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Oncogene
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February 18, 1999
Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation
O Gimm, D S Neuberg, D J Marsh, et al.
Hormone and Metabolic Research. Supplement Series
|
January 1, 1993
Somatostatin receptor scintigraphy and magnetic resonance imaging in recurrent medullary thyroid carcinoma: a comparative study
U Dörr, S Würstlin, K Frank-Raue, et al.
International Journal of Cancer
|
March 10, 2001
Prognostic value of codon 918 (ATG-->ACG) RET proto-oncogene mutations in sporadic medullary thyroid carcinoma
T Schilling, J Bürck, H P Sinn, et al.
Deutsche Medizinische Wochenschrift (1946)
|
September 26, 2003
[Hereditary medullary thyroid carcinoma--genotype-phenotype characterization]
K Frank-Raue, C Heimbach, S Rondot, et al.
Clinical Endocrinology
|
July 1, 1995
Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma
C Eng, L M Mulligan, D P Smith, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
November 30, 1999
Cholecystokinin-B/gastrin receptor binding peptides: preclinical development and evaluation of their diagnostic and therapeutic potential
T M Behr, M Béhé, C Angerstein, et al.
Cancer Research
|
December 11, 1997
Improved treatment of medullary thyroid cancer in a nude mouse model by combined radioimmunochemotherapy: doxorubicin potentiates the therapeutic efficacy of radiolabeled antibodies in a radioresistant tumor type
T M Behr, E Wulst, S Radetzky, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association
|
May 18, 2006
Late diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
K Müssig, S Kaltenbach, C Maser-Gluth, et al.
Genes, Chromosomes & Cancer
|
March 1, 1995
Mutation of the RET protooncogene in sporadic medullary thyroid carcinoma
C Eng, L M Mulligan, D P Smith, et al.
Archives of Internal Medicine
|
June 1, 1992
The natural course of multiple endocrine neoplasia type IIb. A study of 18 cases
H F Vasen, M van der Feltz, F Raue, et al.
Page
of 22
Search research articles
Search
Showing results (201-210 of 215) with videos related to
Sort By:
Page
of 22
Oncogene
|
February 18, 1999
Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation
O Gimm, D S Neuberg, D J Marsh, et al.
Hormone and Metabolic Research. Supplement Series
|
January 1, 1993
Somatostatin receptor scintigraphy and magnetic resonance imaging in recurrent medullary thyroid carcinoma: a comparative study
U Dörr, S Würstlin, K Frank-Raue, et al.
International Journal of Cancer
|
March 10, 2001
Prognostic value of codon 918 (ATG-->ACG) RET proto-oncogene mutations in sporadic medullary thyroid carcinoma
T Schilling, J Bürck, H P Sinn, et al.
Deutsche Medizinische Wochenschrift (1946)
|
September 26, 2003
[Hereditary medullary thyroid carcinoma--genotype-phenotype characterization]
K Frank-Raue, C Heimbach, S Rondot, et al.
Clinical Endocrinology
|
July 1, 1995
Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma
C Eng, L M Mulligan, D P Smith, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
November 30, 1999
Cholecystokinin-B/gastrin receptor binding peptides: preclinical development and evaluation of their diagnostic and therapeutic potential
T M Behr, M Béhé, C Angerstein, et al.
Cancer Research
|
December 11, 1997
Improved treatment of medullary thyroid cancer in a nude mouse model by combined radioimmunochemotherapy: doxorubicin potentiates the therapeutic efficacy of radiolabeled antibodies in a radioresistant tumor type
T M Behr, E Wulst, S Radetzky, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association
|
May 18, 2006
Late diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
K Müssig, S Kaltenbach, C Maser-Gluth, et al.
Genes, Chromosomes & Cancer
|
March 1, 1995
Mutation of the RET protooncogene in sporadic medullary thyroid carcinoma
C Eng, L M Mulligan, D P Smith, et al.
Archives of Internal Medicine
|
June 1, 1992
The natural course of multiple endocrine neoplasia type IIb. A study of 18 cases
H F Vasen, M van der Feltz, F Raue, et al.
Page
of 22