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

303 related items for PubMed ID: 16918956

  • 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. A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia.
    Hirai H, Nakajima S, Miyauchi A, Nishimura K, Shimizu N, Shima M, Michigami T, Ozono K, Okada S.
    J Hum Genet; 2001; 46(1):41-4. PubMed ID: 11289719
    [Abstract] [Full Text] [Related]

  • 5. Parathyroid hormone gene polymorphism and sporadic idiopathic hypoparathyroidism.
    Goswami R, Mohapatra T, Gupta N, Rani R, Tomar N, Dikshit A, Sharma RK.
    J Clin Endocrinol Metab; 2004 Oct; 89(10):4840-5. PubMed ID: 15472173
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Glial cells missing-2 (GCM2) transactivates the calcium-sensing receptor gene: effect of a dominant-negative GCM2 mutant associated with autosomal dominant hypoparathyroidism.
    Canaff L, Zhou X, Mosesova I, Cole DE, Hendy GN.
    Hum Mutat; 2009 Jan; 30(1):85-92. PubMed ID: 18712808
    [Abstract] [Full Text] [Related]

  • 8. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. [Familial hypoparathyroidism due to activating mutations in the calcium-sensing receptor gene].
    Watanabe T, Minagawa M.
    Nihon Rinsho; 2002 Feb; 60(2):331-7. PubMed ID: 11857922
    [Abstract] [Full Text] [Related]

  • 12. A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor.
    Pearce SH, Williamson C, Kifor O, Bai M, Coulthard MG, Davies M, Lewis-Barned N, McCredie D, Powell H, Kendall-Taylor P, Brown EM, Thakker RV.
    N Engl J Med; 1996 Oct 10; 335(15):1115-22. PubMed ID: 8813042
    [Abstract] [Full Text] [Related]

  • 13. CASRdb: calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.
    Pidasheva S, D'Souza-Li L, Canaff L, Cole DE, Hendy GN.
    Hum Mutat; 2004 Aug 10; 24(2):107-11. PubMed ID: 15241791
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 16. Pancreatitis in primary hyperparathyroidism-related hypercalcaemia is not associated with mutations in the CASR gene.
    Felderbauer P, Karakas E, Fendrich V, Bulut K, Werner I, Dekomien G, Klein W, Bartsch D, Schmidt WE.
    Exp Clin Endocrinol Diabetes; 2007 Sep 10; 115(8):527-9. PubMed ID: 17853337
    [Abstract] [Full Text] [Related]

  • 17. MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1.
    Balogh K, Hunyady L, Patocs A, Gergics P, Valkusz Z, Toth M, Racz K.
    Clin Endocrinol (Oxf); 2007 Nov 10; 67(5):727-34. PubMed ID: 17953629
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.