O. Gimm

M. Klintschar, H. Dralle, C. Hoang‐Vu, 2005, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Expression of the Epidermal Growth Factor Seven-Transmembrane Member CD 97 Correlates with Grading and Staging in Human Oral Squamous Cell Carcinomas

M. Klintschar, H. Dralle, C. Hoang‐Vu, 2005 .

Extent of surgery in clinically evident but operable MTC – when is central and/or lateral lympadenectomy indicated?

O. Gimm, 2013, Thyroid Research.

Outcome after surgery for primary hyperaldosteronism may depend on KCNJ5 tumor mutation status: a population-based study from Western Norway

S. Knappskog, L. Akslen, T. Arnesen, 2013, Langenbeck's Archives of Surgery.

Premonitory symptoms preceding metastatic medullary thyroid cancer in MEN 2B: An exploratory analysis.

S. Hess, C. Sekulla, K. Lorenz, 2008, Surgery.

Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation

D. Neuberg, C. Eng, R. Hinze, 1999, Oncogene.

GBS-MeDIP: A protocol for parallel identification of genetic and epigenetic variation in the same reduced fraction of genomes across individuals

M. H. Hosseinpour Feizi, C. Guerrero-Bosagna, L. Coutinho, 2022, STAR protocols.

Multiple endocrine neoplasia: types 1 and 2.

D. Marsh, O. Gimm, 2011, Advances in oto-rhino-laryngology.

RET proto-oncogene mutations affecting codon 790/791: A mild form of multiple endocrine neoplasia type 2A syndrome?

H. Dralle, B. Niederle, J. Ukkat, 2002, Surgery.

Reoperation in metastasizing medullary thyroid carcinoma: is a tumor stage-oriented approach justified?

H. Dralle, O. Gimm, Henning Dralle, 1997, Surgery.

Prophylactic Thyroidectomy in 75 Children and Adolescents with Hereditary Medullary Thyroid Carcinoma: German and Austrian Experience

R. Hinze, H. Dralle, B. Niederle, 1998, World Journal of Surgery.

Evidence for a role of the amyloid precursor protein in thyroid carcinogenesis.

R. Kursawe, T. Aigner, K. Schmid, 2008, The Journal of endocrinology.

Multiple endocrine neoplasia type 1 (MEN1): loss of one MEN1 allele in tumors and monohormonal endocrine cell clusters but not in islet hyperplasia of the pancreas.

W. Knoefel, G. Klöppel, H. Dralle, 2007, The Journal of clinical endocrinology and metabolism.

The development of a Swedish Nurse Practitioner Program - a request from clinicians and a process supported by US experience

C. Juhlin, E. Jangland, O. Gimm, 2013 .

Preoperative and surgical therapy in sporadic and familial pheochromocytoma.

H. Dralle, M. Brauckhoff, O. Gimm, 2004, Frontiers of hormone research.

Technical aspects of subtotal endoscopic adrenalectomy

H. Dralle, K. Kaczirek, B. Niederle, 2003, European Surgery.

Repeat Adrenocortical-Sparing Adrenalectomy for Recurrent Hereditary Pheochromocytoma

H. Dralle, M. Brauckhoff, O. Gimm, 2004, Surgery Today.

Critical size of residual adrenal tissue and recovery from impaired early postoperative adrenocortical function after subtotal bilateral adrenalectomy.

H. Dralle, J. Ukkat, M. Brauckhoff, 2003, Surgery.

Functional Results After Endoscopic Subtotal Cortical-Sparing Adrenalectomy

H. Dralle, M. Brauckhoff, O. Gimm, 2003, Surgery Today.

Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.

D. Marsh, A. Richardson, J. Cardinal, 2006, The Journal of molecular diagnostics : JMD.

Challenges of training in adrenal surgery.

Q. Duh, O. Gimm, 2019, Gland surgery.

Medullary Thyroid Carcinoma

K. Lorenz, H. Dralle, J. Ukkat, 2004, Scandinavian journal of surgery : SJS : official organ for the Finnish Surgical Society and the Scandinavian Surgical Society.

Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation.

L. Mulligan, C. Eng, D. Marsh, 1997, The Journal of clinical endocrinology and metabolism.

Long-term results and functional outcome after cervical evisceration in patients with thyroid cancer.

