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Idiopathic Inflammatory Myopathies -- See Myositis


Inflammation of a muscle or muscle tissue
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Idiopathic Inflammatory Myopathy -- See Myositis


Inflammation of a muscle or muscle tissue
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Idiopathic Inflammatory Myositis -- See Myositis


Inflammation of a muscle or muscle tissue
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Idiopathic Interstitial Pneumonia -- See Idiopathic Interstitial Pneumonias


A group of interstitial lung diseases with no known etiology. There are several entities with varying patterns of inflammation and fibrosis. They are classified by their distinct clinical-radiological-pathological features and prognosis. They include IDIOPATHIC PULMONARY FIBROSIS; CRYPTOGENIC ORGANIZING PNEUMONIA; and others
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Your entry Idiopathic Interstitial Pneumonias would be here -- Search as Words
 

Idiopathic Interstitial Pneumonitis - from Asbestos Exposure -- See Asbestosis


A form of pneumoconiosis caused by inhalation of asbestos fibers which elicit potent inflammatory responses in the parenchyma of the lung. The disease is characterized by interstitial fibrosis of the lung, varying from scattered sites to extensive scarring of the alveolar interstitium
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Idiopathic Parkinson Disease -- See Parkinson Disease


A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75)
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Idiopathic Parkinson's Disease -- See Parkinson Disease


A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75)
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Idiopathic Proctocolitis -- See Colitis, Ulcerative


Inflammation of the COLON that is predominantly confined to the MUCOSA. Its major symptoms include DIARRHEA, rectal BLEEDING, the passage of MUCUS, and ABDOMINAL PAIN
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Idiopathic Pulmonary Fibroses -- See Idiopathic Pulmonary Fibrosis


A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change
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Idiopathic Pulmonary Fibrosis   3
Idiopathic Pulmonary Fibrosis -- diagnosis.   2
 

Idiopathic Pulmonary Fibrosis, Familial -- See Idiopathic Pulmonary Fibrosis


A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change
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Idiopathic Pulmonary Fibrosis -- therapy.   2
 

Idiopathic Sexual Precocities -- See Puberty, Precocious


Development of SEXUAL MATURATION in boys and girls at a chronological age that is 2.5 standard deviations below the mean age at onset of PUBERTY in the population. This early maturation of the hypothalamic-pituitary-gonadal axis results in sexual precocity, elevated serum levels of GONADOTROPINS and GONADAL STEROID HORMONES such as ESTRADIOL and TESTOSTERONE
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Idiopathic Sexual Precocity -- See Puberty, Precocious


Development of SEXUAL MATURATION in boys and girls at a chronological age that is 2.5 standard deviations below the mean age at onset of PUBERTY in the population. This early maturation of the hypothalamic-pituitary-gonadal axis results in sexual precocity, elevated serum levels of GONADOTROPINS and GONADAL STEROID HORMONES such as ESTRADIOL and TESTOSTERONE
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Idiopathic Thrombocytopenic Purpura -- See Purpura, Thrombocytopenic, Idiopathic


Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms
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Idiopathic Thrombocytopenic Purpuras -- See Purpura, Thrombocytopenic, Idiopathic


Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms
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Idiopathic Torsion Dystonia -- See Dystonia Musculorum Deformans


A condition characterized by focal DYSTONIA that progresses to involuntary spasmodic contractions of the muscles of the legs, trunk, arms, and face. The hands are often spared, however, sustained axial and limb contractions may lead to a state where the body is grossly contorted. Onset is usually in the first or second decade. Familial patterns of inheritance, primarily autosomal dominant with incomplete penetrance, have been identified. (Adams et al., Principles of Neurology, 6th ed, p1078)
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Idiopathic Torsion Dystonias -- See Dystonia Musculorum Deformans


