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Serveur d'exploration sur le lymphœdème - Corpus (PubMed)

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

Number of relevant bibliographic references: 17.
Ident.Authors (with country if any)Title
001B77 (2013) F C Connell ; K. Gordon ; G. Brice ; V. Keeley ; S. Jeffery ; P S Mortimer ; S. Mansour ; P. OstergaardThe classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.
001C09 (2013) G. Brice ; P. Ostergaard ; S. Jeffery ; K. Gordon ; P S Mortimer ; S. MansourA novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family.
001C43 (2013) K D Gordon ; G. Brice ; Y. Walker ; R. Pollok ; P. Mortimer ; C. SlaterGenital lymphoedema due to ano-genital granulomatosis.
002315 (2012) F C Connell ; K. Kalidas ; P. Ostergaard ; G. Brice ; V. Murday ; P S Mortimer ; I. Jeffrey ; S. Jeffery ; Sahar MansourCCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis.
002A85 (2010) F. Connell ; G. Brice ; S. Jeffery ; V. Keeley ; P. Mortimer ; S. MansourA new classification system for primary lymphatic dysplasias based on phenotype.
003090 (2009) F C Connell ; P. Ostergaard ; C. Carver ; G. Brice ; N. Williams ; S. Mansour ; P S Mortimer ; Steve JefferyAnalysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.
003753 (2007) S. Kumar ; C. Carver ; S. Mccall ; G. Brice ; P. Ostergaard ; P. Mortimer ; S. JefferyA family with lymphoedema-distichiasis where identical twins have a discordant phenotype.
003774 (2007) C. Carver ; G. Brice ; S. Mansour ; P. Ostergaard ; P. Mortimer ; S. JefferyThree children with Milroy disease and de novo mutations in VEGFR3.
003D87 (2005) G. Brice ; A H Child ; A. Evans ; R. Bell ; S. Mansour ; K. Burnand ; M. Sarfarazi ; S. Jeffery ; P. MortimerMilroy disease and the VEGFR-3 mutation phenotype.
004041 (2004) B B Patil ; R. Bell ; G. Brice ; S. Jeffery ; S P DesaiDistichiasis without lymphoedema?
004180 (2003) A L Evans ; R. Bell ; G. Brice ; P. Comeglio ; C. Lipede ; S. Jeffery ; P. Mortimer ; M. Sarfarazi ; A H ChildIdentification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema.
004236 (2003) M. Ameen ; G. Brice ; P S MortimerClinicopathological case 2: lymphoedema-distichiasis syndrome.
004532 (2002) G. Brice ; S. Mansour ; R. Bell ; J R O. Collin ; A H Child ; A F Brady ; M. Sarfarazi ; K G Burnand ; S. Jeffery ; P. Mortimer ; V A MurdayAnalysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.
004758 (2001) R. Bell ; G. Brice ; A H Child ; V A Murday ; S. Mansour ; C J Sandy ; J R Collin ; A F Brady ; D F Callen ; K. Burnand ; P. Mortimer ; S. JefferyAnalysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene.
004909 (2000) R. Bell ; G. Brice ; A H Child ; V A Murday ; S. Mansour ; C J Sandy ; J R Collin ; P. Mortimer ; D F Callen ; K. BurnandReduction of the genetic interval for lyphoedema-distichiasis to below 2 Mb.
004C28 (1999) J. Mangion ; N. Rahman ; S. Mansour ; G. Brice ; J. Rosbotham ; A H Child ; V A Murday ; P S Mortimer ; R. Barfoot ; A. Sigurdsson ; S. Edkins ; M. Sarfarazi ; K. Burnand ; A L Evans ; T O Nunan ; M R Stratton ; S. JefferyA gene for lymphedema-distichiasis maps to 16q24.3.
004D23 (1999) A L Evans ; G. Brice ; V. Sotirova ; P. Mortimer ; J. Beninson ; K. Burnand ; J. Rosbotham ; A. Child ; M. SarfaraziMapping of primary congenital lymphedema to the 5q35.3 region.

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