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.
[0-50] [0 - 20][0 - 50][50-70]

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
005135 (2011)	Sanjeeva Goli ; Vijay Kandimalla ; Omar Khan	A case of Noonan's syndrome with anomalous lymphorenal communication
005202 (2011)	M. Bakker [Pays-Bas] ; E. Pajkrt [Pays-Bas] ; I. B. Mathijssen [Pays-Bas] ; C. M. Bilardo [Pays-Bas]	Targeted ultrasound examination and DNA testing for Noonan syndrome, in fetuses with increased nuchal translucency and normal karyotype
005732 (2010)	M. Tartaglia [Italie] ; G. Zampino [Italie] ; B. D. Gelb [États-Unis]	Noonan Syndrome: Clinical Aspects and Molecular Pathogenesis
005C54 (2010)	Woo Jin Lee [Corée du Sud] ; Deok Woo Lee [Corée du Sud] ; Ji Hye Yang [Corée du Sud] ; Sung Eun Chang [Corée du Sud] ; Mi Woo Lee [Corée du Sud] ; Jee Ho Choi [Corée du Sud] ; Kee Chan Moon [Corée du Sud]	Novel occurrence of microcystic lymphatic malformation and linear port‐wine stain in patients with Noonan syndrome
006138 (2009)	Siying Wang [États-Unis] ; Wen-Mei Yu [États-Unis] ; Wanming Zhang [États-Unis] ; Keith R. Mccrae [États-Unis] ; Benjamin G. Neel [États-Unis] ; Cheng-Kui Qu [États-Unis]	Noonan Syndrome/Leukemia-associated Gain-of-function Mutations in SHP-2 Phosphatase (PTPN11) Enhance Cell Migration and Angiogenesis*
006220 (2009)	Kosei Hasegawa [Japon] ; Yoshiharu Nagaoka [Japon] ; Hidehiko Maruyama [Japon] ; Kunihiko Aya [Japon] ; Hiroyuki Tanaka [Japon] ; Tsuneo Morishima [Japon]	Late-onset Lymphedema and Protein-losing Enteropathy with Noonan Syndrome
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.
006D80 (2008)	Willem Verhoeven [Pays-Bas] ; Ellen Wingbermühle [Pays-Bas] ; Jos Egger [Pays-Bas] ; Ineke Van Der Burgt [Pays-Bas] ; Siegfried Tuinier [Pays-Bas]	Noonan syndrome: Psychological and psychiatric aspects
006E68 (2008)	Oleg A. Shchelochkov [États-Unis] ; Ankita Patel [États-Unis] ; George M. Weissenberger [États-Unis] ; A. Craig Chinault [États-Unis] ; Joanna Wiszniewska [États-Unis] ; Priscilla H. Fernandes [États-Unis] ; Christine Eng [États-Unis] ; Mary K. Kukolich [États-Unis] ; V. Reid Sutton [États-Unis]	Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome
006F22 (2008)	Lize V. Ferreira [Brésil] ; Silvia C. A. L. Souza [Brésil] ; Luciana R. Montenegro [Brésil] ; Alexsandra C. Malaquias [Brésil] ; Ivo J. P. Arnhold [Brésil] ; Berenice B. Mendonca [Brésil] ; Alexander A. L. Jorge [Brésil]	Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients
007176 (2007)	Ineke Van Der Burgt [Pays-Bas]	Noonan syndrome
007421 (2007)	A C Shaw [Royaume-Uni] ; K. Kalidas [Royaume-Uni] ; A H Crosby [Royaume-Uni] ; S. Jeffery [Royaume-Uni] ; M A Patton [Royaume-Uni]	The natural history of Noonan syndrome: a long-term follow-up study
007546 (2007)	Judith E. Allanson	Noonan syndrome
007553 (2007)	S-T Lee ; C-S Ki [États-Unis] ; Hj Lee [Corée du Sud]	Mutation analysis of the genes involved in the Ras‐mitogen‐activated protein kinase (MAPK) pathway in Korean patients with Noonan syndrome
007621 (2007)	Kristin Becker [Royaume-Uni] ; Helen Hughes [Royaume-Uni] ; Karol Howard [Royaume-Uni] ; Maggie Armstrong [Royaume-Uni] ; Devender Roberts [Royaume-Uni] ; Edgar J. Lazda [Royaume-Uni] ; John P. Short [Royaume-Uni] ; Adam Shaw [Royaume-Uni] ; Michael A. Patton [Royaume-Uni] ; Marco Tartaglia [Italie]	Early fetal death associated with compound heterozygosity for Noonan syndrome‐causative PTPN11 mutations
007B70 (2006)	Jean-Marc Levaillant [France] ; Marion Gérard-Blanluet [France] ; Muriel Holder-Espinasse [France] ; Anne-Sylvie Valat-Rigot [France] ; Louise Devisme [France] ; Hélène Cavé [France] ; Sylvie Manouvrier-Hanu [France]	Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri‐dimensional ultrasonography
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?
007D47 (2006)	Ulrike Hüffmeier [Allemagne] ; Martin Zenker [Allemagne] ; Juliane Hoyer [Allemagne] ; Raimund Fahsold [Allemagne] ; Anita Rauch [Allemagne]	A variable combination of features of Noonan syndrome and neurofibromatosis type I are caused by mutations in the NF1 gene
008216 (2005)	J S Lee [États-Unis] ; M. Tartaglia [Italie, États-Unis] ; B D Gelb [États-Unis] ; K. Fridrich [États-Unis] ; S. Sachs ; C A Stratakis ; M. Muenke ; P G Robey [États-Unis] ; M T Collins [États-Unis] ; A. Slavotinek	Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndrome
008449 (2005)	Lindy Peta Fox [États-Unis] ; Adam S. Geyer [États-Unis] ; Kwame Anyane-Yeboa [États-Unis] ; Maria C. Garzon [États-Unis]	Cutis Verticis Gyrata in a Patient with Noonan Syndrome
008C05 (2004)	G. Weiss [Israël] ; Y. Confino ; A. Shemer [Israël] ; H. Trau [Israël]	Cutaneous manifestations in the cardiofaciocutaneous syndrome, a variant of the classical Noonan syndrome. Report of a case and review of the literature
008C26 (2004)	Débora Romeo Bertola [Brésil] ; Alexandre C. Pereira [Brésil] ; Paulo S. L. De Oliveira [Brésil] ; Chong A. Kim [Brésil] ; José Eduardo Krieger [Brésil]	Clinical variability in a Noonan syndrome family with a new PTPN11 gene mutation
008C82 (2004)	Rie Yoshida [Japon] ; Masafumi Miyata [Japon] ; Toshiro Nagai [Japon] ; Toshio Yamazaki [Japon] ; Tsutomu Ogata [Japon]	A 3‐bp deletion mutation of PTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia
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
009531 (2002)	Na Tramboo [Inde] ; K. Iqbal [Inde] ; Ma Dar [Inde] ; Ra Malik [Inde] ; Ba Naikoo [Inde] ; Ma Andrabi [Inde]	Unusual dysmorphic features in five patients with Noonan's syndrome: A brief review
009591 (2002)	I. Witters [Belgique] ; B. Spitz [Belgique] ; C. Van Hole [Belgique] ; K. Devriendt [Belgique] ; J. P. Fryns [Belgique] ; K. Verbek [Belgique]	Resolution of non‐immune hydrops in Noonan syndrome with favorable outcome
009640 (2002)	Edmond G. Lemire [Canada]	Noonan syndrome or new autosomal dominant condition with coarctation of the aorta, hypertrophic cardiomyopathy, and minor anomalies
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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