Syndactyly < Syndrome < Synovial Cyst

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

List of bibliographic references indexed by Syndrome

Number of relevant bibliographic references: 401.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
001046 (2016)	Toshiki Takenouchi [Japon] ; Nobuhiko Okamoto [Japon] ; Shinobu Ida [Japon] ; Tomoko Uehara [Japon] ; Kenjiro Kosaki [Japon]	Further evidence of a mutation in CDC42 as a cause of a recognizable syndromic form of thrombocytopenia.
001299 (2016)	Timothy J. Tausch ; Isamu Tachibana ; Jordan A. Siegel ; Ronald Hoxworth ; Jeremy M. Scott ; Allen F. Morey	Classification System for Individualized Treatment of Adult Buried Penis Syndrome.
001373 (2016)	Darryl Schuitevoerder [États-Unis] ; Ian White [États-Unis] ; Jeanine Fortino [États-Unis] ; John Vetto [États-Unis]	Axillary web syndrome: an underappreciated complication of sentinel node biopsy in melanoma.
001501 (2016)	Fatma Bastaki [Émirats arabes unis] ; Madiha Mohamed [Émirats arabes unis] ; Pratibha Nair [Émirats arabes unis] ; Fatima Saif [Émirats arabes unis] ; Nafisa Tawfiq [Émirats arabes unis] ; Mahmoud Taleb Al-Ali [Émirats arabes unis] ; Oliver Brandau [Allemagne] ; Abdul Rezzak Hamzeh [Émirats arabes unis]	A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis-lymphedema-telangiectasia syndrome by Whole Exome Sequencing.
001600 (2015)	Xiao-Lu Deng [République populaire de Chine] ; Fei Yin ; Guo-Yuan Zhang ; Yuan-Dong Duan	[A complicated case study: Hennekam syndrome].
001815 (2015)	Aladdin H. Hassanein [États-Unis] ; Javier A. Couto [États-Unis] ; John B. Mulliken [États-Unis] ; Arin K. Greene [États-Unis]	Stewart-Treves Phenomenon: Lymphangiosarcoma Arising in Lymphedematous Tissue Is not a Syndrome.
002253 (2015)	Kelly L. Jones [États-Unis] ; Ulrike Schwarze [États-Unis] ; Margaret P. Adam [États-Unis] ; Peter H. Byers [États-Unis] ; Heather C. Mefford [États-Unis]	A Homozygous B3GAT3 Mutation Causes a Severe Syndrome with Multiple Fractures, Extending the Number of Linkeropathy Syndromes
002286 (2014)	S. Collet [France] ; A. Forli [France] ; P-H Carpentier [France] ; F. Laviolette [France] ; B. Imbert [France] ; S. Blaise [France]	[Secretan's syndrome: myth or pathomimia?].
002881 (2014)	Spring Golden [États-Unis] ; Dawn M. Davis ; Jerry D. Brewer	Lymphedema in a patient with distichiasis.
002A11 (2014)	O. Leduc ; E. Fumière ; S. Banse ; C. Vandervorst ; A. Clément ; T. Parijs ; F. Wilputte ; F. Maquerlot ; M. Ezquer Echandia ; A. Tinlot ; A. Leduc	Identification and description of the axillary web syndrome (AWS) by clinical signs, MRI and US imaging.
002C19 (2014)	Ghayda M. Mirzaa [États-Unis] ; Laura Enyedi [États-Unis] ; Gretchen Parsons [États-Unis] ; Sarah Collins [États-Unis] ; Livija Medne [États-Unis] ; Carissa Adams [États-Unis] ; Thomas Ward [États-Unis] ; Bradley Davitt [États-Unis] ; Alma Bicknese [États-Unis] ; Elaine Zackai [États-Unis] ; Helga Toriello [États-Unis] ; William B. Dobyns [États-Unis] ; Susan Christian [États-Unis]	Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature
002C48 (2014)	Carlo Bellini [Italie] ; Raoul C M. Hennekam	Clinical disorders of primary malfunctioning of the lymphatic system.
002C88 (2014)	L. A. Koehler ; D. W. Hunter ; T. C. Haddad ; A. H. Blaes ; A. T. Hirsch ; P. M. Ludewig	CHARACTERIZING AXILLARY WEB SYNDROME: ULTRASONOGRAPHIC EFFICACY
002D20 (2014)	M J Bernas	Axillary web syndrome, the lost cord, and lingering questions.
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.
002F37 (2013)	M. Marc [France] ; M. Barreau ; M. Gerard ; L. Verneuil ; L. Derieux ; A. Dompmartin	[Lymphoedema distichiasis].
002F60 (2013)	C. Courtin [France] ; L. Mathieu ; F. Rongiéras ; A. Bertani ; F. Chauvin	[Comorbid puffy hand syndrome and factitious disorders: an unusual association with poor prognosis].
003D05 (2012)	E. Archier [France] ; J C Grillo ; S. Fourcade ; C. Gaudy ; J J Grob ; M A Richard	[Morel-Lavallee syndrome of the lower leg].
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.
004257 (2012)	Gwendolyn De Bruyn [Belgique] ; Alexandra Casaer ; Katrien Devolder ; Geert Van Acker ; Hilde Logghe ; Koen Devriendt ; Luc Cornette	Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression.
004290 (2012)	Hiroyuki Ishida [Japon] ; Kosuke Imai ; Kenichi Honma ; Shin-Ichi Tamura ; Toshihiko Imamura ; Masafumi Ito ; Shigeaki Nonoyama	GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia.

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