Lymphedema (etiology) < Lymphedema (genetics) < Lymphedema (history)

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List of bibliographic references

Number of relevant bibliographic references: 377.
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Ident.	Authors (with country if any)	Title
000078 (1999)	A H Child [Royaume-Uni] ; J. Beninson ; M. Sarfarazi	Cause of primary congenital lymphedema.
000081 (1999)	D. Mowat [Australie] ; A. Jauch ; L. Robson ; A. Smith	Duplication within chromosome 5q characterized by fluorescence in situ hybridization.
000143 (1999)	J. Mangion ; N. Rahman ; S. Mansour ; G. Brice ; J. Rosbotham ; A H Child ; V A Murday ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; R. Barfoot ; A. Sigurdsson ; S. Edkins ; M. Sarfarazi ; K. Burnand ; A L Evans ; T O Nunan ; M R Stratton ; S. Jeffery	A gene for lymphedema-distichiasis maps to 16q24.3.
000174 (1999)	C. Limwongse [États-Unis] ; R E Wyszynski ; L H Dickerman ; N H Robin	Microcephaly-lymphedema-chorioretinal dysplasia: a unique genetic syndrome with variable expression and possible characteristic facial appearance.
000205 (1999)	S G Gragnani ; F. Michelotti ; R. Rocca ; R. Sardi ; N. Bardini	Primary congenital lymphedema. A case report.
000246 (2000)	J L Rosbotham [Royaume-Uni] ; G W Brice ; A H Child ; T O Nunan ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; K G Burnand	Distichiasis-lymphoedema: clinical features, venous function and lymphoscintigraphy.
000337 (2000)	S C Robertson [États-Unis] ; J A Tynan ; D J Donoghue	RTK mutations and human syndromeswhen good receptors turn bad.
000341 (2000)	M J Karkkainen [Finlande] ; R E Ferrell ; E C Lawrence ; M A Kimak ; K L Levinson ; M A Mctigue ; Kari Alitalo [Finlande] ; D N Finegold	Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema.
000352 (2000)	Alexandre Irrthum ; Marika J. Karkkainen ; Koen Devriendt [Belgique] ; Kari Alitalo [Finlande] ; Miikka Vikkula [Belgique]	Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase
000414 (2000)	S. Jacquemont [France] ; S. Barbarot ; M. Bocéno ; J F Stalder ; A. David	Familial congenital pulmonary lymphangectasia, non-immune hydrops fetalis, facial and lower limb lymphedema: confirmation of Njolstad's report.
000424 (2000)	Laura N. Bull ; Erin Roche ; Eyun J. Song ; Jan Pedersen ; A. S. Knisely ; C. B. Van Der Hagen ; Kristin Eiklid ; Ystein Aagenaes [États-Unis] ; Nelson B. Freimer	Mapping of the Locus for Cholestasis-Lymphedema Syndrome (Aagenaes Syndrome) to a 6.6-cM Interval on Chromosome 15q
000486 (2000)	Jianming Fang ; Susan L. Dagenais ; Robert P. Erickson ; Martin F. Arlt ; Michael W. Glynn ; Jerome L. Gorski ; Laurie H. Seaver [États-Unis] ; Thomas W. Glover	Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome
000529 (2001)	C J Holberg [États-Unis] ; R P Erickson ; M J Bernas ; M H Witte ; K E Fultz ; M. Andrade ; C L Witte	Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families.
000535 (2000)	R. Bell ; G. Brice ; A. Child ; V. Murday ; S. Mansour ; C. Sandy ; J. Collin ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; D. Callen ; K. Burnand ; S. Jeffery	Reduction of the genetic interval for lymphoedema-distichiasis to below 2 Mb
000564 (2001)	Y. Fatinni [Arabie saoudite] ; A. Asindi ; Y. Al Falki ; A. Al Harthi ; S. Al Fifi ; S. Al-Daama	Possible new autosomal recessive syndrome of congenital lymphoedema, nail dystrophy and esotropia in a Saudi family.
000599 (2001)	L R Osborne	'Forkhead' gene expression balanced on a knife-edge.
000615 (2001)	I. Casteels ; K. Devriendt ; A. Leys ; H. Van Cleynenbreuge. ; P. Demaerel ; F. De Tavernier ; J. Fryns	Autosomal dominant microcephaly—lymphoedema-chorioretinal dysplasia syndrome
000621 (2001)	R P Erickson	Lymphedema-distichiasis and FOXC2 gene mutations.
000659 (2001)	D N Finegold [États-Unis] ; M A Kimak ; E C Lawrence ; K L Levinson ; E M Cherniske ; B R Pober ; J W Dunlap ; R E Ferrell	Truncating mutations in FOXC2 cause multiple lymphedema syndromes.
000661 (2001)	S. Aradhya [États-Unis] ; D L Nelson	NF-kappaB signaling and human disease.
000683 (2001)	M J Karkkainen [Finlande] ; L. Jussila ; R E Ferrell ; D N Finegold ; Kari Alitalo [Finlande]	Molecular regulation of lymphangiogenesis and targets for tissue oedema.

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