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 *

287 related articles for article (PubMed ID: 14646405)

  • 21. "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]  

  • 22. A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomalies.
    Durmaz B; Cogulu O; Dizdarer C; Stobbe H; Pfaeffle R; Ozkinay F
    J Pediatr Endocrinol Metab; 2011; 24(9-10):779-82. PubMed ID: 22145475
    [TBL] [Abstract][Full Text] [Related]  

  • 23. LHX3 and LHX4 transcription factors in pituitary development and disease.
    Colvin SC; Mullen RD; Pfaeffle RW; Rhodes SJ
    Pediatr Endocrinol Rev; 2009 Jan; 6 Suppl 2():283-90. PubMed ID: 19337183
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary].
    Halász Z
    Orv Hetil; 2011 Feb; 152(6):221-32. PubMed ID: 21278027
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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; 92(5):1909-19. PubMed ID: 17327381
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Adrenocorticotrope deficiency with clinical evidence for late onset in combined pituitary hormone deficiency caused by a homozygous 301-302delAG mutation of the PROP1 gene.
    Lamesch C; Neumann S; Pfäffle R; Kiess W; Paschke R
    Pituitary; 2002; 5(3):163-8. PubMed ID: 12812307
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Functional SNPs within the intron 1 of the PROP1 gene contribute to combined growth hormone deficiency (CPHD).
    Godi M; Mellone S; Tiradani L; Marabese R; Bardelli C; Salerno M; Prodam F; Bellone S; Petri A; Momigliano-Richiardi P; Bona G; Giordano M
    J Clin Endocrinol Metab; 2012 Sep; 97(9):E1791-7. PubMed ID: 22745233
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A critical functional missense mutation (H173R) in the bovine PROP1 gene significantly affects growth traits in cattle.
    Pan C; Wu C; Jia W; Xu Y; Lei C; Hu S; Lan X; Chen H
    Gene; 2013 Dec; 531(2):398-402. PubMed ID: 24029076
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Pituitary transcription factors in the aetiology of combined pituitary hormone deficiency.
    Pfäffle R; Klammt J
    Best Pract Res Clin Endocrinol Metab; 2011 Feb; 25(1):43-60. PubMed ID: 21396574
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency.
    Cogan JD; Wu W; Phillips JA; Arnhold IJ; Agapito A; Fofanova OV; Osorio MG; Bircan I; Moreno A; Mendonca BB
    J Clin Endocrinol Metab; 1998 Sep; 83(9):3346-9. PubMed ID: 9745452
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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; 65(3):294-300. PubMed ID: 16918947
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene.
    Pernasetti F; Toledo SP; Vasilyev VV; Hayashida CY; Cogan JD; Ferrari C; Lourenço DM; Mellon PL
    J Clin Endocrinol Metab; 2000 Jan; 85(1):390-7. PubMed ID: 10634415
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel OTX2 mutation in a patient with combined pituitary hormone deficiency, pituitary malformation, and an underdeveloped left optic nerve.
    Gorbenko Del Blanco D; Romero CJ; Diaczok D; de Graaff LC; Radovick S; Hokken-Koelega AC
    Eur J Endocrinol; 2012 Sep; 167(3):441-52. PubMed ID: 22715480
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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]  

  • 37. OTX2 loss of function mutation causes anophthalmia and combined pituitary hormone deficiency with a small anterior and ectopic posterior pituitary.
    Tajima T; Ohtake A; Hoshino M; Amemiya S; Sasaki N; Ishizu K; Fujieda K
    J Clin Endocrinol Metab; 2009 Jan; 94(1):314-9. PubMed ID: 18854396
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 58(6):785-94. PubMed ID: 12780757
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene.
    Mendonca BB; Osorio MG; Latronico AC; Estefan V; Lo LS; Arnhold IJ
    J Clin Endocrinol Metab; 1999 Mar; 84(3):942-5. PubMed ID: 10084575
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Long-Term Outcomes, Genetics, and Pituitary Morphology in Patients with Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiencies: A Single-Centre Experience of Four Decades of Growth Hormone Replacement.
    Rohayem J; Drechsel H; Tittel B; Hahn G; Pfaeffle R; Huebner A
    Horm Res Paediatr; 2016; 86(2):106-116. PubMed ID: 27487097
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.