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Journal Abstract Search

321 related items for PubMed ID: 18174732

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  • 22. Congenital Hypopituitarism During the Neonatal Period: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome.
    Bosch I Ara L, Katugampola H, Dattani MT.
    Front Pediatr; 2020; 8():600962. PubMed ID: 33634051
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  • 27. Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.
    Reynaud R, Gueydan M, Saveanu A, Vallette-Kasic S, Enjalbert A, Brue T, Barlier A.
    J Clin Endocrinol Metab; 2006 Sep; 91(9):3329-36. PubMed ID: 16735499
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  • 28. HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype.
    Fang Q, Benedetti AF, Ma Q, Gregory L, Li JZ, Dattani M, Sadeghi-Nejad A, Arnhold IJ, Mendonca BB, Camper SA, Carvalho LR.
    Clin Endocrinol (Oxf); 2016 Sep; 85(3):408-14. PubMed ID: 27000987
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  • 29. Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency.
    Turton JP, Reynaud R, Mehta A, Torpiano J, Saveanu A, Woods KS, Tiulpakov A, Zdravkovic V, Hamilton J, Attard-Montalto S, Parascandalo R, Vella C, Clayton PE, Shalet S, Barton J, Brue T, Dattani MT.
    J Clin Endocrinol Metab; 2005 Aug; 90(8):4762-70. PubMed ID: 15928241
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  • 30. A novel missense mutation (P366T) of the LHX4 gene causes severe combined pituitary hormone deficiency with pituitary hypoplasia, ectopic posterior lobe and a poorly developed sella turcica.
    Tajima T, Hattori T, Nakajima T, Okuhara K, Tsubaki J, Fujieda K.
    Endocr J; 2007 Aug; 54(4):637-41. PubMed ID: 17527005
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  • 32. A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism.
    Castinetti F, Saveanu A, Reynaud R, Quentien MH, Buffin A, Brauner R, Kaffel N, Albarel F, Guedj AM, El Kholy M, Amin M, Enjalbert A, Barlier A, Brue T.
    J Clin Endocrinol Metab; 2008 Jul; 93(7):2790-9. PubMed ID: 18445675
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  • 33. Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery.
    Correa FA, Nakaguma M, Madeira JLO, Nishi MY, Abrão MG, Jorge AAL, Carvalho LR, Arnhold IJP, Mendonça BB.
    Arch Endocrinol Metab; 2019 May 13; 63(2):167-174. PubMed ID: 31090814
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  • 34. Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort.
    Jullien N, Saveanu A, Vergier J, Marquant E, Quentien MH, Castinetti F, Galon-Faure N, Brauner R, Marrakchi Turki Z, Tauber M, El Kholy M, Linglart A, Rodien P, Fedala NS, Bergada I, Cortet-Rudelli C, Polak M, Nicolino M, Stuckens C, Barlier A, Brue T, Reynaud R, Genhypopit Network.
    Clin Endocrinol (Oxf); 2021 Feb 13; 94(2):277-289. PubMed ID: 33098107
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  • 35. Heritable disorders of pituitary development.
    Parks JS, Brown MR, Hurley DL, Phelps CJ, Wajnrajch MP.
    J Clin Endocrinol Metab; 1999 Dec 13; 84(12):4362-70. PubMed ID: 10599689
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  • 36. Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency.
    Bulut FD, Özdemir Dilek S, Kotan D, Mengen E, Gürbüz F, Yüksel B.
    J Clin Res Pediatr Endocrinol; 2020 Sep 02; 12(3):261-268. PubMed ID: 31948187
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  • 37. Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates.
    McLennan K, Jeske Y, Cotterill A, Cowley D, Penfold J, Jones T, Howard N, Thomsett M, Choong C.
    Clin Endocrinol (Oxf); 2003 Jun 02; 58(6):785-94. PubMed ID: 12780757
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  • 38. Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient.
    Tajima T, Hattorri T, Nakajima T, Okuhara K, Sato K, Abe S, Nakae J, Fujieda K.
    J Clin Endocrinol Metab; 2003 Jan 02; 88(1):45-50. PubMed ID: 12519827
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  • 40. Four novel mutations of the LHX3 gene cause combined pituitary hormone deficiencies with or without limited neck rotation.
    Pfaeffle RW, Savage JJ, Hunter CS, Palme C, Ahlmann M, Kumar P, Bellone J, Schoenau E, Korsch E, Brämswig JH, Stobbe HM, Blum WF, Rhodes SJ.
    J Clin Endocrinol Metab; 2007 May 02; 92(5):1909-19. PubMed ID: 17327381
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