List of bibliographic references indexed by Syndrome de Noonan
Number of relevant bibliographic references: 41.
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Ident. | Authors (with country if any) | Title |
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000B79 (2016) |
Kei Suzuki [Japon] ; Akiko Nakamura [Japon] ; Ken Ishikura [Japon] ; Hiroshi Imai [Japon] | Recurrent SDSE bacteraemia resulting in streptococcal toxic shock syndrome in a patient with Noonan syndrome. |
001627 (2015) |
S. Fuchs [Israël] ; G. Gat-Yablonski [Israël] ; B. Shtaif [Israël] ; L. Lazar [Israël] ; M. Phillip [Israël] ; Y. Lebenthal [Israël] | Vascular endothelial growth factor (VEGF) levels in short, GH treated children: a distinct pattern of VEGF-C in Noonan syndrome. |
001708 (2015) |
Sarah Joyce [Royaume-Uni] ; Kristiana Gordon [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Pia Ostergaard [Royaume-Uni] ; Rani Nagaraja [Royaume-Uni] ; John Short [Royaume-Uni] ; Sandra Moore [Royaume-Uni] ; Peter Mortimer (dermatologue) [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] | The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome |
001A72 (2015) |
Martin Koenighofer [Autriche] ; Christina Y. Hung [États-Unis] ; Jacob L. Mccauley [États-Unis] ; Julia Dallman [États-Unis] ; Emma J. Back [États-Unis] ; Ivana Mihalek [Singapour] ; Karen W. Gripp [États-Unis] ; Katia Sol-Church [États-Unis] ; Paolo Rusconi [États-Unis] ; Zhaiyi Zhang [États-Unis] ; Geng-Xian Shi [États-Unis] ; Douglas A. Andres [États-Unis] ; Olaf A. Bodamer [États-Unis] | Mutations in RIT1 cause Noonan syndrome – additional functional evidence and expanding the clinical phenotype |
002770 (2014) |
Vikas Bhambhani ; Maximilian Muenke | Noonan Syndrome |
002909 (2014) |
Llana Pootrakul [États-Unis] ; Michael R. Nazareth ; Richard T. Cheney ; Marcelle A. Grassi | Lymphangioma circumscriptum of the vulva in a patient with Noonan syndrome. |
002F55 (2013) |
N. Khen-Dunlop [France] ; J. Amiel ; C. Delacourt ; Y. Révillon | [Enigmatic lymphatic diseases involving the lung]. |
003A78 (2013) |
Yan Zhao [République populaire de Chine] ; Dongjie Zang [République populaire de Chine] ; Hongjun Xu [République populaire de Chine] ; Shi-Jun Shan [République populaire de Chine] ; Cheng Zhou [République populaire de Chine] ; Jianzhong Zhang [République populaire de Chine] | Poikiloderma, hyperpigmentation, alopecia, hypohidrosis, malformed bones, lymphedema of the legs and decreased cortisol level: A new entity? |
004733 (2012) |
Patroula Smpokou [États-Unis] ; Erica Tworog-Dube [États-Unis] ; Raju S. Kucherlapati [États-Unis] ; Amy E. Roberts [États-Unis] | Medical complications, clinical findings, and educational outcomes in adults with Noonan syndrome |
005247 (2011) |
John S. Ferguson [Royaume-Uni] ; Shymalar Gunatheesan [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Rob Hastings [Royaume-Uni] ; Ruth Newbury-Ecob [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] | Primary lymphedema with coarctation of the aorta: Possible new syndrome or variant of Irons–Bianchi syndrome? |
005522 (2010) |
Moritz Felcht [Allemagne] ; Nicola Dikow [Allemagne] ; Matthias Goebeler [Allemagne] ; Philipp Stroebel [Allemagne] ; Nina Booken [Allemagne] ; Urs Vo Merb Umer [Allemagne] ; Kirsten Merx [Allemagne] ; Thomas Henzler [Allemagne] ; Alexander Marx [Allemagne] ; Ute Moog [Allemagne] ; Sergij Goerdt [Allemagne] ; Claus-Detlev Klemke [Allemagne] | Warty skin changes, chronic scrotal lymphoedema, and facial dysmorphism |
006870 (2008) |
Mei-Fang Cheng [Taïwan] ; Yen-Wen Wu ; Kai-Yuan Tzen ; Ruoh-Fang Yen | Usefulness of lymphoscintigraphy in demonstrating lymphedema in patients with Noonan syndrome. |
006D53 (2008) |
Robert E. Ferrell [États-Unis] ; David N. Finegold [États-Unis] | Research Perspectives in Inherited Lymphatic Disease |
007B94 (2006) |
Natalia Pastor [Espagne] ; Isabel Betlloch [Espagne] ; Mar Blanes [Espagne] ; Javier Mataix [Espagne] ; José Ba Uls [Espagne] ; Isabel Belinch N [Espagne] | Noonan Syndrome and Scrotal Lymphedema: Primary or Secondary? |
008E51 (2003) |
Tsutomu Ogata [Japon] ; Seiji Sato ; Yukihiro Hasegawa ; Kenjiro Kosaki | Lymphstasis in a boy with Noonan syndrome: implication for the development of skeletal features. |
009250 (2003) |
Wan-Ling Ho [Taïwan] ; Jou-Kou Wang [Taïwan] ; Yiu-Wah Li [Taïwan] | Radiological features of late-onset lymphoedema in Noonan's syndrome |
009592 (2002) |
Robert E. Ferrell [États-Unis] | Research Perspectives in Inherited Lymphatic Disease |
009609 (2002) |
Imad R. Makhoul [Israël] ; Polo Sujov [Israël] ; Nadir Ghanem [Israël] ; Moshe Bronshtein [Israël] | Prenatal diagnosis of Milroy's primary congenital lymphedema |
009924 (2001) |
G. Lorette [France] ; L. Vaillant ; F. Baulieu | [Lymphedema in children]. |
009994 (2001) |
A. Aggarwal [États-Unis] ; J. Krishnan ; A. Kwart ; D. Perry | Noonan's syndrome and seminoma of undescended testicle. |
00A270 (2000) |
M. Keberle [Allemagne] ; H. Mörk ; M. Jenett ; D. Hahn ; M. Scheurlen | Computed tomography after lymphangiography in the diagnosis of intestinal lymphangiectasia with protein-losing enteropathy in Noonan's syndrome. |
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