¼±Åà - È­»ìǥŰ/¿£ÅÍŰ ´Ý±â - ESC

 
"muco"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
KMLE ¾àǰ/ÀǾàǰ ¸ÂÃã °Ë»ö °á°ú : 14 ÆäÀÌÁö: 2
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • mucoid colony
    Á¡¾×Áý¶ô
  • mucolipidosis
    Á¡¾×ÁöÁúÁõ
  • mucolytic
    1. Á¡¾×¿ëÇØ- 2. Á¡¾×¿ëÇØÁ¦
  • mucolytic agent
    Á¡¾×¿ëÇØÁ¦
  • mucoperiosteal flap
    Á¡¸·»À¸·ÇÇÆÇ, Á¡¸·°ñ¸·ÇÇÆÇ
  • mucoperiosteum
    Á¡¸·»À¸·, Á¡¸·°ñ¸·
  • mucopolysaccharide
    Á¡¾×´Ù´ç·ù, ¹ÂÄÚ´Ù´ç·ù
  • mucopolysaccharidosis
    Á¡¾×´Ù´ç·ùÁõ, ¹ÂÄÚ´Ù´ç·ùÁõ
  • mucoprotein
    Á¡¾×´Ü¹éÁú, ¹ÂÄڴܹéÁú
  • mucopurulent
    Á¡¾×°í¸§-, Á¡¾×³ó-
  • mucopus
    °í¸§¸ð¾çÁ¡¾×, Á¡¾×³ó
  • Mucor
    ÅаõÆÎÀÌ(¼Ó)
  • Mucor corymbifer
    »ñ°«ÅаõÆÎÀ̱Õ
  • Mucoraceae
    ÅаõÆÎÀÌ(°ú)
  • mucormycosis
    ÅаõÆÎÀÌÁõ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • mucolipidosis
    Á¡¾×ÁöÁúÁõ
  • mucolytic
    Á¡¾×¿ëÇØÁ¦, Á¡¾×¿ëÇØ-
  • mucolytic agent
    Á¡¾×¿ëÇØÁ¦
  • mucolytic enzyme
    Á¡¾×ºÐÇØÈ¿¼Ò
  • mucoperiosteal flap
    Á¡¸·°ñ¸·ÇÇÆÇ
  • mucoperiosteum
    Á¡¸·»À¸·, Á¡¸·°ñ¸·
  • mucoperiostitis
    Á¡¸·»À¸·¿°, Á¡¸·°ñ¸·¿°
  • mucopolysaccharide
    Á¡¾×´Ù´ç·ù
  • mucopolysaccharidosis
    Á¡¾×´Ù´ç·ùÁõ
  • mucoprotein
    Á¡¾×´Ü¹éÁú
  • mucopurulent
    Á¡¾×°í¸§-
  • mucopurulent sputum
    Á¡¾×°í¸§°¡·¡, Á¡¾×³ó°¡·¡
  • Mucor
    ÅаõÆÎÀÌ
  • Mucor corymbifer
    »ñ°«ÅаõÆÎÀ̱Õ
  • Mucoraceae
    ÅаõÆÎÀÌ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • mucocutaneous
    Á¡¸·ÇǺÎ(ïÄØ¯ù«Ý±)ÀÇ
  • mucocutaneous
    Á¡¸·ÇǺÎÀÇ
  • mucocutaneous candidiasis
    Á¡¸· ÇǺΠĭµð´ÙÁõ
  • mucocutaneous candidiasis
    Á¡¸·ÇǺΠĭµð´Ù(Áõ)
  • mucocutaneous end-organ
    Á¡¸· ÇǺΠ¸»´Ü±â°ü
  • mucocutaneous junction
    Á¡¸·ÇǺÎÁ¢ÇÕºÎ(ïÄØ¯ù«Ý±ïÈùêÝ»).
  • mucocutaneous junction
    Á¡¸·ÇǺÎÁ¢ÇÕºÎ(¡­ïÈùêÝ»)
  • mucocutaneous leishmaniasis
    ÇǺΠÁ¡¸·¸®½´¸¶´Ï¾ÆÁõ
  • mucocutaneous lymph node syndrome
    ÇǺÎÁ¡¸·¸²ÇÁÀýÁõÈıº.
