(New medical branch of treatment in mathematical machine of Sikander Aqeel)
Daily population is increasing of earth, where your need is easy faster and cheap medical science for treatment own body,
First you should understand about treatment, (That what is the treatment)
actually treatment is an appetite of sick cells, such as you gathers all things (milk, sugar, coffee, tea pack, bread, **er) before cook breakfast, if you will not gather this all things, then you cannot get breakfast, so the here breakfast is an appetite of stomach cells,
If you take medicines from one hole of mouth, here I am introducing fifteen thousand billion holes to take medicines, and this process will work like super-sonic speed for health,
Treatment of Galea Aponeurotica Tendon (3/29/2016)
The Calcium and Galea Aponeurotica Tendon
Here we have three compounds to the treatment of Galea Aponeurotica Tendon, (Frontal bone + Parietal bone + Occipital bone) with marrow of brain;
If we are treating of Galea Aponeurotica Tendon, then we are treating of brain and hairs of head with marrow of brain,
First compound = calcium phosphate = Ca3 (PO4)2
Second compound = calcium sulfate = CaSO4
Third compound = furs sulfate = FeSO4
Calcium = (Ca)4 = calcium found in vegetables,
Calcium phosphate = Ca3 (PO4)2 = phosphorus found in cow milk
Calcium sulfate = CaSO4 = sulfur found in milk
Furs sulfate = FeSO4 = sulfur found in milk,
Iron = Fe = Iron found in vegetables,
Oxygen = (O2)6 = Oxygen found in milk,
Medicines for bath-tub = nearly six vegetables powder + milk liquid + powder of poultry, and powder of Spinach for Iron,
1 = Iron is involved in DNA synthesis and may also play roles in normal brain development,
Iron found in sops of poultry and specific vegetables
2 = Phosphorous (P) increase the ability to take up oxygen,
And Phosphorous found 60% from milk
3 = sulfur found in milk,
4 = calcium found in vegetables,
5 = oxygen found in milk,
AFTER GRIND OF FORMULAS,
GRIND OF (Ca)4 = 160 MOLE
= a2 / b3 = c2
= a3800 round / b160 % = c2
= a3800 / b25600 % = c2
= a14440000 / b655360000 = c2
-----------
= 655360000 / 14440000 = 45.38 Carboxyl group
= a / b = 45.25 / 6.75 = 6.7
= a / b = 6.7 – 1 pH = 6.6
= a / b = 6.6 pH of cow’s milk after grind,
Calcium = (Ca)4 = calcium found in vegetables = 6.6 pH of cow’s milk
GRIND OF (PO4)2 = 190 MOLE
= a2 / b3 = c2
= a3800 round / b190 % = c2
= a3800 / b36100 % = c2
= a14440000 / b1303210000 = c2
-----------
= 1303210000 / 14440000 = 90.25
= a / b = 90.25 / 9.5 = 9.5
= a / b = 9.5 + 2 pH = 9.7
= a / b = 9.7 Optimum pH of Arginase enzymes after grind,
Phosphate = (PO4)2 = Arginase enzymes = 9.7 Optimum pH, regulate the activity of enzymes in milk,
GRIND OF SO4 = 96 MOLE
= a2 / b3 = c2
= a3800 round / b 96 % = c2
= a3800 / b 9216 % = c2
= a14440000 / b 84934656 = c2
-----------
= 84934656 / 14440000 = 5.88
= a / b = 5.88 / 2.4 = 2.4
= a / b = 2.4 pH of lemon juice after grind,
Sulfate = SO4 = lemon juice = 2.4 pH,
GRIND OF Fe = 56 MOLE
= a2 / b3 = c2
= a3800 round / b 56 % = c2
= a3800 / b 3136 % = c2
= a14440000 / b 9834496 = c2
= 14440000 / 9834496 = 1.46
= a / b = 1.5 Optimum pH of Pepsin enzymes after grind,
Iron = Fe = Pepsin enzymes = 1.5 Optimum pH,
GRIND OF (O2)6 = 192 MOLE
= a2 / b3 = c2
= a3800 round / b 192 % = c2
= a3800 / b 36864 % = c2
= a14440000 / b 1358954496 = c2
-----------
= 1358954496 / 14440000 = 94.11
= a / b = 94.11 / 9.7 = 9.7
= a / b = 9.7 Optimum pH of Arginase enzymes after grind,
Oxygen = (O2)6 = Arginase enzymes = 9.7 Optimum pH, regulate the activity of enzymes in milk,
Effect of treatment from Optimum pH and normal pH
Calcium = 6.6 pH of cow’s milk after grind
Phosphate = 9.7 Optimum pH of Arginase enzymes after grind
Sulfate = 2.4 pH of lemon juice after grind
Iron = 1.5 Optimum pH of Pepsin enzymes after grind
Oxygen = 9.7 Optimum pH of Arginase enzymes after grind
Medicines for bath-tub =
1 = nearly six vegetables powder
2 = milk liquid
3 = powder of poultry
4 = powder of Spinach for Iron
5 = 25 centigrade warm water
Treatment of
• frontal bone
• Parietal bone
• occipital bone
• Occipitalis muscles
• Frontalis muscle
• Central Galea Aponeurotica tendon
Related Disorders of arginase enzymes
Symptoms of the following disorders may be similar to those of arginase deficiency. Comparisons may be useful for a differential diagnosis:
The urea cycle disorders are a group of rare disorders affecting the urea cycle, a series of biochemical processes in which nitrogen is converted into urea and removed from the body through the urine. Nitrogen is a waste product of protein metabolism. The symptoms of all urea cycle disorders vary in severity and result from the excessive ac**ulation of ammonia in the blood and body tissues (hyperammonemia). Common symptoms include lack of appetite, vomiting, drowsiness, seizures, and/or coma. The liver may be abnormally enlarged (hepatomegaly). In some cases, life-threatening complications may result. In addition to arginase deficiency, the other urea cycle disorders are: carbamyl phosphate synthetase (CPS) deficiency; argininosuccinate synthetase deficiency (citrullinemia); argininosuccinate lyase (ASL) deficiency; ornithine transcarbamylase (OTC) deficiency; and N-acetylglutamate synthetase (NAGS) deficiency
Cerebral palsy is a neurological movement disorder characterized by a lack of muscle control and impaired ability to coordinate movement (ataxia). This disorder is usually a result of injury to the brain during early development in the uterus or at birth. Cerebral palsy is not a progressive disease. An infant with cerebral palsy may experience developmental delays during the first or second year of life. As an affected child grows, additional symptoms may develop, including drooling, speech impairment, difficulty maintaining bladder and/or bowel control, convulsive seizures, hand tremors, and/or difficulty coordinating voluntary movement. Spastic cerebral palsy is characterized by involuntary contractions of the muscles in the arms and legs and an awkward “scissor” gait. These muscle movements may be accompanied by facial grimacing and/or abnormal tongue movements. (For more information on this disorder,
Reye syndrome is a rare childhood disease characterized by liver failure, abnormal brain function (encephalopathy), abnormally low levels of glucose (hypoglycemia), and high levels of ammonia in the blood. This disorder usually follows a viral infection.