K. Lorenz, H. Dralle, M. Brauckhoff, 2006, Surgery.

Surgery for Medullary Thyroid Cancer

O. Gimm, 2007 .

C-cell cancer – prevention and treatment

H. Dralle, O. Gimm, Oliver Gimm, 1999, Langenbeck's Archives of Surgery.

Primary hereditary medullary thyroid carcinoma – C-cell morphology and correlation with preoperative calcitonin levels

R. Hinze, H. Holzhausen, F. Rath, 1998, Virchows Archiv.

Ectopic intrathyroidal thymus diagnosed as a solid thyroid lesion: case report and review of the literature.

H. Dralle, O. Gimm, U. Krause, 1997, Journal of pediatric surgery.

Epigenetic PTEN silencing in malignant melanomas without PTEN mutation.

C. Eng, M. Walker, H. Hampel, 2000, The American journal of pathology.

M2-macrophage infiltration and macrophage traits of tumor cells in urinary bladder cancer.

I. Shabo, H. Olsson, F. Aljabery, 2017, Urologic oncology.

Risk factors of paralysis and functional outcome after recurrent laryngeal nerve monitoring in thyroid surgery.

Johannes Haerting, Hans Lippert, J. Haerting, 2004, Surgery.

Voice Changes Without Laryngeal Nerve Alterations After Thyroidectomy: The Need For Prospective Trials - A Review Study.

O. Gimm, E. Beka, Ervin Beka, 2021, Journal of voice : official journal of the Voice Foundation.

Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma.

Jenny Welander, Adam Andreasson, C. Larsson, 2014, The Journal of clinical endocrinology and metabolism.

Over-representation of PPARγ sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general population

C. Plass, A. von Deimling, C. Eng, 2000, Journal of medical genetics.

Differential nuclear and cytoplasmic expression of PTEN in normal thyroid tissue, and benign and malignant epithelial thyroid tumors.

J. Yeh, C. Eng, R. Hinze, 2000, The American journal of pathology.

Regulatory subunit type I‐α of protein kinase A (PRKAR1A): A tumor‐suppressor gene for sporadic thyroid cancer

C. Stratakis, O. Gimm, N. Sarlis, 2002, Genes, chromosomes & cancer.

Distinct pattern of oxidative DNA damage and DNA repair in follicular thyroid tumours.

K. Schmid, C. Weidinger, K. Krause, 2012, Journal of molecular endocrinology.

CDC73/HRPT2 CpG island hypermethylation and mutation of 5'-untranslated sequence are uncommon mechanisms of silencing parafibromin in parathyroid tumors.

B. Teh, A. Gill, D. Marsh, 2010, Endocrine-related cancer.

Biomarkers in Thyroid Tumor Research: New Diagnostic Tools and Potential Targets of Molecular-Based Therapy

E. Kebebew, M. Castellone, C. Hoang‐Vu, 2012, Journal of thyroid research.

Frequent epigenetic silencing of the CpG island promoter of RASSF1A in thyroid carcinoma.

G. Pfeifer, H. Dralle, C. Hoang‐Vu, 2002, Cancer research.

Germ-line mutations in nonsyndromic pheochromocytoma.

J. Schipper, K. Zerres, C. Eng, 2002, The New England journal of medicine.

Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array‐CGH

C. Langford, C. Larsson, S. Gregory, 2006, International journal of cancer.

Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia.

Louise Izatt, Marc Tischkowitz, Anneke Lucassen, 2007, The Journal of clinical endocrinology and metabolism.

HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours

K Hammje, B. Teh, S. Khoo, 2003, Journal of medical genetics.

Frequent RASSF1A promoter hypermethylation and K-ras mutations in pancreatic carcinoma

B. Boehm, G. Pfeifer, Limin Liu, 2003, Oncogene.

CpG island methylation of tumor-related promoters occurs preferentially in undifferentiated carcinoma.

H. Dralle, C. Hoang‐Vu, R. Dammann, 2006, Thyroid : official journal of the American Thyroid Association.

Papillary and follicular thyroid carcinomas show distinctly different microarray expression profiles and can be distinguished by a minimum of five genes.

S. Liyanarachchi, A. de la Chapelle, R. Davuluri, 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas

Jenny Welander, Diana E. Benn, Patricia L. M. Dahia, 2017, Nature Reviews Endocrinology.

Dual energy 4D-CT of parathyroid adenomas not clearly localized by sestamibi scintigraphy and ultrasonography - a retrospective study.

G. Wallin, O. Gimm, M. Woisetschläger, 2020, European journal of radiology.

The NF1 gene: a frequent mutational target in sporadic pheochromocytomas and beyond.

