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Oliver Gimm

Showing results (61-70 of 113) with videos related to

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The Journal of Molecular Diagnostics : JMD|October 27, 2006
Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidismViive M Howell, John W Cardinal, Anne-Louise Richardson, et al.
Endocrine-Related Cancer|November 2, 2013
Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomasRavi Kumar Dutta, Jenny Welander, Michael Brauckhoff, et al.
The American Journal of Surgical Pathology|August 26, 2006
Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasiasAnthony J Gill, Adele Clarkson, Oliver Gimm, et al.
Surgery|December 12, 2003
Critical size of residual adrenal tissue and recovery from impaired early postoperative adrenocortical function after subtotal bilateral adrenalectomyMichael Brauckhoff, Oliver Gimm, Phuong Nguyen Thanh, et al.
Langenbeck'S Archives of Surgery|April 4, 2007
Riedel's thyroiditis: impact and strategy of a challenging surgeryKerstin Lorenz, Oliver Gimm, Hans Jürgen Holzhausen, et al.
World Journal of Surgery|November 2, 2004
Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset diseaseMichael Brauckhoff, Oliver Gimm, Carl-Ludwig Weiss, et al.
Oncogene|May 31, 2003
Peroxisome proliferator-activated receptor gamma is frequently downregulated in a diversity of sporadic nonmedullary thyroid carcinomasMicheala A Aldred, Carl Morrison, Oliver Gimm, et al.
Biomedical Optics Express|September 14, 2020
Optical coherence tomography for thyroid pathology: 3D analysis of tissue microstructureIulian Emil Tampu, Michaela Maintz, Daniela Koller, et al.
Cancers|January 21, 2022
Genetic Alterations in Mitochondrial DNA Are Complementary to Nuclear DNA Mutations in PheochromocytomasMouna Tabebi, Małgorzata Łysiak, Ravi Kumar Dutta, et al.
World Journal of Surgery|November 2, 2004
Timing and extent of surgery in patients with familial medullary thyroid carcinoma/multiple endocrine neoplasia 2A-related RET mutations not affecting codon 634Oliver Gimm, Jörg Ukkat, Barbara E Niederle, et al.
Pageof 12

Showing results (61-70 of 113) with videos related to

Sort By:
Pageof 12
The Journal of Molecular Diagnostics : JMD|October 27, 2006
Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidismViive M Howell, John W Cardinal, Anne-Louise Richardson, et al.
Endocrine-Related Cancer|November 2, 2013
Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomasRavi Kumar Dutta, Jenny Welander, Michael Brauckhoff, et al.
The American Journal of Surgical Pathology|August 26, 2006
Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasiasAnthony J Gill, Adele Clarkson, Oliver Gimm, et al.
Surgery|December 12, 2003
Critical size of residual adrenal tissue and recovery from impaired early postoperative adrenocortical function after subtotal bilateral adrenalectomyMichael Brauckhoff, Oliver Gimm, Phuong Nguyen Thanh, et al.
Langenbeck'S Archives of Surgery|April 4, 2007
Riedel's thyroiditis: impact and strategy of a challenging surgeryKerstin Lorenz, Oliver Gimm, Hans Jürgen Holzhausen, et al.
World Journal of Surgery|November 2, 2004
Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset diseaseMichael Brauckhoff, Oliver Gimm, Carl-Ludwig Weiss, et al.
Oncogene|May 31, 2003
Peroxisome proliferator-activated receptor gamma is frequently downregulated in a diversity of sporadic nonmedullary thyroid carcinomasMicheala A Aldred, Carl Morrison, Oliver Gimm, et al.
Biomedical Optics Express|September 14, 2020
Optical coherence tomography for thyroid pathology: 3D analysis of tissue microstructureIulian Emil Tampu, Michaela Maintz, Daniela Koller, et al.
Cancers|January 21, 2022
Genetic Alterations in Mitochondrial DNA Are Complementary to Nuclear DNA Mutations in PheochromocytomasMouna Tabebi, Małgorzata Łysiak, Ravi Kumar Dutta, et al.
World Journal of Surgery|November 2, 2004
Timing and extent of surgery in patients with familial medullary thyroid carcinoma/multiple endocrine neoplasia 2A-related RET mutations not affecting codon 634Oliver Gimm, Jörg Ukkat, Barbara E Niederle, et al.
Pageof 12