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Journal Abstract Search

198 related items for PubMed ID: 27386973

  • 1. Pituitary stalk interruption syndrome: cause, clinical manifestations, diagnosis, and management.
    Voutetakis A, Sertedaki A, Dacou-Voutetakis C.
    Curr Opin Pediatr; 2016 Aug; 28(4):545-50. PubMed ID: 27386973
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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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  • 5. Pituitary stalk interruption syndrome and isolated pituitary hypoplasia may be caused by mutations in holoprosencephaly-related genes.
    Tatsi C, Sertedaki A, Voutetakis A, Valavani E, Magiakou MA, Kanaka-Gantenbein C, Chrousos GP, Dacou-Voutetakis C.
    J Clin Endocrinol Metab; 2013 Apr 01; 98(4):E779-84. PubMed ID: 23476075
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  • 6. 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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  • 7. Pituitary Stalk Interruption Syndrome: From Clinical Findings to Pathogenesis.
    Wang CZ, Guo LL, Han BY, Su X, Guo QH, Mu YM.
    J Neuroendocrinol; 2017 Jan 01; 29(1):. PubMed ID: 27917547
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  • 10. Digenic Inheritance of PROKR2 and WDR11 Mutations in Pituitary Stalk Interruption Syndrome.
    McCormack SE, Li D, Kim YJ, Lee JY, Kim SH, Rapaport R, Levine MA.
    J Clin Endocrinol Metab; 2017 Jul 01; 102(7):2501-2507. PubMed ID: 28453858
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  • 12. 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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  • 14. Pituitary stalk interruption syndrome and liver changes: From clinical features to mechanisms.
    Wu ZY, Li YL, Chang B.
    World J Gastroenterol; 2020 Nov 28; 26(44):6909-6922. PubMed ID: 33311939
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  • 16. Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndrome.
    Karaca E, Buyukkaya R, Pehlivan D, Charng WL, Yaykasli KO, Bayram Y, Gambin T, Withers M, Atik MM, Arslanoglu I, Bolu S, Erdin S, Buyukkaya A, Yaykasli E, Jhangiani SN, Muzny DM, Gibbs RA, Lupski JR.
    J Clin Endocrinol Metab; 2015 Jan 28; 100(1):E140-7. PubMed ID: 25322266
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  • 17. Pituitary stalk interruption syndrome in Chinese people: clinical characteristic analysis of 55 cases.
    Guo Q, Yang Y, Mu Y, Lu J, Pan C, Dou J, Lv Z, Ba J, Wang B, Zou X, Yang L, Ouyang J, Yang G, Wang X, Du J, Gu W, Jin N, Chen K, Zang L, Erickson BJ.
    PLoS One; 2013 Jan 28; 8(1):e53579. PubMed ID: 23341953
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  • 19. Re-analysis of gene mutations found in pituitary stalk interruption syndrome and a new hypothesis on the etiology.
    Wang S, Qin Q, Jiang D, Xiao Y, Ye L, Jiang X, Guo Q.
    Front Endocrinol (Lausanne); 2024 Jan 28; 15():1338781. PubMed ID: 38464967
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  • 20. Delayed Diagnosis of Congenital Combined Pituitary Hormone Deficiency including Severe Growth Hormone Deficiency in Children with Persistent Neonatal Hypoglycemia-Case Reports and Review.
    Smyczyńska J, Pawelak N, Hilczer M, Lewiński A.
    Int J Mol Sci; 2022 Sep 21; 23(19):. PubMed ID: 36232371
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