Ara
Toplam kayıt 379, listelenen: 121-140
Evaluation Of Apical Root Resorption Following Extraction Therapy In Subjects With Class I And Class Ii Malocclusions
(Oxford Univ Press, 1999)
The purpose of this study was to determine the amount of root resorption during orthodontic treatment, and to examine the relationship between tooth movement and apical root resorption. Twenty-seven Class I and 27 Class ...
Pelvic-Peritoneal Tuberculosis with Elevated Serum and Peritoneal-Fluid Ca-125 Levels - A Report of 2 Cases
(Karger, 1993)
We report 2 patients with pelvic-peritoneal tuberculosis and elevated serum and peritoneal fluid levels of Ca-125. The first was a young and infertile women who had cul-de-sac nodularity and dysmenorrhea. The other was ...
Müteferrika Matbaası’nın Düşündürdükleri ve Avrupa’da Basımcılığın Etkileri: Gelecek İçin Geçmişi Anlamak
(1998)
The existing developments in information technology have led to enormous changes concerning the entire humanity. A similar transformation took place in Europe soon after the invention of Gutenberg’s printing press in the ...
Altered Apoptotic Profiles in Irradiated Patients with Increased Toxicity
(Elsevier Science Inc, 1999)
Purpose: A retrospective study of radiation-induced apoptosis in CD4 and CD8 T-lymphocytes, from 12 cancer patients who displayed enhanced toxicity to radiation therapy and 9 ataxia telangiectasia patients, was performed ...
Alice in Wonderland Syndrome As An Initial Manifestation of Epstein-Barr Virus Infection
(British Med Journal Publ Group, 1992)
We present a patient with serologically confirmed Epstein-Barr virus (EBV) infection who had illusions of size, shape, and colour of objects but none of the typical symptoms and signs peculiar to infectious mononucleosis ...
Genetic Linkage Study Of Familial Mediterranean Fever (Fmf) To 16P13.3 And Evidence For Genetic Heterogeneity In The Turkish Population
(British Med Journal Publ Group, 1997)
Familial Mediterranean fever (FMF) is an autosomal recessive condition that is almost entirely restricted to the non-Askhenazi Jews, Arabs, Armenians, and Turks. Genetic linkage study of a large group of non-Turkish families ...
Kaposi Sarcoma In A Paediatric Renal Transplant Recipient
(Oxford Univ Press United Kingdom, 1996)
Cerebral Infarct Associated With Factor V Leiden Mutation In A Boy With Hemophilia A
(Wiley-Liss, 1997)
An 11-year-old boy with mild hemophilia A was admitted to our hospital because of focal convulsions, Magnetic resonance imaging showed an old occipital infarct. Protein C, S, antithrombin ill, anticardiolipin antibodies ...
Factor V Q 506 Mutation In Children With Thrombosis
(Wiley-Liss, 1996)
The factor V Leiden mutation in 12-children with thrombosis and in 20 controls was investigated, Five heterozygous individuals and 1 homozygous individual among the cases with thrombosis and 1 heterozygous individual among ...
Heterogeneous Spectrum Of Mutations In The Fanconi Anaemia Group A Gene
(Stockton Press, 1999)
Fanconi anaemia (FA) is a genetically heterogeneous autosomal recessive disorder associated with chromosomal fragility, bone-marrow failure, congenital abnormalities and cancer. The gene for complementation group A (FAA), ...
Effect of Formoterol on Clinical Parameters and Lung Functions in Patients With Bronchial Asthma: A Randomised Controlled Trial
(British Med Journal Publ Group, 1999)
Aims-To determine the role of formoterol in the treatment of children with bronchial asthma who are symptomatic despite regular use of inhaled corticosteroids. Methods-A randomised, double blind, parallel group, placebo ...