here < hereditary < heritable

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List of bibliographic references

Number of relevant bibliographic references: 31.
[0-20] [0 - 20][0 - 31][20-30][20-40]

Ident.	Authors (with country if any)	Title
001738 (2006)	A. Ghalamkarpour [Belgique] ; S. Morlot [Allemagne] ; A. Raas-Rothschild [Israël] ; A. Utkus [Lituanie] ; Jb Mulliken [États-Unis] ; Lm Boon [Belgique] ; M. Vikkula [Belgique]	Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations
001879 (2005)	Fred B. Berry ; Yahya Tamimi [Canada] ; Michelle V. Carle ; Ordan J. Lehmann [Canada] ; Michael A. Walter [Canada]	The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis
001B15 (2005)	Y. Goto [Japon] ; S. Anan [Japon] ; M. Yamaguchi-Yamada [Japon] ; C. Sakata [Japon] ; N. Manabe [Japon]	Increased Smad4‐Mediated Acceleration of TGF‐β1 Signaling and Myofibroblastic Differentiation in Tubulointerstitial Cells in Kidneys of Hereditary Nephrotic Mice
001B33 (2005)	Etty Daniel-Spiegel [Israël] ; Arash Ghalamkarpour [Belgique] ; Ronen Spiegel [Israël] ; Ehud Weiner [Israël] ; Miikka Vikkula [Belgique] ; Eliezer Shalev [Israël] ; Stavit Alon Shalev [Israël]	Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema
001B90 (2005)	S. Anan [Japon] ; Y. Goto [Japon] ; M. Yamaguchi-Yamada [Japon] ; C. Sakata [Japon] ; N. Manabe [Japon]	European Tissue Repair Society Focus MeetingTissue Repair, Contraction, and the MyofibroblastNyon, SwitzerlandNovember 18–20, 2004The following compilation of abstracts represents a partial list of submissions received for presentation at the meeting. Please note the abstracts are arranged in alphabetical order (by presenter's name). Communications by the invited speakers will be published in a book by Landes Bioscience.: TGF‐β1 Signaling is Regulated by Negative Feedback Mechanism of BMP‐7 in Fibrotic Kidneys of Hereditary Nephrotic Mice
001C63 (2005)	Seiji Mizuno [Japon] ; Yasukazu Yamada [Japon] ; Kenichiro Yamada [Japon] ; Noriko Nomura [Japon] ; Nobuaki Wakamatsu [Japon]	Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation
001F95 (2004)	M. A. M. Van Steensel [Pays-Bas] ; M. Van Geel ; P. M. Steijlen	Molecular genetics of hereditary hair and nail disease
002040 (2004)	Aaltje Schram [Pays-Bas] ; Hester Y. Kroes [Pays-Bas] ; Krystyna Sollie [Pays-Bas] ; Bert Timmer [Pays-Bas] ; Peter Barth [Pays-Bas] ; Ton Van Essen [Pays-Bas]	Hereditary fetal brain degeneration resembling fetal brain disruption sequence in two sibships
002072 (2004)	G. Herrmann [Allemagne] ; L. Schneider [Allemagne] ; T. Krieg [Allemagne] ; N. Hunzelmann [Allemagne] ; K. Scharffetter-Kochanek [Allemagne]	Efficacy of danazol treatment in a patient with the new variant of hereditary angio‐oedema (HAE III)
002162 (2004)	Cagri Yildirim-Toruner [États-Unis] ; Kavitha Subramanian [États-Unis] ; Lamya El Manjra [États-Unis] ; Emily Chen [États-Unis] ; Stanley Goldstein ; Emilia Vitale [États-Unis, Italie]	A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema‐distichiasis syndrome associated with renal disease and diabetes mellitus
002D08 (2001)	Katja Aktan-Collan ; Ari Haukkala ; Jukka-Pekka Mecklin ; Antti Uutela ; Helena K Ri Inen	Comprehension of cancer risk one and 12 months after predictive genetic testing for hereditary non-polyposis colorectal cancer
003107 (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 [États-Unis]	Mutations in FOXC2 ( MFH-1 ), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome
003270 (2000)	Alexandre Irrthum [Belgique] ; Marika J. Karkkainen ; Koen Devriendt ; Kari Alitalo [Finlande] ; Miikka Vikkula [Belgique]	Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase
004833 (1995)	Hans C. Andersson [États-Unis] ; Dilys M. Parry [États-Unis] ; John J. Mulvihill [États-Unis]	Lymphangiosarcoma in late‐onset hereditary lymphedema: Case report and nosological implications
004F10 (1993)	T. W. Offori ; C. C. Platt [Royaume-Uni] ; M. Stephens [Royaume-Uni] ; G. B. Hopkinson	Angiosarcoma in congenital hereditary lymphoedema (Milroy's disease)—diagnostic beacons and a review of the literature
005594 (1990)	J. Bazex [France] ; R. Baran [France] ; F. Monbrun ; N. Grigorieff-Larrue ; M. C. Marguery	Hereditary distal onycholysis—a case report
005984 (1988)	M. Thrusfield	Is it hereditary?: 2. Types and characteristic patterns of hereditary disease
005A46 (1988)	R. Curley [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; R. A. Marsden [Royaume-Uni]	(9) Hereditary multiple fibrofolliculomas: Syndrome of Birt, Hogg and Dubé
005B97 (1987)	G E Morris ; B M Slavin ; N L Browse	Hereditary angioneurotic oedema: a neglected diagnosis.
006139 (1984)	Helena K Ri Inen	Hereditary lymphedema: a new combination of symptoms not fitting into present classifications
006140 (1984)	Marvin J. Fritzler [Canada] ; John P. Ariette [Canada] ; Alan R. Behm [Canada] ; T. Douglas Kinsella [Canada]	Hereditary hemorrhagic telangiectasia versus CREST syndrome: Can serology aid diagnosis?

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