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Journal Abstract Search

204 related items for PubMed ID: 31448886

  • 21. Pituitary Stalk Interruption Syndrome in a 54-year Adult Male.
    Wen-Lu W, Fen-Fan X, You-Yu G, Lin-Wu G.
    J Coll Physicians Surg Pak; 2022 Mar; 32(3):389-391. PubMed ID: 35148598
    [Abstract] [Full Text] [Related]

  • 22. 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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  • 23. 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 Jul 01; 8(1):e53579. PubMed ID: 23341953
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  • 24. Partial growth hormone deficiency with pituitary stalk transection.
    Hasegawa T, Hasegawa Y, Yokoyama T, Koto S, Tsuchiya Y.
    Endocrinol Jpn; 1991 Oct 01; 38(5):573-5. PubMed ID: 1668835
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  • 25. Relationship between pituitary stalk (PS) visibility and the severity of hormone deficiencies: PS interruption syndrome revisited.
    Wang W, Wang S, Jiang Y, Yan F, Su T, Zhou W, Jiang L, Zhang Y, Ning G.
    Clin Endocrinol (Oxf); 2015 Sep 01; 83(3):369-76. PubMed ID: 25845766
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  • 30. Pituitary stalk interruption syndrome: cause, clinical manifestations, diagnosis, and management.
    Voutetakis A, Sertedaki A, Dacou-Voutetakis C.
    Curr Opin Pediatr; 2016 Aug 01; 28(4):545-50. PubMed ID: 27386973
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  • 32. 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 01; 100(1):E140-7. PubMed ID: 25322266
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  • 33. Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes.
    Osorio MG, Marui S, Jorge AA, Latronico AC, Lo LS, Leite CC, Estefan V, Mendonca BB, Arnhold IJ.
    J Clin Endocrinol Metab; 2002 Nov 01; 87(11):5076-84. PubMed ID: 12414875
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  • 34. Anterior and posterior hypopituitarism with pituitary stalk abnormalities.
    Carlier R, Monnet O, Idir AB, Halimi P, Simon P, Bouchard P, Schaison G, Doyon D.
    J Neuroradiol; 1991 Nov 01; 18(1):49-60. PubMed ID: 1880561
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  • 36. Pituitary stalk interruption syndrome in 59 children: the value of MRI in assessment of pituitary functions.
    Wang Q, Hu Y, Li G, Sun X.
    Eur J Pediatr; 2014 May 01; 173(5):589-95. PubMed ID: 24257915
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  • 37. Osteogenesis Imperfecta Due to Combined Heterozygous Mutations in Both COL1A1 and COL1A2, Coexisting With Pituitary Stalk Interruption Syndrome.
    Wang D, Zhang M, Guan H, Wang X.
    Front Endocrinol (Lausanne); 2019 May 01; 10():193. PubMed ID: 30984112
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  • 38. Transection of the pituitary stalk: development of an ectopic posterior lobe assessed with MR imaging.
    Fujisawa I, Kikuchi K, Nishimura K, Togashi K, Itoh K, Noma S, Minami S, Sagoh T, Hiraoka T, Momoi T.
    Radiology; 1987 Nov 01; 165(2):487-9. PubMed ID: 3659371
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  • 39. Clues for Polygenic Inheritance of Pituitary Stalk Interruption Syndrome From Exome Sequencing in 20 Patients.
    Zwaveling-Soonawala N, Alders M, Jongejan A, Kovacic L, Duijkers FA, Maas SM, Fliers E, van Trotsenburg ASP, Hennekam RC.
    J Clin Endocrinol Metab; 2018 Feb 01; 103(2):415-428. PubMed ID: 29165578
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