Parma J - Search Results

1

Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas.

Parma J, Duprez L, Van Sande J, Cochaux P, Gervy C, Mockel J, Dumont J, Vassart G. Parma J, et al. Nature. 1993 Oct 14;365(6447):649-51. doi: 10.1038/365649a0. Nature. 1993. PMID: 8413627

2

Somatic and germline mutations of the TSH receptor gene in thyroid diseases.

Van Sande J, Parma J, Tonacchera M, Swillens S, Dumont J, Vassart G. Van Sande J, et al. Among authors: parma j. J Clin Endocrinol Metab. 1995 Sep;80(9):2577-85. doi: 10.1210/jcem.80.9.7673398. J Clin Endocrinol Metab. 1995. PMID: 7673398 Review. No abstract available.

3

Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism.

Duprez L, Parma J, Van Sande J, Allgeier A, Leclère J, Schvartz C, Delisle MJ, Decoulx M, Orgiazzi J, Dumont J, et al. Duprez L, et al. Among authors: parma j. Nat Genet. 1994 Jul;7(3):396-401. doi: 10.1038/ng0794-396. Nat Genet. 1994. PMID: 7920658

4

[Thyrotropin receptor. Control of the gene expression and structure function relationships].

Vassart G, Parma J, Duprez L, Maenhaut C, Ledent C, Van Sande J, Brabant G, Dumont J. Vassart G, et al. Among authors: parma j. Ann Endocrinol (Paris). 1993;54(6):367-8. Ann Endocrinol (Paris). 1993. PMID: 7944277 French. No abstract available.

5

Identification and functional characterization of two new somatic mutations causing constitutive activation of the thyrotropin receptor in hyperfunctioning autonomous adenomas of the thyroid.

Paschke R, Tonacchera M, Van Sande J, Parma J, Vassart G. Paschke R, et al. Among authors: parma j. J Clin Endocrinol Metab. 1994 Dec;79(6):1785-9. doi: 10.1210/jcem.79.6.7989485. J Clin Endocrinol Metab. 1994. PMID: 7989485

6

Somatic mutations causing constitutive activity of the thyrotropin receptor are the major cause of hyperfunctioning thyroid adenomas: identification of additional mutations activating both the cyclic adenosine 3',5'-monophosphate and inositol phosphate-Ca2+ cascades.

Parma J, Van Sande J, Swillens S, Tonacchera M, Dumont J, Vassart G. Parma J, et al. Mol Endocrinol. 1995 Jun;9(6):725-33. doi: 10.1210/mend.9.6.8592518. Mol Endocrinol. 1995. PMID: 8592518

7

Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia.

Tonacchera M, Van Sande J, Cetani F, Swillens S, Schvartz C, Winiszewski P, Portmann L, Dumont JE, Vassart G, Parma J. Tonacchera M, et al. Among authors: parma j. J Clin Endocrinol Metab. 1996 Feb;81(2):547-54. doi: 10.1210/jcem.81.2.8636266. J Clin Endocrinol Metab. 1996. PMID: 8636266

8

Activating mutations of the TSH receptor gene cause thyroid diseases.

Vassart G, Van Sande J, Parma J, Tonacchera M, Duprez L, Swillens S, Dumont J. Vassart G, et al. Among authors: parma j. Ann Endocrinol (Paris). 1996;57(1):50-4. Ann Endocrinol (Paris). 1996. PMID: 8734289 Review.

9

The TSH receptor and thyroid diseases.

Paschke R, Van Sande J, Parma J, Vassart G. Paschke R, et al. Among authors: parma j. Baillieres Clin Endocrinol Metab. 1996 Jan;10(1):9-27. doi: 10.1016/s0950-351x(96)80266-7. Baillieres Clin Endocrinol Metab. 1996. PMID: 8734449 Review.

10

Two autonomous nodules of a patient with multinodular goiter harbor different activating mutations of the thyrotropin receptor gene.

Duprez L, Hermans J, Van Sande J, Dumont JE, Vassart G, Parma J. Duprez L, et al. Among authors: parma j. J Clin Endocrinol Metab. 1997 Jan;82(1):306-8. doi: 10.1210/jcem.82.1.3691. J Clin Endocrinol Metab. 1997. PMID: 8989278 No abstract available.

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