A condition characterized by focal DYSTONIA that progresses to involuntary spasmodic contractions of the muscles of the legs, trunk, arms, and face. The hands are often spared, however, sustained axial and limb contractions may lead to a state where the body is grossly contorted. Onset is usually in the first or second decade. Familial patterns of inheritance, primarily autosomal dominant with incomplete penetrance, have been identified. (Adams et al., Principles of Neurology, 6th ed, p1078)
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Idiopathic Trigeminal Neuralgia -- See Trigeminal Neuralgia


A syndrome characterized by recurrent episodes of excruciating pain lasting several seconds or longer in the sensory distribution of the TRIGEMINAL NERVE. Pain may be initiated by stimulation of trigger points on the face, lips, or gums or by movement of facial muscles or chewing. Associated conditions include MULTIPLE SCLEROSIS, vascular anomalies, ANEURYSMS, and neoplasms. (Adams et al., Principles of Neurology, 6th ed, p187)
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Idiopathic Trigeminal Neuralgias -- See Trigeminal Neuralgia


A syndrome characterized by recurrent episodes of excruciating pain lasting several seconds or longer in the sensory distribution of the TRIGEMINAL NERVE. Pain may be initiated by stimulation of trigger points on the face, lips, or gums or by movement of facial muscles or chewing. Associated conditions include MULTIPLE SCLEROSIS, vascular anomalies, ANEURYSMS, and neoplasms. (Adams et al., Principles of Neurology, 6th ed, p187)
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Idiopathic ventricular fibrillation -- See Brugada syndrome


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Idiostomidae -- See Scarabaeidae


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Idiosyncratic drug reactions -- See Also the narrower term Drug allergy


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Idiosyncratic drug reactions. : Q and A : February 18, 2019  2019 1
Idiot de la familie Sartre, Jean-Paul, 1905-1980 : Sartre & Flaubert / Hazel E. Barnes  1981 1
Idiot de la famille Sartre, Jean-Paul, 1905-1980 : Sartre & Flaubert / Hazel E. Barnes  1981 1
Idiot de la famille Sartre, Jean-Paul, 1905-1980 English : Sartre & Flaubert / Hazel E. Barnes  1981 1
Idiot Dostoyevsky, Fyodor, 1821-1881   2
Idiot Dostoyevsky, Fyodor, 1821-1881 Criticism and interpretation : Subordinated Ethics Natural Law and Moral Miscellany in Aquinas and Dostoyevsky  2020 1
 

Idiot (Motion picture) -- See Hakuchi (Motion picture)


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Idiot-savant.   2
 

Idiot savant syndrome -- See Savant syndrome


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Idiot savants -- See Savants (Savant syndrome)


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Idioterne (Motion picture) : The idiots / John Rockwell  2003 1
Idiotismes Fraņcais (Langue) Canada : Les Francais dici en perspective  2020 1
 

Idiotopes, Immunoglobulin -- See Immunoglobulin idiotypes


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Idiotyp -- Antikörper -- Immunsystem. : The network collective : rise and fall of a scientific paradigm / Klaus Eichmann  2008 1
Idiotyp Immunsystem Antikörper : The network collective : rise and fall of a scientific paradigm / Klaus Eichmann  2008 1
 

Idiotype immune networks -- See Idiotypic networks


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Idiotype networks -- See Idiotypic networks


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Idiotypes, Antibody -- See Immunoglobulin idiotypes


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Idiotypes, Immunoglobulin -- See Immunoglobulin idiotypes


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Idiotypic immune networks -- See Idiotypic networks


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Idiotypic networks -- See Also the narrower term Immune response Regulation


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Idiotypic networks. : The network collective : rise and fall of a scientific paradigm / Klaus Eichmann  2008 1
Idiotypic networks -- Research. : The network collective : rise and fall of a scientific paradigm / Klaus Eichmann  2008 1
 

Idioverse -- See Idiodynamics


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Idj-Inadjana language (Y17) (Qld SD54-04) -- See Itinadyana language Y17


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Idj-Inadjana people (Y17) (Qld SD54-04) -- See Itinadyana people Y17


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