B. Bausch

发表

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.

Clinical decision making in small non-functioning VHL-related incidentalomas

C. Bode, T. Krauss, H. Neumann, 2020, Endocrine connections.

with Pheochromocytoma and Neurofibromatosis Type 1 Mutational Spectra and Loss-of-Heterozygosity Analyses in Patients NF1 Germline

A. Fassina, V. Mautner, S. Calvieri, 2007 .

Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1.

G. Arnaldi, C. Eng, A. Fassina, 2007, The Journal of clinical endocrinology and metabolism.

Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytoma.

C. Eng, M. Fassnacht, H. Neumann, 2006, The Journal of clinical endocrinology and metabolism.

A registry-based study of thyroid paraganglioma: histological and genetic characteristics.

L. Akslen, C. Eng, A. Fassina, 2015, Endocrine-related cancer.

SDHD mutations in carotid body tumors and pheochromocytomas: paraganglioma syndrome type 1

H. Neumann, D. Berger, S. Hoegerle, 2003 .

Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention

C. Larsson, C. Eng, P. Söderkvist, 2017, JAMA oncology.

Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene.

C. Eng, F. Forrer, H. Neumann, 2005, JAMA.

Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma.

H. Neumann, W. Borozdin, B. Bausch, 2006, The New England journal of medicine.

Mutations of the SDHB and SDHD genes

H. Neumann, Christian Pawlu, B. Bausch, 2004, Familial Cancer.

Genetic and Clinical Investigation of Pheochromocytoma

C. Eng, H. Neumann, A. Januszewicz, 2006, Annals of the New York Academy of Sciences.

Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy

W. Young, C. Eng, T. Krauss, 2019, JAMA network open.

Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study.

A. Tabarin, E. Baudin, C. Eng, 2019, The lancet. Diabetes & endocrinology.

The penetrance of MEN2 pheochromocytoma is not only determined by RET mutations.

T. Zelinka, C. Eng, H. Neumann, 2017, Endocrine-related cancer.

Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study.

T. Zelinka, C. Eng, J. Plukker, 2014, The Lancet. Oncology.

Minimally Invasive Surgery (MIS) in Children and Adolescents with Pheochromocytomas and Retroperitoneal Paragangliomas: Experiences in 42 Patients

H. Neumann, M. Walz, H. Groeben, 2018, World Journal of Surgery.

Evaluation of Laboratory and Sonographic Parameters for Detection of Portal Hypertension in Patients with Common Variable Immunodeficiency

M. Karsdal, D. Schuppan, D. Bettinger, 2022, Journal of Clinical Immunology.

Current Diagnostic and Therapeutic Strategies in Treatment of CNS Hemangioblastomas in Patients with VHL

C. Jilg, M. T. Krüger, S. Gläsker, 2014 .

Genetic testing for pheochromocytoma-associated syndromes.

H. Neumann, N. Reisch, Christian Pawlu, 2005, Annales d'endocrinologie.

Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment

H. Urbach, J. Beck, C. Jilg, 2020, Child's Nervous System.

Characterization of endolymphatic sac tumors and von Hippel–Lindau disease in the International Endolymphatic Sac Tumor Registry

S. Richard, C. Eng, T. Krauss, 2016, Head & neck.

Malignant Head and Neck Paragangliomas in SDHB Mutation Carriers

H. Neumann, J. Schipper, C. Boedeker, 2007, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Somatic deletion of the NF1 gene in a neurofibromatosis type 1-associated malignant melanoma demonstrated by digital PCR

A. Nikkels, A. Rübben, B. Bausch, 2006, Molecular Cancer.

Germ-line mutations in nonsyndromic pheochromocytoma.

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

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.

C. Eng, T. Bley, H. Neumann, 2004, JAMA.

Renal cancer in von Hippel–Lindau disease and related syndromes

A. Vortmeyer, C. Eng, C. Jilg, 2013, Nature Reviews Nephrology.

Alu‐Alu recombination underlies the vast majority of large VHL germline deletions: Molecular characterization and genotype–phenotype correlations in VHL patients

H. Neumann, G. Scherer, J. Kohlhase, 2009, Human mutation.

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

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

Long-term prognosis of patients with pediatric pheochromocytoma.

C. Eng, K. Schmid, K. Rácz, 2013, Endocrine-related cancer.

Pheochromocytoma and NF1

H. Neumann, B. Bausch, 2012 .

Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma–paraganglioma

P. Devilee, H. Neumann, D. Ascher, 2019, Journal of Medical Genetics.

Max Schottelius: Pioneer in Pheochromocytoma

A. Tischler, C. Eng, K. Schmid, 2017, Journal of the Endocrine Society.

Evidence of MEN-2 in the original description of classic pheochromocytoma.

A. Vortmeyer, C. Eng, H. Neumann, 2007, The New England journal of medicine.

Therapy Algorithm for Portal Vein Thrombosis in Liver Cirrhosis: The Internist's Point of View

M. Rössle, C. Klinger, B. Bausch, 2014, Visceral Medicine.

Germline Mutations in Non-syndromic Pheochromocytoma

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

von Hippel-Lindau Disease Associated Pancreatic Neuroendocrine Tumors – Molecular Genetics and Clinical Aspects

K. Rácz, A. Patócs, G. Weryha, 2014 .

Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions

K. Huoponen, M. Pöyhönen, C. Saloranta, 2007, Genetics in Medicine.

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.