Sobol H - Search Results

1

[Endocrine polyadenomatosis of 2a type (MEN 2a). Clinical and genetic study of a family].

Guillausseau PJ, Guillausseau C, Calmettes C, Feingold N, Demenais F, Sobol H, Gony J, Hors J, Schaison G, Seret D, et al. Guillausseau PJ, et al. Among authors: sobol h. Ann Endocrinol (Paris). 1988;49(1):17-21. Ann Endocrinol (Paris). 1988. PMID: 2900619 French.

2

[Multiple endocrine neoplasms type 2. Recent aspects].

Guillausseau PJ, Calmettes C, Feingold N, Franc B, Guillausseau-Scholer C, Modigliani E, Sobol H. Guillausseau PJ, et al. Among authors: sobol h. Presse Med. 1991 Dec 21-28;20(44):2256-62. Presse Med. 1991. PMID: 1685777 Review. French.

3

Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A.

Narod SA, Lavoué MF, Morgan K, Calmettes C, Sobol H, Goodfellow PJ, Lenoir GM. Narod SA, et al. Among authors: sobol h. Am J Hum Genet. 1992 Sep;51(3):469-77. Am J Hum Genet. 1992. PMID: 1353939 Free PMC article.

4

[Familial medullary thyroid cancer. Contribution of genealogy and genetics to the study of two families].

Houdent C, Avronsart B, Dubuisson M, Ozenne G, Testard J, Calmettes C, Chaventre A, Sobol H, Lenoir GM, Wolf LM. Houdent C, et al. Among authors: sobol h. Presse Med. 1990 Mar 31;19(12):549-52. Presse Med. 1990. PMID: 2139215 French.

5

Screening for multiple endocrine neoplasia type 2a with DNA-polymorphism analysis.

Sobol H, Narod SA, Nakamura Y, Boneu A, Calmettes C, Chadenas D, Charpentier G, Chatal JF, Delepine N, Delisle MJ. Sobol H, et al. N Engl J Med. 1989 Oct 12;321(15):996-1001. doi: 10.1056/NEJM198910123211502. N Engl J Med. 1989. PMID: 2571086

6

Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma.

Narod SA, Sobol H, Nakamura Y, Calmettes C, Baulieu JL, Bigorgne JC, Chabrier G, Couette J, de Gennes JL, Duprey J, et al. Narod SA, et al. Among authors: sobol h. Hum Genet. 1989 Nov;83(4):353-8. doi: 10.1007/BF00291380. Hum Genet. 1989. PMID: 2572534

7

[Cutaneous lesion associated with multiple endocrine neoplasms type 2A (Sipple's syndrome). An early clinical marker].

Chabre O, Labat-Moleur F, Berthod F, Tarel V, Stoebner P, Sobol H, Bachelot I. Chabre O, et al. Among authors: sobol h. Presse Med. 1992 Feb 22;21(7):299-303. Presse Med. 1992. PMID: 1348355 French.

8

Linked markers flanking the gene for multiple endocrine neoplasia type 2A.

Nakamura Y, Mathew CG, Sobol H, Easton DF, Telenius H, Bragg T, Chin K, Clark J, Jones C, Lenoir GM, et al. Nakamura Y, et al. Among authors: sobol h. Genomics. 1989 Aug;5(2):199-203. doi: 10.1016/0888-7543(89)90046-3. Genomics. 1989. PMID: 2571570

9

The gene for MEN 2A is tightly linked to the centromere of chromosome 10.

Narod SA, Sobol H, Schuffenecker I, Lavoué MF, Lenoir GM. Narod SA, et al. Among authors: sobol h. Hum Genet. 1991 Mar;86(5):529-30. doi: 10.1007/BF00194649. Hum Genet. 1991. PMID: 1673115

10

Genetic screening of endocrine tumour syndromes with DNA probes: the example of medullary thyroid carcinoma.

Sobol H, Narod SA, Assouline D, Lenoir GM. Sobol H, et al. Horm Res. 1989;32(1-3):34-40. doi: 10.1159/000181240. Horm Res. 1989. PMID: 2575577 Review.

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