P. Söderkvist, O. Gimm, J. Welander, 2013, Endocrine-related cancer.

Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas.

P. Söderkvist, O. Gimm, J. Welander, 2011, Endocrine-related cancer.

Preventive medicine of von Hippel-Lindau disease-associated pancreatic neuroendocrine tumors.

H. Amthauer, E. Jonasch, W. Young, 2018, Endocrine-related cancer.

Risk‐Oriented Approach to Hereditary Adrenal Pheochromocytoma

H. Dralle, A. Machens, M. Brauckhoff, 2006, Annals of the New York Academy of Sciences.

First experiences in intraoperative neurostimulation of the recurrent laryngeal nerve during thyroid surgery of children and adolescents.

H. Dralle, J. Ukkat, M. Brauckhoff, 2002, Journal of pediatric surgery.

Super-selective venous sampling in conjunction with quickPTH for patients with persistent primary hyperparathyroidism: report of five cases

C. Juhlin, O. Gimm, L. Arnesson, 2012, Surgery Today.

The genetic basis of pheochromocytoma.

H. Neumann, A. Januszewicz, O. Gimm, 2004, Frontiers of hormone research.

Heat Production, Nerve Function, and Morphology following Nerve Close Dissection with Surgical Instruments

C. Nordborg, C. Nordborg, L. Brudin, 2012, World Journal of Surgery.

RET-familial medullary thyroid carcinoma mutants Y791F and S891A activate a Src/JAK/STAT3 pathway, independent of glial cell line-derived neurotrophic factor.

J. Osinga, H. Hollema, R. Hofstra, 2005, Cancer research.

Allelic deletion of the MEN1 gene in duodenal gastrin and somatostatin cell neoplasms and their precursor lesions

W. Knoefel, G. Klöppel, H. Dralle, 2006, Gut.

Case report: Two sisters with a germline CHEK2 variant and distinct endocrine neoplasias

J. Bishop, P. Söderkvist, A. Alli, 2022, Frontiers in Endocrinology.

Frequent EPAS1 / HIF2 a exons 9 and 12 mutations in non-familial pheochromocytoma

C. Larsson, M. Bäckdahl, P. Söderkvist, 2014 .

Frequent promoter methylation of tumor-related genes in sporadic and men2-associated pheochromocytomas.

G. Pfeifer, H. Dralle, C. Hoang‐Vu, 2005, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Molecular Profiling of Pheochromocytoma and Abdominal Paraganglioma Stratified by the PASS Algorithm Reveals Chromogranin B as Associated With Histologic Prediction of Malignant Behavior

C. Larsson, P. Söderkvist, A. Stenman, 2019, The American journal of surgical pathology.

Multiple Endocrine Neoplasia 2B Syndrome due to Codon 918 Mutation: Clinical Manifestation and Course in Early and Late Onset Disease

C. Sekulla, H. Dralle, J. Ukkat, 2004, World Journal of Surgery.

Genetic Alterations in Mitochondrial DNA Are Complementary to Nuclear DNA Mutations in Pheochromocytomas

P. Söderkvist, L. Brunaud, M. Turkina, 2022, Cancers.

Activating FGFR1 Mutations in Sporadic Pheochromocytomas

P. Söderkvist, L. Brunaud, M. Brauckhoff, 2017, World Journal of Surgery.

Whole‐exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene

Jenny Welander, Gerald Goh, Stefano Caramuta, 2015, Genes, chromosomes & cancer.

Role of SDHAF2 and SDHD in von Hippel–Lindau Associated Pheochromocytomas

C. Larsson, M. Bäckdahl, A. Fassina, 2014, World Journal of Surgery.

Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma.

C. Eng, H. Neumann, H. Dziema, 2000, Cancer research.

Dissecting molecular events in thyroid neoplasia provides evidence for distinct evolution of follicular thyroid adenoma and carcinoma.

M. Eszlinger, K. Schmid, C. Ihling, 2011, The American journal of pathology.

RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease

S. Borrego, G. Antiñolo, C. Eng, 2000, Journal of medical genetics.

Expression of telomerase genes in thyroid carcinoma.

C. Poremba, F. Rath, J. Köhrle, 2002, International journal of oncology.

Germline SDHA mutation detected by next-generation sequencing in a young index patient with large paraganglioma.

