Serveur d'exploration sur le lymphœdème - Curation (Ncbi)

Index « Keywords » - entrée « Lymphedema (congenital) »
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Lymphedema (complications) < Lymphedema (congenital) < Lymphedema (diagnosis)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 302.
[0-20] [0 - 20][0 - 50][20-40]
Ident.Authors (with country if any)Title
000041 (1998) M. De Los Santos [États-Unis] ; A. Szuba ; S G RocksonImages in vascular medicine. Lymphoscintigraphy in congenital lymphedema.
000078 (1999) A H Child [Royaume-Uni] ; J. Beninson ; M. SarfaraziCause of primary congenital lymphedema.
000101 (1976) V. Torres ; G. Mascar Galy ; E. Jorda[A case of Nonne-Milroy syndrome associated with chyloabdomen. Immunologic study].
000205 (1999) S G Gragnani ; F. Michelotti ; R. Rocca ; R. Sardi ; N. BardiniPrimary congenital lymphedema. A case report.
000235 (????) R J Hirsch ; N B Silverberg ; T. Laude ; J M WeinbergTuberous sclerosis associated with congenital lymphedema.
000284 (????) O H Haugen [Norvège] ; J. KrohnBilateral congenital glaucoma in a child with hydrops fetalis, congenital pulmonary lymphangiectasia, and lymphoedema.
000326 (1975) W J DoddsFurther studies of canine von Willebrand's disease.
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 FinegoldMissense 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
000472 (2000) H. Nogami [Japon] ; H. Ito ; K. Arao ; T. Oki ; M. FutamuraCongenital balloon digits in two neonates caused by constriction rings.
000517 (2000) T. Watanabe [Japon]Congenital penoscrotal lymphedema complicated by sepsis associated with a streptococcal infection.
000529 (2001) C J Holberg [États-Unis] ; R P Erickson ; M J Bernas ; M H Witte ; K E Fultz ; M. Andrade ; C L WitteSegregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families.
000540 (1975) J J Laskas ; W B Shelley ; M G WoodLymphangiosarcoma arising in congenital lymphedema.
000564 (2001) Y. Fatinni [Arabie saoudite] ; A. Asindi ; Y. Al Falki ; A. Al Harthi ; S. Al Fifi ; S. Al-DaamaPossible new autosomal recessive syndrome of congenital lymphoedema, nail dystrophy and esotropia in a Saudi family.
000580 (2001) M. Kamble [Inde] ; N C PrajapatiCongenital lymphedema.
000589 (????) J B Kinmonth ; S J CoxProtein-losing enteropathy in lymphoedema. Surgical investigation and treatment.
000645 (2001) O. Butenandt[Lymphedema. In Ullrich-Turner syndrome it is congenital].
000679 (2001) A. Zenciroglu ; A. Uckun ; C. Akincioglu ; M. Unlü ; T. TezicPrimary congenital lymphoedema with unilateral arm involvement.
000698 (2001) R. Kato[Hennekam syndrome].
000748 (2001) Y. Izumikawa[Lymphedema].
000755 (2001) P. Franceschini ; D. Licata ; G. Rapello ; A. Guala ; G. Di Cara ; D. FranceschiniPrenatal diagnosis of Nonne-Milroy lymphedema.

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