Genetic Markers < Genetic Predisposition to Disease < Genetic Research

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List of bibliographic references

Number of relevant bibliographic references: 56.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000008 (2017)	S. Vignes [France]	[Lymphedema: From diagnosis to treatment].
000391 (2017)	Francoise Pujol [Suède] ; Tina Hodgson [Suède] ; Ines Martinez-Corral [Suède] ; Anne-Catherine Prats [Suède] ; Danelle Devenport [Suède] ; Masatoshi Takeichi [Suède] ; Elisabeth Genot [Suède] ; Taija M Kinen [Suède] ; Philippa Francis-West [Suède] ; Barbara Garmy-Susini [Suède] ; Florence Tatin [France]	Dachsous1-Fat4 Signaling Controls Endothelial Cell Polarization During Lymphatic Valve Morphogenesis-Brief Report.
000446 (2017)	André Viveiros [Autriche] ; Marion Reiterer [Autriche] ; Benedikt Schaefer [Autriche] ; Armin Finkenstedt [Autriche] ; Stefan Schneeberger [Autriche] ; Hubert Schwaighofer [Autriche] ; Patrizia Moser [Autriche] ; Rudolf Sprenger [Autriche] ; Bernhard Glodny [Autriche] ; Wolfgang Vogel [Autriche] ; Andreas R. Janecke [Autriche] ; Heinz Zoller [Autriche]	CCBE1 mutation causing sclerosing cholangitis: Expanding the spectrum of lymphedema-cholestasis syndrome.
000904 (2016)	Sang Kyung Seo [Corée du Sud] ; Kyu Yeun Kim [Corée du Sud] ; Seo Ae Han [Corée du Sud] ; Joon Seok Yoon [Corée du Sud] ; Sang-Yong Shin [Corée du Sud] ; Sang Kyun Sohn [Corée du Sud] ; Joon Ho Moon [Corée du Sud]	First Korean case of Emberger syndrome (primary lymphedema with myelodysplasia) with a novel GATA2 gene mutation.
000E97 (2015)	Matthew Collin [Royaume-Uni] ; Rachel Dickinson ; Venetia Bigley	Haematopoietic and immune defects associated with GATA2 mutation.
000F08 (2015)	Amy P. Hsu [États-Unis] ; Lisa J. Mcreynolds ; Steven M. Holland	GATA2 deficiency.
000F30 (2015)	Yasmeen Sheik [Inde] ; Sameera Fatima Qureshi [Inde] ; Basheeruddin Mohhammed [Inde] ; Pratibha Nallari [Inde]	FOXC2 and FLT4 Gene Variants in Lymphatic Filariasis.
001026 (2015)	K. De Keyser [Belgique] ; S. Janssens ; N. Buys	Chronic progressive lymphoedema in draught horses.
001138 (2015)	N F Liu ; Z. Yu ; Y. Luo ; D. Sun ; Z. Yan	A NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE.
001379 (2014)	Peter S. Mortimer ; Stanley G. Rockson	New developments in clinical aspects of lymphatic disease.
001449 (2014)	R. Gupta ; M. Kitaichi ; Y. Inoue ; R. Kotloff ; F X Mccormack	Lymphatic manifestations of lymphangioleiomyomatosis.
001530 (2014)	Pascal Brouillard ; Laurence Boon ; Miikka Vikkula	Genetics of lymphatic anomalies.
001531 (2014)	Julie Blatt [États-Unis] ; Cynthia M. Powell ; Craig N. Burkhart ; Joseph Stavas ; Arthur S. Aylsworth	Genetics of hemangiomas, vascular malformations, and primary lymphedema.
001591 (2014)	Geraldine Leung [États-Unis] ; Christina Baggott ; Claudia West ; Charles Elboim ; Steven M. Paul ; Bruce A. Cooper ; Gary Abrams ; Anand Dhruva ; Brian L. Schmidt ; Kord Kober ; John D. Merriman ; Heather Leutwyler ; John Neuhaus ; Dale Langford ; Betty J. Smoot ; Bradley E. Aouizerat ; Christine Miaskowski	Cytokine candidate genes predict the development of secondary lymphedema following breast cancer surgery.
001666 (2014)	Steven M. Dean [États-Unis] ; Jean Starr [États-Unis]	An unusual case of familial lymphedema.
001696 (2014)	Emilia Balboa-Beltran [Espagne] ; María J. Fernández-Seara [Espagne] ; Alejandro Pérez-Mu Uzuri [Espagne] ; Ram N Lago [Espagne] ; Carlos García-Magán [Espagne] ; María L. Couce [Espagne] ; Beatriz Sobrino [Espagne] ; Jorge Amigo [Espagne] ; Angel Carracedo [Arabie saoudite] ; Francisco Barros [Espagne]	A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease.
001698 (2014)	R M Digiovanni ; R P Erickson ; E C Ohlson ; M. Bernas ; M H Witte	A novel FLT4 mutation identified in a patient with Milroy disease.
001830 (2013)	Stanley G. Rockson [États-Unis]	The lymphatics and the inflammatory response: lessons learned from human lymphedema.
001A51 (2013)	Christine Miaskowski [États-Unis] ; Marylin Dodd ; Steven M. Paul ; Claudia West ; Deborah Hamolsky ; Gary Abrams ; Bruce A. Cooper ; Charles Elboim ; John Neuhaus ; Brian L. Schmidt ; Betty Smoot ; Bradley E. Aouizerat	Lymphatic and angiogenic candidate genes predict the development of secondary lymphedema following breast cancer surgery.
001B31 (2013)	Kristiana Gordon [Royaume-Uni] ; Sarah L. Spiden ; Fiona C. Connell ; Glen Brice ; Sally Cottrell ; John Short ; Rohan Taylor ; Steve Jeffery ; Peter S. Mortimer ; Sahar Mansour ; Pia Ostergaard	FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.
001C64 (2013)	Leonid L. Nikitenko [Royaume-Uni] ; Tatsuo Shimosawa ; Stephen Henderson ; Taija M Kinen ; Hiromi Shimosawa ; Uzma Qureshi ; R Barbara Pedley ; Margaret C P. Rees ; Toshiro Fujita ; Chris Boshoff	Adrenomedullin haploinsufficiency predisposes to secondary lymphedema.

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