P. Söderkvist, R. Wiseman, L. Isaksson, 2013, The Journal of clinical endocrinology and metabolism.

Prognostic Significance of Disseminated Tumor Cells in the Connective Tissue of Patients with Medullary Thyroid Carcinoma

C. Sekulla, H. Dralle, J. Ukkat, 2006, World Journal of Surgery.

Timing and Extent of Surgery in Patients with Familial Medullary Thyroid Carcinoma/Multiple Endocrine Neoplasia 2A-related RET Mutations Not Affecting Codon 634

Phuong Nguyen Thanh, H. Dralle, B. Niederle, 2004, World Journal of Surgery.

Does a somatic deletion in RET clarify the sporadic nature of medullary thyroid carcinoma?

D. Marsh, O. Gimm, 2003, Journal of endocrinological investigation.

Riedel’s thyroiditis: impact and strategy of a challenging surgery

H. Holzhausen, K. Lorenz, H. Dralle, 2007, Langenbeck's Archives of Surgery.

Relationship Between RKIP Protein Expression and Clinical Staging in Thyroid Carcinoma

B. Trojanowicz, C. Sekulla, R. Finke, 2008 .

Primary hyperparathyroidism, C-cell hyperplasia and papillary thyroid carcinoma in a patient with RET germline polymorphism S836S

R. Hinze, H. Dralle, M. Brauckhoff, 2002, Langenbeck's Archives of Surgery.

pheochromocytomas and paragangliomas

P. Söderkvist, O. Gimm, J. Welander, 2011 .

Gene Expression of Parathyroid Tumors

P. Eilers, K. Furge, B. Teh, 2004, Cancer Research.

Distinct Expression of Galectin‐3 in Pheochromocytomas

H. Dralle, C. Hoang‐Vu, M. Brauckhoff, 2006, Annals of the New York Academy of Sciences.

Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas.

P. Reynolds, C. Eng, R. Hinze, 2001, The Journal of clinical endocrinology and metabolism.

FOXO3a: a novel player in thyroid carcinogenesis?

T. Aigner, K. Schmid, C. Weidinger, 2008, Endocrine-related cancer.

Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx

O. Gimm, 2004, Familial Cancer.

Limitations of Intraoperative Adrenal Remnant Volume Measurement in Patients Undergoing Subtotal Adrenalectomy

R. Spielmann, C. Sekulla, K. Lorenz, 2008, World Journal of Surgery.

CD82, and CD63 in thyroid cancer.

H. Holzhausen, J. Köhrle, B. Trojanowicz, 2004, International journal of molecular medicine.

Management of incidental gallbladder cancer in a national cohort

B. Andersson, O. Gimm, P. Sandström, 2019, The British journal of surgery.

Extrathyroidal manifestations of multiple endocrine neoplasia type 2.

M. Brauckhoff, O. Gimm, 2009, Thyroid : official journal of the American Thyroid Association.

Small-bowel endoscopy is crucial for diagnosis of melanoma metastases to the small bowel: a case of metachronous small-bowel metastases and review of the literature.

P. Helmbold, U. Bilkenroth, O. Gimm, 2007, Melanoma research.

X-chromosome variants are associated with aldosterone producing adenomas

T. Arnesen, P. Söderkvist, M. Larsson, 2021, Scientific Reports.

Current Primary Surgery of Thyroid Carcinoma

H. Dralle, O. Gimm, 1995 .

The expression of CD97EGF and its ligand CD55 on marginal epithelium is related to higher stage and depth of tumor invasion of gastric carcinomas.

R. Finke, C. Hoang‐Vu, O. Gimm, 2005, Oncology reports.

Clinical Spectrum of Primary Adrenal Lymphoma: Results of a Multicenter Cohort Study.

F. Beuschlein, C. Antke, M. Rudelius, 2020, European journal of endocrinology.

Germline Mutations in Non-syndromic Pheochromocytoma

J. Schipper, K. Zerres, C. Eng, 2004 .

Absence of the BRAF V600E mutation in pheochromocytoma

P. Söderkvist, C. Juhlin, A. Stenman, 2016, Journal of Endocrinological Investigation.

Adrenal and extra-adrenal pheochromocytomas in a family with germline RET V804L mutation.

C. Eng, O. Nilsson, H. Ahlman, 1999, JAMA.

Diagnosis and therapy of sporadic and familial medullary thyroid carcinoma

H. Dralle, O. Gimm, T. Sutter, 2001, Journal of Cancer Research and Clinical Oncology.

TFF3-based candidate gene discrimination of benign and malignant thyroid tumors in a region with borderline iodine deficiency.

M. Eszlinger, K. Krause, D. Fuhrer, 2008, The Journal of clinical endocrinology and metabolism.

Expression of CD97 and CD55 in human medullary thyroid carcinomas.

