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324 related items for PubMed ID: 31948187

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.
    Baş F, Uyguner ZO, Darendeliler F, Aycan Z, Çetinkaya E, Berberoğlu M, Şiklar Z, Öcal G, Darcan Ş, Gökşen D, Topaloğlu AK, Yüksel B, Özbek MN, Ercan O, Evliyaoğlu O, Çetinkaya S, Şen Y, Atabek E, Toksoy G, Aydin BK, Bundak R.
    Endocrine; 2015 Jun 02; 49(2):479-91. PubMed ID: 25500790
    [Abstract] [Full Text] [Related]

  • 3. Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
    Turton JP, Mehta A, Raza J, Woods KS, Tiulpakov A, Cassar J, Chong K, Thomas PQ, Eunice M, Ammini AC, Bouloux PM, Starzyk J, Hindmarsh PC, Dattani MT.
    Clin Endocrinol (Oxf); 2005 Jul 02; 63(1):10-8. PubMed ID: 15963055
    [Abstract] [Full Text] [Related]

  • 4. Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD).
    Kelberman D, Turton JP, Woods KS, Mehta A, Al-Khawari M, Greening J, Swift PG, Otonkoski T, Rhodes SJ, Dattani MT.
    Clin Endocrinol (Oxf); 2009 Jan 02; 70(1):96-103. PubMed ID: 19128366
    [Abstract] [Full Text] [Related]

  • 5. PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.
    Lemos MC, Gomes L, Bastos M, Leite V, Limbert E, Carvalho D, Bacelar C, Monteiro M, Fonseca F, Agapito A, Castro JJ, Regateiro FJ, Carvalheiro M.
    Clin Endocrinol (Oxf); 2006 Oct 02; 65(4):479-85. PubMed ID: 16984240
    [Abstract] [Full Text] [Related]

  • 6. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion.
    Abrão MG, Leite MV, Carvalho LR, Billerbeck AE, Nishi MY, Barbosa AS, Martin RM, Arnhold IJ, Mendonca BB.
    Clin Endocrinol (Oxf); 2006 Sep 02; 65(3):294-300. PubMed ID: 16918947
    [Abstract] [Full Text] [Related]

  • 7. Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea.
    Choi JH, Jung CW, Kang E, Kim YM, Heo SH, Lee BH, Kim GH, Yoo HW.
    Yonsei Med J; 2017 May 02; 58(3):527-532. PubMed ID: 28332357
    [Abstract] [Full Text] [Related]

  • 8. Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency.
    Avbelj Stefanija M, Kotnik P, Bratanič N, Žerjav Tanšek M, Bertok S, Bratina N, Battelino T, Trebušak Podkrajšek K.
    Horm Res Paediatr; 2015 May 02; 84(3):153-8. PubMed ID: 26111865
    [Abstract] [Full Text] [Related]

  • 9. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.
    Madeira JL, Nishi MY, Nakaguma M, Benedetti AF, Biscotto IP, Fernandes T, Pequeno T, Figueiredo T, Franca MM, Correa FA, Otto AP, Abrão M, Miras MB, Santos S, Jorge AA, Costalonga EF, Mendonca BB, Arnhold IJ, Carvalho LR.
    Clin Endocrinol (Oxf); 2017 Dec 02; 87(6):725-732. PubMed ID: 28734020
    [Abstract] [Full Text] [Related]

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  • 11. Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion.
    Agarwal G, Bhatia V, Cook S, Thomas PQ.
    J Clin Endocrinol Metab; 2000 Dec 02; 85(12):4556-61. PubMed ID: 11134108
    [Abstract] [Full Text] [Related]

  • 12. Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency.
    Kandemir N, Vurallı D, Taşkıran E, Gönç N, Özön A, Alikaşifoğlu A, Yılmaz E.
    Turk J Pediatr; 2012 Dec 02; 54(6):570-5. PubMed ID: 23692781
    [Abstract] [Full Text] [Related]

  • 13. Comparison of clinical characteristics of a pediatric cohort with combined pituitary hormone deficiency caused by mutation of the PROP1 gene or of other origins.
    Zygmunt-Górska A, Wójcik M, Gilis-Januszewska A, Starmach A, Bik-Multanowski M, Starzyk JB.
    Hormones (Athens); 2024 Mar 02; 23(1):69-79. PubMed ID: 38147295
    [Abstract] [Full Text] [Related]

  • 14. Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.
    Rainbow LA, Rees SA, Shaikh MG, Shaw NJ, Cole T, Barrett TG, Kirk JM.
    Clin Endocrinol (Oxf); 2005 Feb 02; 62(2):163-8. PubMed ID: 15670191
    [Abstract] [Full Text] [Related]

  • 15. Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency.
    Vieira TC, Boldarine VT, Abucham J.
    Arq Bras Endocrinol Metabol; 2007 Oct 02; 51(7):1097-103. PubMed ID: 18157385
    [Abstract] [Full Text] [Related]

  • 16. Congenital combined pituitary hormone deficiency attributable to a novel PROP1 mutation (467insT).
    Nose O, Tatsumi K, Nakano Y, Amino N.
    J Pediatr Endocrinol Metab; 2006 Apr 02; 19(4):491-8. PubMed ID: 16759034
    [Abstract] [Full Text] [Related]

  • 17. PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency.
    de Graaff LC, Argente J, Veenma DC, Drent ML, Uitterlinden AG, Hokken-Koelega AC.
    Horm Res Paediatr; 2010 Apr 02; 73(5):363-71. PubMed ID: 20389107
    [Abstract] [Full Text] [Related]

  • 18. Mutations in PROP1 cause familial combined pituitary hormone deficiency.
    Wu W, Cogan JD, Pfäffle RW, Dasen JS, Frisch H, O'Connell SM, Flynn SE, Brown MR, Mullis PE, Parks JS, Phillips JA, Rosenfeld MG.
    Nat Genet; 1998 Feb 02; 18(2):147-9. PubMed ID: 9462743
    [Abstract] [Full Text] [Related]

  • 19. Hypopituitarism in five PROP1 mutation siblings: long-lasting natural course and the effects of growth hormone replacement introduction in middle adulthood.
    Doknic M, Gasic V, Stojanovic M, Pavlovic S, Marinkovic S, Miljic D, Pekic S, Manojlovic-Gacic E, Damjanovic D, Soldatovic I, Petakov M.
    Pituitary; 2020 Aug 02; 23(4):400-408. PubMed ID: 32415500
    [Abstract] [Full Text] [Related]

  • 20. Identification of Novel PROP1 and POU1F1 Mutations in Patients with Combined Pituitary Hormone Deficiency.
    Birla S, Khadgawat R, Jyotsna VP, Jain V, Garg MK, Bhalla AS, Sharma A.
    Horm Metab Res; 2016 Dec 02; 48(12):822-827. PubMed ID: 27756091
    [Abstract] [Full Text] [Related]

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