Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas.

[1]  R. Ramos,et al.  Mutation of SDHB is a Cause of Hypoxia-Related High-Altitude Paraganglioma , 2010, Clinical Cancer Research.

[2]  A. Chou,et al.  Immunohistochemistry for SDHB triages genetic testing of SDHB, SDHC, and SDHD in paraganglioma-pheochromocytoma syndromes. , 2010, Human pathology.

[3]  Steven P. Gygi,et al.  SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma , 2009, Science.

[4]  E. van Marck,et al.  An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis. , 2009, The Lancet. Oncology.

[5]  C. Stratakis,et al.  SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma–paraganglioma syndromes , 2009, Journal of internal medicine.

[6]  K. Pacak,et al.  Clinical aspects of SDHx-related pheochromocytoma and paraganglioma. , 2009, Endocrine-related cancer.

[7]  M. Weiss,et al.  Chromosomal changes in sporadic and familial head and neck paragangliomas , 2009, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

[8]  O. Haas,et al.  Novel SDHD germ‐line mutations in pheochromocytoma patients , 2007, European journal of clinical investigation.

[9]  R. Ma,et al.  A Chinese family with familial paraganglioma syndrome due to succinate dehydrogenase deficiency. , 2007, Hong Kong medical journal = Xianggang yi xue za zhi.

[10]  Peter Devilee,et al.  The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency , 2005, BMC Medical Genetics.

[11]  M. Mascalchi,et al.  Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109X , 2005, Journal of Medical Genetics.

[12]  J. Netterville,et al.  Paragangliomas of the head and neck. , 2004, Oral oncology.

[13]  K. Sotlar,et al.  Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. , 2004, Cancer genetics and cytogenetics.

[14]  P. Taschner,et al.  Hereditary Paraganglioma Due to the SDHD M1I Mutation in a Second Chinese Family: A Founder Effect? , 2003, The Laryngoscope.

[15]  W. Dinjens,et al.  Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma. , 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.

[16]  E S Husebye,et al.  Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. , 2001, American journal of human genetics.

[17]  P. Schofield,et al.  Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss , 2001, Genes, chromosomes & cancer.

[18]  P. Devilee,et al.  Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene , 2001, Genes, chromosomes & cancer.

[19]  Ulrich Müller,et al.  Mutations in SDHC cause autosomal dominant paraganglioma, type 3 , 2000, Nature Genetics.

[20]  B. Devlin,et al.  Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. , 2000, Science.