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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

212 related items for PubMed ID: 36780067

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Genetics of parathyroid tumours.
    Thakker RV.
    J Intern Med; 2016 Dec; 280(6):574-583. PubMed ID: 27306766
    [Abstract] [Full Text] [Related]

  • 6. Hyperparathyroidism in hereditary syndromes: special expressions and special managements.
    Marx SJ, Simonds WF, Agarwal SK, Burns AL, Weinstein LS, Cochran C, Skarulis MC, Spiegel AM, Libutti SK, Alexander HR, Chen CC, Chang R, Chandrasekharappa SC, Collins FS.
    J Bone Miner Res; 2002 Nov; 17 Suppl 2():N37-43. PubMed ID: 12412776
    [Abstract] [Full Text] [Related]

  • 7. Clinical and molecular genetics of parathyroid neoplasms.
    Sharretts JM, Simonds WF.
    Best Pract Res Clin Endocrinol Metab; 2010 Jun; 24(3):491-502. PubMed ID: 20833339
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Evolution of Our Understanding of the Hyperparathyroid Syndromes: A Historical Perspective.
    Marx SJ, Goltzman D.
    J Bone Miner Res; 2019 Jan; 34(1):22-37. PubMed ID: 30536424
    [Abstract] [Full Text] [Related]

  • 10. Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.
    Dwight T, Twigg S, Delbridge L, Wong FK, Farnebo F, Richardson AL, Nelson A, Zedenius J, Philips J, Larsson C, Teh BT, Robinson B.
    Clin Endocrinol (Oxf); 2000 Jul; 53(1):85-92. PubMed ID: 10931084
    [Abstract] [Full Text] [Related]

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

  • 12. Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome.
    Wassif WS, Farnebo F, Teh BT, Moniz CF, Li FY, Harrison JD, Peters TJ, Larsson C, Harris P.
    Clin Endocrinol (Oxf); 1999 Feb; 50(2):191-6. PubMed ID: 10396361
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue.
    Marx SJ, Lourenço DM.
    Horm Metab Res; 2017 Nov; 49(11):805-815. PubMed ID: 29136674
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Absence of somatic RET gene mutation in sporadic parathyroid tumors and hyperplasia secondary to uremia, and absence of somatic Men1 gene mutation in MEN2A-associated hyperplasia.
    Uchino S, Noguchi S, Nagatomo M, Sato M, Yamashita H, Yamashita H, Watanabe S, Murakami T, Toda M, Wakiya S, Adachi M.
    Biomed Pharmacother; 2000 Jun; 54 Suppl 1():100s-103s. PubMed ID: 10915003
    [Abstract] [Full Text] [Related]

  • 18. MEN1 intragenic deletions may represent the most prevalent somatic event in sporadic primary hyperparathyroidism.
    Alvelos MI, Vinagre J, Fonseca E, Barbosa E, Teixeira-Gomes J, Sobrinho-Simões M, Soares P.
    Eur J Endocrinol; 2013 Feb; 168(2):119-28. PubMed ID: 23093699
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma.
    Cardoso L, Stevenson M, Thakker RV.
    Hum Mutat; 2017 Dec; 38(12):1621-1648. PubMed ID: 28881068
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.