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Items: 1 to 20 of 104

1.

Von hippel-lindau disease and erythrocytosis.

Capodimonti S, Teofili L, Martini M, Cenci T, Iachininoto MG, Nuzzolo ER, Bianchi M, Murdolo M, Leone G, Larocca LM.

J Clin Oncol. 2012 May 1;30(13):e137-9. doi: 10.1200/JCO.2011.38.6797. Epub 2012 Mar 5. No abstract available.

2.

A novel von Hippel-Lindau point mutation presents as apparently sporadic pheochromocytoma.

Rich TA, Jonasch E, Matin S, Waguespack SG, Gombos DS, Santarpia L, Stolle C, Jimenez C.

Cancer Invest. 2008 Jul;26(6):642-6. doi: 10.1080/07357900701802527.

PMID:
18584357
3.

Familial isolated pheochromocytoma presenting a new mutation in the von Hippel-Lindau gene.

Sansó G, Rudaz MC, Levin G, Barontini M.

Am J Hypertens. 2004 Dec;17(12 Pt 1):1107-11.

PMID:
15607616
4.

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
5.

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
6.

[Genetic detection and analysis of the VHL gene in patients with sporadic pheochromocytoma].

Zhang B, Wang YM, Wang N, Ha XQ, Dong YC, Zhou DH.

Zhonghua Zhong Liu Za Zhi. 2009 May;31(5):361-5. Chinese.

PMID:
19799085
7.

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.

8.

Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.

Gergics P, Patocs A, Toth M, Igaz P, Szucs N, Liko I, Fazakas F, Szabo I, Kovacs B, Glaz E, Racz K.

Eur J Endocrinol. 2009 Sep;161(3):495-502. doi: 10.1530/EJE-09-0399. Epub 2009 Jul 2.

9.

[Pheochromocytoma in Von Hippel Lindau disease. 3 cases].

Tourniaire J, Pradat P, Chalendar D.

Ann Endocrinol (Paris). 1995;56(6):609-12. French.

PMID:
8787353
10.

Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma.

Walther MM, Reiter R, Keiser HR, Choyke PL, Venzon D, Hurley K, Gnarra JR, Reynolds JC, Glenn GM, Zbar B, Linehan WM.

J Urol. 1999 Sep;162(3 Pt 1):659-64.

PMID:
10458336
11.

Pheochromocytoma in von Hippel-Lindau disease and neurofibromatosis type 1.

Opocher G, Conton P, Schiavi F, Macino B, Mantero F.

Fam Cancer. 2005;4(1):13-6. Review.

PMID:
15883705
12.

Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patient.

Gonc N, Engiz O, Neumann HP, Demirbilek H, Ozon A, Alikasifoglu A, Kandemir N.

J Pediatr Endocrinol Metab. 2011;24(1-2):109-12.

PMID:
21528828
13.

Intrathoracic and multiple abdominal pheochromocytomas in von Hippel-Lindau disease.

Hoffman RW, Gardner DW, Mitchell FL.

Arch Intern Med. 1982 Oct;142(10):1962-4.

PMID:
7125783
14.

Bilateral pheochromocytoma as first presentation of von Hippel-Lindau disease in a Chinese family.

Tong AL, Zeng ZP, Zhou YR, Yuan T, Cao CX, Zhang J, Li M.

Chin Med Sci J. 2009 Dec;24(4):197-201.

PMID:
20120764
15.

Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma.

Crossey PA, Eng C, Ginalska-Malinowska M, Lennard TW, Wheeler DC, Ponder BA, Maher ER.

J Med Genet. 1995 Nov;32(11):885-6.

16.

von Hippel-Lindau disease type 2A in a family with a duplicated 21-base-pair in-frame insertion mutation in the VHL gene.

Miyagawa Y, Nakazawa M, Noda Y, Ito S, Ohguro H.

Graefes Arch Clin Exp Ophthalmol. 2003 Mar;241(3):241-4. Epub 2003 Feb 20.

PMID:
12644949
17.

Molecular analysis of the Von Hippel-Lindau (VHL) gene in a family with non-syndromic pheochromocytoma: the importance of genetic testing.

Cruz JB, Fernandes LP, Clara SA, Conde SJ, Perone D, Kopp P, Nogueira CR.

Arq Bras Endocrinol Metabol. 2007 Dec;51(9):1463-7.

18.

Genotype-phenotype correlation in von Hippel-Lindau disease: identification of a mutation associated with VHL type 2A.

Chen F, Slife L, Kishida T, Mulvihill J, Tisherman SE, Zbar B.

J Med Genet. 1996 Aug;33(8):716-7.

19.

Bilateral pheochromocytomas in a child who had hemihypertrophy and alteration in the VHL gene.

Amini Z, Babovic-Vuksanovic D, Lteif A.

J Pediatr Endocrinol Metab. 2013;26(3-4):369-72. doi: 10.1515/jpem-2012-0255.

PMID:
23327821
20.

Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.

Neumann HP, Berger DP, Sigmund G, Blum U, Schmidt D, Parmer RJ, Volk B, Kirste G.

N Engl J Med. 1993 Nov 18;329(21):1531-8. Erratum in: N Engl J Med 1994 Dec 1;331(22):1535.

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