  • mucocutaneous lymph node syndrome
    ÇǺÎÁ¡¸·¸²ÇÁÀýÁõÈıº
  • mucocutaneous lymphadenopathy syndrome, acute febrile
    Á¡¸·ÇǺθ²ÇÁÀý ÁõÈıº (±Þ¼º¿­¼º), °¡¿Í»ç³¢º´
  • mucocutaneous ocular syndrome
    ÇǺÎÁ¡¸·´«ÁõÈıº(ù«Ý±ïÄØ¯äÑñøý¦ÏØ).
  • mucocutaneous ocular syndrome
    ÇǺÎÁ¡¸·¾ÈÁõÈıº(ù«Ý±ïÄØ¯äÑñøý¦ÏØ)
  • mucoderm
    Á¡¸·ÀÇ °íÀ¯¸·(¡­Í³êóد).
  • mucoenteritis
    ¼ÒÀåÁ¡¸·¿°(á³íóïÄØ¯æú).
KI ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 9 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
  • mucous bronchogram
    Á¡¾×±â°üÁöÁ¶¿µ»ó
  • mucous cyst
    Á¡¾×³¶
  • mucous gland
    Á¡¾×»ù, Á¡¾×¼±
  • mucous membrane
    Á¡¸·
  • mucous polyp
    Á¡¾×¼ºÆú¸³
  • mucous secretion
    Á¡¾×ºÐºñ
  • mucous stool
    Á¡¾×º¯
  • mucous tumor
    Á¡¾×Á¾
  • mucoviscidosis
    ¹ÂÄÚºñ½Ãµµ½Ã½º
Çѱ¹Ç¥ÁØÁúº´»çÀκзù ¾àÀÚ ¸ÂÃã °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
  • ÄÚµå
    ¿µ¹®
    ÇѱÛ
  • E76.3
    Mucopolysaccharidosis, unspecified
    »ó¼¼ºÒ¸íÀÇ Á¡¾×´Ù´çÁúÁõ
  • J41.1
    Mucopurulent chronic bronchitis
    Á¡¾×³ó¼º ¸¸¼º ±â°üÁö¿°
  • H10.0
    Mucopurulent conjunctivitis
    Á¡¾×È­³ó¼º °á¸·¿°
  • B46.5
    Mucormycosis, unspecified
    »ó¼¼ºÒ¸íÀÇ ÅаõÆÎÀÌÁõ
  • K51.5
    Mucosal proctocolitis
    Á¡¸·¼º Á÷Àå°áÀå¿°
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • mucoperiostitis
    Á¡¸· °ñ¸·¿°
  • mucopolysaccharide
    Á¡¾× ´Ù´ç·ù
  • mucopus
    ³ó¾ç Á¡¾×
    ¹éÇ÷±¸°¡ Á¸ÀçÇϱ⠶§¹®¿¡ °í¸§°ú °°Àº ¿Ü°üÀ» ³ªÅ¸³»´Â Á¡¾×.
  • mucosa
    Á¡¸·, Á¡¸·Ãþ
  • mucosal area
    Á¡¸· ºÎÀ§
  • mucosal barrier to acid back-diffusion

    mucosal bleeding (Á¡¸· ÃâÇ÷

  • mucosal change
    Á¡¸· º¯È­
  • mucosal disease
    Á¡¸· º´
  • mucosal immunity
    Á¡¸· ¸é¿ª
  • mucosal insert
    Á¡¸· »ðÀÔ
  • mucosal level
    Á¡¸· ¼öÁØ
  • mucosal neuroma
    Á¡¸· ½Å°æÁ¾
    ÀüÇüÀûÀÎ ¼öÁú ¾ÏÁ¾°ú Å©·Ò ģȭ ¼¼Æ÷Á¾À» µ¿¹ÝÇϸ鼭 ±× À§¿¡ ÀÔ¼ú, ±¸°­, ´«, ±âµµ, ¼ÒÈ­±â°è, ¹æ±¤ µî ¿©·¯ Àå¼Ò¿¡ ½Å°æÁ¾ ¶Ç´Â ½Å°æÀý ½Å°æÁ¾À» µ¿¹ÝÇÏ´Â °ÍÀ» Ư¡À¸·Î ÇÑ´Ù.
