| thalamocortical | Relating to the efferent connections of the thalamus with the cerebral cortex. (05 Mar 2000) |
|---|---|
| thalamocortical fibres | A general term identifying nerve fibres arising from nuclei of the thalamus and projecting to, and terminating in, the cerebral cortex. (05 Mar 2000) |
| thalamolenticular | Relating to the thalamus, usually the dorsal thalamus, and the lenticular nucleus (putamen and globus pallidus). (05 Mar 2000) |
| thalamophora | <zoology> Same as Foraminifera. Origin: NL, fr. Gr. Chamber + to bear. Source: Websters Dictionary (01 Mar 1998) |
| thalamostriate veins | See: inferior thalamostriate veins, superior thalamostriate vein. (05 Mar 2000) |
| thalamotomy | Destruction of a selected portion of the thalamus by stereotaxy for the relief of pain, involuntary movements, epilepsy, and, rarely, emotional disturbances; produces few, if any, neurological deficits or undesirable personality changes. Origin: thalamus + G. Tome, incision (05 Mar 2000) |
| thalamus | <anatomy> Either of two large, ovoid masses, consisting chiefly of grey substance, situated one on each side of and forming part of the lateral wall of the third ventricle. It is divided into two major parts: dorsal and ventral, each of which contains many nuclei. Origin: L., Gr. Thalamos = inner chamber (18 Nov 1997) |
| thalassaemia | <haematology> A genetic form of anaemia in which there is abnormality of the globin portion of haemoglobin. Affected individuals cannot synthesise haemoglobin properly, and they produce small, pale, short-lived red blood cells. Widespread in Mediterranean countries. Origin: Gr. Haima = blood (11 Jan 1998) |
| thalassaemia intermedia | A clinical variant of thalassaemia characterised by an intermediate degree of severity. These patients have severe anaemia but usually do not require regular blood transfusions. Intermedia disorders represented a heterogeneous group of genetic disorders and may include cases with homozygous or heterozygous abnormalities in the beta-globin chain gene. (05 Mar 2000) |
| thalassaemia major | The dire disease also known as beta thalassaemia. The clinical picture of this form of anaemia was first described in 1925 by the paediatrician thomas benton cooley. Other names for the disease are cooley's anaemia and mediterranean anaemia. The term thalassaemia was coined by the nobel prise winning pathologist george whipple and the professor of paediatrics william bradford at u. Of rochester because thalassa in greek means the sea (like the mediterrranean sea) + -aemia means in the blood so thalassaemia means sea in the blood. Thalassaemia is not just one disease. It is a complex contingent of genetic (inherited) disorders all of which involve underproduction of haemoglobin, the indispensable molecule in red blood cells that carries oxygen. The globin part of normal adult haemoglobin is made up of 2 alpha and 2 beta polypeptide chains. In beta thalassaemia, there is a mutation (change) in both beta globin chains leading to underproduction (or absence) of beta chains, underproduction of haemoglobin, and profound anaemia. The gene for beta thalassaemia is relatively frequent in people of mediterranean origin (for example, from italy and greece). Children with this disease inherit one gene for it from each parent (and so are said to be homozygous for beta thalassaemia). The parents are carriers (heterozygotes) with just one thalassaemia gene, are said to have thalassaemia minor, and are essentially normal. Their children affected with beta thalassaemia seem entirely normal at birth (because at birth we still have predominantly foetal haemoglobin which does not contain beta chains) but the anaemia emerges in the first few months of life and becomes progressively more severe leading to pallor and easy fatiguability, failure to thrive (grow), bouts of fever (due to infections) and diarrhoea. Treatment based on blood transfusions is helpful but not curative. Gene therapy will, it is hoped, be applicable to this disease. (12 Dec 1998) |
| thalassaemia minor | Also called thalassaemia trait, thalassaemia minor is the carrier state for beta thalassaemia. People who are carriers (heterozygotes) have just one thalassaemia gene, are said to have thalassaemia minor, and are essentially normal. (12 Dec 1998) |
