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Journal Abstract Search

178 related items for PubMed ID: 9329368

  • 21. Endocrine manifestations of von Hippel-Lindau disease.
    Cassol C, Mete O.
    Arch Pathol Lab Med; 2015 Feb; 139(2):263-8. PubMed ID: 25611110
    [Abstract] [Full Text] [Related]

  • 22. 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; 94(5):1701-5. PubMed ID: 19258401
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  • 23. Concurrent bilateral pheochromocytoma and thoracic paraganglioma during pregnancy.
    Snabboon T, Plengpanich W, Houngngam N, Buranasupkajorn P, Plengvidhya N, Sereepapong W, Sunthornyothin S, Shotelersuk V.
    Endocrine; 2010 Apr; 37(2):261-4. PubMed ID: 20960261
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  • 24. [Pheochromocytoma, first manifestation of Von Hippel-Lindau disease: a possibility to be considered].
    Richard S, Resche F, Vermesse B, Fendler JP, Francillard M, Laroche F, Luton JP, Méry JP, Proye C, Redondo A.
    Arch Mal Coeur Vaiss; 1992 Aug; 85(8):1153-6. PubMed ID: 1482250
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  • 25. Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.
    Currás-Freixes M, Inglada-Pérez L, Mancikova V, Montero-Conde C, Letón R, Comino-Méndez I, Apellániz-Ruiz M, Sánchez-Barroso L, Aguirre Sánchez-Covisa M, Alcázar V, Aller J, Álvarez-Escolá C, Andía-Melero VM, Azriel-Mira S, Calatayud-Gutiérrez M, Díaz JÁ, Díez-Hernández A, Lamas-Oliveira C, Marazuela M, Matias-Guiu X, Meoro-Avilés A, Patiño-García A, Pedrinaci S, Riesco-Eizaguirre G, Sábado-Álvarez C, Sáez-Villaverde R, Sainz de Los Terreros A, Sanz Guadarrama Ó, Sastre-Marcos J, Scolá-Yurrita B, Segura-Huerta Á, Serrano-Corredor Mde L, Villar-Vicente MR, Rodríguez-Antona C, Korpershoek E, Cascón A, Robledo M.
    J Med Genet; 2015 Oct; 52(10):647-56. PubMed ID: 26269449
    [Abstract] [Full Text] [Related]

  • 26. Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genes.
    Bar M, Friedman E, Jakobovitz O, Leibowitz G, Lerer I, Abeliovich D, Gross DJ.
    Clin Endocrinol (Oxf); 1997 Dec; 47(6):707-12. PubMed ID: 9497878
    [Abstract] [Full Text] [Related]

  • 27. Familial pheochromocytoma associated with a novel mutation in the von Hippel-Lindau gene.
    Gross DJ, Avishai N, Meiner V, Filon D, Zbar B, Abeliovich D.
    J Clin Endocrinol Metab; 1996 Jan; 81(1):147-9. PubMed ID: 8550742
    [Abstract] [Full Text] [Related]

  • 28. Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease.
    Ritter MM, Frilling A, Crossey PA, Höppner W, Maher ER, Mulligan L, Ponder BA, Engelhardt D.
    J Clin Endocrinol Metab; 1996 Mar; 81(3):1035-7. PubMed ID: 8772572
    [Abstract] [Full Text] [Related]

  • 29. Chromogranin a expression in phaeochromocytomas associated with von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2.
    Cleary S, Phillips JK, Huynh TT, Pacak K, Fliedner S, Elkahloun AG, Munson P, Worrell RA, Eisenhofer G.
    Horm Metab Res; 2007 Dec; 39(12):876-83. PubMed ID: 18046660
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  • 33. Molecular diagnosis of von Hippel-Lindau disease in a kindred with a predominance of familial phaeochromocytoma.
    Garcia A, Matias-Guiu X, Cabezas R, Chico A, Prat J, Baiget M, De Leiva A.
    Clin Endocrinol (Oxf); 1997 Mar; 46(3):359-63. PubMed ID: 9156047
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  • 35. Recurrent polytopic chromaffin paragangliomas in a 9-year-old boy resulting from a novel germline mutation in the von Hippel-Lindau gene.
    Reichardt P, Apel TW, Domula M, Tröbs RB, Krause I, Bierbach U, Neumann HP, Kiess W.
    J Pediatr Hematol Oncol; 2002 Feb; 24(2):145-8. PubMed ID: 11990703
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  • 38. Pheochromocytoma and Von Hippel-Lindau in pregnancy.
    Kolomeyevskaya N, Blazo M, Van den Veyver I, Strehlow S, Aagaard-Tillery KM.
    Am J Perinatol; 2010 Mar; 27(3):257-63. PubMed ID: 19784914
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  • 39. Pheochromocytoma as a catecholamine producing tumor: implications for clinical practice.
    Zelinka T, Eisenhofer G, Pacak K.
    Stress; 2007 Jun; 10(2):195-203. PubMed ID: 17514588
    [Abstract] [Full Text] [Related]

  • 40. Paediatric bilateral adrenal phaeochromocytomas in association with a novel mutation in the von Hippel Lindau gene.
    Kim L, Holland AJ, Srinivasan S, Cowell CT, Benn DE, Robinson BG.
    J Paediatr Child Health; 2008 Sep; 44(9):514-6. PubMed ID: 18928468
    [Abstract] [Full Text] [Related]

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