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Journal Abstract Search

204 related items for PubMed ID: 31448886

  • 1. A Novel Missense Mutation in Human Receptor Roundabout-1 (ROBO1) Gene Associated with Pituitary Stalk Interruption Syndrome.
    Liu Z, Chen X.
    J Clin Res Pediatr Endocrinol; 2020 Jun 03; 12(2):212-217. PubMed ID: 31448886
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  • 2. Familial ROBO1 deletion associated with ectopic posterior pituitary, duplication of the pituitary stalk and anterior pituitary hypoplasia.
    Scala M, Accogli A, Allegri AME, Tassano E, Severino M, Morana G, Maghnie M, Capra V.
    J Pediatr Endocrinol Metab; 2019 Jan 28; 32(1):95-99. PubMed ID: 30530901
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  • 3. Mutations in the Human ROBO1 Gene in Pituitary Stalk Interruption Syndrome.
    Bashamboo A, Bignon-Topalovic J, Moussi N, McElreavey K, Brauner R.
    J Clin Endocrinol Metab; 2017 Jul 01; 102(7):2401-2406. PubMed ID: 28402530
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  • 13. Dynamic MRI in the congenital agenesis of the neural pituitary stalk syndrome: the role of the vascular pituitary stalk in predicting residual anterior pituitary function.
    Maghnie M, Genovese E, Villa A, Spagnolo L, Campan R, Severi F.
    Clin Endocrinol (Oxf); 1996 Sep 01; 45(3):281-90. PubMed ID: 8949565
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  • 15. Pituitary stalk interruption syndrome in 58 Chinese patients: clinical features and genetic analysis.
    Yang Y, Guo QH, Wang BA, Dou JT, Lv ZH, Ba JM, Lu JM, Pan CY, Mu YM.
    Clin Endocrinol (Oxf); 2013 Jul 01; 79(1):86-92. PubMed ID: 23199197
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  • 18. Exome sequencing in 16 patients with pituitary stalk interruption syndrome: A monocentric study.
    Brauner R, Bignon-Topalovic J, Bashamboo A, McElreavey K.
    PLoS One; 2023 Jul 01; 18(12):e0292664. PubMed ID: 38096238
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  • 19. CDON gene contributes to pituitary stalk interruption syndrome associated with unilateral facial and abducens nerve palsy.
    Obara-Moszyńska M, Budny B, Kałużna M, Zawadzka K, Jamsheer A, Rohde A, Ruchała M, Ziemnicka K, Niedziela M.
    J Appl Genet; 2021 Dec 01; 62(4):621-629. PubMed ID: 34235642
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  • 20. Magnetic resonance imaging in the diagnosis of growth hormone deficiency.
    Argyropoulou M, Perignon F, Brauner R, Brunelle F.
    J Pediatr; 1992 Jun 01; 120(6):886-91. PubMed ID: 1593348
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