| thalassaemia, beta | Also known as thalassaemia major.The clinical picture of this important type of anaemia was first described in 1925 by the paediatrician thomas benton cooley. Other names for the disease are cooley's anaemia and mediterranean anaemia. The name thalassaemia was coined by the nobel prise winning pathologist george whipple and the professor of paediatrics wm bradford at u. Of rochester because thalassa in greek means the sea (like the mediterrranean sea) + -aemia means in the blood so thalassaemia means sea in the blood. Thalassaemia is not just one disease. It is a complex contingent of genetic (inherited) disorders all of which involve underproduction of haemoglobin, the indispensable molecule in red blood cells that carries oxygen. The globin part of normal adult haemoglobin is made up of 2 alpha and 2 beta polypeptide chains. In beta thalassaemia, there is a mutation (change) in both beta globin chains leading to underproduction (or absence) of beta chains, underproduction of haemoglobin, and profound anaemia. The gene for beta thalassaemia is relatively frequent in people of mediterranean origin (for example, from italy and greece). Children with this disease inherit one gene for it from each parent. The parents are carriers (heterozygotes) with just one thalassaemia gene, are said to have thalassaemia minor, and are essentially normal. Their children affected with beta thalassaemia seem entirely normal at birth because at birth we still have predominantly foetal haemoglobin which does not contain beta chains. The anaemia surfaces in the first few months after birth and becomes progressively more severe leading to pallor and easy fatiguability, failure to thrive (grow), bouts of fever (due to infections) and diarrhoea. Treatment based on blood transfusions is helpful but not curative. Gene therapy will, it is hoped, be applicable to this disease. (12 Dec 1998) |
| thalassian | <zoology> Any sea tortoise. Origin: From Gr. The sea. Source: Websters Dictionary (01 Mar 1998) |
| thalassic | <geology> Of or pertaining to the sea; sometimes applied to rocks formed from sediments deposited upon the sea bottom. Origin: Gr. The sea. Source: Websters Dictionary (01 Mar 1998) |
| thalassinian | <zoology> Any species of Thalaassinidae, a family of burrowing macrurous Crustacea, having a long and soft abdomen. Source: Websters Dictionary (01 Mar 1998) |
Synonyms : Thalassotherapies
Synonyms :
Synonyms : Celgene Brand of Thalidomide, Sedoval, Thalomid
Synonyms :
Synonyms : Radioisotopes, Thallium
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|---|---|---|---|
|
한국원자력연구소염화탈륨(Tl-201)주사액 - 새창
|
원자력병원 |
A37190211 | Thallium chloride(Tl-201) | 전문의약품 | 급여 | 분업예외의약품 |
|
파미온탈리도마이드캡슐50mg - 새창
|
비엘엔에이치 |
E26130071 | Thalidomide | 전문의약품 | 급여 | 분업예외의약품 |
|
싱코르에이알아이염화탈륨주사액13.5mCi - 새창
|
싱코르코리아 |
E30950163 | Thallium chloride(Tl-201) | 전문의약품 | 급여 |
|
싱코르에이알아이염화탈륨주사액20.3mCi - 새창
|
싱코르코리아 |
E30950164 | Thallium chloride(Tl-201) | 전문의약품 | 급여 |
|
싱코르에이알아이염화탈륨주사액27mCi - 새창
|
싱코르코리아 |
E30950165 | Thallium chloride(Tl-201) | 전문의약품 | 급여 |
| thalassemia major |
Cooley's anemia: a fatal form of homozygous thalassemia (inherited from both parents) in which there is no hemoglobin; skeletal deformations; heart and spleen and liver enlarged
출처: wordnet.princeton.edu/perl/webwn
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|---|---|
| Thallophyta |
used only in former classifications: comprising what is now considered a heterogeneous assemblage of flowerless and seedless organisms: algae; bacteria; fungi; lichens
출처: wordnet.princeton.edu/perl/webwn
|
| thallophyte |
any of a group of cryptogamic organisms consisting principally of a thallus and thus showing no differentiation into stem and root and leaf
출처: wordnet.princeton.edu/perl/webwn
|
| thalidomide |
a sedative and hypnotic drug; withdrawn from sale after discovered to cause severe birth defects because it inhibits angiogenesis
출처: wordnet.princeton.edu/perl/webwn
|
| thallium |
a soft grey malleable metallic element that resembles tin but discolors on exposure to air; it is highly toxic and is used in rodent and insect poisons; occurs in zinc blende and some iron ores
출처: wordnet.princeton.edu/perl/webwn
|
| THA | large egg-shaped structures of gray matter that form the dorsal subdivision of the diencephalon |
|---|---|
| THA | polar bears |
| THA | white bear of arctic regions |
| THA | an inherited form of anemia caused by faulty synthesis of hemoglobin |
| THA | a fatal form of homozygous thalassemia (inherited from both parents) in which there is no hemoglobin |
| THA | an inherited form of anemia caused by faulty synthesis of hemoglobin |
| THA | a fatal form of homozygous thalassemia (inherited from both parents) in which there is no hemoglobin |
| THA | relating to the seas, especially smaller or inland seas |
| THA | a genus of Labridae |
| THA | small Atlantic wrasse the male of which has a brilliant blue head |
| THA | Greek philosopher and astronomer (who predicted an eclipse in 585 BC) who was said by Aristotle to be the founder of physical science |
| THA | Greek philosopher and astronomer (who predicted an eclipse in 585 BC) who was said by Aristotle to be the founder of physical science |