BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 17937064)

  • 21. Molecular analysis of a mutated FSH receptor detected in a patient with spontaneous ovarian hyperstimulation syndrome.
    Uchida S; Uchida H; Maruyama T; Kajitani T; Oda H; Miyazaki K; Kagami M; Yoshimura Y
    PLoS One; 2013; 8(9):e75478. PubMed ID: 24058690
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Spontaneous ovarian hyperstimulation syndrome in a pregnancy with hypothyroidism].
    Delabaere A; Tran X; Jardon K; Pouly JL; Bourdel N
    Gynecol Obstet Fertil; 2011 Mar; 39(3):e64-7. PubMed ID: 21377389
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Does elevated human chorionic gonadotropin alone trigger spontaneous ovarian hyperstimulation syndrome?
    Michaelson-Cohen R; Altarescu G; Beller U; Reens R; Halevy-Shalem T; Eldar-Geva T
    Fertil Steril; 2008 Nov; 90(5):1869-74. PubMed ID: 18166181
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutation analysis of the follicle-stimulating hormone receptor gene in girls with gonadotropin-independent precocious puberty resulting from autonomous cystic ovaries.
    Batista MC; Kohek MB; Frazzatto ES; Fragoso MC; Mendonça BB; Latronico AC
    Fertil Steril; 2000 Feb; 73(2):280-3. PubMed ID: 10685529
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Activating mutations of the gonadotrophin receptors].
    Beck-Peccoz P; Persani L; Romoli R; Asteria C; Borgato S
    Arch Pediatr; 1998; 5 Suppl 4():380S-384S. PubMed ID: 9853088
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The molecular basis of impaired follicle-stimulating hormone action: evidence from human mutations and mouse models.
    Siegel ET; Kim HG; Nishimoto HK; Layman LC
    Reprod Sci; 2013 Mar; 20(3):211-33. PubMed ID: 23184658
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Pediatric pituitary adenoma with mixed FSH and TSH immunostaining and FSH hypersecretion in a 6 year-old girl with precocious puberty: case report and multidisciplinary management.
    Ceraudo M; Criminelli Rossi D; Di Iorgi N; Cama A; Piatelli G; Consales A
    Int J Neurosci; 2022 Apr; 132(4):362-369. PubMed ID: 32842843
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: evidence for a new inactivating mutation of the TSH receptor gene.
    Tonacchera M; Agretti P; Pinchera A; Rosellini V; Perri A; Collecchi P; Vitti P; Chiovato L
    J Clin Endocrinol Metab; 2000 Mar; 85(3):1001-8. PubMed ID: 10720030
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The immature HPO axis.
    Buttram VC
    J Reprod Med; 1975 Jan; 14(1):21-5. PubMed ID: 1089157
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A mutation in the follicle-stimulating hormone receptor as a cause of familial spontaneous ovarian hyperstimulation syndrome.
    Montanelli L; Delbaere A; Di Carlo C; Nappi C; Smits G; Vassart G; Costagliola S
    J Clin Endocrinol Metab; 2004 Apr; 89(4):1255-8. PubMed ID: 15080154
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A mutation in the follicle-stimulating hormone receptor as a cause of familial spontaneous ovarian hyperstimulation syndrome.
    Montanelli L; Delbaere A; Di Carlo C; Nappi C; Smits G; Vassart G; Costagliola S
    J Clin Endocrinol Metab; 2004 Mar; 89(3):1255-8. PubMed ID: 15001619
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Elevated plasma TSH and hypothyroidism in children with hypothalamic hypopituitarism.
    Illig R; Krawczyńska H; Torresani T; Prader A
    J Clin Endocrinol Metab; 1975 Oct; 41(4):722-8. PubMed ID: 809459
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Ovarian hyperstimulation syndrome (OHSS) due to mutations in the follicle-stimulating hormone receptor.
    Rodien P; Beau I; Vasseur C
    Ann Endocrinol (Paris); 2010 May; 71(3):206-9. PubMed ID: 20362966
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Primary hypothyroidism of childhood: evaluation of the hypothalamic-pituitary gonadal axis before and during L-thyroxine replacement.
    Kugler JA; Huseman CA
    Clin Endocrinol (Oxf); 1983 Aug; 19(2):213-22. PubMed ID: 6411394
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Delayed puberty and primary amenorrhea associated with a novel mutation of the human follicle-stimulating hormone receptor: clinical, histological, and molecular studies.
    Meduri G; Touraine P; Beau I; Lahuna O; Desroches A; Vacher-Lavenu MC; Kuttenn F; Misrahi M
    J Clin Endocrinol Metab; 2003 Aug; 88(8):3491-8. PubMed ID: 12915623
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Pathologic manifestations of hormonal receptor mutations].
    Milgrom E
    Bull Acad Natl Med; 2000; 184(3):605-16; discussion 617-9. PubMed ID: 10989556
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Functional characterization of two naturally occurring mutations V
    Banerjee AA; Achrekar SK; Joseph S; Pathak BR; Mahale SD
    Mol Cell Endocrinol; 2017 Jan; 440():69-79. PubMed ID: 27889471
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Association of primary hypothyroidism with preconcious puberty. Presentation of clinical case and the effect of acute inhibition of thyrotropin on the gonadal activity].
    Cos Welsh J
    Bol Med Hosp Infant Mex; 1976; 33(5):1007-20. PubMed ID: 973854
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A case of ovarian torsion in a patient carrier of a FSH receptor gene mutation previously affected by spontaneous ovarian hyperstimulation syndrome.
    Di Carlo C; Savoia F; Fabozzi A; Gargano V; Nappi C
    Gynecol Endocrinol; 2015 Feb; 31(2):105-8. PubMed ID: 25495063
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility.
    Tapanainen JS; Aittomäki K; Min J; Vaskivuo T; Huhtaniemi IT
    Nat Genet; 1997 Feb; 15(2):205-6. PubMed ID: 9020851
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.