Syndactyly < Syndrome < Synovial Cyst

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

List of bibliographic references

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

Ident.	Authors (with country if any)	Title
000897 (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.
000A09 (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.
000A49 (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.
000B08 (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.
000B69 (2015)	Xiao-Lu Deng [République populaire de Chine] ; Fei Yin ; Guo-Yuan Zhang ; Yuan-Dong Duan	[A complicated case study: Hennekam syndrome].
000C65 (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.
001121 (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, expanding the phenotype of linkeropathy syndromes.
001147 (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?].
001436 (2014)	Spring Golden [États-Unis] ; Dawn M. Davis ; Jerry D. Brewer	Lymphedema in a patient with distichiasis.
001511 (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.
001602 (2014)	Ghayda M. Mirzaa [États-Unis] ; Laura Enyedi ; Gretchen Parsons ; Sarah Collins ; Livija Medne ; Carissa Adams ; Thomas Ward ; Bradley Davitt ; Alma Bicknese ; Elaine Zackai ; Helga Toriello ; William B. Dobyns ; Susan Christian	Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature.
001618 (2014)	Carlo Bellini [Italie] ; Raoul C M. Hennekam	Clinical disorders of primary malfunctioning of the lymphatic system.
001627 (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.
001649 (2014)	M J Bernas	Axillary web syndrome, the lost cord, and lingering questions.
001660 (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.
001741 (2013)	M. Marc [France] ; M. Barreau ; M. Gerard ; L. Verneuil ; L. Derieux ; A. Dompmartin	[Lymphoedema distichiasis].
001765 (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].
001D15 (2012)	E. Archier [France] ; J C Grillo ; S. Fourcade ; C. Gaudy ; J J Grob ; M A Richard	[Morel-Lavallee syndrome of the lower leg].
001F06 (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.
001F77 (2012)	Jan Kazenwadel [Australie] ; Genevieve A. Secker ; Yajuan J. Liu ; Jill A. Rosenfeld ; Robert S. Wildin ; Jennifer Cuellar-Rodriguez ; Amy P. Hsu ; Sarah Dyack ; Conrad V. Fernandez ; Chan-Eng Chong ; Milena Babic ; Peter G. Bardy ; Akiko Shimamura ; Michael Y. Zhang ; Tom Walsh ; Steven M. Holland ; Dennis D. Hickstein ; Marshall S. Horwitz ; Christopher N. Hahn ; Hamish S. Scott ; Natasha L. Harvey	Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature.
002026 (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.

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