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

Index « Auteurs » - entrée « G. Brice »
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List of bibliographic references

Number of relevant bibliographic references: 18.
Ident.Authors (with country if any)Title
000399 (2013) K D Gordon ; G. Brice ; Y. Walker ; R. Pollok ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; C. SlaterGenital lymphoedema due to ano-genital granulomatosis.
000440 (2013) Fc Connell [Royaume-Uni] ; K. Gordon [Royaume-Uni] ; G. Brice [Royaume-Uni] ; V. Keeley [Royaume-Uni] ; S. Jeffery [Royaume-Uni] ; Ps Mortimer [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; P. Ostergaard [Royaume-Uni]The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings
000461 (2013) G. Atton [Royaume-Uni] ; K. Gordon [Royaume-Uni] ; G. Brice [Royaume-Uni] ; V. Keeley [Royaume-Uni] ; K. Riches [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. Mansour [Royaume-Uni]G27 The Lymphatic Phenotype in Turner Syndrome: An Evaluation of Patients Presenting to Three Specialist Primary Lymphoedema Clinics and Literature Review
000477 (2013) G. Brice [Royaume-Uni] ; P. Ostergaard ; S. Jeffery ; K. Gordon [Royaume-Uni] ; Ps Mortimer [Royaume-Uni] ; S. MansourA novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family
000582 (2012) Fc Connell [Royaume-Uni] ; K. Kalidas ; P. Ostergaard ; G. Brice [Royaume-Uni] ; V. Murday [Royaume-Uni] ; Ps Mortimer ; I. Jeffrey [Royaume-Uni] ; S. Jeffery ; Sahar Mansour [Royaume-Uni]CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non‐immune hydrops fetalis
000786 (2010) F. Connell ; G. Brice [Royaume-Uni] ; S. Jeffery ; V. Keeley [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. Mansour [Royaume-Uni]A new classification system for primary lymphatic dysplasias based on phenotype
000839 (2009) F C Connell [Royaume-Uni] ; P. Ostergaard ; C. Carver ; G. Brice ; N. Williams ; S. Mansour ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Steve JefferyAnalysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.
000888 (2009) F. C. Connell [Royaume-Uni] ; P. Ostergaard [Royaume-Uni] ; C. Carver [Royaume-Uni] ; G. Brice [Royaume-Uni] ; N. Williams [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Steve Jeffery [Royaume-Uni]Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas
000A00 (2007) C. Carver ; G. Brice ; S. Mansour ; P. Ostergaard ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. JefferyThree children with Milroy disease and de novo mutations in VEGFR3
000A30 (2007) S. Kumar [Arabie saoudite] ; C. Carver ; S. Mccall ; G. Brice ; P. Ostergaard ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. Jeffery [Royaume-Uni]A family with lymphoedema‐distichiasis where identical twins have a discordant phenotype
000B59 (2005) G. Brice [Royaume-Uni] ; A H Child [Royaume-Uni] ; A. Evans [Royaume-Uni] ; R. Bell [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; K. Burnand [Royaume-Uni] ; M. Sarfarazi [États-Unis] ; S. Jeffery [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni]Milroy disease and the VEGFR-3 mutation phenotype
000C70 (2003) M. Ameen [Royaume-Uni] ; G. Brice ; Peter Mortimer (dermatologue)‎ [Royaume-Uni]Clinicopathological case 2: lymphoedema-distichiasis syndrome.
000C91 (2003) A L Evans [Royaume-Uni] ; R. Bell ; G. Brice [Royaume-Uni] ; P. Comeglio [Royaume-Uni] ; C. Lipede ; S. Jeffery ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; M. Sarfarazi [États-Unis] ; A H Child [Royaume-Uni]Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema
000D07 (2003) M. Ameen [Royaume-Uni] ; G. Brice [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni]Case 2
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
000E70 (2001) R. Bell [Royaume-Uni] ; G. Brice [Royaume-Uni] ; A. H. Child [Royaume-Uni] ; V. A. Murday [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; C. J. Sandy [Royaume-Uni] ; J. R. O. Collin [Royaume-Uni] ; A. F. Brady [Royaume-Uni] ; D. F. Callen [Australie] ; K. Burnand [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. Jeffery [Royaume-Uni]Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene
000F09 (2000) R. Bell ; G. Brice ; A H Child ; V A Murday ; S. Mansour ; C J Sandy ; J R O. Collin ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; D F Callen ; K. Burnand ; S. JefferyReduction of the genetic interval for lymphoedema-distichiasis to below 2 Mb
001031 (1999) J. Mangion [Royaume-Uni] ; N. Rahman [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; G. Brice [Royaume-Uni] ; J. Rosbotham [Royaume-Uni] ; A. H. Child [Royaume-Uni] ; V. A. Murday [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; R. Barfoot [Royaume-Uni] ; A. Sigurdsson [Royaume-Uni] ; S. Edkins [Royaume-Uni] ; M. Sarfarazi ; K. Burnand [Royaume-Uni] ; A. L. Evans [Royaume-Uni] ; T. O. Nunan [Royaume-Uni] ; M. R. Stratton [Royaume-Uni] ; S. Jeffery [Royaume-Uni]A Gene for Lymphedema-Distichiasis Maps to 16q24.3

