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 *

162 related articles for article (PubMed ID: 20694410)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. Panhypopituitarism: genetic versus acquired etiological factors.
    Coya R; Vela A; Pérez de Nanclares G; Rica I; Castaño L; Busturia MA; Martul P;
    J Pediatr Endocrinol Metab; 2007 Jan; 20(1):27-36. PubMed ID: 17315526
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation in HESX1 causes combined pituitary hormone deficiency without septo optic dysplasia phenotypes.
    Takagi M; Takahashi M; Ohtsu Y; Sato T; Narumi S; Arakawa H; Hasegawa T
    Endocr J; 2016 Apr; 63(4):405-10. PubMed ID: 26781211
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 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. 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; 87(6):725-732. PubMed ID: 28734020
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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; 49(2):479-91. PubMed ID: 25500790
    [TBL] [Abstract][Full Text] [Related]  

  • 13. "Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency.
    Deladoëy J; Flück C; Büyükgebiz A; Kuhlmann BV; Eblé A; Hindmarsh PC; Wu W; Mullis PE
    J Clin Endocrinol Metab; 1999 May; 84(5):1645-50. PubMed ID: 10323394
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 85(12):4556-61. PubMed ID: 11134108
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 63(2):167-174. PubMed ID: 31090814
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heterozygous mutation of HESX1 causing hypopituitarism and multiple anatomical malformations without features of septo-optic dysplasia.
    Corneli G; Vivenza D; Prodam F; Di Dio G; Vottero A; Rapa A; Bellone S; Bernasconi S; Bona G
    J Endocrinol Invest; 2008 Aug; 31(8):689-93. PubMed ID: 18852528
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 51(7):1097-103. PubMed ID: 18157385
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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; 70(1):96-103. PubMed ID: 19128366
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.