It's ALL in the diagnosis.
نویسنده
چکیده
The molecular diagnosis of human cancer will hasten the development of treatments tailored to the abnormalities present in each patient's tumor cells. Recent gene expression profiling studies of pediatric acute lymphoblastic leukemia (ALL) suggest that the molecular diagnosis of these diseases is right around the corner.
منابع مشابه
Children\'s Deafness
This is an article about children's deafness, it's ethiology, diagnosis, treatment, and educational treatment. Here I have given a brief account about the deafness itself and it's individual and social complications, also it's impression on the psychological well baing of the child. Then I have discussed, rather in detail, the ethiology of .children's deafness and I have given some statistic...
متن کاملdesign and evaluation PCR primer for type 1 tyrosinemia patient from yasuj
Tyrosinemia is a rare autosomal recessive genetic disease caused by fumarylacetoacetate hydrolase deficiency. 40 different mutation have been recognized related to Tyrosinemia that could be found in all extend of the gene with higher frequency from exon 8 to 14. Because of the size of FAH gene it's impossible to Sequence whole length of the gene by one round of sequencing reaction. Aim of this ...
متن کاملP 3: The Study about MRI Images of Encephalitis and Diagnosis by Using the Software Ways
Introduction: Encephalitis is inflammation of the brain. Viral infections are the most common cause of the condition .Encephalitis can cause flu-like symptoms, such as a fever or severe headache. It can also cause confused thinking, seizures, or problems with senses or movement. However, many cases of encephalitis result in only mild flu-like symptoms or even no symptoms. It's important to get ...
متن کاملگزارش یک مورد سندروم نادر Susac از بخش نورولوژی بیمارستان امام خمینی، سال 1378
This syndrome is a very rare neurological presentation which was first reported by Susac in 1975, and usually involves the young women with triad of: (1) Visual loss due to occlusion of retinal artery branches. (2) Subacute encephalopathy with psychic manifestation, personality disorders, involvement of the cortico-spianal tracts, pseudo-bulbar, focal or generalized seizures and myoclonic jerks...
متن کاملمعرفی یک بیمار مبتلا به Giant cell tumor استخوان کشکک همراه با متاستازی ریوی
This syndrome is a very rare neurological presentation which was first reported by Susac in 1975, and usually involves the young women with triad of: (1) Visual loss due to occlusion of retinal artery branches. (2) Subacute encephalopathy with psychic manifestation, personality disorders, involvement of the cortico-spianal tracts, pseudo-bulbar, focal or generalized seizures and myoclonic jerks...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Cancer cell
دوره 1 2 شماره
صفحات -
تاریخ انتشار 2002