List of associated KwdEn.i

Nombre de
documents		Descripteur
15Humans
13Male
12Female
12Lymphedema (genetics)
11Lymphedema (diagnosis)
9Phenotype
8Mutation
6Child, Preschool
6Infant
6Lymphedema
5Pedigree
4Adult
4Child
4Distichiasis
4Eyelashes (abnormalities)
4Family study
4Human
4Lymphedema (pathology)
4Syndrome
4Vascular Endothelial Growth Factor Receptor-3 (genetics)
3Adolescent
3Age of Onset
3Chromosomes, Human, Pair 16 (genetics)
3DNA (genetics)
3DNA Mutational Analysis
3Family Health
3Lymphedema (congenital)
2Abnormalities, Multiple (genetics)
2Chromosome E16
2Craniofacial Abnormalities (diagnosis)
2Craniofacial Abnormalities (genetics)
2DNA (chemistry)
2DNA-Binding Proteins (genetics)
2Diagnosis, Differential
2Eyelid Diseases (genetics)
2Eyelid Diseases (pathology)
2Forkhead Transcription Factors
2Genetic Linkage (genetics)
2Genetic determinism
2Genetics
2Haplotypes
2Infant, Newborn
2Linkage
2Lymphedema (classification)
2Sequence Deletion
2Transcription Factors (genetics)
2VEGFR-3
1Abnormalities, Multiple (diagnostic imaging)
1Abnormalities, Multiple (etiology)
1Algorithms
1Amino Acid Substitution
1Anal Canal (pathology)
1Calcium-Binding Proteins (genetics)
1Chromosome 16
1Classification
1Codon
1Congenital
1Connexin 43 (genetics)
1Crohn Disease (diagnosis)
1Deletion
1Diseases in Twins (diagnosis)
1Diseases in Twins (genetics)
1Diseases in Twins (pathology)
1Dysplasia
1Edema (pathology)
1Exons
1Eye Abnormalities (diagnosis)
1Eye Abnormalities (genetics)
1Eyelashes (diagnostic imaging)
1Eyelid Diseases (etiology)
1FOXC2
1Facies
1Fetus
1Foot Deformities, Congenital (diagnosis)
1Foot Deformities, Congenital (genetics)
1Forkhead Transcription Factors (genetics)
1Gene
1Gene Frequency
1Genes, Dominant
1Genetic Markers (genetics)
1Genetic Predisposition to Disease
1Genetic mapping
1Genital Diseases, Male (diagnosis)
1Genital Diseases, Male (genetics)
1Genome
1Genotype
1Heterozygote Detection
1Hydrops Fetalis (diagnosis)
1Hydrops Fetalis (genetics)
1Identification
1Insertion
1Leg
1Locus
1Long arm
1Lymph node
1Lymphangiectasis
1Lymphangiectasis, Intestinal (diagnosis)
1Lymphangiectasis, Intestinal (genetics)
1Lymphatic
1Lymphatic Abnormalities (diagnosis)

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