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PUBMED FOR HANDHELDS

Journal Abstract Search


280 related items for PubMed ID: 9821430

  • 1. Congenital heart disease in patients with Turner's syndrome. Italian Study Group for Turner Syndrome (ISGTS).
    Mazzanti L, Cacciari E.
    J Pediatr; 1998 Nov; 133(5):688-92. PubMed ID: 9821430
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  • 2. Turner's syndrome: cardiologic profile according to the different chromosomal patterns and long-term clinical follow-Up of 136 nonpreselected patients.
    Prandstraller D, Mazzanti L, Picchio FM, Magnani C, Bergamaschi R, Perri A, Tsingos E, Cacciari E.
    Pediatr Cardiol; 1999 Nov; 20(2):108-12. PubMed ID: 9986886
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  • 4. 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. PubMed ID: 3170246
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  • 8. [Heart malformations and vascular complications associated with Turner's syndrome. Prospective study of 26 patients].
    Douchin S, Rossignol AM, Klein SK, Siché JP, Baguet JP, Bost M.
    Arch Mal Coeur Vaiss; 2000 May; 93(5):565-70. PubMed ID: 10858854
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  • 10. [Rare association of a bicuspid aortic valve and accessory azygous lobe in Turner syndrome. Echocardiographic and clinical findings].
    Biferali F, Paventi S, Taglieri C.
    Minerva Cardioangiol; 1996 May; 44(7-8):361-4. PubMed ID: 8965992
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  • 12. Aortic distensibility and dilation in Turner's syndrome.
    Sharma J, Friedman D, Dave-Sharma S, Harbison M.
    Cardiol Young; 2009 Dec; 19(6):568-72. PubMed ID: 19857368
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  • 13. Spontaneous pubertal development in Turner's syndrome. Italian Study Group for Turner's Syndrome.
    Pasquino AM, Passeri F, Pucarelli I, Segni M, Municchi G.
    J Clin Endocrinol Metab; 1997 Jun; 82(6):1810-3. PubMed ID: 9177387
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  • 14. Turner's syndrome in fetal life.
    Surerus E, Huggon IC, Allan LD.
    Ultrasound Obstet Gynecol; 2003 Sep; 22(3):264-7. PubMed ID: 12942498
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  • 16. Phenotype in girls and women with Turner syndrome: Association between dysmorphic features, karyotype and cardio-aortic malformations.
    Noordman I, Duijnhouwer A, Kapusta L, Kempers M, Roeleveld N, Schokking M, Smeets D, Freriks K, Timmers H, van Alfen-van der Velden J.
    Eur J Med Genet; 2018 Jun; 61(6):301-306. PubMed ID: 29339108
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  • 18. Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families.
    Larizza D, Cuccia M, Martinetti M, Maghnie M, Dondi E, Salvaneschi L, Severi F.
    Clin Endocrinol (Oxf); 1994 Jan; 40(1):39-45. PubMed ID: 8306479
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  • 19. 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. PubMed ID: 15757080
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  • 20. Aortic dissection and Turner's syndrome: case report and review of the literature.
    Bordeleau L, Cwinn A, Turek M, Barron-Klauninger K, Victor G.
    J Emerg Med; 1998 Feb; 16(4):593-6. PubMed ID: 9696176
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