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Cerebelloparenchymal Disorder I -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Cerebelloparenchymal Disorder Is -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Cerebellopontile angle -- Surgery.   2
 

Cerebellopontine angle -- See Cerebellopontile angle


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Cerebellopontine Angle -- surgery. : Surgery of cerebellopontine lesions / Madjid Samii, Venelin Gerganov  2013 1
 

Cerebelloretinal Angiomatoses, Familial -- See von Hippel-Lindau Disease


An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions
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Cerebelloretinal Angiomatosis, Familial -- See von Hippel-Lindau Disease


An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions
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  Cerebellum -- 2 Related Subjects   2
Cerebellum   10
 

Cerebellum Abnormalities -- See Also the narrower term Arnold-Chiari deformity


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Cerebellum -- Anatomy. : The neuronal codes of the cerebellum / edited by Detlef H. Heck  2016 1
Cerebellum -- anatomy & histology. : Duvernoy's atlas of the human brain stem and cerebellum : high-field MRI : surface anatomy, internal structure, vascularization and 3D sectional anatomy / Thomas P. Naiedich [and others] ; with contributions by T. Benner [and others] ; drawings by Jean-Louis Vannson  2009 1
Cerebellum -- Atlases. : Duvernoy's atlas of the human brain stem and cerebellum : high-field MRI : surface anatomy, internal structure, vascularization and 3D sectional anatomy / Thomas P. Naiedich [and others] ; with contributions by T. Benner [and others] ; drawings by Jean-Louis Vannson  2009 1
 

Cerebellum Degeneration -- See Also the narrower term Friedreich's ataxia


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Cerebellum Disease -- See Cerebellar Diseases


Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA
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  Cerebellum Diseases -- 2 Related Subjects   2
Cerebellum -- Diseases.   7
Cerebellum -- Diseases -- Diagnosis. : Paediatric neurological disorders with cerebellar involvement : diagnosis and management / edited by Stefano D'Arrigo, Daria Riva and Enza Maria Valente  2014 1
Cerebellum -- Diseases -- Handbooks, manuals, etc. : Handbook of the cerebellum and cerebellar disorders / Mario Manto [and others], editors  2013 1
Cerebellum -- Diseases -- Periodicals : Cerebellum & ataxias  2014- 1
 

Cerebellum Dysplastic Gangliocytoma -- See Hamartoma Syndrome, Multiple


A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE
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Cerebellum Dysplastic Gangliocytomas -- See Hamartoma Syndrome, Multiple


A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE
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Cerebellum -- embryology : The cerebellum : from embryology to diagnostic investigations / edited by Mario Manto, Thierry A.G.M. Huisman  2018 1
Cerebellum -- Growth. : Development of the cerebellum from molecular aspects to diseases / Hassan Marzban, editor  2017 1
Cerebellum -- growth & development. : Development of the cerebellum from molecular aspects to diseases / Hassan Marzban, editor  2017 1
Cerebellum -- Handbooks, manuals, etc. : Handbook of the cerebellum and cerebellar disorders / Mario Manto [and others], editors  2013 1
Cerebellum -- Magnetic resonance imaging -- Atlases. : MRI atlas of the human cerebellum / [edited by] Jeremy D. Schmahmann [and others]  2000 1
Cerebellum -- Periodicals   2
Cerebellum -- Physiology.   6
Cerebellum -- physiopathology. : Speech and language disorders associated with subcortical pathology / Bruce E. Murdoch, Brooke-Mai Whelan  2009 1
Cerebellum -- Surgery. : Surgery of the cerebellopontine angle / by Nicholas, C Bambakidis, Cliff A. Megerian [and] Robert F. Spetzler  2009 1
 

Cerebellum Tumors -- See Also the narrower term Medulloblastoma


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Cerebellums -- See Cerebellum


