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

553 related items for PubMed ID: 19953642

  • 1. 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]

  • 2. Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical management.
    Cetani F, Pardi E, Ambrogini E, Lemmi M, Borsari S, Cianferotti L, Vignali E, Viacava P, Berti P, Mariotti S, Pinchera A, Marcocci C.
    Clin Endocrinol (Oxf); 2006 Feb; 64(2):146-52. PubMed ID: 16430712
    [Abstract] [Full Text] [Related]

  • 3. Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome.
    Mizusawa N, Uchino S, Iwata T, Tsuyuguchi M, Suzuki Y, Mizukoshi T, Yamashita Y, Sakurai A, Suzuki S, Beniko M, Tahara H, Fujisawa M, Kamata N, Fujisawa K, Yashiro T, Nagao D, Golam HM, Sano T, Noguchi S, Yoshimoto K.
    Clin Endocrinol (Oxf); 2006 Jul; 65(1):9-16. PubMed ID: 16817812
    [Abstract] [Full Text] [Related]

  • 4. Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias.
    Marx SJ, Agarwal SK, Kester MB, Heppner C, Kim YS, Skarulis MC, James LA, Goldsmith PK, Saggar SK, Park SY, Spiegel AM, Burns AL, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Emmert-Buck MR, Guru SC, Manickam P, Crabtree J, Erdos MR, Collins FS, Chandrasekharappa SC.
    Recent Prog Horm Res; 1999 Jul; 54():397-438; discussion 438-9. PubMed ID: 10548885
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Molecular pathogenesis of primary hyperparathyroidism.
    Cetani F, Pardi E, Borsari S, Marcocci C.
    J Endocrinol Invest; 2011 Jul; 34(7 Suppl):35-9. PubMed ID: 21985978
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. 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; 67(5):727-34. PubMed ID: 17953629
    [Abstract] [Full Text] [Related]

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

  • 10. Multiple endocrine neoplasia type 1.
    Marini F, Falchetti A, Del Monte F, Carbonell Sala S, Gozzini A, Luzi E, Brandi ML.
    Orphanet J Rare Dis; 2006 Oct 02; 1():38. PubMed ID: 17014705
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Somatic mutation of the MEN1 gene in parathyroid tumours.
    Heppner C, Kester MB, Agarwal SK, Debelenko LV, Emmert-Buck MR, Guru SC, Manickam P, Olufemi SE, Skarulis MC, Doppman JL, Alexander RH, Kim YS, Saggar SK, Lubensky IA, Zhuang Z, Liotta LA, Chandrasekharappa SC, Collins FS, Spiegel AM, Burns AL, Marx SJ.
    Nat Genet; 1997 Aug 02; 16(4):375-8. PubMed ID: 9241276
    [Abstract] [Full Text] [Related]

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

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

  • 15. Characteristics of the Danish families with multiple endocrine neoplasia type 1.
    Jäger AC, Friis-Hansen L, Hansen TV, Eskildsen PC, Sølling K, Knigge U, Hansen CP, Andersen PH, Brixen K, Feldt-Rasmussen U, Kroustrup JP, Mollerup CL, Rehfeld JF, Blichert-Toft M, Nielsen FC.
    Mol Cell Endocrinol; 2006 Apr 25; 249(1-2):123-32. PubMed ID: 16563611
    [Abstract] [Full Text] [Related]

  • 16. Multiple endocrine neoplasia type 1 (MEN1) in Austria.
    Weinhäusel A, Kaserer K, Vierhapper H, Niederle B, Haas OA, Study Group of Multiple Endocrine Neoplasia Austria.
    Wien Klin Wochenschr; 2002 Apr 15; 114(7):252-7. PubMed ID: 12089860
    [Abstract] [Full Text] [Related]

  • 17. Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families.
    Agarwal SK, Debelenko LV, Kester MB, Guru SC, Manickam P, Olufemi SE, Skarulis MC, Heppner C, Crabtree JS, Lubensky IA, Zhuang Z, Kim YS, Chandrasekharappa SC, Collins FS, Liotta LA, Spiegel AM, Burns AL, Emmert-Buck MR, Marx SJ.
    Hum Mutat; 1998 Apr 15; 12(2):75-82. PubMed ID: 9671267
    [Abstract] [Full Text] [Related]

  • 18. Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours.
    Bergman L, Boothroyd C, Palmer J, Grimmond S, Walters M, Teh B, Shepherd J, Hartley L, Hayward N.
    Br J Cancer; 2000 Oct 15; 83(8):1003-8. PubMed ID: 10993646
    [Abstract] [Full Text] [Related]

  • 19. Somatic mutations of the multiple endocrine neoplasia type 1 (MEN1) gene in patients with sporadic, nonfamilial primary hyperparathyroidism.
    Sato K, Yamazaki K, Zhu H, Kanbe M, Iihara M, Wada Y, Tanaka R, Okamoto T, Ito Y, Obara T.
    Surgery; 2000 Mar 15; 127(3):337-41. PubMed ID: 10715991
    [Abstract] [Full Text] [Related]

  • 20. MEN1 mutation analysis in Chinese patients with multiple endocrine neoplasia type 1.
    Jiang XH, Lu JL, Cui B, Zhao YJ, Wang WQ, Liu JM, Fang WQ, Cao YN, Ge Y, Zhang CX, Casse H, Li XY, Ning G.
    Endocr Relat Cancer; 2007 Dec 15; 14(4):1073-9. PubMed ID: 18045958
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 28.