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

Index « Keywords » - entrée « Turner Syndrome (genetics) »
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Turner Syndrome (epidemiology) < Turner Syndrome (genetics) < Turner Syndrome (immunology)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 36.
[0-20] [0 - 20][0 - 36][20-35][20-40]
Ident.Authors (with country if any)Title
000221 (1999) F. Haverkamp [Allemagne] ; J. Wölfle ; K. Zerres ; O. Butenandt ; P. Amendt ; B P Hauffa ; E. Weimann ; M. Bettendorf ; E. Keller ; R. Mühlenberg ; C J Partsch ; W G Sippell ; C. HoppeGrowth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failure.
000260 (1999) A. Tsezou [Grèce] ; C. Hadjiathanasiou ; D. Gourgiotis ; A. Galla ; E. Kavazarakis ; A. Pasparaki ; M. Kapsetaki ; C. Sismani ; C. Theodoridis ; P C Patsalis ; N. Moschonas ; S. KitsiouMolecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy.
000461 (2000) L. S Vendahl [Suède] ; M L DavenportDelayed diagnoses of Turner's syndrome: proposed guidelines for change.
000655 (2001) M. Sood [Inde] ; A. TrehanTurner's syndrome in infancy.
000683 (2001) M J Karkkainen [Finlande] ; L. Jussila ; R E Ferrell ; D N Finegold ; Kari Alitalo [Finlande]Molecular regulation of lymphangiogenesis and targets for tissue oedema.
000714 (2001) K A Leppig [États-Unis] ; C M DistecheRing X and other structural X chromosome abnormalities: X inactivation and phenotype.
000754 (2001) C. Boucher ; C. Sargent ; T. Ogata ; N. AffaraBreakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location
000B36 (????) Daniela Larizza [Italie] ; Miryam Martinetti ; Jean Michel Dugoujon ; Carmine Tinelli ; Valeria Calcaterra ; Mariaclara Cuccia ; Laura Salvaneschi ; Francesca SeveriParental GM and HLA genotypes and reduced birth weight in patients with Turner's syndrome.
001969 (2004) Eve J. Lowenstein [États-Unis] ; Karen H. Kim ; Sharon A. GlickTurner's syndrome in dermatology.
001B14 (2004) Valeria Brazzelli [Italie] ; Daniela Larizza ; Miriam Martinetti ; Sara Martinoli ; Valeria Calcaterra ; Annalisa De Silvestri ; Roberta Pandolfi ; Giovanni BorroniHalo nevus, rather than vitiligo, is a typical dermatologic finding of turner's syndrome: clinical, genetic, and immunogenetic study in 72 patients.
001D35 (2005) Melissa L. Loscalzo [États-Unis] ; Phillip L. Van ; Vincent B. Ho ; Vladimir K. Bakalov ; Douglas R. Rosing ; Carol A. Malone ; Harry C. Dietz ; Carolyn A. BondyAssociation between fetal lymphedema and congenital cardiovascular defects in Turner syndrome.
001E57 (2005) A. Debeer [Belgique] ; E. Steenkiste ; K. Devriendt ; M. MorrenScalp skin lesion in Turner syndrome: more than lymphoedema?
002024 (2006) K L Lachlan [Royaume-Uni] ; S. Youings ; T. Costa ; P A Jacobs ; N S ThomasA clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions.
002596 (2007) S. Cabrol [France][Turner syndrome].
002852 (2007) Thomas Morgan [États-Unis]Turner syndrome: diagnosis and management.
002A67 (????) D. Simm [Allemagne] ; K. Degenhardt ; C. Gerdemann ; T M K. Völkl ; A. Rauch ; H G Dörr[Chronological age of patients with Turner syndrome at diagnosis].
002E10 (2008) Melissa L. Loscalzo [États-Unis]Turner syndrome.
002F70 (2008) Carolyn A. BondyAortic Dissection in Turner Syndrome
003945 (2010) Rosa Fernandez [Espagne] ; Eduardo PasaroTall stature and gonadal dysgenesis in a non-mosaic girl 45,X.
004D77 (1990) J G Hall [Canada] ; D M GilchristTurner syndrome and its variants.
004E37 (2012) Jolanta Wierzba [Pologne] ; María Concepci N Gil-Rodríguez [Espagne] ; Anna Polucha [Pologne] ; Beatriz Puisac [Espagne] ; María Arnedo [Espagne] ; María Esperanza Teresa-Rodrigo [Espagne] ; Dorota Winnicka [Pologne] ; Fausto G. Hegardt [Espagne] ; Feliciano J. Ramos [Espagne] ; Janusz Limon [Pologne] ; Juan Pié [Espagne]Cornelia de Lange syndrome with NIPBL mutation and mosaic Turner syndrome in the same individual

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