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N Wohllk

Showing results (11-20 of 19) with videos related to

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Revista Medica De Chile|June 1, 1993
[Thyroid profile in normal pregnancy]N Wohllk, M Osorio, J Aguayo, et al.
Bailliere'S Clinical Endocrinology and Metabolism|July 1, 1995
RET proto-oncogene mutations in multiple endocrine neoplasia type 2 and medullary thyroid carcinomaG J Cote, N Wohllk, D Evans, et al.
Revista Medica De Chile|September 13, 2001
[Germline mutations of the ret proto-oncogene in Chilean patients with hereditary and sporadic medullary thyroid carcinoma]N Wohllk, P Becker, R Youlton, et al.
Proceedings of the Association of American Physicians|January 1, 1996
The molecular basis for familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.
Endocrinology and Metabolism Clinics of North America|March 1, 1996
Application of genetic screening information to the management of medullary thyroid carcinoma and multiple endocrine neoplasia type 2N Wohllk, G J Cote, D B Evans, et al.
American Journal of Human Genetics|September 1, 1996
Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, N Wohllk, E Huang, et al.
Endocrine|January 25, 2012
Reproducibility and performance of one or two samples of salivary cortisol in the diagnosis of Cushing's syndrome using an automated immunoassay systemC A Carrasco, M García, M Goycoolea, et al.
Science (New York, N.Y.)|April 21, 1995
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Relevance of RET proto-oncogene mutations in sporadic medullary thyroid carcinomaN Wohllk, G J Cote, M M Bugalho, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Revista Medica De Chile|June 1, 1993
[Thyroid profile in normal pregnancy]N Wohllk, M Osorio, J Aguayo, et al.
Bailliere'S Clinical Endocrinology and Metabolism|July 1, 1995
RET proto-oncogene mutations in multiple endocrine neoplasia type 2 and medullary thyroid carcinomaG J Cote, N Wohllk, D Evans, et al.
Revista Medica De Chile|September 13, 2001
[Germline mutations of the ret proto-oncogene in Chilean patients with hereditary and sporadic medullary thyroid carcinoma]N Wohllk, P Becker, R Youlton, et al.
Proceedings of the Association of American Physicians|January 1, 1996
The molecular basis for familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.
Endocrinology and Metabolism Clinics of North America|March 1, 1996
Application of genetic screening information to the management of medullary thyroid carcinoma and multiple endocrine neoplasia type 2N Wohllk, G J Cote, D B Evans, et al.
American Journal of Human Genetics|September 1, 1996
Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, N Wohllk, E Huang, et al.
Endocrine|January 25, 2012
Reproducibility and performance of one or two samples of salivary cortisol in the diagnosis of Cushing's syndrome using an automated immunoassay systemC A Carrasco, M García, M Goycoolea, et al.
Science (New York, N.Y.)|April 21, 1995
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Relevance of RET proto-oncogene mutations in sporadic medullary thyroid carcinomaN Wohllk, G J Cote, M M Bugalho, et al.
Pageof 2