Richard S - Search Results

1

Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors.

Prowse AH, Webster AR, Richards FM, Richard S, Olschwang S, Resche F, Affara NA, Maher ER. Prowse AH, et al. Among authors: richard s. Am J Hum Genet. 1997 Apr;60(4):765-71. Am J Hum Genet. 1997. PMID: 9106522 Free PMC article.

2

[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. Richard S, et al. Arch Mal Coeur Vaiss. 1992 Aug;85(8):1153-6. Arch Mal Coeur Vaiss. 1992. PMID: 1482250 Review. French.

3

DNA-based presymptomatic diagnosis for the von Hippel-Lindau disease by linkage analysis.

Olschwang S, Boisson C, Richard S, Resche F, Thomas G. Olschwang S, et al. Among authors: richard s. Eur J Hum Genet. 1995;3(2):108-15. doi: 10.1159/000472284. Eur J Hum Genet. 1995. PMID: 7552140

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. Richard S, et al. Surgery. 1994 Dec;116(6):1076-81. Surgery. 1994. PMID: 7985090

5

Haemangioblastoma, haemangioblastomatosis, and von Hippel-Lindau disease.

Resche F, Moisan JP, Mantoura J, de Kersaint-Gilly A, Andre MJ, Perrin-Resche I, Menegalli-Boggelli D, Lajat Y, Richard S. Resche F, et al. Among authors: richard s. Adv Tech Stand Neurosurg. 1993;20:197-304. doi: 10.1007/978-3-7091-6912-4_6. Adv Tech Stand Neurosurg. 1993. PMID: 8397535 Review. No abstract available.

6

[Variety of pancreatic lesions observed in von Hippel-Lindau disease. Apropos of 8 cases].

Hammel P, Beigelman C, Chauveau D, Resche F, Bougerolles E, Flejou JF, Bernades P, Delchier JC, Richard S. Hammel P, et al. Among authors: richard s. Gastroenterol Clin Biol. 1995 Dec;19(12):1011-7. Gastroenterol Clin Biol. 1995. PMID: 8729413 French.

7

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.

Zbar B, Kishida T, Chen F, Schmidt L, Maher ER, Richards FM, Crossey PA, Webster AR, Affara NA, Ferguson-Smith MA, Brauch H, Glavac D, Neumann HP, Tisherman S, Mulvihill JJ, Gross DJ, Shuin T, Whaley J, Seizinger B, Kley N, Olschwang S, Boisson C, Richard S, Lips CH, Lerman M, et al. Zbar B, et al. Among authors: richard s. Hum Mutat. 1996;8(4):348-57. doi: 10.1002/(SICI)1098-1004(1996)8:4<348::AID-HUMU8>3.0.CO;2-3. Hum Mutat. 1996. PMID: 8956040

8

Haemangioblastoma of the central nervous system in von Hippel-Lindau disease. French VHL Study Group.

Richard S, Campello C, Taillandier L, Parker F, Resche F. Richard S, et al. J Intern Med. 1998 Jun;243(6):547-53. doi: 10.1046/j.1365-2796.1998.00337.x. J Intern Med. 1998. PMID: 9681857 Free article. Review.

9

[Von Hippel-Lindau disease: a hereditary disease that impacts multiple tissues].

Richard S, Giraud S, Hammel P, Beroud C, Joly D, Olschwang S, Resche F. Richard S, et al. Presse Med. 1998 Jun 20;27(22):1112-20. Presse Med. 1998. PMID: 9767816 Review. French. No abstract available.

10

Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma.

Olschwang S, Richard S, Boisson C, Giraud S, Laurent-Puig P, Resche F, Thomas G. Olschwang S, et al. Among authors: richard s. Hum Mutat. 1998;12(6):424-30. doi: 10.1002/(SICI)1098-1004(1998)12:6<424::AID-HUMU9>3.0.CO;2-H. Hum Mutat. 1998. PMID: 9829912

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