These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 19844116)

  • 1. Growth without growth hormone and similar dysmorphic features in three patients with sporadic combined pituitary hormone deficiencies.
    Gat-Yablonski G; Lazar L; Bar M; de Vries L; Weintrob N; Phillip M
    Horm Res; 2009; 72(5):302-9. PubMed ID: 19844116
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 62(2):163-8. PubMed ID: 15670191
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 88(1):45-50. PubMed ID: 12519827
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 73(5):363-71. PubMed ID: 20389107
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel HESX1 mutations associated with a life-threatening neonatal phenotype, pituitary aplasia, but normally located posterior pituitary and no optic nerve abnormalities.
    Sobrier ML; Maghnie M; Vié-Luton MP; Secco A; di Iorgi N; Lorini R; Amselem S
    J Clin Endocrinol Metab; 2006 Nov; 91(11):4528-36. PubMed ID: 16940453
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe.
    Melo ME; Marui S; Carvalho LR; Arnhold IJ; Leite CC; Mendonça BB; Knoepfelmacher M
    Clin Endocrinol (Oxf); 2007 Jan; 66(1):95-102. PubMed ID: 17201807
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular analysis of LHX3 and PROP-1 in pituitary hormone deficiency patients with posterior pituitary ectopia.
    Sloop KW; Walvoord EC; Showalter AD; Pescovitz OH; Rhodes SJ
    J Clin Endocrinol Metab; 2000 Aug; 85(8):2701-8. PubMed ID: 10946868
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?
    Dattani MT
    Clin Endocrinol (Oxf); 2005 Aug; 63(2):121-30. PubMed ID: 16060904
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genetic aspects of growth hormone deficiency].
    Reynaud R; Castinetti F; Galon-Faure N; Albarel-Loy F; Saveanu A; Quentien MH; Jullien N; Khammar A; Enjalbert A; Barlier A; Brue T
    Arch Pediatr; 2011 Jun; 18(6):696-706. PubMed ID: 21497494
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical characteristics and molecular analysis of PIT1, PROP1,LHX3, and HESX1 in combined pituitary hormone deficiency patients with abnormal pituitary MR imaging.
    Kim SS; Kim Y; Shin YL; Kim GH; Kim TU; Yoo HW
    Horm Res; 2003; 60(6):277-83. PubMed ID: 14646405
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 65(4):479-85. PubMed ID: 16984240
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 58(3):527-532. PubMed ID: 28332357
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 84(3):153-8. PubMed ID: 26111865
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 63(1):10-8. PubMed ID: 15963055
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction.
    Carvalho LR; Woods KS; Mendonca BB; Marcal N; Zamparini AL; Stifani S; Brickman JM; Arnhold IJ; Dattani MT
    J Clin Invest; 2003 Oct; 112(8):1192-201. PubMed ID: 14561704
    [TBL] [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; 18(2):147-9. PubMed ID: 9462743
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis of the PROP1 and HESX1 genes in patients with septo-optic dysplasia and/or pituitary hormone deficiency.
    Cruz JB; Nunes VS; Clara SA; Perone D; Kopp P; Nogueira CR
    Arq Bras Endocrinol Metabol; 2010; 54(5):482-7. PubMed ID: 20694410
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinical and genetic aspects of combined pituitary hormone deficiencies].
    Castinetti F; Reynaud R; Saveanu A; Quentien MH; Albarel F; Barlier A; Enjalbert A; Brue T
    Ann Endocrinol (Paris); 2008 Feb; 69(1):7-17. PubMed ID: 18291347
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.