Tür "info:eu-repo/semantics/article" Tıp Fakültesi için listeleme
Toplam kayıt 3962, listelenen: 81-100
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A Double-Blind, Placebo Controlled, Cross-Over Trial of Adjunctive Donepezil For Cognitive Impairment In Schizophrenia
(Oxford Univ Press, 2004)Although there have been several case reports suggesting the beneficial effect of acetylcholinesterase inhibitors in the cognitive deficits seen in schizophrenia, controlled studies have revealed contradictory results. The ... -
A European Organization for Research and Treatment of Cancer - International Antimicrobial Therapy Group Study of Secondary Infections in Febrile, Neutropenic Patients with Cancer
(Univ Chicago Press, 2005)Background. Neutropenic patients with cancer may develop several episodes of fever and infection during chemotherapy-induced myeloaplasia. Methods. To identify risk factors for secondary infectious episodes among patients ... -
A Fully Liquid Dtap-Ipv-Hb-Prp-T Hexavalent Vaccine for Primary and Booster Vaccination of Healthy Turkish Infants and Toddlers
(Tubitak Scientific & Technical Research Council Turkey, 2017)Background/aim: Immunogenicity and safety of a primary series of a fully liquid, hexavalent DTaP-IPV-HB-PRP-T vaccine given at 2, 3, and 4 months of age compared to licensed comparators and a DTaP-IPV-HB-PRP-T booster at ... -
A Gamma-Distribution Convolution Model of 99Mtc-Mibi Thyroid Time-Activity Curves
(2016)Background The convolution approach to thyroid time-activity curve (TAC) data fitting with a gamma distribution convolution (GDC) TAC model following bolus intravenous injection is presented and applied to 99mTc-MIBI data. ... -
A Gene for Congenital Generalized Lipodystrophy Maps to Human Chromosome 9Q34
(Endocrine Soc, 1999)Congenital generalized lipodystrophy (CGL, Berardinelli-Seip Syndrome, OMIM # 269700) is a rare autosomal recessive disorder characterized by near complete absence of adipose tissue from birth. Affected individuals have ... -
A Giant Short Arm Of No. 21 Chromosome In Mother Of 21/21 Translocation Mongol
(British Med Journal Publ Group, 1976) -
A Homologous Genetic Basis of the Murine Cpfl1 Mutant and Human Achromatopsia Linked to Mutations in the Pde6C Gene
(Natl Acad Sciences, 2009)Retinal cone photoreceptors mediate fine visual acuity, daylight vision, and color vision. Congenital hereditary conditions in which there is a lack of cone function in humans cause achromatopsia, an autosomal recessive ... -
A Hypokalemic Muscular Weakness After Licorice Ingestion: A Case Report
(2009)A 21-year-old male presented to the emergency department with the complaint of muscle weakness. The patient had used a powderized over-the-counter product named 'Tekumut' for 2 weeks to quit smoking. The granulated product ... -
A Large Turkish Kindred with Syndactyly Type-II (Synpolydactyly) .1. Field Investigation, Clinical and Pedigree Data
(British Med Journal Publ Group, 1995)A very large Turkish family with syndactyly type II (synpolydactyly (SPD)) is described, which originated from and is mainly concentrated in the village of Derbent, Afyon. The kindred consists of 425 subjects over seven ... -
A Large Turkish Kindred With Syndactyly Type-II (Synpolydactyly) .2. Homozygous Phenotype
(British Med Journal Publ Group, 1995)Syndactyly type II (synpolydactyly (SPD)) is an autosomal dominant condition with typical abnormalities of the distal parts of both upper and lower limbs. We report here a previously undescribed phenotypic feature of people ... -
A Logistic Regression Model Including Dna Status and Morphology of Spermatozoa for Prediction of Fertilization in Vitro
(Oxford Univ Press, 1998)To determine predictive values of routine semen analysis, sperm morphology evaluation using strict criteria and DNA status for in-vitro fertilization (IVF), 66 consecutive couples undergoing IVF in a university hospital ... -
A Model of Complaint Based for Overcrowding Emergency Department: Five-Level Hacettepe Emergency Triage System
(Turkish Assoc Trauma Emergency Surgery, 2013)BACKGROUND To compare ESI Five-Level Triage System with 5-Level Hacettepe Emergency Triage System (HETS), which was developed for Overcrowded EDs in our country. METHODS Over a period of six days, patients were assessed ... -
A Molecular and Clinical Study of Larsen Syndrome Caused by Mutations in FLNB
(BMJ, 2007)Background: Larsen syndrome is an autosomal dominant osteochondrodysplasia characterised by large-joint dislocations and craniofacial anomalies. Recently, Larsen syndrome was shown to be caused by missense mutations or ... -
A Molecular Genetic and Statistical Approach for the Diagnosis of Dual-Site Cancers
(Oxford Univ Press, 2004)Background: Concurrent tumors can be synchronous, independently derived, non-metastatic tumors or metastatic tumors. The prognosis and clinical management of patients with these different concurrent tumor types are different. ...