  • mucosal pattern
    Àḷ »ó, Á¡¸·Çü
  • mucosal ridging
    Á¡¸· ¾ÐÈç, Á¡¸·ÀÇ ¾ÐÈç
  • mucosal thickening
    Á¡¸· ºñÈÄ
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
mucoenteritis 1. Inflammation of the intestinal mucous membrane.
Synonym: mucomembranous enteritis.
(05 Mar 2000)
mucoepidermoid Denoting a mixture of mucus-secreting and epithelial cells, as in mucoepidermoid carcinoma.
(05 Mar 2000)
mucoepidermoid carcinoma <tumour> Most commonly a salivary gland carcinoma of low grade malignancy in children, but with variable malignancy in adults; composed of mucous, epidermoid, and intermediate cells, with mucous cells abundant only in low grade carcinoma's; recurrence is frequent, and high grade carcinoma's metastasize to cervical nodes.
Synonym: mucoepidermoid tumour.
(05 Mar 2000)
mucoepidermoid tumour A malignant epithelial tumour of glandular tissue, especially the salivary glands, characterised by acini with mucus-producing cells and by the presence of malignant squamous elements. most mucoepidermoid tumours are low-grade lesions readily cured by adequate excision. They may appear in any age group. They grow slowly. If high-grade, they behave aggressively, widely infiltrating the salivary gland and producing lymph node and distant metastases.
(12 Dec 1998)
mucoepithelial dysplasia An epithelial cell dishesive disease characterised by red, periorificial mucosal lesions of oral, nasal, vaginal, urethral, anal, bladder, and conjunctival mucosa, with cataracts, follicular keratosis, non-scarring alopecia, frequent pulmonary infections, pneumothorax, and sometimes cor pulmonale; autosomal dominant inheritance.
(05 Mar 2000)
mucoglobulin A glycoprotein or mucoprotein in which the protein component is a globulin.
(05 Mar 2000)
mucoid Resembling mucus.
(27 Sep 1997)
mucoid adenocarcinoma <tumour> Sometimes applied to mucinous carcinoma, or adenocarcinoma containing mucin secreting neoplastic cells.
(05 Mar 2000)
mucoid colony A colony showing viscous or sticky growth typical of an organism producing large quantities of a carbohydrate capsule.
(05 Mar 2000)
mucoid degeneration A conversion of any of the connective tissues into a gelatinous or mucoid substance.
Synonym: myxoid degeneration, myxomatous degeneration, myxomatosis.
(05 Mar 2000)
mucoid impaction of bronchus Plugging of the lumen of bronchi due to thickened mucus, interfering with ventilation of corresponding lung segments and leading to characteristic clustered linear and grape-like radiologic densities and occasionally atelectasis and pneumonia; characteristically seen in cystic fibrosis but it can occur in a variety of disease states.
(05 Mar 2000)
mucoid medial degeneration Loss of elastic and muscle fibres in the aortic media, with accumulation of mucopolysaccharide, sometimes in cystlike spaces between the fibres; a disease of unknown cause, which may be inherited and which predisposes to dissecting aneurysms.
Synonym: Erdheim disease, medionecrosis aortae idiopathica cystica, medionecrosis of the aorta, mucoid medial degeneration.
(05 Mar 2000)
mucolipidosis <biochemistry> A group of inherited metabolic diseases characterised by the accumulation of excessive amounts of acid mucopolysaccharides, sphingolipids, and/or glycolipids in visceral and mesenchymal cells. Abnormal amounts of sphingolipids or glycolipids are present in neural tissue. Mental retardation and skeletal changes are common.
