「Deficiency」の共起表現一覧(1語右で並び替え)
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| e have been associated with specific granule | deficiency, a rare congenital disorder. |
| rder is classified as a multiple carboxylase | deficiency, a group of disorders characterized by impai |
| ced the Radnor Report, leading to the Mental | Deficiency Act of 1913. |
| The Act was repealed by the Mental | Deficiency Act 1913, by which time two further classifi |
| Commissioner, under the terms of the Mental | Deficiency Act, 1913. |
| On the average, primary carnitine | deficiency affects 1 in every 40,000 live births in Jap |
| omatic parents have been diagnosed with MCAD | deficiency after a child's diagnosis. |
| It is possible that a retinol (vitamin A) | deficiency alone could cause albumin levels to become r |
| Adenylosuccinate lyase | deficiency, also called adenylosuccinase deficiency, is |
| Tetrahydrobiopterin | deficiency also disrupts the levels of certain neurotra |
| Phosphofructokinase | deficiency, also known as Glycogen storage disease type |
| Aldolase A | deficiency, also called ALDOA deficiency and red cell a |
| Phosphofructokinase | deficiency also presents in a rare infantile form. |
| Guanidinoacetate methyltransferase | deficiency, also called GAMT deficiency, is an autosoma |
| Mevalonate kinase | deficiency, also called mevalonic aciduria, is an autos |
| This | deficiency, an X-linked recessive hereditary disease, i |
| this gene are associated with 3-ketothiolase | deficiency, an inborn error of isoleucine catabolism ch |
| sed to replenish thyroid hormones in thyroid | deficiency and hypothyroidism. |
| of those with limb amputation or congenital | deficiency, and those with neurological disabilities ar |
| ich he decides that Hannah has a vitamin B12 | deficiency and that the B12 she was given earlier was b |
| There are some associated risks of Vitamin | deficiency and stomach ulcer formation requiring preven |
| al symptoms and signs suggestive of androgen | deficiency and decreased testosterone levels are presen |
| on, and is used for treatment of the vitamin | deficiency, and also (because of its afinity for cyanid |
| These spots are a sign of vitamin A | deficiency and are associated with conjunctival xerosis |
| Symptoms are very similar to biotinidase | deficiency and treatment - large doses of biotin - is a |
| alled aniridia, cerebellar ataxia and mental | deficiency and Gillespie's syndrome II, is a rare genet |
| Mutations in this gene can result in B cell | deficiency and agammaglobulinemia, an autosomal recessi |
| rap more iodide, compensating for the iodine | deficiency and allowing it to produce adequate amounts |
| These include hypothyroidism, growth hormone | deficiency and hypopituitarism. |
| rphyria (CEP), uroporphyrinogen III synthase | deficiency and UROS deficiency, is a congenital form of |
| iron to the bloodstream helps solve the iron | deficiency and rectal prolapse. |
| ferlin in muscle, the pathology of dysferlin | deficiency, and approaches to treatment. |
| the rats had been suffering from a vitamin A | deficiency and this was the main cause of the tumors. |
| upplementation with omega-3 may correct this | deficiency and improve the clinical outcome. |
| spectrum exhibit the characteristic hydrogen | deficiency and other features typical of RCB:s. |
| r, with 30% of the control group showing the | deficiency and 6% of alcoholics displaying it. |
| der is associated with ornithine translocase | deficiency, and a form of hyperammonemia. |
| eading to thrombocytopenia or blood platelet | deficiency and/or leukopenia or white blood cell (WBC) |
| In iron | deficiency anemia (microcytic anemia), it can be as low |
| s, present in large numbers, produce an iron | deficiency anemia by sucking blood from the host's inte |
| "The diagnosis of iron | deficiency anemia". |
| Increased RDW is seen in iron | deficiency anemia, Thalassemia Major (Cooley's anemia), |
| itin is the most sensitive lab test for iron | deficiency anemia, however serum ferritin can be elevat |
| tb, DMT1 and ferroportin in response to iron | deficiency anemia. |
| this state is uncorrected, it leads to iron | deficiency anemia. |
| ffects of guanidinoacetate methyltransferase | deficiency are most severe in organs and tissues that r |
| of GABA in the brains of patients with SSADH | deficiency as compared to normal brain concentrations o |
