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  • ¿µ¹®
    ÇѱÛ
  • neurolemma
    ½Å°æÁý, ½Å°æÃÊ
  • neuroleptanalgesia
    ½Å°æÀÌ¿ÏÁøÅë
  • neuroleptanesthesia
    ½Å°æÀ̿ϸ¶Ãë(¹ý)
  • neuroleptic
    ½Å°æÀÌ¿ÏÁ¦
  • neuroleptic malignant syndrome
    ½Å°æÀÌ¿ÏÁ¦¾Ç¼ºÁõÈıº
  • neuroleptic-induced disorder
    Ç×Á¤½Åº´¾à¹°À¯¹ßÀå¾Ö
  • neuroleptization
    ½Å°æÀÌ¿ÏÈ­
  • neurolipomatosis
    ½Å°æÁö¹æÁ¾Áõ
  • neurologic
    ½Å°æÇÐÀû-
  • neurologic examination
    ½Å°æÇÐÀû°Ë»ç
  • neurological disorder
    ½Å°æ°èÀå¾Ö, ½Å°æ°èÁúȯ
  • neurologist
    ½Å°æ°úÀÇ»ç, ½Å°æÇÐÀÚ
  • neurology
    ½Å°æÇÐ
  • neurolysin
    ½Å°æ¿ëÇØ¼Ò
  • neurolysis
    ½Å°æ¹Ú¸®(¼ú)
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 11
  • ¿µ¹®
    ÇѱÛ
  • neurolysin
    ½Å°æ¿ëÇØ¼Ò
  • neurolysis
    ½Å°æ¹Ú¸®¼ú
  • neuroma
    ½Å°æÁ¾
  • neuromalacia
    ½Å°æ¿¬È­(Áõ)
  • neuromatosis
    ½Å°æÁ¾Áõ
  • neuromelanocyte
    ½Å°æ¸á¶ó´Ñ¼¼Æ÷
  • neuromere
    ½Å°æºÐÀý
  • neuromotor
    ½Å°æ¿îµ¿-
  • neuromuscular
    ½Å°æ±ÙÀ°-
  • neuromuscular antagonist
    ½Å°æ±ÙÀ°´ëÇ×Á¦
  • neuromuscular blocker
    ½Å°æ±ÙÀ°Â÷´ÜÁ¦
  • neuromuscular coordination
    ½Å°æ±ÙÀ°Çùµ¿
  • neuromuscular disease
    ½Å°æ±ÙÀ°º´
  • neuromuscular disorder
    ½Å°æ±ÙÀ°Àå¾Ö, ½Å°æ±ÙÀ°Áúȯ
  • neuromuscular dysfunction
    ½Å°æ±ÙÀ°±â´ÉÀå¾Ö
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 11
  • ¿µ¹®
    ÇѱÛ
  • neurochoroiditis
    ¸Æ¶ô¸·½Ã½Å°æ¿°(ØæÕ©Ø¯ãÊãêÌèæú).
  • neurocirculatory
    ½Å°æ¼øÈ¯(ãêÌèâàü»)ÀÇ.
  • neurocirculatory asthenia
    ½Å°æ¼øÈ¯¹«·ÂÁõ(~Ùíæ³ñø).
  • neurocirculatory collapse
    ½Å°æ¼øÈ¯ÇãÅ»(~úÈ÷­).
  • neurocirculatory dystonia
    ½Å°æ¼øÈ¯¼º À̱äÀåÁõ.
  • neuroclonic
    ½Å°æ°æ·Ã(ãêÌèÌâÕý)ÀÇ.
  • neurocoel
    ½Å°æ°­(ãêÌèË·).
  • neurocranium
    ³ú¸Ó¸®»À (³úµÎ°³°ñ)
  • neurocranium
    ³úµÎ°³°ñ, ½Å°æµÎ°³(~ÔéËÏ).
  • neurocranium
    ³ú¸Ó¸®»À
  • neurocrine
    ½Å°æºÐºñ(ÀÇ), ½Å°æÀۿ뼺 ºÐºñ.
  • neurocrinia
    ½Å°æÀۿ뼺 ÀÛ¿ë.
  • neurocutaneous
    ½Å°æ ÇǺÎÀÇ
  • neurocutaneous syndrome
    ½Å°æÇǺÎÁõÈıº(¡­ù«Ý±ñøý¦ÏØ)
  • neurocyte
    ½Å°æ¼¼Æ÷(ãêÌèá¬øà).
ÀÇÇÐ³í¹® ¾àÀÚ(Pubmed/Entrez) °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 5 ÆäÀÌÁö: 11
  • JrId: 6086
    JournalTitle: Neurosciences research.
    MedAbbr: Neurosci Res (N Y)
    ISSN: 0077-7846
    ESSN:
    IsoAbbr: Neurosci. Res.
    NlmId: 435453
  • JrId: 6087
    JournalTitle: Neuroscience.