H. Dralle, C. Hoang‐Vu, T. Klonisch, 2004, International journal of oncology.

Characterisation of DEHAL1 expression in thyroid pathologies.

K. Schmid, A. Tannapfel, K. Krause, 2007, European journal of endocrinology.

Case report: A somatic mutation in CLCN2 identified in a sporadic aldosterone producing adenoma.

T. Arnesen, P. Söderkvist, M. Walz, 2019, European journal of endocrinology.

Over-representation of a germline variant in the gene encoding RET co-receptor GFRalpha-1 but not GFRalpha-2 or GFRalpha-3 in cases with sporadic medullary thyroid carcinoma.

L. Mulligan, C. Eng, R. Hinze, 2001, Oncogene.

syndromes Clinical presentation and penetrance of Pheochromocytoma/ Paraganglioma

K. Byth, X. Jeunemaître, J. Bertherat, 2005 .

Total Parathyroidectomy Without Autotransplantation for Renal Hyperparathyroidism: Experience with a qPTH-controlled Protocol

C. Sekulla, K. Lorenz, H. Dralle, 2006, World Journal of Surgery.

Medullary thyroid cancer — Reoperation

H. Dralle, O. Gimm, 2007, Acta Chirurgica Austriaca.

The Transcriptional Regulation of FOXO Genes in Thyrocytes

C. Weidinger, K. Krause, H. Dralle, 2016, Hormone and Metabolic Research.

Chapter 34 – Surgical Management of Advanced Thyroid Cancer Invading the Aerodigestive Tract

H. Dralle, A. Machens, M. Brauckhoff, 2005 .

Calcitonin kinetics in the early postoperative period of medullary thyroid carcinoma

H. Dralle, J. Ukkat, M. Brauckhoff, 2001, Langenbeck's Archives of Surgery.

["Physiological" and "neoplastic" C-cell hyperplasia of the thyroid. Morphologically and biologically distinct entities?].

R. Hinze, H. Holzhausen, H. Dralle, 2001, Der Pathologe.

Repeat mediastinal lymph-node dissection for palliation in advanced medullary thyroid carcinoma

H. Dralle, A. Machens, J. Ukkat, 1999, Langenbeck's Archives of Surgery.

Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas.

T. Arnesen, P. Söderkvist, M. Brauckhoff, 2014, Endocrine-related cancer.

Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas.

T. Arnesen, P. Söderkvist, M. Brauckhoff, 2014, Endocrine-related cancer.

Germline V804M Mutation in the RET Proto-oncogene in Two Apparently Sporadic Cases of MTC Presenting in the Seventh Decade of Life

C. Eng, R. Hinze, O. Gimm, 1999 .

pheochromocytomas and paragangliomas

P. Söderkvist, O. Gimm, J. Welander, 2011 .

Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas The NGS in PPGL ( NGSnPPGL ) Study Group

Benn, T. Dwight, H. Firth, 2016 .

Multiple Endocrine Neoplasia Type 4 (MEN 4)

N. Pellegata, O. Gimm, 2021, Endocrine Surgery Comprehensive Board Exam Guide.

Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.

D. Petillo, D. Marsh, H. Dralle, 2004, Human Genetics.

[Lymph node excision in thyroid carcinoma].

H. Dralle, O. Gimm, 1996, Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen.

Nuclear and mitochondrial DNA alterations in pheochromocytomas and paragangliomas and their potential treatment.

P. Söderkvist, O. Gimm, Mouna Tabebi, 2022, Endocrine-Related Cancer.

Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas.

P. Söderkvist, O. Gimm, J. Welander, 2011, Endocrine-related cancer.

65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma.

A. Tischler, W. Young, C. Eng, 2018, Endocrine-related cancer.

Domain landscapes of somatic NF1 mutations in pheochromocytoma and paraganglioma.

P. Söderkvist, F. Frikha, O. Gimm, 2023, Gene.

Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas.

T. Arnesen, P. Söderkvist, M. Brauckhoff, 2014, Endocrine-related cancer.

Genetics of primary hyperaldosteronism.

P. Söderkvist, O. Gimm, Ravi Kumar Dutta, 2016, Endocrine-related cancer.

CDC73/HRPT2 CpG island hypermethylation and mutation of 5'-untranslated sequence are uncommon mechanisms of silencing parafibromin in parathyroid tumors.

B. Teh, A. Gill, D. Marsh, 2010, Endocrine-related cancer.