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 *

123 related articles for article (PubMed ID: 21765099)

  • 21. [Molecular aspects of the etiopathogenesis of the parathyroid gland diseases].
    Lacka K
    Endokrynol Pol; 2005; 56(3):327-33. PubMed ID: 16350727
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Molecular heterogeneity of congenital forms of insulin resistance].
    van der Vorm ER; Lindhout D; Wit JM; Odink RJ; Krans HM; Maassen JA
    Ned Tijdschr Geneeskd; 1991 Jun; 135(26):1165-70. PubMed ID: 1650430
    [No Abstract]   [Full Text] [Related]  

  • 23. Multiple endocrine neoplasia (MEN)--an overview and case report--patient with sporadic bilateral pheochromocytoma, hyperparathyroidism and marfanoid habitus.
    Fassbender WJ; Krohn-Grimberghe B; Görtz B; Litzlbauer D; Stracke H; Raue F; Kaiser HE
    Anticancer Res; 2000; 20(6C):4877-87. PubMed ID: 11205236
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic testing in multiple endocrine neoplasia and related syndromes.
    Calender A
    Forum (Genova); 1998; 8(2):146-59. PubMed ID: 9666051
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Diagnostic challenges due to phenocopies: lessons from Multiple Endocrine Neoplasia type1 (MEN1).
    Turner JJ; Christie PT; Pearce SH; Turnpenny PD; Thakker RV
    Hum Mutat; 2010 Jan; 31(1):E1089-101. PubMed ID: 19953642
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Inherited endocrine diseases involving G proteins and G protein-coupled receptors.
    Spiegel AM
    Endocr Dev; 2007; 11():133-144. PubMed ID: 17986833
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Heritable forms of primary hyperparathyroidism: a current perspective.
    DeLellis RA; Mangray S
    Histopathology; 2018 Jan; 72(1):117-132. PubMed ID: 29239035
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic testing in presymptomatic diagnosis of multiple endocrine neoplasia.
    Calender A; Giraud S; Schuffenecker I; Lenoir GM; Gaudray P; Courseaux A; Porchet N; Aubert JP; Zhang CX
    Horm Res; 1997; 47(4-6):199-210. PubMed ID: 9167953
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Primary hyperparathyroidism with multiple parathyroid gland enlargement: review of 53 cases.
    Scholz DA; Purnell DC; Edis AJ; van Heerden JA; Woolner LB
    Mayo Clin Proc; 1978 Dec; 53(12):792-7. PubMed ID: 32439
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Multiple endocrine neoplasia: genetic aspects].
    Calender A;
    Bull Acad Natl Med; 2010 Jan; 194(1):81-95; discussion 95-6. PubMed ID: 20669561
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Management of familial hyperparathyroidism syndromes: MEN1, MEN2, MEN4, HPT-Jaw tumour, Familial isolated hyperparathyroidism, FHH, and neonatal severe hyperparathyroidism.
    Cristina EV; Alberto F
    Best Pract Res Clin Endocrinol Metab; 2018 Dec; 32(6):861-875. PubMed ID: 30665551
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Multiple endocrine neoplasia type 1 (MEN-1). Clinical, biochemical and genetical investigations.
    Oberg K; Skogseid B; Eriksson B
    Acta Oncol; 1989; 28(3):383-7. PubMed ID: 2568120
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications.
    Warner J; Epstein M; Sweet A; Singh D; Burgess J; Stranks S; Hill P; Perry-Keene D; Learoyd D; Robinson B; Birdsey P; Mackenzie E; Teh BT; Prins JB; Cardinal J
    J Med Genet; 2004 Mar; 41(3):155-60. PubMed ID: 14985373
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31.
    Szabó J; Heath B; Hill VM; Jackson CE; Zarbo RJ; Mallette LE; Chew SL; Besser GM; Thakker RV; Huff V
    Am J Hum Genet; 1995 Apr; 56(4):944-50. PubMed ID: 7717405
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome.
    Haven CJ; Wong FK; van Dam EW; van der Juijt R; van Asperen C; Jansen J; Rosenberg C; de Wit M; Roijers J; Hoppener J; Lips CJ; Larsson C; Teh BT; Morreau H
    J Clin Endocrinol Metab; 2000 Apr; 85(4):1449-54. PubMed ID: 10770180
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Parathyroid surgery in familial hyperparathyroid disorders.
    Carling T; Udelsman R
    J Intern Med; 2005 Jan; 257(1):27-37. PubMed ID: 15606374
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular pathogenesis of primary hyperparathyroidism.
    Arnold A; Shattuck TM; Mallya SM; Krebs LJ; Costa J; Gallagher J; Wild Y; Saucier K
    J Bone Miner Res; 2002 Nov; 17 Suppl 2():N30-6. PubMed ID: 12412775
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Parathyroid-Targeted Overexpression of Regulator of G-Protein Signaling 5 (RGS5) Causes Hyperparathyroidism in Transgenic Mice.
    Balenga N; Koh J; Azimzadeh P; Hogue J; Gabr M; Stains JP; Olson JA
    J Bone Miner Res; 2019 May; 34(5):955-963. PubMed ID: 30690792
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Calcium-sensing receptor (CaSR) mutations and disorders of calcium, electrolyte and water metabolism.
    Hannan FM; Thakker RV
    Best Pract Res Clin Endocrinol Metab; 2013 Jun; 27(3):359-71. PubMed ID: 23856265
    [TBL] [Abstract][Full Text] [Related]  

  • 40. GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism.
    Guan B; Welch JM; Sapp JC; Ling H; Li Y; Johnston JJ; Kebebew E; Biesecker LG; Simonds WF; Marx SJ; Agarwal SK
    Am J Hum Genet; 2016 Nov; 99(5):1034-1044. PubMed ID: 27745835
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.