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Journal Abstract Search

212 related items for PubMed ID: 36780067

  • 21. 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
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  • 23. Familial isolated hyperparathyroidism caused by single adenoma: a distinct entity different from multiple endocrine neoplasia.
    Watanabe T, Tsukamoto F, Shimizu T, Sugimoto T, Taguchi T, Nishisho I, Nakazawa H, Shiba E, Shishiba Y, Takai S.
    Endocr J; 1998 Oct; 45(5):637-46. PubMed ID: 10395244
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  • 24. Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasias.
    Gill AJ, Clarkson A, Gimm O, Keil J, Dralle H, Howell VM, Marsh DJ.
    Am J Surg Pathol; 2006 Sep; 30(9):1140-9. PubMed ID: 16931959
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  • 28. Genetic testing in multiple endocrine neoplasia and related syndromes.
    Calender A.
    Forum (Genova); 1998 Sep; 8(2):146-59. PubMed ID: 9666051
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  • 32. Familial and Hereditary Forms of Primary Hyperparathyroidism.
    Cetani F, Saponaro F, Borsari S, Marcocci C.
    Front Horm Res; 2019 Sep; 51():40-51. PubMed ID: 30641519
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  • 35. Primary Hyperparathyroidism Focused on Molecular Pathogenesis.
    Gómez Sáez JM.
    Eur Endocrinol; 2014 Aug; 10(2):153-156. PubMed ID: 29872481
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  • 36. Tumor suppressor gene mutation in a patient with a history of hyperparathyroidism-jaw tumor syndrome and healed generalized osteitis fibrosa cystica: a case report and genetic pathophysiology review.
    Parfitt J, Harris M, Wright JM, Kalamchi S.
    J Oral Maxillofac Surg; 2015 Jan; 73(1):194.e1-9. PubMed ID: 25511968
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  • 37. Genetics of Hyperparathyroidism, Including Parathyroid Cancer.
    Simonds WF.
    Endocrinol Metab Clin North Am; 2017 Jun; 46(2):405-418. PubMed ID: 28476229
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  • 38. Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism.
    Villablanca A, Wassif WS, Smith T, Höög A, Vierimaa O, Kassem M, Dwight T, Forsberg L, Du Q, Learoyd D, Jones K, Stranks S, Juhlin C, Teh BT, Carling T, Robinson B, Larsson C.
    Eur J Endocrinol; 2002 Sep; 147(3):313-22. PubMed ID: 12213668
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  • 39. 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; 16(4):375-8. PubMed ID: 9241276
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  • 40. A MEN1 Patient Presenting With Multiple Parathyroid Adenomas and Transient Hypercortisolism: A Case Report and Literature Review.
    Chen F, Xu Q, Yue W, Yu X, Shao S.
    Front Endocrinol (Lausanne); 2022 Aug; 13():802453. PubMed ID: 35370956
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