(12 Dec 1998)
mucolipidosis I <biochemistry> Mucolipidosis somewhat like a mild form of Hurler's syndrome with mild dysostosis multiplex, and moderate mental retardation due to neuraminidase deficiency.
Inheritance: autosomal recessive.
Synonym: lipomucopolysaccharidosis.
(05 Mar 2000)
mucolipidosis II <biochemistry> Mucolipidosis of early onset and with severe symptoms like those in Hurler's syndrome but with normal urinary mucopolysaccharides, vacuolated lymphocytes, and inclusion bodies in cultured fibroblasts (I-cells).
The lysosomes lack hydrolases but high concentrations of lysosomal enzymes are found in the extracellular fluids such as serum, spinal fluid, and urine.
It is associated with a deficiency of N-acetylglucosaminyl-1-phosphotransferase. The gene defect responsible probably prevents the addition of the lysosome recognition marker mannose 6 phosphate) to these enzymes so that they are not directed into the lysosomes but are released.
Inheritance: autosomal recessive.
Synonym: I-cell disease, inclusion cell disease.
(12 Jul 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 2
  • Mucopolysaccharidoses - »õâ Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
    Synonyms : Mucopolysaccharidosis
  • Mucopolysaccharidosis I - »õâ Systemic lysosomal storage disease caused by a deficiency of alpha-L-iduronidase (IDURONIDASE) and characterized by progressive physical deterioration with urinary excretion of DERMATAN SULFATE and HEPARAN SULFATE. There are three recognized phenotypes representing a spectrum of clinical severity from severe to mild: Hurler's syndrome, Hurler-Scheie syndrome and Scheie's syndrome (formerly mucopolysaccharidosis V). Symptoms may include DWARFISM, hepatosplenomegaly, gargoyle-like facies, corneal clouding, cardiac complications, and noisy breathing. Hunter syndrome (MUCOPOLYSACCHARIDOSIS II) and Hurler syndrome were each originally called "gargoylism" because of the coarseness of the facial features of affected individuals.
    Synonyms : Gargoylism, Hurler Syndrome, Hurler Disease, Hurler's Disease, MPS I H, MPS I H-S, MPS I S, MPS I-S, Mucopolysaccharidosis 1, Mucopolysaccharidosis 5, Mucopolysaccharidosis I-S, Mucopolysaccharidosis IS, Scheie Syndrome, Disease, Hurler, Disease, Hurler's, MPS I H S
  • Mucopolysaccharidosis II - »õâ Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15.
    Synonyms : Hunter Syndrome Gargoylism, Mucopolysaccharidosis 2, Gargoylisms, Hunter Syndrome, Hunter Syndrome, Hunter Syndrome Gargoylisms, Hunters Syndrome, IIs, Mucopolysaccharidosis, Mucopolysaccharidosis IIs, Syndrome, Hunter's
  • Mucopolysaccharidosis III - »õâ Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme.
    Synonyms : MPS III A, MPS III B, MPS III C, MPS III D, Mucopolysaccharidosis 3, San Filippo's Syndrome, IIIs, Mucopolysaccharidosis, Mucopolysaccharidosis IIIs, Oligophrenia, Polydystrophic, Oligophrenias, Polydystrophic, Polydystrophic Oligophrenias, San Filippo Syndrome
  • Mucopolysaccharidosis IV - »õâ Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint instability, development of cervical myelopathy, and excessive urinary keratan sulfate. There are two biochemically distinct forms, each due to a deficiency of a different enzyme.
