Genes < Genes, Dominant < Genes, Helminth

Facettes : Author.f

List of bibliographic references

Number of relevant bibliographic references: 33.
[0-20] [0 - 20][0 - 33][20-32][20-40]

Ident.	Authors (with country if any)	Title
001896 (2013)	M. Marc ; M. Barreau ; M. Gerard ; L. Verneuil ; L. Derieux ; A. Dompmartin	[Lymphoedema distichiasis].
002464 (2012)	Gwendolyn De Bruyn ; Alexandra Casaer ; Katrien Devolder ; Geert Van Acker ; Hilde Logghe ; Koen Devriendt ; Luc Cornette	Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression.
002B55 (2010)	Pranoot Tanpaiboon ; Piranit Kantaputra ; Karn Wejathikul ; Wirawit Piyamongkol	c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient.
003090 (2009)	F C Connell ; P. Ostergaard ; C. Carver ; G. Brice ; N. Williams ; S. Mansour ; P S Mortimer ; Steve Jeffery	Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.
003416 (2008)	Sajid Malik ; Karl-Heinz Grzeschik	Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family.
003715 (2007)	Russell H. Mellor ; Glen Brice ; Anthony W B. Stanton ; Jane French ; Alberto Smith ; Steve Jeffery ; J Rodney Levick ; Kevin G. Burnand ; Peter S. Mortimer	Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb.
003C70 (2005)	Pradeep C. Vasudevan ; Sixto Garcia-Minaur ; Maria Pilar Botella ; Antonio Perez-Aytes ; Nora L. Shannon ; Oliver W J. Quarrell	Microcephaly-lymphoedema-chorioretinal dysplasia: three cases to delineate the facial phenotype and review of the literature.
003E11 (2003)	Michael S. Pepper	Literature watch. FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.
003E27 (2004)	Naoyuki Miura	[Multiple roles of forkhead genes in development and metabolism].
004034 (2004)	H R Dürr ; C. Pellengahr ; A. Nerlich ; A. Baur ; M. Maier ; V. Jansson	Stewart-Treves syndrome as a rare complication of a hereditary lymphedema.
004265 (2003)	Alexandre Irrthum ; Koenraad Devriendt ; David Chitayat ; Gert Matthijs ; Conrad Glade ; Peter M. Steijlen ; Jean-Pierre Fryns ; Maurice A M. Van Steensel ; Miikka Vikkula	Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.
004270 (2003)	Benjamin M. Kriederman ; Teressa L. Myloyde ; Marlys H. Witte ; Susan L. Dagenais ; Charles L. Witte ; Margaret Rennels ; Michael J. Bernas ; Michelle T. Lynch ; Robert P. Erickson ; Mark S. Caulder ; Naoyuki Miura ; David Jackson ; Brian P. Brooks ; Thomas W. Glover	FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.
004851 (2001)	I. Casteels ; K. Devriendt ; H. Van Cleynenbreugel ; P. Demaerel ; F. De Tavernier ; J P Fryns	Autosomal dominant microcephaly--lymphoedema-chorioretinal dysplasia syndrome.
004A59 (2000)	A. Irrthum ; M J Karkkainen ; K. Devriendt ; K. Alitalo ; M. Vikkula	Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.
004A66 (2000)	M J Karkkainen ; R E Ferrell ; E C Lawrence ; M A Kimak ; K L Levinson ; M A Mctigue ; K. Alitalo ; D N Finegold	Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema.
004B48 (2000)	J L Rosbotham ; G W Brice ; A H Child ; T O Nunan ; P S Mortimer ; K G Burnand	Distichiasis-lymphoedema: clinical features, venous function and lymphoscintigraphy.
005413 (1995)	H C Andersson ; D M Parry ; J J Mulvihill	Lymphangiosarcoma in late-onset hereditary lymphedema: case report and nosological implications.
005610 (1994)	M. Hausmann ; R. Keller	[Yellow nail syndrome].
005699 (1993)	L S Sadler ; L K Robinson	Chorioretinal dysplasia-microcephaly-mental retardation syndrome: report of an American family.
005813 (1993)	M. Chery ; C. Philippe ; A M Worms ; S. Gilgenkrantz	The Noonan syndrome. The Nancy experience revisited.
006078 (1989)	D D Farhud ; I. Farhud ; G R Walizadeh ; M. Djaber-Ansari	Congenital hereditary lymphedema (Nonne/Milroy).

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