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 *

371 related articles for article (PubMed ID: 11079449)

  • 21. Autosomal recessive idiopathic hypogonadotropic hypogonadism: genetic analysis excludes mutations in the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes.
    Bo-Abbas Y; Acierno JS; Shagoury JK; Crowley WF; Seminara SB
    J Clin Endocrinol Metab; 2003 Jun; 88(6):2730-7. PubMed ID: 12788881
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Combined hypothalamic-pituitary-gonadal defect in a hypogonadic man with a novel mutation in the DAX-1 gene.
    Caron P; Imbeaud S; Bennet A; Plantavid M; Camerino G; Rochiccioli P
    J Clin Endocrinol Metab; 1999 Oct; 84(10):3563-9. PubMed ID: 10522996
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
    Pedersen-White JR; Chorich LP; Bick DP; Sherins RJ; Layman LC
    Mol Hum Reprod; 2008 Jun; 14(6):367-70. PubMed ID: 18463157
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Exaggerated free alpha-subunit levels during pulsatile gonadotropin-releasing hormone replacement in women with idiopathic hypogonadotropic hypogonadism.
    Lavoie HB; Martin KA; Taylor E; Crowley WF; Hall JE
    J Clin Endocrinol Metab; 1998 Jan; 83(1):241-7. PubMed ID: 9435449
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Physiologic and genetic insights into the pathophysiology and management of hypogonadotropic hypogonadism.
    Hall JE
    Ann Endocrinol (Paris); 1999 Jul; 60(2):93-101. PubMed ID: 10456179
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical manifestations of impaired GnRH neuron development and function.
    Kim HG; Bhagavath B; Layman LC
    Neurosignals; 2008; 16(2-3):165-82. PubMed ID: 18253056
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.
    Oliveira LM; Seminara SB; Beranova M; Hayes FJ; Valkenburgh SB; Schipani E; Costa EM; Latronico AC; Crowley WF; Vallejo M
    J Clin Endocrinol Metab; 2001 Apr; 86(4):1532-8. PubMed ID: 11297579
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel mutation in DAX1 causes delayed-onset adrenal insufficiency and incomplete hypogonadotropic hypogonadism.
    Tabarin A; Achermann JC; Recan D; Bex V; Bertagna X; Christin-Maitre S; Ito M; Jameson JL; Bouchard P
    J Clin Invest; 2000 Feb; 105(3):321-8. PubMed ID: 10675358
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genomic sequence of the DAX1 gene: an orphan nuclear receptor responsible for X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.
    Guo W; Burris TP; Zhang YH; Huang BL; Mason J; Copeland KC; Kupfer SR; Pagon RA; McCabe ER
    J Clin Endocrinol Metab; 1996 Jul; 81(7):2481-6. PubMed ID: 8675564
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations.
    Seminara SB; Hayes FJ; Crowley WF
    Endocr Rev; 1998 Oct; 19(5):521-39. PubMed ID: 9793755
    [No Abstract]   [Full Text] [Related]  

  • 31. Minipuberty of infancy and adolescent pubertal function in adrenal hypoplasia congenita.
    Kaiserman KB; Nakamoto JM; Geffner ME; McCabe ER
    J Pediatr; 1998 Aug; 133(2):300-2. PubMed ID: 9709728
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genotype and phenotype of patients with gonadotropin-releasing hormone receptor mutations.
    Kim HG; Pedersen-White J; Bhagavath B; Layman LC
    Front Horm Res; 2010; 39():94-110. PubMed ID: 20389088
    [TBL] [Abstract][Full Text] [Related]  

  • 33. New mutations of DAX-1 genes in two Japanese patients with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism.
    Yanase T; Takayanagi R; Oba K; Nishi Y; Ohe K; Nawata H
    J Clin Endocrinol Metab; 1996 Feb; 81(2):530-5. PubMed ID: 8636263
    [TBL] [Abstract][Full Text] [Related]  

  • 34. GnRH receptor mutations in isolated gonadotropic deficiency.
    Chevrier L; Guimiot F; de Roux N
    Mol Cell Endocrinol; 2011 Oct; 346(1-2):21-8. PubMed ID: 21645587
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [DAX-1 abnormality].
    Kinoshita E
    Nihon Rinsho; 2002 Feb; 60(2):391-6. PubMed ID: 11857932
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Novel mutation of the DAX1 gene in a patient with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.
    Hamaguchi K; Arikawa M; Yasunaga S; Kakuma T; Fukagawa K; Yanase T; Nawata H; Sakata T
    Am J Med Genet; 1998 Feb; 76(1):62-6. PubMed ID: 9508067
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Role of sequence variations of the GnRH receptor and G protein-coupled receptor 54 gene in male idiopathic hypogonadotropic hypogonadism.
    Lanfranco F; Gromoll J; von Eckardstein S; Herding EM; Nieschlag E; Simoni M
    Eur J Endocrinol; 2005 Dec; 153(6):845-52. PubMed ID: 16322390
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repression.
    Achermann JC; Ito M; Silverman BL; Habiby RL; Pang S; Rosler A; Jameson JL
    J Clin Endocrinol Metab; 2001 Jul; 86(7):3171-5. PubMed ID: 11443184
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita.
    Reutens AT; Achermann JC; Ito M; Ito M; Gu WX; Habiby RL; Donohoue PA; Pang S; Hindmarsh PC; Jameson JL
    J Clin Endocrinol Metab; 1999 Feb; 84(2):504-11. PubMed ID: 10022408
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Progressive onset of adrenal insufficiency and hypogonadism of pituitary origin caused by a complex genetic rearrangement within DAX-1.
    Salvi R; Gomez F; Fiaux M; Schorderet D; Jameson JL; Achermann JC; Gaillard RC; Pralong FP
    J Clin Endocrinol Metab; 2002 Sep; 87(9):4094-100. PubMed ID: 12213854
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.