Now showing items 1-10 of 131
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
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
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 ...
Fish Studies In 45 Patients With Rubinstein-Taybi Syndrome: Deletions Associated With Polysplenia, Hypoplastic Left Heart And Death In Infancy
(Nature Publishing Group, 1999)
Rubinstein-Taybi syndrome (RTS) is a dominant Mendelian disorder characterised by mental retardation, a typical facies, broad thumbs and short stature. Previous reports indicated that 4-25% of RTS patients have a submicroscopic ...