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

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List of bibliographic references indexed by Lymphedema (genetics)

Number of relevant bibliographic references: 377.
[20-40] [0 - 20][0 - 50][40-60]

Ident.	Authors (with country if any)	Title
001D77 (2015)	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
002100 (2015)	Katrina Mears [États-Unis] ; Benjamin Bakall [États-Unis] ; Lisa A. Harney [États-Unis] ; Jessica A. Penticoff [États-Unis] ; Edwin M. Stone [États-Unis]	Autosomal Dominant Microcephaly Associated With Congenital Lymphedema and Chorioretinopathy Due to a Novel Mutation in KIF11.
002213 (2015)	Patrick Frosk [Canada] ; Bernard Chodirker [Canada] ; Louise Simard [Canada] ; Wael El-Matary [Canada] ; Ana Hanlon-Dearman [Canada] ; Jeremy Schwartzentruber [Canada] ; Jacek Majewski [Canada] ; Cheryl Rockman-Greenberg [Canada]	A novel CCBE1 mutation leading to a mild form of hennekam syndrome: case report and review of the literature
002248 (2015)	Svetlana Melikhan-Revzin [Israël] ; Alina Kurolap [Israël] ; Efrat Dagan [Israël] ; Adi Mory [Israël] ; Ruth Gershoni-Baruch [Israël]	A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary Lymphedema.
002251 (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.
002252 (2015)	Carolyn C. Jackson [États-Unis] ; Lucy Best [États-Unis] ; Lazaro Lorenzo [France] ; Jean-Laurent Casanova [États-Unis, France] ; Jochen Wacker [Allemagne] ; Simone Bertz [Allemagne] ; Abbas Agaimy [Allemagne] ; Thomas Harrer [Allemagne]	A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression
002711 (2014)	Johane M. Robitaille [Canada] ; Roxanne M. Gillett [Canada] ; Marissa A. Leblanc [Canada] ; Daniel Gaston [Canada] ; Mathew Nightingale [Canada] ; Michael P. Mackley [Canada] ; Sandhya Parkash [Canada] ; Julie Hathaway [Canada] ; Aidan Thomas [Canada] ; Anna Ells [Canada] ; Elias I. Traboulsi [États-Unis] ; Elise Héon [Canada] ; Mélanie Roy [Canada] ; Stavit Shalev [Israël] ; Conrad V. Fernandez [Canada] ; Christine Macgillivray [Canada] ; Karin Wallace [Canada] ; Somayyeh Fahiminiya [Canada] ; Jacek Majewski [Canada] ; Christopher R. Mcmaster [Canada] ; Karen Bedard [Canada]	Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.
002777 (2014)	R P Erickson	Next generation sequencing is here now.
002778 (2014)	Peter S. Mortimer [Royaume-Uni] ; Stanley G. Rockson [États-Unis]	New developments in clinical aspects of lymphatic disease
002880 (2014)	Alexandra L. Geffrey [États-Unis] ; Julianna E. Shinnick ; Brigid A. Staley ; Susana Boronat ; Elizabeth A. Thiele	Lymphedema in tuberous sclerosis complex.
002A33 (2014)	Mariëlle Alders [Pays-Bas] ; Lihadh Al-Gazali ; Isabelle Cordeiro ; Bruno Dallapiccola ; Livia Garavelli ; Beyhan Tuysuz ; Faranak Salehi ; Martin A. Haagmans ; Olaf R. Mook ; Charles B. Majoie ; Marcel M. Mannens ; Raoul C. Hennekam	Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome.
002A45 (2014)	Helen L. Hanson [Royaume-Uni] ; Meredith J. Wilson ; John P. Short ; Barry A. Chioza ; Andrew H. Crosby ; Ruth M. Nash ; Karen J. Marks ; Sahar Mansour	Germline CBL mutation associated with a noonan-like syndrome with primary lymphedema and teratoma associated with acquired uniparental isodisomy of chromosome 11q23.
002A51 (2014)	Pascal Brouillard ; Laurence Boon ; Miikka Vikkula [Belgique]	Genetics of lymphatic anomalies
002A52 (2014)	Julie Blatt [États-Unis] ; Cynthia M. Powell ; Craig N. Burkhart ; Joseph Stavas ; Arthur S. Aylsworth	Genetics of hemangiomas, vascular malformations, and primary lymphedema.
002A53 (2014)	K. De Keyser [Belgique] ; S. Janssens ; L M Peeters ; N. Foqué ; F. Gasthuys ; M. Oosterlinck ; N. Buys	Genetic parameters for chronic progressive lymphedema in Belgian Draught Horses.
002A66 (2014)	Akihiro Yamauchi [Japon] ; Takayuki Sakurai [Japon] ; Akiko Kamiyoshi [Japon] ; Yuka Ichikawa-Shindo [Japon] ; Hisaka Kawate [Japon] ; Kyoko Igarashi [Japon] ; Yuichi Toriyama [Japon] ; Megumu Tanaka [Japon] ; Tian Liu [Japon] ; Xian Xian [Japon] ; Akira Imai [Japon] ; Liuyu Zhai [Japon] ; Shinji Owa [Japon] ; Takuma Arai [Japon] ; Takayuki Shindo [Japon]	Functional differentiation of RAMP2 and RAMP3 in their regulation of the vascular system.
002B05 (2014)	Germaine D. Agollah [États-Unis] ; Manuel L. Gonzalez-Garay [États-Unis] ; John C. Rasmussen [États-Unis] ; I-Chih Tan [États-Unis] ; Melissa B. Aldrich [États-Unis] ; Chinmay Darne [États-Unis] ; Caroline E. Fife [États-Unis] ; Renie Guilliod [États-Unis] ; Erik A. Maus [États-Unis] ; Philip D. King [États-Unis] ; Eva M. Sevick-Muraca [États-Unis]	Evidence for SH2 Domain-Containing 5′-Inositol Phosphatase-2 (SHIP2) Contributing to a Lymphatic Dysfunction
002B94 (2014)	Geraldine Leung ; 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
002C15 (2014)	Merlijn J. Meens [Suisse] ; Amélie Sabine [Suisse] ; Tatiana V. Petrova [Suisse] ; Brenda R. Kwak [Suisse]	Connexins in lymphatic vessel physiology and disease.
002D38 (2014)	Joëlle Kartopawiro [Australie] ; Neil I. Bower ; Tara Karnezis ; Jan Kazenwadel ; Kelly L. Betterman ; Emmanuelle Lesieur ; Katarzyna Koltowska ; Jonathan Astin ; Philip Crosier ; Sonja Vermeren ; Marc G. Achen ; Steven A. Stacker ; Kelly A. Smith ; Natasha L. Harvey ; Mathias François ; Benjamin M. Hogan	Arap3 is dysregulated in a mouse model of hypotrichosis-lymphedema-telangiectasia and regulates lymphatic vascular development.
002D59 (2014)	Steven M. Dean [États-Unis] ; Jean Starr [États-Unis]	An unusual case of familial lymphedema.

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