    Synonyms : Eccentroosteochondrodysplasia, MPS IV A, MPS IV B, Morquio Disease, Morquio's Syndrome, Mucopolysaccharidosis 4, Disease, Morquio, Disease, Morquio's, Eccentro Osteochondrodysplasia, Eccentro-Osteochondrodysplasias, Eccentroosteochondrodysplasias
¿ÜºÎ ¸µÅ© - Merriam-Webster's ÀÇÇлçÀü ¸ÂÃã °Ë»ö (https://www.merriam-webster.com) °á°ú: 5 ÆäÀÌÁö: 2
¿ÜºÎ ¸µÅ© - A.D.A.M. Medical Encyclopedia ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú: 6 ÆäÀÌÁö: 2
¿ÜºÎ ¸µÅ© - µå·¯±×ÀÎÆ÷ ¾àÇÐ Á¤º¸ ¸ÂÃã °Ë»ö (http://www.druginfo.co.kr) °á°ú: 10 ÆäÀÌÁö: 2
Á¦Ç°¸í
ÆÇ¸Å»ç
º¸ÇèÄÚµå ¼ººÐ/ÇÔ·®
±¸ºÐ/º¸Çè±Þ¿©
¹ÂÄÚÆåÆ®Á¤ - »õâ
Çѱ¹º£¸µ°ÅÀΰÖÇÏÀÓ
A07600351 Ambroxol HCl
ÀϹÝÀǾàǰ | ±Þ¿©
¹ÂÄÚÅ׳îÁ¤ - »õâ
ÇѸ²Á¦¾à
A37802131 Ambroxol HCl, Clenbuterol HCl
Àü¹®ÀǾàǰ | ±Þ¿©
¹ÂÄÚÅõ½ÅÁ¤ - »õâ
¿µÀÏÁ¦¾à
A16601711 Ambroxol HCl, Clenbuterol HCl
Àü¹®ÀǾàǰ | »èÁ¦
¹ÂÄÚº¥½ÇÁ¤ - »õâ
µ¿±¤Á¦¾à
A01302761 Ambroxol HCl, Clenbuterol HCl
Àü¹®ÀǾàǰ | »èÁ¦
¹ÂÄÚÆåÆ®½Ã·´ - »õâ
Çѱ¹º£¸µ°ÅÀΰÖÇÏÀÓ
A07600371 Ambroxol HCl
ÀϹÝÀǾàǰ | »èÁ¦
¹ÂÄÚÁ¹Á¤ - »õâ
ºÎ±¤¾àǰ
A13100831 Bromhexine HCl
ÀϹÝÀǾàǰ | ±Þ¿©
¼Ò¾Æ¿ë¹ÂÄڷн÷´ - »õâ
ºÎ±¤¾àǰ
A13101471 S-carboxymethylcysteine
ÀϹÝÀǾàǰ | ±Þ¿©
¹ÂÄÚ·Ðݼ¿375mg - »õâ
ºÎ±¤¾àǰ
A13101421 S-carboxymethylcysteine
ÀϹÝÀǾàǰ | ±Þ¿©
¹ÂÄÚ·Ð5%½Ã·´ - »õâ
ºÎ±¤¾àǰ
A13150221 S-carboxymethylcysteine
ÀϹÝÀǾàǰ | ±Þ¿©
¹Â°íÁüÁ¤30mg - »õâ
»ï°øÁ¦¾à
A14100281 Lysozyme Chloride
ÀϹÝÀǾàǰ | ºñ±Þ¿©
¿ÜºÎ ¸µÅ© - WebMD.com Drug Reference ¸ÂÃã °Ë»ö (http://www.webmd.com) °á°ú: 4 ÆäÀÌÁö: 2
KMLE À¥ ¿ë¾î ¸ÂÃã °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
mucoid relating to or resembling mucus; "a mucoid substance" any of several glycoproteins similar to mucin
Ãâó: wordnet.princeton.edu/perl/webwn
mucopolysaccharide complex polysaccharides containing an amino group; occur chiefly as components of connective tissue
Ãâó: wordnet.princeton.edu/perl/webwn
mucopolysaccharidosis any of a group of genetic disorders involving a defect in the metabolism of mucopolysaccharides resulting in greater than normal levels of mucopolysaccharides in tissues
Ãâó: wordnet.princeton.edu/perl/webwn
mucopurulent containing or composed of mucus and pus
Ãâó: wordnet.princeton.edu/perl/webwn
Mucor any mold of the genus Mucor
Ãâó: wordnet.princeton.edu/perl/webwn
WordNet ÀÏ¹Ý ¿µ¿µ »çÀü °Ë»ö °á°ú : 8 ÆäÀÌÁö: 2
muco mucus-secreting membrane lining all body cavities or passages that communicate with the exterior
muco of or relating to mucous membranes
muco of or secreting or covered with or resembling mucus
