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 |
|---|
| 000844 (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. |
| 000924 (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. |
| 000A89 (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. |
| 000B16 (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. |
| 000E31 (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. |
| 000F22 (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. |
| 000F23 (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. |
| 000F24 (2014) |
M J Bernas | Axillary web syndrome, the lost cord, and lingering questions. |
| 001062 (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. |
| 001075 (2015) |
Xiao-Lu Deng [République populaire de Chine] ; Fei Yin ; Guo-Yuan Zhang ; Yuan-Dong Duan | [A complicated case study: Hennekam syndrome]. |
| 001241 (????) |
Rafael Fabiano Machado Rosa [Brésil] ; Flávia Enk [Brésil] ; Korine Camargo [Brésil] ; Giovanni Marco Travi [Brésil] ; André Freitas [Brésil] ; Rosana Cardoso Manique Rosa [Brésil] ; Carla Graziadio [Brésil] ; Vinicius Freitas De Mattos [Brésil] ; Paulo Ricardo Gazzola Zen [Brésil] | Microcephaly-chorioretinopathy syndrome, autosomal recessive form. A case report. |
| 001398 (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. |
| 001810 (2014) |
Carlo Bellini [Italie] ; Raoul C M. Hennekam | Clinical disorders of primary malfunctioning of the lymphatic system. |
| 001845 (2014) |
Spring Golden [États-Unis] ; Dawn M. Davis ; Jerry D. Brewer | Lymphedema in a patient with distichiasis. |
| 001850 (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?]. |
| 001867 (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. |
| 001896 (2013) |
M. Marc [France] ; M. Barreau ; M. Gerard ; L. Verneuil ; L. Derieux ; A. Dompmartin | [Lymphoedema distichiasis]. |
| 001A22 (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]. |
| 002067 (????) |
Maria N. Kelly [États-Unis] ; Nausheen Khuddus ; Silus Motamarry ; Sanjeev Tuli | Microcephaly, lymphedema, chorioretinal dysplasia (MLCRD) syndrome. |
| 002212 (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. |
| 002234 (2012) |
E. Archier [France] ; J C Grillo ; S. Fourcade ; C. Gaudy ; J J Grob ; M A Richard | [Morel-Lavallee syndrome of the lower leg]. |
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