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Toplam kayıt 72, listelenen: 21-30
Age-Related Changes in Human Tendo Calcaneus Collagen Fibrils
(Saudi Med J, 2005)
Objectives: The ruptures of tendo calcaneus often occur between the age of 30 - 45 years as described by several textbooks. It is also described that some diseases and drugs are said to be responsible in the etiology; ...
Scanning Electron Microscopic Observation Of The Brown Tumor Of The Head Of Mandible
(Saudi Med J, 2005)
Brown tumors are tumor-like, expansile osteolytic lesions of bone which are seen in both primary and secondary hyperparathyroidism. They generally resolve after surgical treatment of the parathyroid adenoma. Here, we report ...
Removal of Hydrosalpinges Increases Endometrial Leukaemia Inhibitory Factor (Lif) Expression At The Time of The Implantation Window
(Oxford Univ Press, 2005)
BACKGROUND: The presence of hydrosalpinges is associated with lower implantation and pregnancy rates in women undergoing IVF-embryo transfer, while salpingectomy improves these parameters. Although the mechanism by which ...
Functional Capacity In Severe Chronic Obstructive Pulmonary Disease
(Saudi Med J, 2005)
Objective: To investigate the functional capacity in patients with severe chronic obstructive pulmonary disease (COPD) and healthy subjects. Methods: The present study was conducted in the School of Physical Therapy and ...
Extensive Scanning Of The Calpain-3 Gene Broadens The Spectrum Of Lgmd2A Phenotypes
(B M J Publishing Group, 2005)
Background: The limb girdle muscular dystrophies ( LGMD) are a heterogeneous group of Mendelian disorders highlighted by weakness of the pelvic and shoulder girdle muscles. Seventeen autosomal loci have been so far identified ...
High Cystine In Platelets From Patients With Nephropathic Cystinosis: A Chemical, Ultrastructural, And Functional Evaluation
(B M J Publishing Group, 2005)
Aim: To investigate the morphology and function of platelets in nephropathic cystinosis (NC). Methods: Seven patients ( mean age, 6.5 years; SD, 20 months) with NC were investigated. Their platelets were examined by ...
Genotype-Phenotype Analysis Of Human Frontoparietal Polymicrogyria Syndromes
(Wiley, 2005)
Human cerebral cortical polymicrogyria is a heterogeneous disorder, with only one known gene (GPR56) associated with an apparently distinctive phenotype, termed bilateral frontoparietal polymicrogyria (BFPP). To define the ...