| ee diets had nearly twice the bone thickness | deficiency as boys with minimally restricted or unrestr |
| Adenylosuccinate lyase | deficiency at NIH's Office of Rare Diseases |
| ataxia-telangiectasia, ataxia with vitamin E | deficiency, ataxia with oculomotor apraxia (AOA), spast |
| cy-2 (LAD-2) is a type of leukocyte adhesion | deficiency attributable to the absence of neutrophil si |
| cy-1 (LAD-1) is a type of leukocyte adhesion | deficiency attributable to mutations in the gene on chr |
| nyone with glucose-6-phosphate dehydrogenase | deficiency because there can be a severe reaction with |
| rugs must not be given to patients with G6PD | deficiency, because they cause potentially fatal haemol |
| hould be avoided in those affected by biotin | deficiency, because egg whites contain high levels of a |
| Carbamoyl phosphate synthetase I | deficiency belongs to a class of genetic diseases calle |
| Osteolathyrism is a collagen cross-linking | deficiency brought on by dietary over-reliance on the s |
| bout 60 patients had been diagnosed with ASL | deficiency, but many more are thought to be undiagnosed |
| r supplying it through fertilizer cures iron | deficiency, but phytoplasma-infected sugarcane does not |
| that lack vend counters compensate for this | deficiency by occasionally checking the amount of cash |
| holding capacity (sands and peats) potassium | deficiency can lead to a rapid, premature desiccation o |
| counterpart, triiodothyronine, and as such a | deficiency can cause symptoms of hypothyroidism, includ |
| However, nitrogen | deficiency can also be detected non-destructively by me |
| Biotin | deficiency can result in behavioral disorders, lack of |
| Episodes of LCHAD | deficiency can be triggered by periods of fasting or by |
| THB | deficiency can be caused by mutations in one of several |
| Symptoms of iron | deficiency can occur even before the condition has prog |
| The | deficiency can be in biotinidase or holocarboxylase syn |
| Deficiency can cause Hyper-IgM syndrome type 3. | |
| Nitrogen | deficiency can be detected with a chlorophyll content m |
| This | deficiency can be systemic or limited to red blood cell |
| Heparin Cofactor II | deficiency can lead to increased thrombin generation an |
| ecreased or absent IgA, termed selective IgA | deficiency, can be a clinically significant immunodefic |
| eople with later-onset ornithine translocase | deficiency cannot tolerate high-protein foods, such as |
| resulting in alpha-N-acetylgalactosaminidase | deficiency, cause an infantile neuroaxonal dystrophy kn |
| ) in JBS can be attributed to growth hormone | deficiency caused by diminished anterior pituitary func |
| The | deficiency causes the near absence of T lymphocytes and |
| Mevalonate kinase | deficiency causes an accumulation of mevalonic acid in |
| Fumarase | deficiency causes encephalopathy, severe mental retarda |
| hat low-dose GH treatment for adults with GH | deficiency changes the body composition by increasing m |
| Although MPO | deficiency classically presents with immune deficiency |
| vegetables, and made illnesses from vitamin | deficiency common among ships' crews. |
| ynthesis of PHA is usually caused by certain | deficiency conditions (e.g. |
| In 11-beta-hydroxylase | deficiency, cortodoxone levels increase dramatically, c |
| ndrome is a syndrome characterised by mental | deficiency, craniosynostosis, blepharophimosis, ptosis, |
| As a result of the potassium | deficiency developed in his childhood, he eats four ban |
| Carbamoyl-phosphate synthase I | deficiency disease |
| re general idea that colon cancer is a fiber | deficiency disease is now generally considered incorrec |
| babies can be caused by molybdenum cofactor | deficiency disease which leads to neurological damage a |
| exhausted and seven men died of the vitamin | deficiency disease. |
| of five vitamins associated with a pandemic | deficiency disease: niacin deficiency (pellagra), vitam |
| spectrometry for newborn screening of enzyme | deficiency diseases (together with Professors Frank Tur |
| Other | deficiency diseases with similar signs and symptoms inc |
| In addition to these classical vitamin | deficiency diseases, some evidence has also suggested l |
| 78-1952), U.S. Army physician, researcher of | deficiency diseases, and medical educator |
| Although glycogen synthase | deficiency does not result in storage of extra glycogen |
| acillus, Staphylococcus and Streptococcus, a | deficiency due to infant formula feeding can lead to in |
