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Items: 1 to 20 of 88

1.

A case of turner syndrome associated with severe coarctation of the aorta.

Luca AC, Iordache C, Braha E.

Rev Med Chir Soc Med Nat Iasi. 2013 Jul-Sep;117(3):670-3.

PMID:
24502033
3.

[Coarctation of the aorta in patients with the Shereshevskiĭ-Turner syndrome].

Pokrovskiĭ AV, Zhunkova OT, Vdovichenko AS.

Probl Endokrinol (Mosk). 1971 Sep-Oct;17(5):47-50. Russian. No abstract available.

PMID:
5148297
4.

Turner Syndrome in Girls Presenting with Coarctation of the Aorta.

Eckhauser A, South ST, Meyers L, Bleyl SB, Botto LD.

J Pediatr. 2015 Nov;167(5):1062-6. doi: 10.1016/j.jpeds.2015.08.002.

PMID:
26323199
5.

The prevalence of turner syndrome in girls presenting with coarctation of the aorta.

Wong SC, Burgess T, Cheung M, Zacharin M.

J Pediatr. 2014 Feb;164(2):259-63. doi: 10.1016/j.jpeds.2013.09.031.

PMID:
24172638
6.

Prevalence of cardiovascular malformations and association with karyotypes in Turner's syndrome.

Gøtzsche CO, Krag-Olsen B, Nielsen J, Sørensen KE, Kristensen BO.

Arch Dis Child. 1994 Nov;71(5):433-6.

7.

Pattern of Turner syndrome in Singapore (1999-2004).

Tan KB, Yeo GS.

Singapore Med J. 2009 Jun;50(6):587-90.

8.

Pseudocoarctation of the aortic arch in a patient with Turner's syndrome.

Klein LW, Levin JL, Weintraub WS, Agarwal JB, Helfant RH.

Clin Cardiol. 1984 Nov;7(11):621-3.

9.

Further delineation of aortic dilation, dissection, and rupture in patients with Turner syndrome.

Lin AE, Lippe B, Rosenfeld RG.

Pediatrics. 1998 Jul;102(1):e12.

PMID:
9651464
10.

Characteristic cardiovascular anomalies of XO Turner syndrome, XX and XY phenotype and XO-XX Turner mosaic.

Nora JJ, Torres FG, Sinha AK, McNamara DG.

Am J Cardiol. 1970 Jun;25(6):639-41. No abstract available.

PMID:
5420904
11.

Turner syndrome: diagnosis and management.

Morgan T.

Am Fam Physician. 2007 Aug 1;76(3):405-10. Review.

12.

[Rare variant of a Turner-Ullrich syndrome].

Allemann J, Müller G, Legat M.

Schweiz Med Wochenschr. 1982 Sep 4;112(36):1249-55. German.

PMID:
7134952
13.

Turner syndrome and associated problems in Turkish children: a multicenter study.

Yeşilkaya E, Bereket A, Darendeliler F, Baş F, Poyrazoğlu Ş, Küçükemre Aydın B, Darcan Ş, Dündar B, Büyükinan M, Kara C, Sarı E, Adal E, Akıncı A, Atabek ME, Demirel F, Çelik N, Özkan B, Özhan B, Orbak Z, Ersoy B, Doğan M, Ataş A, Turan S, Gökşen D, Tarım Ö, Yüksel B, Ercan O, Hatun Ş, Şimşek E, Ökten A, Abacı A, Döneray H, Özbek MN, Keskin M, Önal H, Akyürek N, Bulan K, Tepe D, Emeksiz HC, Demir K, Kızılay D, Topaloğlu AK, Eren E, Özen S, Abalı S, Akın L, Selver Eklioğlu B, Kaba S, Anık A, Baş S, Ünüvar T, Sağlam H, Bolu S, Özgen T, Doğan D, Deniz Çakır E, Şen Y, Andıran N, Çizmecioğlu F, Evliyaoğlu O, Karagüzel G, Pirgon Ö, Çatlı G, Can HD, Gürbüz F, Binay Ç, Baş VN, Fidancı K, Polat A, Gül D, Açıkel C, Demirbilek H, Cinaz P, Bondy C.

J Clin Res Pediatr Endocrinol. 2015 Mar;7(1):27-36. doi: 10.4274/jcrpe.1771.

14.

False aneurysm on distal part of coarctation of the aorta in a parous Turner syndrome patient.

Oi K, Yoshida T, Takeshita M, Tsuruta G.

Gen Thorac Cardiovasc Surg. 2013 Sep;61(9):531-3. doi: 10.1007/s11748-012-0189-x.

PMID:
23207878
15.

Cardiovascular anomalies in children and young adults with Ullrich-Turner syndrome the Erlangen experience.

Völkl TM, Degenhardt K, Koch A, Simm D, Dörr HG, Singer H.

Clin Cardiol. 2005 Feb;28(2):88-92.

16.

Cardiovascular malformations and complications in Turner syndrome.

Sybert VP.

Pediatrics. 1998 Jan;101(1):E11.

PMID:
9417175
17.

No evidence for angiotensin type 2 receptor gene polymorphism in intron 1 in patients with coarctation of the aorta and Ullrich-Turner syndrome.

Struwe E, Krammer K, Dötsch J, Metzler M, Dörr HG, Cesnjevar R, Rascher W, Koch A.

Pediatr Cardiol. 2006 Sep-Oct;27(5):636-9.

PMID:
16944335
18.

Spontaneous resolution of fetal cystic hygroma and hydrops in Turner syndrome.

Mostello DJ, Bofinger MK, Siddiqi TA.

Obstet Gynecol. 1989 May;73(5 Pt 2):862-5.

PMID:
2649827
19.

Heart disease in Turner's syndrome.

Mazzanti L, Prandstraller D, Tassinari D, Rubino I, Santucci S, Picchio FM, Forabosco A, Cacciari E.

Helv Paediatr Acta. 1988 Aug;43(1-2):25-31.

PMID:
3170246
20.

Variable X chromosomal abnormalities in patients with stigmata of Turner syndrome.

Verma RS, Khan F, Dosik H.

Int J Gynaecol Obstet. 1979 Nov-Dec;17(3):234-42.

PMID:
42576
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