    MedAbbr: Neuroscience
    ISSN: 0306-4522
    ESSN:
    IsoAbbr: Neuroscience
    NlmId: 7605074
  • JrId: 6088
    JournalTitle: Neurosciences Research Program bulletin.
    MedAbbr: Neurosci Res Program Bull
    ISSN: 0028-3967
    ESSN:
    IsoAbbr:
    NlmId: 7509226
  • JrId: 6166
    JournalTitle: Neuroscience and biobehavioral reviews.
    MedAbbr: Neurosci Biobehav Rev
    ISSN: 0149-7634
    ESSN:
    IsoAbbr:
    NlmId: 7806090
  • JrId: 6167
    JournalTitle: the official journal of the Japan Neuroscience Society.
    MedAbbr: Neurosci Res Suppl
    ISSN: 0921-8696
    ESSN:
    IsoAbbr: Neurosci. Res. Suppl.
    NlmId: 8508422
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 11
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • neuronal heterotopia
    À̼Ҽº ½Å°æ¿ø
  • neuronal representation
    ´º¿ì·± Ç¥Çö
  • neuronal storage disease
    ½Å°æ ÃàÀûÁõ
  • neuronephric
    ½Å°æ ½ÅÀÇ
    ½Å°æ°è ¹× ½Å°è¿¡ °ü°èµÈ.
  • neuronitis
    ´º¿ì·Ð¿°, ½Å°æ¿ø¿°
    ô¼ö³»ÀÇ ½Å°æ±Ù ¹× ¼¼Æ÷¿¡ ¿°ÁõÀ» ÀÏÀ¸Å°´Â Áúȯ.
  • neuronophage
    ½Å°æ¿ø ½Ä¼¼Æ÷
    µ¿ÀǾî=neuro
  • neuronophagia
    ´º·Î³ëÆÄ±â¾Æ, ½Å°æ¿ø ½ÄÇö»ó, ½Å°æ ¼¼Æ÷ ½ÄÇö»ó
    µ¿ÀǾî=neurono
  • neuronophagocytosis =neuronophagia
    ½Å°æ ¼¼Æ÷ ħ½Ä
    ½ÄÀÛ¿ë¿¡ ÀÇÇÑ ½Å°æ ¼¼Æ÷ÀÇ ÆÄ±«.
  • neuronotropic
    ½Å°æ¿ø ģȭ¼ºÀÇ
    ´º·Ð¿¡ ´ëÇØ¼­ Ưº°ÇÑ Ä£È­¼ºÀ» °¡Áø.
  • neuroparalytic keratitis
    ½Å°æ ¸¶ºñ¼º °¢¸·¿°, ¿µ¾ç ½Å°æ¼º °¢¸·¿°
    »ïÂ÷ ½Å°æÀÇ Àå¾Ö·Î, ¾È°ËÀÇ Æó¼â¿¡ ÁöÀåÀ» ¹ÞÀ¸¸ç °¢¸· »óÇÇ¿¡´Â °ÇÁ¶¿Í ±Õ¿­ÀÌ »ý±â´Â »óÅÂ.
  • neuropathic disorder
    ½Å°æ Àå¾Ö
  • neuropathic pain
    ½Å°æº´º¯¼º µ¿Åë, ½Å°æº´¼º ÅëÁõ, ½Å°æº´Áõ¼º ÅëÁõ
    µ¿ÀǾî=neurogenous
  • neuropathic pain disorder
    ½Å°æ¼º µ¿Åë Àå¾Ö, ½Å°æº´¼º µ¿Åë Àå¾Ö
  • neuropathic process
    ½Å°æº´Áõ¼º °úÁ¤
  • neuropathogenesis
    ½Å°æº´ ¹ß»ý, ½Å°æº´ ¹ßº´·Ð
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 11
neuroendocrinology The study of the anatomical and functional relationships between the nervous system and the endocrine system.
(12 Dec 1998)
neuroepithelial Relating to the neuroepithelium.
(05 Mar 2000)
neuroepithelial body A corpuscular aggregate of nonciliated cells containing neurosecretory substance found in normal bronchial epithelium.
(05 Mar 2000)
neuroepithelial cells neuroectoderm
neuroepithelial layer of retina The outermost layer of the cerebral layer of retina, composed of the primary receptor cells of the retina; the stratum consists of two sublayers: 1) an external layer made up of the rods and cones, the photosensitive processes of the receptor cells, and 2) the external nuclear layer containing the cell bodies of these cells; the external limiting membrane forms a perforated supporting plate between the two sublayers; the name refers to the fact that the retinal receptor cells are a specialised form of (epithelial) ependyma cell and thus, in a sense, are comparable to the neuroepithelial cells (e.g., hair cells) of other sense organs.
Synonym: external nuclear layer of retina, stratum neuroepitheliale retinae, stratum nucleare externum retinae.
(05 Mar 2000)
neuroepithelium <embryology> Ectoderm on the dorsal surface of the early vertebrate embryo that gives rise to the cells (neurons and glia) of the nervous system.
Synonym: neural plate.