| oral solution for the treatment of vitamin E | deficiency due to digestive malabsorption in paediatric |
| rosis suffer from essential fatty acid (EFA) | deficiency due to malabsorption, it was hypothesized th |
| ilirubinemia are Gilbert's syndrome and G6PD | deficiency, especially if they are present concurrently |
| House wonders if a Vitamin K | deficiency explains the delay between the blood test an |
| ore, correction with mixing indicates factor | deficiency; failure to correct indicates an inhibitor. |
| hy (MLD), Krabbe disease, multiple sulfatase | deficiency, Farber disease, and Wolman disease. |
| Type 89 50 mm shell, in retrospect a serious | deficiency for an army lacking effective hand-carried i |
| adaptation to L-gulonolactone oxidase (GULO) | deficiency, found only in certain lines of mammals. |
| Medium-chain acyl-coenzyme A dehydrogenase | deficiency has an autosomal recessive pattern of inheri |
| Tyk2 | deficiency has more dramatic effects in human cells tha |
| AMACR | deficiency has recently been discovered. |
| Aldolase A | deficiency has an autosomal recessive pattern of inheri |
| Holocarboxylase synthetase | deficiency has an autosomal recessive pattern of inheri |
| Galactokinase | deficiency has autosomal recessive pattern of inheritan |
| Leukocyte-adhesion | deficiency has an autosomal recessive pattern of inheri |
| Tetrahydrobiopterin | deficiency has an autosomal recessive pattern of inheri |
| Pyruvate carboxylase | deficiency has an autosomal recessive pattern of inheri |
| ALA dehydratase | deficiency has an autosomal recessive pattern of inheri |
| Beta-ketothiolase | deficiency has an autosomal recessive pattern of inheri |
| Adenine phosphoribosyltransferase | deficiency has an autosomal recessive pattern of inheri |
| Guanidinoacetate methyltransferase | deficiency has an autosomal recessive pattern of inheri |
| Mevalonate kinase | deficiency has an autosomal recessive pattern of inheri |
| e current understanding of primary carnitine | deficiency has been greatly influenced by the research |
| DBH | deficiency has been treated effectively with L-threo-3, |
| Short-chain acyl-coenzyme A dehydrogenase | deficiency has an autosomal recessive pattern of inheri |
| Purine nucleoside phosphorylase | deficiency has an autosomal recessive pattern of inheri |
| Isobutyryl-coenzyme A dehydrogenase | deficiency has an autosomal recessive pattern of inheri |
| Mitochondrial trifunctional protein | deficiency has an autosomal recessive pattern of inheri |
| Systemic primary carnitine | deficiency has an autosomal recessive pattern of inheri |
| es of anemia, possibly related to folic acid | deficiency, have been described. |
| Patients with MPO | deficiency have a respiratory burst with a normal NBT d |
| Though genetic defects causing iron | deficiency have been studied in rodents, there are no k |
| Very few cases (<20) of A2AP | deficiency have been described. |
| d soul of the island, but in 1817, a serious | deficiency having been discovered in the treasury accou |
| a doctor's prescription for HGH to counter a | deficiency he had been diagnosed with, and had previous |
| epsy, Myasthenia gravis, Alpha 1-antitrypsin | deficiency, heart disease, pulmonary hypertension, Lyme |
| understanding of megaloblastic anemias, iron | deficiency, hemolytic disease of newborn infants, blood |
| toacidosis is usually accompanied by insulin | deficiency, hyperglycemia, and dehydration. |
| inium toxicity, i.e. necrosis, and phosphate | deficiency, i.e. anthocyanosis (reddening of the leaves |
| 943 but was turned back a year in 1944 for a | deficiency in mathematics). |
| is often used as an indicator of vitamin B12 | deficiency in serum. |
| Enzymatic | deficiency in alpha-oxidation (most frequently in phyta |
| d national begin to solve for a considerable | deficiency in consequence management, a universal langu |
| There appears to be a strong | deficiency in neutral hydrogen near the region of the g |
| ids by mitochondria in the mother, caused by | deficiency in the LCHAD (long-chain 3-hydroxyacyl-coenz |
| To make up for this | deficiency, in the late 1890s, they constructed five Pr |
| langeal joints of the hands and feet, mental | deficiency in approximately 90% of affected children, a |
| eep breed, especially in areas with selenium | deficiency in soils. |
| ogramme in Pudukottai district for assessing | deficiency in texture, nutrient and other ingredients f |
