Phenobarbital (therapeutic use) < Phenotype < Phenprocoumon (administration & dosage)

Facettes : Author.f AffPays.f AffRegion.f AffVille.f AffOrg.f KwdFr.f Mesh.f MeshFr.f

List of bibliographic references indexed by Phenotype

Number of relevant bibliographic references: 132.
[60-80] [0 - 20][0 - 50][80-100]

Ident.	Authors (with country if any)	Title
006586 (2009)	M. A. M. Van Steensel [Pays-Bas] ; R. J. Damstra [Pays-Bas] ; M. Heitink [Pays-Bas] ; R. S. Bladergroen [Pays-Bas] ; J. Veraart [Pays-Bas] ; Peter M. Steijlen [Pays-Bas] ; M. Van Geel [Pays-Bas]	Novel missense mutations in the FOXC2 gene alter transcriptional activity
006599 (2009)	Smadar Eventov-Friedman [Israël] ; Amihood Singer [Israël] ; Eric S. Shinwell [Israël]	Microcephaly, lymphedema, chorioretinopathy and atrial septal defect: a case report and review of the literature
006858 (2008)	Hélène Pendeville [Belgique] ; Marie Winandy ; Isabelle Manfroid ; Olivier Nivelles ; Patrick Motte ; Vincent Pasque ; Bernard Peers ; Ingrid Struman ; Joseph A. Martial ; Marianne L. Voz	Zebrafish Sox7 and Sox18 function together to control arterial-venous identity.
006912 (2008)	Leah N. Cueni ; Michael Detmar	The Lymphatic System in Health and Disease
006A47 (2008)	Rui-Cheng Ji [Japon]	Lymphatic endothelial cells, lymphedematous lymphangiogenesis, and molecular control of edema formation.
006B60 (2008)	Paula Haiko ; Taija Makinen ; Salla Keskitalo ; Jussi Taipale ; Marika J. Karkkainen ; Megan E. Baldwin ; Steven A. Stacker ; Marc G. Achen ; Kari Alitalo [Finlande]	Deletion of Vascular Endothelial Growth Factor C (VEGF-C) and VEGF-D Is Not Equivalent to VEGF Receptor 3 Deletion in Mouse Embryos▿
006C50 (2008)	Carla Danussi ; Paola Spessotto ; Alessandra Petrucco ; Bruna Wassermann ; Patrizia Sabatelli ; Monica Montesi ; Roberto Doliana ; Giorgio M. Bressan ; Alfonso Colombatti	Emilin1 Deficiency Causes Structural and Functional Defects of Lymphatic Vasculature ▿
006D68 (2008)	Fiona Connell ; Glen Brice ; Peter Mortimer (dermatologue)‎ [Royaume-Uni]	Phenotypic Characterization of Primary Lymphedema
006E08 (2008)	V. L. Keeley [Royaume-Uni]	Lymphoedema and cellulitis: chicken or egg?
007258 (2007)	Mylène Béri-Deixheimer [France] ; Marie-José Gregoire ; Annick Toutain ; Karène Brochet ; Sylvain Briault ; Jean-Luc Schaff ; Bruno Leheup ; Philippe Jonveaux	Genotype-phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française'.
007320 (2007)	Michael T. Dellinger [États-Unis] ; Robert J. Hunter ; Michael J. Bernas ; Marlys H. Witte ; Robert P. Erickson	Chy-3 mice are Vegfc haploinsufficient and exhibit defective dermal superficial to deep lymphatic transition and dermal lymphatic hypoplasia.
007418 (2007)	C. Carver ; G. Brice ; S. Mansour ; P. Ostergaard ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. Jeffery	Three children with Milroy disease and de novo mutations in VEGFR3
007559 (2007)	Karmen M. Trzupek [États-Unis] ; Rena E. Falk [États-Unis] ; Joseph L. Demer [États-Unis] ; Richard G. Weleber [États-Unis]	Microcephaly with chorioretinopathy in a brother–sister pair: Evidence for germ line mosaicism and further delineation of the ocular phenotype
007571 (2007)	M. A. M. Van Steensel [Pays-Bas] ; M. Van Geel [Pays-Bas] ; C. Schrander-Stumpel [Pays-Bas] ; P. M. Steijlen [Pays-Bas] ; J. C. J. M. Veraart [Pays-Bas]	Lymphedema, cardiac septal defects, and characteristic facies: Possible new case of Irons–Bianchi syndrome
007644 (2007)	Anita Rauch [Allemagne] ; Helmuth-Günther Dörr	Chromosome 5q subtelomeric deletion syndrome
007686 (2007)	S. Kumar [Arabie saoudite] ; C. Carver ; S. Mccall ; G. Brice ; P. Ostergaard ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. Jeffery [Royaume-Uni]	A family with lymphoedema‐distichiasis where identical twins have a discordant phenotype
007760 (2007)	Karmen M. Trzupek [États-Unis] ; Rena E. Falk [États-Unis] ; Joseph L. Demer [États-Unis] ; Richard G. Weleber [États-Unis]	Clinical report. Microcephaly with chorioretinopathy in a brother-sister pair: Evidence for germ line mosaicism and further delineation of the ocular phenotype
007794 (2006)	Ronen Spiegel [Israël] ; Arash Ghalamkarpour ; Etty Daniel-Spiegel ; Miikka Vikkula ; Stavit A. Shalev	Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3.
007817 (2006)	Tine V. Karlsen ; Marika J. Karkkainen ; Kari Alitalo [Finlande] ; Helge Wiig	Transcapillary fluid balance consequences of missing initial lymphatics studied in a mouse model of primary lymphoedema
008043 (2005)	Melissa L. Loscalzo [États-Unis] ; Phillip L. Van ; Vincent B. Ho ; Vladimir K. Bakalov ; Douglas R. Rosing ; Carol A. Malone ; Harry C. Dietz ; Carolyn A. Bondy	Association between fetal lymphedema and congenital cardiovascular defects in Turner syndrome.
008071 (2005)	Subash Babu ; Carla P. Blauvelt ; V. Kumaraswami [Inde] ; Thomas B. Nutman	Chemokine Receptors of T Cells and of B Cells in Lymphatic Filarial Infection: A Role for CCR9 in Pathogenesis

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