Serveur d'exploration sur le lymphœdème - Curation (Ncbi)

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Noonan Syndrome (complications) < Noonan Syndrome (diagnosis) < Noonan Syndrome (diagnostic imaging)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 15.
Ident.Authors (with country if any)Title
000803 (????) C. Glade [Pays-Bas] ; M A Van Steensel ; P M SteijlenHypotrichosis, lymphedema of the legs and acral telangiectasias--new syndrome?
000A93 (2002) Imad R. Makhoul [Israël] ; Polo Sujov ; Nadir Ghanem ; Moshe BronshteinPrenatal diagnosis of Milroy's primary congenital lymphedema.
000E64 (2003) Tsutomu Ogata [Japon] ; Seiji Sato ; Yukihiro Hasegawa ; Kenjiro KosakiLymphstasis in a boy with Noonan syndrome: implication for the development of skeletal features.
002375 (????) Natalia Pastor ; Isabel Betlloch ; Mar Blanes ; Javier Mataix ; José Ba Uls ; Isabel Belinch NNoonan syndrome and scrotal lymphedema: primary or secondary?
002A14 (1991) D. Lacombe [France] ; A. Taieb ; P. Masson ; M. Fayon ; J L DemarquezNeonatal Noonan syndrome with a molluscoid cutaneous excess over the scalp.
002E65 (1991) G. Neri ; M. Zollino ; J F ReynoldsThe Noonan-CFC controversy.
004F04 (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
005329 (2012) Patroula Smpokou [États-Unis] ; Erica Tworog-Dube ; Raju S. Kucherlapati ; Amy E. RobertsMedical complications, clinical findings, and educational outcomes in adults with Noonan syndrome.
005535 (2013) Yan Zhao ; Dongjie Zang ; Hongjun Xu ; Shi-Jun Shan ; Cheng Zhou ; Jianzhong ZhangPoikiloderma, hyperpigmentation, alopecia, hypohidrosis, malformed bones, lymphedema of the legs and decreased cortisol level: a new entity?
005802 (2013) N. Khen-Dunlop [France] ; J. Amiel ; C. Delacourt ; Y. Révillon[Enigmatic lymphatic diseases involving the lung].
006198 (2014) Vikas Bhambhani ; Maximilian MuenkeNoonan Syndrome
007713 (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
00A970 (1980) J A García Centenera ; J L Lucero ; J M Vilchez ; F. Requejo ; M. Herrán ; A. Fabra[Turner's phenotype in a male with deficit of ACTH and gonadotropins (author's transl)].
00B529 (1993) M. Chery ; C. Philippe ; A M Worms ; S. GilgenkrantzThe Noonan syndrome. The Nancy experience revisited.
00BB69 (1998) J P Fryns ; P. MoermanTrisomy 21 in a second trimester male hydropic fetus with "Noonan-syndrome-phenotype": nuchal and thoracic lymphangiomatosis, oedema of the dorsum of hands and feet, and bicuspid pulmonary valve.

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