「Deficiency」の共起表現(1語右で並び替え)

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「Deficiency」の共起表現一覧(1語右で並び替え)

Deficiency

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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The Act was repealed by the Mental Deficiency Act 1913, by which time two further classifi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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