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Index « PmcKwd.i » - entrée « Turner syndrome »
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Turner Syndrome < Turner syndrome < Turner syndrome (TS)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 24.
[0-20] [0 - 20][0 - 24][20-23][20-40]
Ident.Authors (with country if any)Title
000064 (2017) Imen Mehri Turki [Tunisie]Surgical correction of the webbed neck: an alternative lateral approach
000360 (2017) Simona Bucerzan [Roumanie] ; Diana Miclea [Roumanie] ; Radu Popp [Roumanie] ; Camelia Alkhzouz [Roumanie] ; Cecilia Lazea [Roumanie] ; Ioan Victor Pop [Roumanie] ; Paula Grigorescu-Sido [Roumanie]Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study)
000447 (2017) Serena Gianfaldoni ; Georgi Tchernev ; Uwe Wollina ; Torello LottiA Case of Alopecia Areata in a Patient with Turner Syndrome
000681 (2016) Alessandra Bernadete Trov De Marqui ; Roseane Lopes Da Silva-Grecco ; Marly Aparecida Spadotto BalarinPrevalence of Y-chromosome sequences and gonadoblastoma in Turner syndrome
000770 (2016) Pooja Chauhan [Inde] ; Sushil Kumar Jaiswal [Inde] ; Anjali Rani Lakhotia [Inde] ; Amit Kumar Rai [Inde]Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome
000A94 (2016) Jung Yu [Corée du Sud] ; Ha Young Shin [Corée du Sud] ; Chong Guk Lee [Corée du Sud] ; Jae Hyun Kim [Corée du Sud]Concomitant occurrence of Turner syndrome and growth hormone deficiency
000D46 (2015) Min Kyung Yu [Corée du Sud] ; Mo Kyung Jung [Corée du Sud] ; Ki Eun Kim [Corée du Sud] ; Ah Reum Kwon [Corée du Sud] ; Hyun Wook Chae [Corée du Sud] ; Duk Hee Kim [Corée du Sud] ; Ho-Seong Kim [Corée du Sud]Turner syndrome with spinal hemorrhage due to vascular malformation
000D47 (2015) Go Hun Seo [Corée du Sud] ; Eungu Kang [Corée du Sud] ; Ja Hyang Cho [Corée du Sud] ; Beom Hee Lee [Corée du Sud] ; Jin-Ho Choi [Corée du Sud] ; Gu-Hwan Kim [Corée du Sud] ; Eul-Ju Seo [Corée du Sud] ; Han-Wook Yoo [Corée du Sud]Turner syndrome presented with tall stature due to overdosage of the SHOX gene
000D48 (2015) Alessandra Bernadete Trov De Marqui [Brésil]Turner syndrome and genetic polymorphism: a systematic review
001547 (2015) Bui Phuong Thao ; Vu Chi Dung ; Nguyen Ngoc Khanh ; Can Thi Bich Ngoc ; Nguyen Thi Hoan ; Nguyen Thi PhuongAB155. Clinical presentation and its relationship with chromosomal abnormalities in Turner syndrome
001861 (2014) Toshikazu Tanaka [Japon] ; Takuya Koie [Japon] ; Ikuya Iwabuchi [Japon] ; Masaru Ogasawara [Japon] ; Toshiaki Kawaguchi [Japon] ; Chikara Ohyama [Japon]Primary leiomyosarcoma of a horseshoe kidney in a woman with Turner syndrome: a case report
001D64 (2014) Lauren J. Massingham [États-Unis] ; Kirby L. Johnson [États-Unis] ; Thomas M. Scholl [États-Unis] ; Donna K. Slonim [États-Unis] ; Heather C. Wick ; Diana W. Bianchi [États-Unis]Amniotic fluid RNA gene expression profiling provides insights into the phenotype of Turner syndrome
002571 (2013) Hüseyin An L Korkmaz [Turquie] ; Behzat Özkan [Turquie] ; Filiz Hazan [Turquie] ; Muammer Büyükinan [Turquie] ; Tanju Çelik [Turquie]A Case of Turner Syndrome with Concomitant Transient Hypogammaglobulinaemia of Infancy and Central Diabetes Insipidus
002A78 (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
002B84 (2012) Vladimir K. Bakalov ; Liat Gutin ; Clara M. Cheng ; Jian Zhou ; Puja Sheth ; Kavita Shah ; Sruthi Arepalli ; Vien Vanderhoof ; Lawrence M. Nelson ; Carolyn A. BondyAUTOIMMUNE DISORDERS IN WOMEN WITH TURNER SYNDROME AND WOMEN WITH KARYOTYPICALLY NORMAL PRIMARY OVARIAN INSUFFICIENCY
002C57 (2011) Z. Cetin [Turquie] ; I. Mendilcioglu [Turquie] ; S. Yakut [Turquie] ; S. Berker-Karauzum [Turquie] ; B. Karaman [Turquie] ; G. Luleci [Turquie]Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)
002C58 (2011) G. Witters [Belgique, Pays-Bas] ; J. Van Robays [Belgique] ; C. Willekes [Pays-Bas] ; A. Coumans [Pays-Bas] ; H. Peeters [Belgique] ; W. Gyselaers [Belgique] ; J. P. Fryns [Belgique]Trisomy 13, 18, 21, Triploidy and Turner syndrome: the 5T’s. Look at the hands
003212 (2010) Christina Southern Reh [États-Unis] ; Mitchell E. Geffner [États-Unis]Somatotropin in the treatment of growth hormone deficiency and Turner syndrome in pediatric patients: a review
003853 (2008) Kateri Mccarthy ; Carolyn A. BondyTurner syndrome in childhood and adolescence
003854 (2008) Nighat Butt ; Robin W. PatonTurner Syndrome – An Accidental Finding?
003897 (2008) Bessie E. SpiliotisRecombinant human growth hormone in the treatment of Turner syndrome

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