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Journal Abstract Search

184 related items for PubMed ID: 26529631

  • 41. Pituitary stalk interruption syndrome due to novel ROBO1 mutation presenting as combined pituitary hormone deficiency and central diabetes insipidus.
    Misgar RA, Chhabra A, Qadir A, Arora S, Wani AI, Bashir MI, Masoodi SR.
    J Pediatr Endocrinol Metab; 2024 May 27; 37(5):477-481. PubMed ID: 38444307
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  • 43. A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency.
    Lonero A, Delvecchio M, Primignani P, Caputo R, Bargiacchi S, Penco S, Mauri L, Andreucci E, Faienza MF, Cavallo L.
    J Pediatr Endocrinol Metab; 2016 May 01; 29(5):603-5. PubMed ID: 26974134
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  • 46. 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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  • 48. Regulation by miR181 family of the dependence receptor CDON tumor suppressive activity in neuroblastoma.
    Gibert B, Delloye-Bourgeois C, Gattolliat CH, Meurette O, Le Guernevel S, Fombonne J, Ducarouge B, Lavial F, Bouhallier F, Creveaux M, Negulescu AM, Bénard J, Janoueix-Lerosey I, Harel-Bellan A, Delattre O, Mehlen P.
    J Natl Cancer Inst; 2014 Nov 01; 106(11):. PubMed ID: 25313246
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  • 49. Holoprosencephaly: ZIC2 mutation in a case with panhypopituitarism.
    Tasdemir S, Sahin I, Cayır A, Doneray H, Solomon BD, Muenke M, Yuce I, Tatar A.
    J Pediatr Endocrinol Metab; 2014 Jul 01; 27(7-8):777-81. PubMed ID: 24706429
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  • 52. Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog.
    Solomon BD, Bear KA, Wyllie A, Keaton AA, Dubourg C, David V, Mercier S, Odent S, Hehr U, Paulussen A, Clegg NJ, Delgado MR, Bale SJ, Lacbawan F, Ardinger HH, Aylsworth AS, Bhengu NL, Braddock S, Brookhyser K, Burton B, Gaspar H, Grix A, Horovitz D, Kanetzke E, Kayserili H, Lev D, Nikkel SM, Norton M, Roberts R, Saal H, Schaefer GB, Schneider A, Smith EK, Sowry E, Spence MA, Shalev SA, Steiner CE, Thompson EM, Winder TL, Balog JZ, Hadley DW, Zhou N, Pineda-Alvarez DE, Roessler E, Muenke M.
    J Med Genet; 2012 Jul 01; 49(7):473-9. PubMed ID: 22791840
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  • 53. Gonadotrophic status in adolescents with pituitary stalk interruption syndrome.
    Rottembourg D, Linglart A, Adamsbaum C, Lahlou N, Teinturier C, Bougnères P, Carel JC.
    Clin Endocrinol (Oxf); 2008 Jul 01; 69(1):105-11. PubMed ID: 18088398
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  • 58. Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations.
    Aguilella C, Dubourg C, Attia-Sobol J, Vigneron J, Blayau M, Pasquier L, Lazaro L, Odent S, David V.
    Hum Genet; 2003 Feb 01; 112(2):131-4. PubMed ID: 12522553
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  • 59. 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 01; 32(3):389-391. PubMed ID: 35148598
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