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Toplam kayıt 5759, listelenen: 61-80
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A Case Of Disseminated Hypopigmented Keratoses Improved With Oral Acitretin
(2017)Disseminated hypopigmented keratosis is a distinct clinical entity and only few cases have been reported so far. Here, we present a 21-year-old man with almost 10-year history of hypopigmented, nonfollicular, keratotic ... -
A Case Of Erythema Multiforme Associated With Pustules: Coexistence Of Erythema Multiforme Minor And Acute Generalized Exanthamatous Pustulosis
(2019)Adverse cutaneous drug reactions (ACDRs) can mimic a variety of dermatologic diseases, causing confusion and additional work-up for differential diagnoses. In this report, a case who admitted with non-follicular pustules ... -
A Case of Extensive Wound Myiasis Caused By Lucilia Sericata (Diptera: Calliphoridae) in a Patient with Maxillary Sinus Squamous Cell Carcinoma, in Turkey
(Iranian Scientific Society Medical Entomology, 2016)The larvae causing myiasis can lead extensive tissue destruction, invasion into deep tissues and secondary infections. Poor hygiene, low socioeconomic condition and presence of open wounds are the most important predisposing ... -
A Case of Intracranial Hypotension Complicated with Hydrocephalus
(Turkish Neurosurgical Soc, 2010)AIM: Intracranial hypotension may have variable clinical presentation. The imaging characteristics of intracranial hypotension are especially well depicted on magnetic resonance imaging studies. Although the clinical and ... -
A Case of Kaposi's Sarcoma Following Treatment of Membranoproliferative Glomerulonephritis and a Review of the Literature
(Taylor & Francis Ltd, 2007)Kaposi's sarcoma (KS) is an unusual tumor principally affecting the skin of the lower extremities. Although the association between KS and renal transplant has been well documented, there are a few KS cases in the literature ... -
A Case Of Multifocal Skin Metastases From Lung Cancer Presenting With Vasculitic-Type Cutaneous Nodule
(2015)Although cutaneous metastasis occurs usually at the terminal stage of the disease, it may be rarely concurrent with the diagnosis and may also present as the first sign of the illness. A 55-year-old male patient presented ... -
A Case of Sporotrichoid Cutaneous Leishmaniasis
(Turkish Soc Dermatology Venerology, 2011)Cutaneous leishmaniasis is one of the most important travel diseases in the world and one of the most common vector-mediated diseases with a wide clinical spectrum and is caused by parasites belonging to the genus Leishmania. ... -
A Case Of Tuberculous Meningitis With Paradoxical Response In A 14-Year-Old Boy
(2016)A clinical or radiological worsening of already existing lesions or an emergence of new lesions after beginning treatment in patients with tuberculosis (TB) is referred to as the paradoxical response. This has aroused ... -
A Case Report of Thrombocytopenia-associated Multiple Organ Failure Secondary to Salmonella enterica Serotype Typhi Infection in a Pediatric Patient: Successful Treatment With Plasma Exchange
(2010)A high proportion of the patients with Salmonella enterica serotype Typhi infection develop severe sepsis. The mortality rate is high despite aggressive antimicrobial therapy in these patients. The case of a 10-year-old boy ... -
A Classification of Hemolytic Uremic Syndrome and Thrombotic Thrombocytopenic Purpura and Related Disorders
(Elsevier Science Inc, 2006)The diagnostic terms hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP) are based on historical and overlapping clinical descriptions. Advances in understanding some of the causes of the syndrome ... -
A Clinical Comparison of Etomidate-Lipuro, Propofol and Admixture at Induction
(2011)Objective: The purpose of this study was to compare etomidate-lipuro and propofol and 50%, (1:1) admixture of these agents at induction with special reference to injection pain, hemodynamic changes, and myoclonus. Methods: ... -
A Clinical Trial of Gene Therapy For Mucopolysaccharidosis Vi, A Severe Lysosomal Storage Disorder (Meusix)
(Mary Ann Liebert, Inc, 2015) -
A Clinically Variant Fibrosis Syndrome In A Turkish Family Maps To The Cfeom1 Locus On Chromosome 12
(Amer Medical Assoc, 2000)Objectives: To describe the phenotype of a Turkish family with variably expressed congenital fibrosis of the extraocular muscles (CFEOM), and to determine the genetic location of their disorder. Methods: Participants were ...