(04 Mar 1998)
neuroepithelium cristae ampullaris neuroepithelium of ampullary crest
neuroepithelium maculae The specialised sensory hair cells of the epithelium of the macula sacculi and macula utriculi.
Synonym: neuroepithelium maculae.
(05 Mar 2000)
neuroepithelium of macula The specialised sensory hair cells of the epithelium of the macula sacculi and macula utriculi.
Synonym: neuroepithelium maculae.
(05 Mar 2000)
neurofascin <protein> Axon associated adhesion molecule of the vertebrate nervous system. Contains 6 Ig like motifs and 4 fibronectin type II repeats. (Related to Ng CAM, Nr CAM).
(18 Nov 1997)
neurofibril A filamentous structure seen with the light microscope in the nerve cell's body, dendrites, axon, and sometimes synaptic endings, as aggregations of much finer ultramicroscopic elements, the neurofilaments and microtubules; their functional significance remains to be established.
(05 Mar 2000)
neurofibrillar Relating to neurofibrils.
(05 Mar 2000)
neurofibrillar nerve <anatomy, nerve> The intertwined patterns formed by neurofibrils in the neuron.
(05 Mar 2000)
neurofibrillary degeneration Formation of coarse, argentophilic, intracytoplasmic fibres, often in complex tangles within intracranial nerve cells that are undergoing aging.
See: Alzheimer's disease.
(05 Mar 2000)
neurofibrillary tangle <cell biology> Accumulation of twisted protein fragments inside nerve cells. Neurofibrillary tangles are one of the characteristic structural abnormalities found in the brains of patients with Alzheimer's disease patients.
Upon autopsy, the presence of neuritic plaquesand neurofibrillary tangles is used to positively diagnose Alzheimer's disease.
(22 May 1997)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 11
  • Neurofibroma, Plexiform - »õâ A type of neurofibroma manifesting as a diffuse overgrowth of subcutaneous tissue, usually involving the face, scalp, neck, and chest but occasionally occurring in the abdomen or pelvis. The tumors tend to progress, and may extend along nerve roots to eventually involve the spinal roots and spinal cord. This process is almost always a manifestation of NEUROFIBROMATOSIS 1. (From Adams et al., Principles of Neurology, 6th ed, p1016; J Pediatr 1997 Nov;131(5):678-82)
    Synonyms : Tumor Royale, Elephantiasis Neuromatoses, Neurofibromas, Plexiform, Neuroma, Plexiform, Pachydermatoceles, Plexiform Neurofibroma, Plexiform Neurofibromas, Plexiform Neuroma, Plexiform Neuromas
  • Neurofibromatoses - »õâ A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72)
    Synonyms : Multiple Neurofibromas, Neurofibromatosis 3, Neurofibromatosis Syndrome, Multiple Neurofibroma, Neurofibroma, Multiple, Neurofibromas, Multiple, Neurofibromatosis 3s, Neurofibromatosis Syndromes, Syndrome, Neurofibromatosis, Syndromes, Neurofibromatosis
  • Neurofibromatosis 1 - »õâ An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS).
    Synonyms : NF1 (Neurofibromatosis 1), Neurofibromatosis I, Neurofibromatosis Type 1, Neurofibromatosis Type I, Neurofibromatosis, Peripheral, NF 1, Neurofibromatosis, Peripheral, NF1, Neurofibromatosis, Type 1, Neurofibromatosis, Type I, Recklinghausen's Disease of Nerve
  • Neurofibromatosis 2 - »õâ An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life.
    Synonyms : Bilateral Acoustic Neurofibromatosis, Familial Acoustic Neuromas, NF2 (Neurofibromatosis 2), Neurofibromatosis II, Neurofibromatosis Type 2, Neurofibromatosis Type II, Neurofibromatosis, Central NF2, Neurofibromatosis, Central, NF 2, Neurofibromatosis, Type 2
  • Neurofibromin 1 - »õâ A protein found most abundantly in the nervous system. Defects or deficiencies in this protein are associated with NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome. Mutations in the gene (GENE, NEUROFIBROMATOSIS 1) affect two known functions: regulation of ras-GTPase and tumor suppression.
    Synonyms : NF-1 Protein, NF1 GRP, NF1 Protein, NF1-GAP-Related Protein, Neurofibromatosis Type 1 Gene Product, Neurofibromin, NF 1 Protein, NF1 GAP Related Protein
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neurosarcoma a malignant neoplasm of nerve tissue and fibrous tissue and connective tissue
Ãâó: wordnet.princeton.edu/perl/webwn
neuronal neural: of or relating to neurons; "neural network"
Ãâó: wordnet.princeton.edu/perl/webwn
neuroscience the scientific study of the nervous system
Ãâó: wordnet.princeton.edu/perl/webwn
neurasthenia nervous breakdown (not in technical use)
Ãâó: wordnet.princeton.edu/perl/webwn
neurasthenic a person suffering a nervous breakdown of or relating to or suffering from neurasthenia; "neurasthenic tendencies"
Ãâó: wordnet.princeton.edu/perl/webwn
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