muco of or secreting or covered with or resembling mucus
muco recurrent abdominal pain and diarrhea (often alternating with periods of constipation)
muco mucus-secreting membrane lining all body cavities or passages that communicate with the exterior
muco protective secretion of the mucous membranes
muco the most common congenital disease
¿ÜºÎ ¸µÅ© - American Heritage Dictionary ¿µ¿µ»çÀü ¸ÂÃã °Ë»ö (https://www.ahdictionary.com) °á°ú: 5 ÆäÀÌÁö: 2
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
KMLE ¾àǰ/ÀǾàǰ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
¾Ë±â½¬¿î ÀÇÇпë¾îÇ®ÀÌÁý, ¼­¿ïÀÇ´ë ±³¼ö ÁöÁ¦±Ù, °í·ÁÀÇÇÐ ÃâÆÇ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
¾Ë±â½¬¿î ÀÇÇпë¾îÇ®ÀÌÁý, ¼­¿ïÀÇ´ë ±³¼ö ÁöÁ¦±Ù, °í·ÁÀÇÇÐ ÃâÆÇ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
´ëÇѽŰæ¿Ü°úÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
    ÇÑÀÚ
´ëÇѽŰæ¿Ü°úÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
    ÇÑÀÚ
´ëÇѱâ»ýÃæÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
´ëÇѱâ»ýÃæÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
KMLE ÀÇÇоà¾î »çÀü ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
ÀÇÇÐ³í¹® ¾àÀÚ(Pubmed/Entrez) °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
Çѱ¹Ç¥ÁØÁúº´»çÀκзù ¾àÀÚ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ÄÚµå
    ¿µ¹®
    ÇѱÛ
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 2
¿ÜºÎ ¸µÅ© - Merriam-Webster's ÀÇÇлçÀü À¯»ç °Ë»ö (https://www.merriam-webster.com) °á°ú: 0 ÆäÀÌÁö: 2
¿ÜºÎ ¸µÅ© - A.D.A.M. Medical Encyclopedia À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú: 0 ÆäÀÌÁö: 2
¿ÜºÎ ¸µÅ© - MedlinePlus Health Topics ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú: 0 ÆäÀÌÁö: 2
¿ÜºÎ ¸µÅ© - MedlinePlus Health Topics À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú: 0 ÆäÀÌÁö: 2
¿ÜºÎ ¸µÅ© - µå·¯±×ÀÎÆ÷ ¾àÇÐ Á¤º¸ À¯»ç °Ë»ö (http://www.druginfo.co.kr) °á°ú: 0 ÆäÀÌÁö: 2
Á¦Ç°¸í
ÆÇ¸Å»ç
º¸ÇèÄÚµå ¼ººÐ/ÇÔ·®
±¸ºÐ/º¸Çè±Þ¿©
¿ÜºÎ ¸µÅ© - WebMD.com Drug Reference À¯»ç °Ë»ö (http://www.webmd.com) °á°ú: 0 ÆäÀÌÁö: 2
¿ÜºÎ ¸µÅ© - Drug.com Drugs by Medical Condition ¸ÂÃã °Ë»ö (http://www.drugs.com) °á°ú: 0 ÆäÀÌÁö: 2
¿ÜºÎ ¸µÅ© - Drug.com Drugs by Medical Condition À¯»ç °Ë»ö (http://www.drugs.com) °á°ú: 0 ÆäÀÌÁö: 2
KMLE À¥ ¿ë¾î À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
ÇÑ¿µ/¿µÇÑ »çÀü ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 2
  • ¿µ¹®
    ÇѱÛ
¿ÜºÎ ¸µÅ© - American Heritage Dictionary ¿µ¿µ»çÀü À¯»ç °Ë»ö (https://www.ahdictionary.com) °á°ú: 0 ÆäÀÌÁö: 2
ÅëÇÕ°Ë»ö ¿Ï·á