Eyebrows < Eyelashes < Eyelid Diseases

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List of bibliographic references indexed by Eyelashes

Number of relevant bibliographic references: 69.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000D14 (2016)	F. Vidal [France] ; M. Arrault [France] ; S. Vignes [France]	Paediatric primary lymphoedema: a cohort of 155 children and newborns.
000E37 (2016)	Nadine Sousa Marques [Portugal] ; Ana Miranda [Portugal] ; Sandra Barros [Portugal] ; S Nia Parreira [Portugal]	Lymphoedema-distichiasis syndrome.
000E50 (2016)	Sean Mcdermott ; Conor Lahiff	Lymphedema-distichiasis syndrome
001590 (2015)	Seydou Bakayoko [Mali] ; Nouhoum Guirou [Mali]	[Distichiasis: an anomaly of eyelashes].
001D44 (2015)	Paola Spitalieri [Italie] ; Rosa V. Talarico [Italie] ; Annalisa Botta [Italie] ; Michela Murdocca [Italie] ; Maria Rosaria D'Apice [Italie] ; Augusto Orlandi [Italie] ; Emiliano Giardina [Italie] ; Massimo Santoro [Italie] ; Francesco Brancati [Italie] ; Giuseppe Novelli [Italie] ; Federica Sangiuolo [Italie]	Generation of Human Induced Pluripotent Stem Cells from Extraembryonic Tissues of Fetuses Affected by Monogenic Diseases.
002282 (2014)	S. Vignes [France]	[Treatment of varicose veins and limb lymphedema].
002881 (2014)	Spring Golden [États-Unis] ; Dawn M. Davis ; Jerry D. Brewer	Lymphedema in a patient with distichiasis.
002E70 (2014)	L-L Zhu [République populaire de Chine] ; Y-N Lv ; H-D Chen ; X-H Gao	A Chinese pedigree of lymphoedema-distichiasis syndrome with a novel mutation in the FOXC2 gene.
002F37 (2013)	M. Marc [France] ; M. Barreau ; M. Gerard ; L. Verneuil ; L. Derieux ; A. Dompmartin	[Lymphoedema distichiasis].
002F55 (2013)	N. Khen-Dunlop [France] ; J. Amiel ; C. Delacourt ; Y. Révillon	[Enigmatic lymphatic diseases involving the lung].
004075 (2012)	Edyta Sutkowska [Pologne] ; Justyna Gil ; Agnieszka Stembalska ; Aneta Hill-Bator ; Andrzej Szuba	Novel mutation in the FOXC2 gene in three generations of a family with lymphoedema-distichiasis syndrome.
004225 (2012)	Eileen Stewart [États-Unis] ; Shalea Piteau ; Michael Storr ; Jennifer Mackenzie ; Angela Hartsell ; Suresh Nagappan	Index of suspicion.
004731 (2012)	Matthew G. Butler [États-Unis] ; Susan L. Dagenais [États-Unis] ; José L. Garcia-Perez [États-Unis, Espagne] ; Pascal Brouillard [Belgique] ; Miikka Vikkula [Belgique] ; Peter Strouse [États-Unis] ; Jeffrey W. Innis [États-Unis] ; Thomas W. Glover [États-Unis]	Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation
004C98 (2011)	Russell H. Mellor [Royaume-Uni] ; Naomi Tate ; Anthony W B. Stanton ; Charlotte Hubert ; Taija M Kinen ; Alberto Smith ; Kevin G. Burnand ; Steve Jeffery ; J Rodney Levick ; Peter S. Mortimer	Mutations in FOXC2 in humans (lymphoedema distichiasis syndrome) cause lymphatic dysfunction on dependency.
004F46 (2011)	K. Kaarthigeyan [Inde] ; M. Ramprakash [Inde] ; G. Kalpana [Inde]	Distichiasis-lymphedema syndrome with optic disc pit
005513 (2010)	S. Vignes [France] ; C. Canuel	[Abnormal eyelashes].
005662 (2010)	Mehandi Haran [États-Unis] ; Ankur Lodha ; Malcolm Rose ; Sheldon Greenberg	Rare association of immunoglobulin A nephropathy and lymphedema-distichiasis syndrome.
005953 (2010)	E. Sutkowska [Pologne] ; A. Bator ; K. Trompeta ; A. Szuba	Different lymphscintigraphic patterns in patients with lymphedema distichiasis.
005A56 (2010)	A-L Fauret [France] ; E. Tuleja ; X. Jeunemaitre ; S. Vignes	A novel missense mutation and two microrearrangements in the FOXC2 gene of three families with lymphedema-distichiasis syndrome.
005A67 (2010)	Antonella Fabretto [Italie] ; Alison Shardlow ; Flavio Faletra ; Loredana Lepore ; Uros Hladnik ; Paolo Gasparini	A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation.
005B38 (2010)	Pranoot Tanpaiboon [Thaïlande] ; Piranit Kantaputra [Thaïlande] ; Karn Wejathikul [Thaïlande] ; Wirawit Piyamongkol [Thaïlande]	c. 595‐596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient

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