The part of brain that lies behind the BRAIN STEM in the posterior base of skull (CRANIAL FOSSA, POSTERIOR). It is also known as the "little brain" with convolutions similar to those of CEREBRAL CORTEX, inner white matter, and deep cerebellar nuclei. Its function is to coordinate voluntary movements, maintain balance, and learn motor skills
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Cerebellus, Corpus -- See Cerebellum


The part of brain that lies behind the BRAIN STEM in the posterior base of skull (CRANIAL FOSSA, POSTERIOR). It is also known as the "little brain" with convolutions similar to those of CEREBRAL CORTEX, inner white matter, and deep cerebellar nuclei. Its function is to coordinate voluntary movements, maintain balance, and learn motor skills
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Cerebellus, Tentorium -- See Spinal Cord


A cylindrical column of tissue that lies within the vertebral canal. It is composed of WHITE MATTER and GRAY MATTER

--consider also terms at MYEL-
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Cerebral Aneurysm -- See Intracranial Aneurysm


Abnormal outpouching in the wall of intracranial blood vessels. Most common are the saccular (berry) aneurysms located at branch points in CIRCLE OF WILLIS at the base of the brain. Vessel rupture results in SUBARACHNOID HEMORRHAGE or INTRACRANIAL HEMORRHAGES. Giant aneurysms (>2.5 cm in diameter) may compress adjacent structures, including the OCULOMOTOR NERVE. (From Adams et al., Principles of Neurology, 6th ed, p841)
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  Cerebral Aneurysms -- 2 Related Subjects   2
 

Cerebral Angiographies -- See Cerebral Angiography


Radiography of the vascular system of the brain after injection of a contrast medium
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Cerebral angiography -- See Brain Blood-vessels Radiography


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Cerebral Angiography.   4
Cerebral Angiography -- methods.   2
 

Cerebral Angiospasm -- See Vasospasm, Intracranial


Constriction of arteries in the SKULL due to sudden, sharp, and often persistent smooth muscle contraction in blood vessels. Intracranial vasospasm results in reduced vessel lumen caliber, restricted blood flow to the brain, and BRAIN ISCHEMIA that may lead to hypoxic-ischemic brain injury (HYPOXIA-ISCHEMIA, BRAIN)
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Cerebral Angiospasms -- See Vasospasm, Intracranial


Constriction of arteries in the SKULL due to sudden, sharp, and often persistent smooth muscle contraction in blood vessels. Intracranial vasospasm results in reduced vessel lumen caliber, restricted blood flow to the brain, and BRAIN ISCHEMIA that may lead to hypoxic-ischemic brain injury (HYPOXIA-ISCHEMIA, BRAIN)
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Cerebral anoxia. : Brain hypoxia and ischemia : with special emphasis on development / Gabriel G. Haddad, Shan Ping Yu, editors  2009 1
 

Cerebral Anoxia-Ischemia -- See Hypoxia-Ischemia, Brain


A disorder characterized by a reduction of oxygen in the blood combined with reduced blood flow (ISCHEMIA) to the brain from a localized obstruction of a cerebral artery or from systemic hypoperfusion. Prolonged hypoxia-ischemia is associated with ISCHEMIC ATTACK, TRANSIENT; BRAIN INFARCTION; BRAIN EDEMA; COMA; and other conditions
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Cerebral Anoxia-Ischemias -- See Hypoxia-Ischemia, Brain


A disorder characterized by a reduction of oxygen in the blood combined with reduced blood flow (ISCHEMIA) to the brain from a localized obstruction of a cerebral artery or from systemic hypoperfusion. Prolonged hypoxia-ischemia is associated with ISCHEMIC ATTACK, TRANSIENT; BRAIN INFARCTION; BRAIN EDEMA; COMA; and other conditions
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Cerebral Arteries -- See Also Cerebral Angiography


Radiography of the vascular system of the brain after injection of a contrast medium
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Cerebral arteries -- Abnormalities.   2
Cerebral Arteries -- diagnostic imaging.   2
Cerebral arteries -- Dissection -- Handbooks, manuals, etc. : Handbook on cerebral artery dissection / volume editors, R.W. Baumgartner [and others]  2005 1
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