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Results: 1 to 20 of 97

Similar articles for PubMed (Select 22876661)

1.

[Clinical status of Von Hippel-Lindau disease associated pheochromocytoma in Japan: a national epidemiologic survey].

Shuin T, Yao M, Shinohara N, Yamasaki I, Tamura K.

Nihon Hinyokika Gakkai Zasshi. 2012 May;103(3):557-61. Japanese.

PMID:
22876661
2.

[The current clinical status of kidney cancers in patients with the VHL disease in Japan: a nationwide epidemiological survey].

Shuin T, Shinohara N, Yao M, Yamasaki I, Tamura K, Kamada M.

Nihon Hinyokika Gakkai Zasshi. 2012 May;103(3):552-6. Japanese.

PMID:
22876660
3.

Pheochromocytoma in children.

Ciftci AO, Tanyel FC, Senocak ME, Büyükpamukçu N.

J Pediatr Surg. 2001 Mar;36(3):447-52.

PMID:
11226993
4.

Pheochromocytoma as the first manifestation of von Hippel-Lindau disease.

Richard S, Beigelman C, Duclos JM, Fendler JP, Plauchu H, Plouin PF, Resche F, Schlumberger M, Vermesse B, Proye C.

Surgery. 1994 Dec;116(6):1076-81.

PMID:
7985090
5.

Functional and oncologic outcomes of partial adrenalectomy for pheochromocytoma in patients with von Hippel-Lindau syndrome after at least 5 years of followup.

Benhammou JN, Boris RS, Pacak K, Pinto PA, Linehan WM, Bratslavsky G.

J Urol. 2010 Nov;184(5):1855-9. doi: 10.1016/j.juro.2010.06.102. Epub 2010 Sep 17.

6.

[Bilateral adrenal pheochromocytomas in von Hippel-Lindau disease].

Touiti D, Seket B, Deligne E, Badet L, Colombel M, Dawahra M, Martin X, Maréchal JM, Dubernard JM.

Ann Urol (Paris). 2001 Nov;35(6):323-8. French.

PMID:
11774764
7.

Early identification of patients with von Hippel-Lindau disease at risk for pheochromocytoma.

Maranchie JK, Walther MM.

Curr Urol Rep. 2001 Feb;2(1):24-30. Review.

PMID:
12084291
8.

Pancreatic involvement in Japanese patients with von Hippel-Lindau disease: results of a nationwide survey.

Igarashi H, Ito T, Nishimori I, Tamura K, Yamasaki I, Tanaka M, Shuin T.

J Gastroenterol. 2014 Mar;49(3):511-6. doi: 10.1007/s00535-013-0794-1. Epub 2013 Mar 31.

PMID:
23543325
9.

Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: a role for laparoscopic and cortical-sparing surgery.

Baghai M, Thompson GB, Young WF Jr, Grant CS, Michels VV, van Heerden JA.

Arch Surg. 2002 Jun;137(6):682-8; discussion 688-9.

PMID:
12049539
10.

Abdominal visceral lesions in von Hippel-Lindau disease: incidence and clinical behavior of pancreatic and adrenal lesions at a single center.

Delman KA, Shapiro SE, Jonasch EW, Lee JE, Curley SA, Evans DB, Perrier ND.

World J Surg. 2006 May;30(5):665-9.

PMID:
16617420
11.

A genetic register for von Hippel-Lindau disease.

Maddock IR, Moran A, Maher ER, Teare MD, Norman A, Payne SJ, Whitehouse R, Dodd C, Lavin M, Hartley N, Super M, Evans DG.

J Med Genet. 1996 Feb;33(2):120-7.

12.

[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, et al.

Arch Mal Coeur Vaiss. 1992 Aug;85(8):1153-6. Review. French.

PMID:
1482250
13.

Partial adrenalectomy minimizes the need for long-term hormone replacement in pediatric patients with pheochromocytoma and von Hippel-Lindau syndrome.

Volkin D, Yerram N, Ahmed F, Lankford D, Baccala A, Gupta GN, Hoang A, Nix J, Metwalli AR, Lang DM, Bratslavsky G, Linehan WM, Pinto PA.

J Pediatr Surg. 2012 Nov;47(11):2077-82. doi: 10.1016/j.jpedsurg.2012.07.003.

14.

The von Hippel-Lindau (VHL) germline mutation V84L manifests as early-onset bilateral pheochromocytoma.

Abbott MA, Nathanson KL, Nightingale S, Maher ER, Greenstein RM.

Am J Med Genet A. 2006 Apr 1;140(7):685-90.

PMID:
16502427
15.

[The von Hippel-Lindau syndrome with pheochromocytoma].

Palmar I, Vircburger M, Manojlović D, Radević B, Andjelković Z, Burić B, Savicević M, Nesković G.

Srp Arh Celok Lek. 2002 Jul;130 Suppl 2:43-6. Serbian.

PMID:
12584997
16.

Uncommon clinical presentations of pheochromocytoma and paraganglioma in two different patients affected by two distinct novel VHL germline mutations.

Ercolino T, Becherini L, Valeri A, Maiello M, Gaglianò MS, Parenti G, Ramazzotti M, Piscitelli E, Simi L, Pinzani P, Nesi G, Degl'Innocenti D, Console N, Bergamini C, Mannelli M.

Clin Endocrinol (Oxf). 2008 May;68(5):762-8. Epub 2007 Nov 19.

PMID:
18031321
17.

Cortical-sparing adrenalectomy for patients with bilateral pheochromocytoma.

Lee JE, Curley SA, Gagel RF, Evans DB, Hickey RC.

Surgery. 1996 Dec;120(6):1064-70; discussion 1070-1.

PMID:
8957496
18.

A family with von Hippel-Lindau disease revealed by pheochromocytoma.

Tomita N, Moriguchi A, Yamasaki K, Taniyama Y, Kotani N, Hashiya N, Yoshida M, Yao M, Higaki J, Ogihara T.

Hypertens Res. 2001 Jul;24(4):445-50.

19.

Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease.

Hasani-Ranjbar S, Amoli MM, Ebrahim-Habibi A, Haghpanah V, Hejazi M, Soltani A, Larijani B.

Fam Cancer. 2009;8(4):465-71. doi: 10.1007/s10689-009-9266-4. Epub 2009 Aug 1.

PMID:
19649731
20.

Differential grading of endolymphatic sac tumor extension by virtue of von Hippel-Lindau disease status.

Bambakidis NC, Megerian CA, Ratcheson RA.

Otol Neurotol. 2004 Sep;25(5):773-81.

PMID:
15354010
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