| f Ensign until 1927, because of his academic | deficiency in mathematics. |
| that virtually all PIBI(D)S patients have a | deficiency in the nucleotide excision repair of UV-indu |
| A case study suggested that a | deficiency in myophosphorylase may be linked with cogni |
| Deficiency in the liver isozyme leads to argininemia, w | |
| A moderate iron | deficiency, in contrast, can provide protection against |
| f America tried to make up for an increasing | deficiency in salt by preserving meat and fish in pyrol |
| shiorkor was once attributed to pure protein | deficiency in individuals who were consuming enough cal |
| Iron | deficiency in bacterial cells triggers secretion of ent |
| Deficiency in the number of posts actually held (in res | |
| urine in patients with pentosuria, due to a | deficiency in L-xylulose reductase. |
| Deficiency in N-Acetyl Glutamate Synthase or a genetic | |
| familial LCAT | deficiency in which there is complete LCAT deficiency. |
| A | deficiency in this enzyme results in the build-up of no |
| retations of his experiments show particular | deficiency in his familiarity with the principles of tr |
| Mutations and | deficiency in this enzyme are known to cause familial p |
| The project was developed to fill a | deficiency in information about life in Florida from th |
| Factor I | deficiency in turn leads to low levels of complement co |
| ocated a new theory of central noradrenergic | deficiency in Dyslexia. |
| t Cade speculated that mania was caused by a | deficiency in lithium. |
| Other diseases that result from a | deficiency in the sialidase enzyme are categorized in a |
| Haemolytic anaemia or | deficiency in red blood cells (RBCs) |
| rmanent Government was not due merely to his | deficiency in constructive imagination. |
| However, | deficiency in nitrogen or sulfur could cause the vine t |
| nt formulated to prevent and/or correct zinc | deficiency in animals. |
| c galactosemia, in which there is an extreme | deficiency in galactose-1 phosphate uridyltransferase. |
| ith zinc-deficient soils and widespread zinc | deficiency in humans. |
| He says in these cases FAS is a “growth | deficiency in all aspects of the body; these children a |
| The review concluded that there was a | deficiency in the law as the former tribunal could not |
| A | deficiency in pyruvate kinase, the enzyme that potentia |
| A | deficiency in ASAH1 is associated with Farber disease. |
| intestinal copper absorption with secondary | deficiency in copper-dependent mitochondrial enzymes. |
| Zinc | deficiency in children has been dramatically reduced. |
| Deficiency in alpha-l-fucosidase activity is associated | |
| s are a natural source of pyridoxal, and its | deficiency in the human body can lead to serious compli |
| Glucose-6-phosphate dehydrogenase | deficiency, in which uncontrolled oxidative stress caus |
| a form of mucopolysaccharidosis caused by a | deficiency in arylsulfatase B (ARSB). |
| If iron | deficiency in calcareous soils is a problem, this eleme |
| Deficiency in this enzyme in patients receiving aromati | |
| verse health or cognitive effects due to DHA | deficiency in adult vegetarians or vegans, fetal and br |
| This finding indicates a | deficiency in the Standard Model of particle physics, a |
| The opposite of melanism is amelanism, a | deficiency in or total absence of melanin pigments. |
| a vitamin E supplement or to treat vitamin E | deficiency in individuals who cannot absorb fats due to |
| A | deficiency in any of the enzymes of this complex as wel |
| The major surfactant | deficiency in premature infants relates to the lack of |
| Mutations in this gene and the | deficiency in alpha-N-acetylgalactosaminidase activity |
| muscular disease of lambs and calves due to | deficiency in selenium and / or Vitamin E. |
| storage disease type 0 is characterized by a | deficiency in the glycogen synthase enzyme. |
| The signs and symptoms of HMG-CoA lyase | deficiency include vomiting, dehydration, lethargy, con |
| s/NCBI/NIH/UW entry on Acid Sphingomyelinase | Deficiency Includes: Niemann-Pick Disease Type A, Niema |
| illiams syndrome show characteristics of POR | deficiency, including radio-ulnar synostosis and other |
| However, | deficiency induces deformities in skull and peripheral |
| appear on the pinnae of older leaves; as the | deficiency intensifies, the spots turn orange or reddis |
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