noon < noonan < nor

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

List of bibliographic references indexed by noonan

Number of relevant bibliographic references: 124.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000968 (2016)	Doris Milosavljevi [Pays-Bas] ; Eline Overwater [Pays-Bas] ; Saskia Tamminga [Pays-Bas] ; Karin De Boer [Pays-Bas] ; Mariet W. Elting [Pays-Bas] ; Marion E. Van Hoorn [Pays-Bas] ; Tuula Rinne [Pays-Bas] ; Arjan C. Houweling [Pays-Bas]	Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature.
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.
000D50 (2016)	Alireza Tafazoli [Iran] ; Peyman Eshraghi [Iran] ; Zahra Kamel Koleti [Iran] ; Mohammadreza Abbaszadegan [Iran]	Noonan syndrome – a new survey
000E35 (2016)	Harm Winters ; Hanneke J. P. Tielemans ; Dietmar J. O. Ulrich	Lymphovenous Anastomosis and Secondary Resection for Noonan Syndrome with Vulvar Lymphangiectasia
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
001979 (2015)	Sheetal R. Jagtap [Inde] ; Hemalata R. Iyer [Inde] ; Rochana G. Bakhshi [Inde] ; Hemant N. Lahoti [Inde]	Post-operative airway obstruction in Noonan syndrome: An unusual presentation
002043 (2015)	Bruce D. Gelb [États-Unis] ; Amy E. Roberts [États-Unis] ; Marco Tartaglia [Italie]	Cardiomyopathies in Noonan syndrome and the other RASopathies
002186 (2015)	Viviana Cordeddu [Italie] ; Jiani C. Yin [Canada] ; Cecilia Gunnarsson [Suède] ; Carl Virtanen [Canada] ; Séverine Drunat [France] ; Francesca Lepri [Italie] ; Alessandro De Luca [Italie] ; Cesare Rossi [Italie] ; Andrea Ciolfi [Italie] ; Trevor J. Pugh [Canada] ; Alessandro Bruselles [Italie] ; James R. Priest [États-Unis] ; Len A. Pennacchio [États-Unis] ; Zhibin Lu [Canada] ; Arnavaz Danesh [Canada] ; Rene Quevedo [Canada] ; Alaa Hamid [Canada] ; Simone Martinelli [Italie] ; Francesca Pantaleoni [Italie] ; Maria Gnazzo [Italie] ; Paola Daniele [Italie] ; Christina Lissewski [Allemagne] ; Gianfranco Bocchinfuso [Italie] ; Lorenzo Stella [Italie] ; Sylvie Odent [France] ; Nicole Philip [France] ; Laurence Faivre [France] ; Marketa Vlckova [République tchèque] ; Eva Seemanova [République tchèque] ; Cristina Digilio [Italie] ; Martin Zenker [Allemagne] ; Giuseppe Zampino [Italie] ; Alain Verloes [France] ; Bruno Dallapiccola [Italie] ; Amy E. Roberts [États-Unis] ; Hélène Cavé [France] ; Bruce D. Gelb [États-Unis] ; Benjamin G. Neel [Canada, États-Unis] ; Marco Tartaglia [Italie]	Activating mutations affecting the Dbl homology domain of SOS2 cause Noonan syndrome
002368 (2014)	Deepan Mathur ; Santhosh Somashekar ; Cristina Navarrete ; Maria M. Rodriguez	Twin Infant with Lymphatic Dysplasia Diagnosed with Noonan Syndrome by Molecular Genetic Testing
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.
002A45 (2014)	Helen L. Hanson [Royaume-Uni] ; Meredith J. Wilson ; John P. Short ; Barry A. Chioza ; Andrew H. Crosby ; Ruth M. Nash ; Karen J. Marks ; Sahar Mansour	Germline CBL mutation associated with a noonan-like syndrome with primary lymphedema and teratoma associated with acquired uniparental isodisomy of chromosome 11q23.
003064 (2013)	Pankaj Agarwal ; Rajeev Philip ; Manish Gutch ; K. K. Gupta	The other side of Turner's: Noonan's syndrome
003278 (2013)	Ellen A. Croonen [Pays-Bas] ; Willy M. Nillesen [Pays-Bas] ; Kyra E. Stuurman [Pays-Bas] ; Gretel Oudesluijs [Pays-Bas] ; Ingrid M B M. Van De Laar [Pays-Bas] ; Liesbeth Martens [Pays-Bas] ; Charlotte Ockeloen [Pays-Bas] ; Inge B. Mathijssen [Pays-Bas] ; Marga Schepens [Pays-Bas] ; Martina Ruiterkamp-Versteeg [Pays-Bas] ; Hans Scheffer [Pays-Bas] ; Brigitte H W. Faas [Pays-Bas] ; Ineke Van Der Burgt [Pays-Bas] ; Helger G. Yntema [Pays-Bas]	Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings
003347 (2013)	Amy E. Roberts ; Judith E. Allanson ; Marco Tartaglia ; Bruce D. Gelb	Noonan syndrome
003945 (2013)	Gregor Nosan [Slovénie] ; Sara Bertok [Slovénie] ; Samo Vesel [Slovénie] ; Helger G. Yntema [Pays-Bas] ; Darja Paro-Panjan [Slovénie]	A lethal course of hypertrophic cardiomyopathy in Noonan syndrome due to a novel germline mutation in the KRAS gene: case study
003A73 (2013)	A. Gaudineau [France] ; B. Doray [France] ; E. Schaefer [France] ; N. Sananès [France] ; G. Fritz [France] ; M. Kohler [France] ; Y. Alembik [France] ; B. Viville [France] ; R. Favre [France] ; B. Langer [France]	Postnatal phenotype according to prenatal ultrasound features of Noonan syndrome: a retrospective study of 28 cases
003B45 (2013)	Sj Joyce [Royaume-Uni] ; S. Mansour [Royaume-Uni]	G26 Lymphatic Disorders In Noonan Syndrome
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
004C88 (2011)	Marco Tartaglia [Italie] ; Bruce D. Gelb ; Martin Zenker [Allemagne]	Noonan syndrome and clinically related disorders

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