B E Baysal
Overview
Explore the profile of B E Baysal including associated specialties, affiliations and a list of published articles.
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Articles
21
Citations
1073
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0
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Recent Articles
1.
Baysal B
J Med Genet
. 2008 Nov;
45(11):689-94.
PMID: 18978332
Hereditary paraganglioma (PGL) is characterised by genetic predisposition to the development of highly vascular tumours of the paraganglionic tissues and caused by germ line inactivating mutations in the SDHB, SDHC...
2.
Baysal B, Willett-Brozick J, Filho P, Lawrence E, Myers E, Ferrell R
J Med Genet
. 2004 Sep;
41(9):703-9.
PMID: 15342702
No abstract available.
3.
Baysal B
J Med Genet
. 2002 Sep;
39(9):617-22.
PMID: 12205103
Paragangliomas are highly vascularised and often heritable tumours derived from paraganglia, a diffuse neuroendocrine system dispersed from skull base to the pelvic floor. The carotid body, a small oxygen sensing...
4.
Baysal B, Willett-Brozick J, Lawrence E, Drovdlic C, Savul S, McLeod D, et al.
J Med Genet
. 2002 Mar;
39(3):178-83.
PMID: 11897817
Background: Paragangliomas are rare and highly heritable tumours of neuroectodermal origin that often develop in the head and neck region. Germline mutations in the mitochondrial complex II genes, SDHB, SDHC,...
5.
Drovdlic C, Myers E, Peters J, Baysal B, Brackmann D, Slattery 3rd W, et al.
Laryngoscope
. 2002 Jan;
111(10):1822-7.
PMID: 11801952
Objective/hypothesis: To determine the heritable proportion of paraganglioma (PGL) and identify clinical features associated with heritable PGL. Study Design: Patients diagnosed with head and neck PGLs, identified retrospectively through clinical...
6.
Baysal B, Rubinstein W, Taschner P
J Mol Med (Berl)
. 2001 Nov;
79(9):495-503.
PMID: 11692162
This review presents our current knowledge on the genetic and phenotypic aspects of mitochondrial complex II gene defects. The mutations of the complex II subunits cause two strikingly different group...
7.
Baysal B
Otolaryngol Clin North Am
. 2001 Sep;
34(5):863-79, vi.
PMID: 11557444
Genetic studies of hereditary paraganglioma tumors could increase the understanding of the biology of these fascinating tumors, with important clinical implications for diagnosis and treatment. This article focuses on the...
8.
Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation
Willett-Brozick J, Savul S, Richey L, Baysal B
Hum Genet
. 2001 Aug;
109(2):216-23.
PMID: 11511928
Constitutional chromosomal translocations are relatively common causes of human morbidity, yet the DNA double-strand break (DSB) repair mechanisms that generate them are incompletely understood. We cloned, sequenced and analyzed the...
9.
Taschner P, Jansen J, Baysal B, Bosch A, Rosenberg E, Brocker-Vriends A, et al.
Genes Chromosomes Cancer
. 2001 Jun;
31(3):274-81.
PMID: 11391798
Hereditary paragangliomas or glomus tumors are usually benign slow-growing tumors in the head and neck region. The inheritance pattern of hereditary paraganglioma is autosomal dominant with imprinting. Recently, we have...
10.
Badenhop R, Cherian S, Lord R, Baysal B, Taschner P, Schofield P
Genes Chromosomes Cancer
. 2001 Jun;
31(3):255-63.
PMID: 11391796
Paraganglioma (PGL) is a rare disorder characterized by tumors of the head and neck region. Between 10% and 50% of cases of PGL are familial, and the disease is autosomal...