Vein (physiopathology)
1Skin
1Stress, Physiological
1Varicose Veins (diagnostic imaging)
1Varicose Veins (genetics)
1Varicose Veins (physiopathology)
1Vascular Endothelial Growth Factor Receptor-3 (genetics)
1Vein valve
1Veins (embryology)
1Vesicular Transport Proteins (metabolism)

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