نتایج جستجو برای: genetic disease

تعداد نتایج: 1987847  

Journal: :Journal of Clinical Pathology 1978

Journal: :Nucleic Acids Research 2010

Faezeh Sadeghi Mohammad Amin Kerachian,

Autosomal dominant polycystic kidney disease (ADPKD) is the most common form of inherited kidney disease that results in renal failure. PKD currently has no causative therapy. However, some treatment options are available, ranging from symptomatic therapy to delaying the onset of end-stage renal failure. Early diagnosis of adult polycystic kidney disease is vital in order to prevent its complic...

Journal: :international journal of pediatrics 0
manoochehr karjoo pediatrician and gastroenterologist upstate medical university, syracuse new york usa.

celiac disease also known as gluten-sensitive enteropathy is characterized by intestinal mucosal damage and malabsorption from dietary intake of wheat, rye or barley. symptoms may appear with introduction of cereal in the first 3 years of life. a second peak in symptoms occurs in adults during the third or forth decade and even as late as eight decade of life. the prevalence of this disease is ...

Alzheimer's disease (AD) is the most common form of neurodegenerative disorders. Memory loss in an alert person and impairment in the function of language, attention, perception, judgment or problem solving can occur in patients with AD. However, there are some medications in order to delay the debilitating aspects of the disease; but unfortunately, scientists could not found approaches to cure...

یزدان پناه , پرویز,

The familial spastic paraplegia (FSP) is a heterogeneous group of motor neuron disorders characterized by slow progressive weakness and spasticity of lower limbs. The disorder can appear at any age, but it usually occurs in childhood or early adult life. The genetic pattern of this disease is mainly autosomal dominant trait, but occasionally as an autosomal recessive trait, and very rarely as...

Journal: :genetics in the 3rd millennium 0
حسین کلانی hossein kalanie استاد بیماری های مغز و اعصاب زهرا حسین زاده zahra hosseinzadeh کوروش قره گوزلی kurosh gharagozli امیر رضا کلانی amir reza kalanie مینا کم گویان mina kamgooyan مرجان شکیبا marjan shakiba

multiple sclerosis (ms) is a demyelinating disease of the central nervous system, with unknown etiology in which both genetic and environmental factors are thought to be involved. the human leukocyte antigen (hla) system provides a set of genetic markers which lend themselves to systematic study. in iran, hla-a24, hla-dr2, and hla- dr15 are significantly increased in ms patients. the disease al...

Avin Aghamiri Rahim Mehrabi, Reza Talebi,

Background: The tan spot disease of wheat caused by Pyrenophera tritici-repentis has become a major disease in most wheat growing areas worldwide. Objectives: Here we used ISSR and RAPD markers to study the genetic diversity of 34 P. tritici-repentis isolates collected from North of Iran. Materials and Methods: The leaves having the typical symptoms of tan spot disease were collected and after...

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