4.2 Article

Mutation screening in a Norwegian cohort with pheochromocytoma

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Review Surgery

Malignant pheochromocytomas and paragangliomas: a diagnostic challenge

Oliver Gimm et al.

LANGENBECKS ARCHIVES OF SURGERY (2012)

Article Endocrinology & Metabolism

SDHA Immunohistochemistry Detects Germline SDHA Gene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas

Esther Korpershoek et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2011)

Article Genetics & Heredity

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Inaki Comino-Mendez et al.

NATURE GENETICS (2011)

Article Endocrinology & Metabolism

Genetics of pheochromocytomas and paragangliomas

Giuseppe Opocher et al.

BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM (2010)

Article Medicine, General & Internal

Spectrum and Prevalence of FP/TMEM127 Gene Mutations in Pheochromocytomas and Paragangliomas

Li Yao et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2010)

Article Oncology

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

Jean-Pierre Bayley et al.

LANCET ONCOLOGY (2010)

Article Endocrinology & Metabolism

Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation

Mariola Peczkowska et al.

NATURE CLINICAL PRACTICE ENDOCRINOLOGY & METABOLISM (2008)

Article Endocrinology & Metabolism

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

Birke Bausch et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2007)

Review Endocrinology & Metabolism

Pheochromocytoma: recommendations for clinical practice from the First International Symposium

Karel Pacak et al.

NATURE CLINICAL PRACTICE ENDOCRINOLOGY & METABOLISM (2007)

Article Endocrinology & Metabolism

Phaeochromocytoma, new genes and screening strategies

Anne-Paule Gimenez-Roqueplo et al.

CLINICAL ENDOCRINOLOGY (2006)

Review Genetics & Heredity

Current concepts in RET-related genetics, signaling and therapeutics

Ivan Plaza-Menacho et al.

TRENDS IN GENETICS (2006)

Article Genetics & Heredity

Comprehensive NF1 screening on cultured Schwann cells from neurofibromas

Ophelia Maertens et al.

HUMAN MUTATION (2006)

Article Endocrinology & Metabolism

Adrenal incidentaloma -: follow-up results from a Swedish prospective study

B Bülow et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY (2006)

Article Endocrinology & Metabolism

Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2

A Machens et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2005)

Letter Oncology

G12S and H50R variations are polymorphisms in the SDHD gene

A Cascón et al.

GENES CHROMOSOMES & CANCER (2003)

Letter Oncology

Untitled

J Lima et al.

GENES CHROMOSOMES & CANCER (2003)

Article Medicine, General & Internal

Germ-line mutations in nonsyndromic pheochromocytoma.

HPH Neumann et al.

NEW ENGLAND JOURNAL OF MEDICINE (2002)

Article Biochemistry & Molecular Biology

von Hippel-Lindau protein mutants linked to type 2C VHL disease preserve the ability to downregulate HIF

MA Hoffman et al.

HUMAN MOLECULAR GENETICS (2001)

Article Genetics & Heredity

Mutations in SDHC cause autosomal dominant paraganglioma, type 3

S Niemann et al.

NATURE GENETICS (2000)