Search Results - "ARSEVEN, O"
-
1
The frequency of deep venous thrombosis and pulmonary embolus in acute exacerbation of chronic obstructive pulmonary disease
Published in Respiratory medicine (01-07-2002)“…Infection, pulmonary embolism caused by mostly deep venous thrombosis (DVT), hypoxaemia and drugs, used in the treatment of chronic obstructive pulmonary…”
Get full text
Journal Article -
2
Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene
Published in The journal of clinical endocrinology and metabolism (1999)“…Pendred's syndrome is an autosomal recessive disease characterized by goiter, impaired iodide organification, and congenital sensorineural deafness. The gene…”
Get full text
Journal Article -
3
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
Published in European journal of endocrinology (01-06-2001)“…The autosomal recessive Pendred's syndrome is defined by congenital sensorineural deafness, goiter, and impaired iodide organification. It is caused by…”
Get full text
Journal Article -
4
Evaluation of undergraduate training on tuberculosis at Istanbul Medical School
Published in The international journal of tuberculosis and lung disease (01-02-2003)“…SETTING: Undergraduate training on tuberculosis at Istanbul Medical School.OBJECTIVE: To assess whether tuberculosis-related questions asked in chest medicine…”
Get full text
Journal Article -
5
Impact of Promising Biomarkers on Severity and Outcome of Acute Pulmonary Embolism
Published in International journal of general medicine (31-08-2023)“…Acute pulmonary embolism (APE) is a common clinical condition. Its severity ranges from asymptomatic radiological findings to fatal obstructive shock. The…”
Get full text
Journal Article -
6
Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil
Published in Thyroid (New York, N.Y.) (01-11-1999)“…Constitutively activating mutations in the thyrotropin (TSH) receptor have been identified as a major molecular cause of hyperfunctioning thyroid adenomas. A…”
Get more information
Journal Article -
7
-
8
Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia
Published in Thyroid (New York, N.Y.) (01-06-1999)“…Sporadic congenital hypothyroidism is most commonly caused by developmental abnormalities of the thyroid gland. More rarely, it is due to defects in gene…”
Get more information
Journal Article -
9
Determination of the Etiological Organism During Acute Exacerbations of COPD and Efficacy of Azithromycin, Ampicillin-Sulbactam, Ciprofloxacin and Cefaclor
Published in Journal of chemotherapy (1999)“…Acute exacerbations, most of which are due to lower respiratory tract infections, cause great morbidity and mortality in patients with chronic obstructive…”
Get full text
Journal Article Conference Proceeding -
10
Pulmonary arteriovenous malformation diagnosed with radionuclide angiography
Published in Clinical nuclear medicine (01-12-1995)Get more information
Journal Article -
11
Bilateral facial paralysis secondary to lymphoma
Published in O.R.L. Journal for oto-rhino-laryngology and its related specialties (01-03-1993)“…We report a patient with bilateral facial palsy due to a non-Hodgkin lymphoma. He was initially diagnosed to have a facial paralysis of unknown aetiology…”
Get more information
Journal Article -
12
Insertion/deletion polymorphism of the angiotensin-converting enzyme gene: really a risk factor for venous thromboembolism?
Published in Thrombosis and haemostasis (01-11-2003)Get more information
Journal Article -
13
Substitutions of tyrosine 601 in the human thyrotropin receptor result in increase or loss of basal activation of the cyclic adenosine monophosphate pathway and disrupt coupling to Gq/11
Published in Thyroid (New York, N.Y.) (01-01-2000)“…Constitutively activating mutations of the thyrotropin (TSH) receptor have been identified as a molecular cause of toxic adenomas, nonautoimmune familial…”
Get more information
Journal Article -
14
The thyroid hormone receptor variant alpha2 is a weak antagonist because it is deficient in interactions with nuclear receptor corepressors
Published in Endocrinology (Philadelphia) (01-05-1998)“…The thyroid hormone receptor splice variant, alpha2, is unable to bind thyroid hormone (T3) and has been proposed to function as an endogenous inhibitor of T3…”
Get full text
Journal Article -
15
Phenocopies for Deafness and Goiter Development in a Large Inbred Brazilian Kindred with Pendred’s Syndrome Associated with a Novel Mutation in the PDS Gene1
Published in The journal of clinical endocrinology and metabolism (01-01-1999)“…Pendred’s syndrome is an autosomal recessive disease characterized by goiter, impaired iodide organification, and congenital sensorineural deafness. The gene…”
Get full text
Journal Article -
16
-
17
Proteolysis of the Mismatch Repair Protein MLH1 by Caspase-3 Promotes DNA Damage-induced Apoptosis
Published in The Journal of biological chemistry (25-06-2004)“…Caspases are critical proapoptotic proteases that execute cell death signals by selectively cleaving proteins at Asp residues to alter their function. Caspases…”
Get full text
Journal Article -
18
Determination of the etiological organism during acute exacerbations of COPD and efficacy of azithromycin, ampicillin-sulbactam, ciprofloxacin and cefaclor. Turkish Thoracic Society COPD Working Group
Published in Journal of chemotherapy (Florence) (01-06-1999)“…Acute exacerbations, most of which are due to lower respiratory tract infections, cause great morbidity and mortality in patients with chronic obstructive…”
Get full text
Journal Article -
19
Cloning of the cat TSH receptor and evidence against an autoimmune etiology of feline hyperthyroidism
Published in Endocrinology (Philadelphia) (01-02-2002)“…Cats are the only nonhuman mammalian species with a high incidence of hyperthyroidism, and a better understanding of the pathogenesis of feline hyperthyroidism…”
Get full text
Journal Article -
20
Exogenous allergic alveolitis caused by mouldy hazel nut leaves
Published in Pneumologie (Stuttgart, Germany) (01-01-1992)“…A 62-year old farmer woman from the northeastern, very rainy part of Turkey has been collecting large amounts of green and brown involucral hazel-nut leaves…”
Get more information
Journal Article