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Toplam kayıt 29, listelenen: 1-10
Do Experimentally Induced Ipsilateral Testicular Torsion, Vas Deferens Obstruction, Intra-Abdominal Testis or Venous Obstruction Damage the Contralateral Testis Through a Common Mechanism?
(Blackwell Science Ltd, 2000)
Objective To evaluate if various conditions affecting the ipsilateral testis which also damage the contralateral testis share a common pathway for their effects. Materials and methods The study comprised five groups of 10 ...
Dysplastic Changes in Idiopathic Thrombocytopenic Purpura and The Effect of Corticosteroids to Increase Dysplasia and Cause Hyperdiploid Macropolycytes
(Wiley-Liss, 2000)
This study evaluates the dysplastic hematological changes in nine patients with idiopathic thrombocytopenic purpura (ITP) in 11 attacks, before and after corticosteroid treatment. The pretreatment blood smears of patients ...
Intracranial Ependymomas in Childhood - A Retrospective Review of Sixty-Two Children
(Scandinavian University Press, 2000)
Of the 818 tumours of the central nervous system diagnosed between 1972 and 1991, 62 patients (35 males and 27 females) with histopathologically confirmed ependymomas were treated and followed-up at the Children's Hospital ...
Familial Mediterranean Fever In The 'Chuetas' Of Mallorca: A Question Of Jewish Origin Or Genetic Heterogeneity
(Nature Publishing Group, 2000)
Familial Mediterranean fever (FMF) is a hereditary disease commonly found among Jews, Armenians, Turks and Arabs. Recently, FMF was found in the 'Chuetas', a unique community on the island of Mallorca (Spain). To address ...
Giant Axonal Neuropathy Locus Refinement To A < 590 Kb Critical Interval
(Nature Publishing Group, 2000)
Giant axonal neuropathy (GAN) is a rare autosomal recessive neurodegenerative disorder, characterised clinically by the development of chronic distal polyneuropathy during childhood, mental retardation, kinky or curly hair, ...
The Novel Genetic Disorder Microhydranencephaly Maps To Chromosome 16P13.3-12.1
(Univ Chicago Press, 2000)
We studied a large consanguineous Anatolian family with children who exhibited hydranencephaly associated with microcephaly. The children were severely affected. This novel genetic disorder is autosomal recessive. We used ...
Two New Loci For Autosomal Recessive Ichthyosis On Chromosomes 3P21 And 19P12-Q12 And Evidence For Further Genetic Heterogeneity
(Univ Chicago Press, 2000)
Autosomal recessive ichthyosis (ARI) includes a heterogeneous group of disorders of keratinization characterized by desquamation over the whole body. Two forms largely limited to the skin have been defined: lamellar ...
Residual Type 1 Immunity In Patients Genetically Deficient For Interleukin 12 Receptor Β1 (Il-12Rβ1):Evidence for an IL-12Rb1–independent Pathway of IL-12 Responsiveness in Human T Cells
(2000)
Genetic lack of interleukin 12 receptor β1 (IL-12Rβ1) surface expression predisposes to severe infections by poorly pathogenic mycobacteria or Salmonella and causes strongly decreased, but not completely abrogated, interferon ...
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 ...
Selectin Adhesion Molecules in Behcet's Disease
(Bmj Publishing Group, 2000)
Objectives-The pathogenesis of Behcet's disease (BD) is closely related to endothelial cells, leucocyte functions and autoimmunity. The aim of this study was to investigate circulating selectin adhesion molecules, which ...