List of bibliographic references indexed by Syndrome de Noonan (diagnostic)
Number of relevant bibliographic references: 15.
| Ident. | Authors (with country if any) | Title |
|---|
| 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 |
| 002770 (2014) |
Vikas Bhambhani ; Maximilian Muenke | 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 |
| 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 |
| 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. |
| 009609 (2002) |
Imad R. Makhoul [Israël] ; Polo Sujov [Israël] ; Nadir Ghanem [Israël] ; Moshe Bronshtein [Israël] | Prenatal diagnosis of Milroy's primary congenital lymphedema |
| 00B047 (1998) |
J P Fryns ; P. Moerman | Trisomy 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. |
| 00CC09 (1993) |
M. Chery ; C. Philippe ; A M Worms ; S. Gilgenkrantz | The Noonan syndrome. The Nancy experience revisited. |
| 00D515 (1991) |
D. Lacombe [France] ; A. Taieb ; P. Masson ; M. Fayon ; J L Demarquez | Neonatal Noonan syndrome with a molluscoid cutaneous excess over the scalp. |
| 00D715 (1991) |
Giovanni Neri [Italie] ; Marcella Zollino [Italie] ; James F. Reynolds [Italie, États-Unis] | The Noonan‐CFC controversy |
| 00FA02 (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)]. |
| 012C95 (????) |
C. Glade [Pays-Bas] ; M A Van Steensel ; P M Steijlen | Hypotrichosis, lymphedema of the legs and acral telangiectasias--new syndrome? |
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