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

Index « Keywords » - entrée « Craniofacial Abnormalities (diagnosis) »
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Craniofacial Abnormalities (complications) < Craniofacial Abnormalities (diagnosis) < Craniofacial Abnormalities (diagnostic imaging)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 9.
Ident.Authors (with country if any)Title
004971 (2012) F C Connell ; K. Kalidas ; P. Ostergaard ; G. Brice ; V. Murday ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; I. Jeffrey ; S. Jeffery ; Sahar MansourCCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis.
005339 (2012) Siham Al Sinani ; Yusria Al Rawahi ; Hamed AbdoonOctreotide in Hennekam syndrome-associated intestinal lymphangiectasia
005785 (2013) G. Brice ; P. Ostergaard ; S. Jeffery ; K. Gordon ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. MansourA novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family.
005802 (2013) N. Khen-Dunlop [France] ; J. Amiel ; C. Delacourt ; Y. Révillon[Enigmatic lymphatic diseases involving the lung].
006414 (2014) Abdullah Ozyurt [Turquie] ; Eylem Sevinc ; Ali Baykan ; Duran Arslan ; Mustafa Argun ; Ozge Pamukcu ; Kazim UzumVariable clinical presentation in primary lymphoedema: report of two cases.
006A21 (2014) Imane Elmansour ; Soumia Chiheb ; Hakima BenchikhiHennekam syndrome: a rare cause of primary lymphedema.
006F68 (2015) Xiao-Lu Deng [République populaire de Chine] ; Fei Yin ; Guo-Yuan Zhang ; Yuan-Dong Duan[A complicated case study: Hennekam syndrome].
007437 (2015) Makoto Mihara [Japon] ; Hisako Hara [Japon] ; Jun Shibasaki [Japon] ; Yukio Seki [Japon] ; Akitatsu Hayashi [Japon] ; Takuya Iida [Japon] ; Shinya Adachi [Japon] ; Yasushi Uchida [Japon] ; Hideo Kaneko [Japon] ; Makiko Haragi [Japon] ; Arata Murakami [Japon]Indocyanine green lymphography and lymphaticovenous anastomosis for generalized lymphatic dysplasia with pleural effusion and ascites in neonates.
007C46 (2015) Carolyn C. Jackson [États-Unis] ; Lucy Best [États-Unis] ; Lazaro Lorenzo [France] ; Jean-Laurent Casanova [États-Unis, France] ; Jochen Wacker [Allemagne] ; Simone Bertz [Allemagne] ; Abbas Agaimy [Allemagne] ; Thomas Harrer [Allemagne]A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression

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