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Journal Abstract Search

408 related items for PubMed ID: 32112212

  • 21. [Familial pheochromocytoma].
    Tamura N, Nakao K.
    Nihon Rinsho; 2006 May 28; Suppl 1():730-4. PubMed ID: 16776261
    [No Abstract] [Full Text] [Related]

  • 22. PHEOCHROMOCYTOMA: A GENETIC AND DIAGNOSTIC UPDATE.
    Mercado-Asis LB, Wolf KI, Jochmanova I, Taïeb D.
    Endocr Pract; 2018 Jan 28; 24(1):78-90. PubMed ID: 29144820
    [Abstract] [Full Text] [Related]

  • 23. [Pheochromocytoma - chromaffin cell tumor].
    Szosland K, Kopff B, Lewiński A.
    Endokrynol Pol; 2006 Jan 28; 57(1):54-62. PubMed ID: 16575763
    [Abstract] [Full Text] [Related]

  • 24. Perioperative outcomes of syndromic paraganglioma and pheochromocytoma resection in patients with von Hippel-Lindau disease, multiple endocrine neoplasia type 2, or neurofibromatosis type 1.
    Butz JJ, Yan Q, McKenzie TJ, Weingarten TN, Cavalcante AN, Bancos I, Young WF, Schroeder DR, Martin DP, Sprung J.
    Surgery; 2017 Dec 28; 162(6):1259-1269. PubMed ID: 28919049
    [Abstract] [Full Text] [Related]

  • 25. Phaeochromocytoma: a catecholamine and oxidative stress disorder.
    Pacak K.
    Endocr Regul; 2011 Apr 28; 45(2):65-90. PubMed ID: 21615192
    [Abstract] [Full Text] [Related]

  • 26. Pheochromocytomas and secreting paragangliomas.
    Plouin PF, Gimenez-Roqueplo AP.
    Orphanet J Rare Dis; 2006 Dec 08; 1():49. PubMed ID: 17156452
    [Abstract] [Full Text] [Related]

  • 27. [Genetic diagnosis of phaeochromocytomas and paragangliomas].
    Cardot-Bauters C, Ainaouï M, Coppin L, Pigny P.
    Presse Med; 2014 Apr 08; 43(4 Pt 1):460-7. PubMed ID: 24612707
    [Abstract] [Full Text] [Related]

  • 28. Pheochromocytoma: an update on genetics and management.
    Karagiannis A, Mikhailidis DP, Athyros VG, Harsoulis F.
    Endocr Relat Cancer; 2007 Dec 08; 14(4):935-56. PubMed ID: 18045948
    [Abstract] [Full Text] [Related]

  • 29. Hereditary pheochromocytoma and paraganglioma.
    Mazzaglia PJ.
    J Surg Oncol; 2012 Oct 01; 106(5):580-5. PubMed ID: 22648936
    [Abstract] [Full Text] [Related]

  • 30. The clinical presentation (symptoms and signs) of sporadic and familial chromaffin cell tumours (phaeochromocytomas and paragangliomas).
    Kaltsas GA, Papadogias D, Grossman AB.
    Front Horm Res; 2004 Oct 01; 31():61-75. PubMed ID: 14674305
    [No Abstract] [Full Text] [Related]

  • 31. Pheochromocytoma: a review.
    Tsirlin A, Oo Y, Sharma R, Kansara A, Gliwa A, Banerji MA.
    Maturitas; 2014 Mar 01; 77(3):229-38. PubMed ID: 24472290
    [Abstract] [Full Text] [Related]

  • 32. Pediatric Metastatic Pheochromocytoma and Paraganglioma: Clinical Presentation and Diagnosis, Genetics, and Therapeutic Approaches.
    Kuo MJM, Nazari MA, Jha A, Pacak K.
    Front Endocrinol (Lausanne); 2022 Mar 01; 13():936178. PubMed ID: 35903274
    [Abstract] [Full Text] [Related]

  • 33. Diagnosis and Management of Hereditary Phaeochromocytoma and Paraganglioma.
    Lalloo F.
    Recent Results Cancer Res; 2016 Mar 01; 205():105-24. PubMed ID: 27075351
    [Abstract] [Full Text] [Related]

  • 34. Genetics of pheochromocytoma and paraganglioma in Spanish patients.
    Cascón A, Pita G, Burnichon N, Landa I, López-Jiménez E, Montero-Conde C, Leskelä S, Leandro-García LJ, Letón R, Rodríguez-Antona C, Díaz JA, López-Vidriero E, González-Neira A, Velasco A, Matias-Guiu X, Gimenez-Roqueplo AP, Robledo M.
    J Clin Endocrinol Metab; 2009 May 01; 94(5):1701-5. PubMed ID: 19258401
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. [Diagnostic and therapeutic procedures in pheochromocytoma: current trends].
    Widimský J, Zelinka T, Petrák O, Strauch B, Safarík L, Kasalický M, Vranková A, Holaj R.
    Vnitr Lek; 2007 Apr 01; 53(4):428-33. PubMed ID: 17578179
    [Abstract] [Full Text] [Related]

  • 37.
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  • 38. Pheochromocytoma and paraganglioma in children and adolescents.
    Stachowicz-Stencel T, Pasikowska N, Synakiewicz A.
    Acta Biochim Pol; 2023 Sep 17; 70(3):487-493. PubMed ID: 37717273
    [Abstract] [Full Text] [Related]

  • 39.
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  • 40. Age at diagnosis of pheochromocytoma differs according to catecholamine phenotype and tumor location.
    Eisenhofer G, Timmers HJ, Lenders JW, Bornstein SR, Tiebel O, Mannelli M, King KS, Vocke CD, Linehan WM, Bratslavsky G, Pacak K.
    J Clin Endocrinol Metab; 2011 Feb 17; 96(2):375-84. PubMed ID: 21147885
    [Abstract] [Full Text] [Related]

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