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Items: 1 to 20 of 22

1.

The cerebellar hemangioblastomas; review of fifty-three cases with special reference to cerebellar cysts and the association of polycythemia.

CRAMER F, KIMSEY MW.

AMA Arch Neurol Psychiatry. 1952 Feb;67(2):237-52. No abstract available.

PMID:
14893995
2.

LINDAU'S DISEASE. REVIEW OF THE LITERATURE AND STUDY OF A LARGE KINDRED.

MELMON KL, ROSEN SW.

Am J Med. 1964 Apr;36:595-617. No abstract available.

PMID:
14142412
3.

Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases.

BLANK CE.

Ann Hum Genet. 1960 May;24:151-64. No abstract available.

PMID:
13801313
4.

Lindau's disease in five generations.

NICOL AA.

Ann Hum Genet. 1957 Oct;22(1):7-15. No abstract available.

PMID:
13488179
5.

Cerebellar hemangiomas; a clinico-pathologic study of fourteen cases.

MEREDITH JM, HENNIGAR GR.

Am Surg. 1954 Apr;20(4):410-23. No abstract available.

PMID:
13148555
6.

Complex segregation analysis with pointers.

Lalouel JM, Morton NE.

Hum Hered. 1981;31(5):312-21.

PMID:
7333620
7.

Segregation and linkage analyses of von Hippel Lindau disease among 220 descendants from one kindred.

Go RC, Lamiell JM, Hsia YE, Yuen JW, Paik Y.

Am J Hum Genet. 1984 Jan;36(1):131-42.

8.

[Hemangioblastomas of the central nervous system. A clinical study].

Müller-Jensen A, Zangemeister WH, Küchler J, Herrmann HD.

Eur Arch Psychiatry Neurol Sci. 1984;234(3):149-56. German.

PMID:
6541579
9.

Von Hippel-Lindau syndrome: a report on three kindreds.

Shokeir MH.

J Med Genet. 1970 Jun;7(2):155-7. No abstract available.

10.

[Family study of a classic case of von Hippellindau syndrome].

Piotrowski W, Röhrborn G.

Langenbecks Arch Chir. 1965 Aug 30;311(3):310-22. German. No abstract available.

PMID:
5294976
11.

Lindau's disease. A study of one family through six generations.

Lauritsen JG.

Acta Chir Scand. 1973;139(5):482-6. No abstract available.

PMID:
4795931
12.

Haemangioblastomas. A review of 81 cases.

Palmer JJ.

Acta Neurochir (Wien). 1972;27(3):125-48. No abstract available.

PMID:
4677536
13.

Cerebellar haemangioblastoma and von Hippel-Lindau disease.

Huson SM, Harper PS, Hourihan MD, Cole G, Weeks RD, Compston DA.

Brain. 1986 Dec;109 ( Pt 6):1297-310.

PMID:
3790978
14.

Genetic aspects of tuberous sclerosis in the west of Scotland.

Sampson JR, Scahill SJ, Stephenson JB, Mann L, Connor JM.

J Med Genet. 1989 Jan;26(1):28-31.

15.

Hemangioblastomas of the central nervous system. A 10-year study with special reference to von Hippel-Lindau syndrome.

Neumann HP, Eggert HR, Weigel K, Friedburg H, Wiestler OD, Schollmeyer P.

J Neurosurg. 1989 Jan;70(1):24-30.

PMID:
2909683
16.

Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma.

Seizinger BR, Rouleau GA, Ozelius LJ, Lane AH, Farmer GE, Lamiell JM, Haines J, Yuen JW, Collins D, Majoor-Krakauer D, et al.

Nature. 1988 Mar 17;332(6161):268-9.

PMID:
2894613
17.

Parental origin of mutations of the retinoblastoma gene.

Dryja TP, Mukai S, Petersen R, Rapaport JM, Walton D, Yandell DW.

Nature. 1989 Jun 15;339(6225):556-8.

PMID:
2733786
18.

von Hippel-Lindau disease affecting 43 members of a single kindred.

Lamiell JM, Salazar FG, Hsia YE.

Medicine (Baltimore). 1989 Jan;68(1):1-29. Review.

PMID:
2642584
20.

Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

Jadayel D, Fain P, Upadhyaya M, Ponder MA, Huson SM, Carey J, Fryer A, Mathew CG, Barker DF, Ponder BA.

Nature. 1990 Feb 8;343(6258):558-9.

PMID:
2105472

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