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

Index « Auteurs » - entrée « K G Burnand »
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K E Rogstad < K G Burnand < K G Yoganathan  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 4.
Ident.Authors (with country if any)Title
000825 (2009) S O Ogunbiyi [Royaume-Uni] ; J. Deguara ; C. Moss ; K G BurnandHereditary palmoplantar keratoderma associated with primary (congenital) lymphedema.
000958 (2007) J. Tan [Royaume-Uni] ; A. Smith ; S. Abisi ; D. Eastham ; K G BurnandTissue and urinary haemosiderin in chronic leg ulcers.
000D65 (2002) G. Brice [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; R. Bell [Royaume-Uni] ; J R O. Collin [Royaume-Uni] ; A H Child [Royaume-Uni] ; A F Brady [Royaume-Uni] ; M. Sarfarazi [États-Unis] ; K G Burnand [Royaume-Uni] ; S. Jeffery [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; V A Murday [Royaume-Uni]Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24
000D82 (2001) C L Mcguinness [Royaume-Uni] ; K G BurnandLymphoedema.

List of associated KwdEn.i

Nombre de
documents
Descripteur
4Humans
3Female
3Male
2Child, Preschool
2Diagnosis, Differential
2Lymphedema (complications)
2Lymphedema (genetics)
1Abnormalities, Multiple (diagnostic imaging)
1Abnormalities, Multiple (genetics)
1Adolescent
1Adult
1Anemia, Sickle Cell (complications)
1Anemia, Sickle Cell (diagnosis)
1Anemia, Sickle Cell (metabolism)
1Anemia, Sickle Cell (urine)
1Arthritis, Rheumatoid (complications)
1Arthritis, Rheumatoid (diagnosis)
1Arthritis, Rheumatoid (metabolism)
1Arthritis, Rheumatoid (urine)
1Biomarkers (metabolism)
1Biomarkers (urine)
1Biopsy
1Child
1Chromosome E16
1Chromosomes, Human, Pair 16 (genetics)
1Chronic Disease
1DNA-Binding Proteins (genetics)
1Distichiasis
1Elephantiasis, Filarial (diagnosis)
1Elephantiasis, Filarial (surgery)
1Eyelashes (abnormalities)
1Eyelashes (diagnostic imaging)
1FOXC2
1Family study
1Forkhead Transcription Factors
1Gene
1Genetic Linkage (genetics)
1Genetic determinism
1Genitalia (surgery)
1Hemosiderin (metabolism)
1Hemosiderin (urine)
1Human
1Infant
1Ischemia (complications)
1Ischemia (diagnosis)
1Ischemia (metabolism)
1Ischemia (urine)
1Keratoderma, Palmoplantar (complications)
1Keratoderma, Palmoplantar (congenital)
1Keratoderma, Palmoplantar (genetics)
1Leg (surgery)
1Leg Ulcer (etiology)
1Leg Ulcer (metabolism)
1Leg Ulcer (pathology)
1Leg Ulcer (urine)
1Linkage
1Lymphedema
1Lymphedema (congenital)
1Lymphedema (diagnosis)
1Lymphedema (diagnostic imaging)
1Lymphedema (etiology)
1Lymphedema (metabolism)
1Lymphedema (microbiology)
1Lymphedema (surgery)
1Lymphedema (urine)
1Lymphography (methods)
1Mutation
1Pathogenesis
1Pedigree
1Phenotype
1Predictive Value of Tests
1Prognosis
1Puberty (genetics)
1Radionuclide Imaging
1Reproducibility of Results
1Skin (metabolism)
1Skin (pathology)
1Surgical Procedures, Operative (methods)
1Syndrome
1Transcription Factors (genetics)
1Venous Insufficiency (complications)
1Venous Insufficiency (diagnosis)
1Venous Insufficiency (metabolism)
1Venous Insufficiency (urine)
1distichiasis
1primary lymphoedema
1varicose veins

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HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i  \
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