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Cerebellar Ataxia.   2
 

Cerebellar Ataxias -- See Cerebellar Ataxia


Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
  1
 

Cerebellar Degeneration with Slow Eye Movements -- 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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Cerebellar 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
  1
Cerebellar Diseases.   3
Cerebellar Diseases -- diagnosis   3
Cerebellar Diseases -- therapy   3
 

Cerebellar Disorder -- 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
  1
 

Cerebellar Disorders -- 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
  1
 

Cerebellar Dysfunction -- 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
  1
 

Cerebellar Dysfunctions -- 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
  1
 

Cerebellar Dysmetria -- See Cerebellar Ataxia


Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
  1
 

Cerebellar Dysmetrias -- See Cerebellar Ataxia


Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
  1
 

Cerebellar Hemiataxia -- See Cerebellar Ataxia


Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
  1
 

Cerebellar Hemiataxias -- See Cerebellar Ataxia


Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
  1
 

Cerebellar Incoordination -- See Cerebellar Ataxia


Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
  1
 

Cerebellar Incoordinations -- See Cerebellar Ataxia


Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
  1
 

Cerebellar Mossy Fiber -- See Nerve Fibers


Slender processes of NEURONS, including the AXONS and their glial envelopes (MYELIN SHEATH). Nerve fibers conduct nerve impulses to and from the CENTRAL NERVOUS SYSTEM
  1
 

Cerebellar Mossy Fibers -- See Nerve Fibers


Slender processes of NEURONS, including the AXONS and their glial envelopes (MYELIN SHEATH). Nerve fibers conduct nerve impulses to and from the CENTRAL NERVOUS SYSTEM
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Cerebellar Neoplasms -- genetics. : NF2 & Gorlins / D. Gareth R. Evans  2014 1
 

Cerebellar Syndrome -- 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
  1
 

Cerebellar Syndromes -- 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
  1
 

Cerebellar White Matter -- See White Matter


The region of CENTRAL NERVOUS SYSTEM that appears lighter in color than the other type, GRAY MATTER. It mainly consists of MYELINATED NERVE FIBERS and contains few neuronal cell bodies or DENDRITES
  1
 

Cerebellar White Matters -- See White Matter


The region of CENTRAL NERVOUS SYSTEM that appears lighter in color than the other type, GRAY MATTER. It mainly consists of MYELINATED NERVE FIBERS and contains few neuronal cell bodies or DENDRITES
  1
Cerebelleum -- anatomy & histology : The cerebellum : from embryology to diagnostic investigations / edited by Mario Manto, Thierry A.G.M. Huisman  2018 1
 

Cerebelli, 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
  1
 

Cerebelli, 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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Cerebello-pontile angle -- See Cerebellopontile angle


  1
 

Cerebello-Retinal 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
  1
 

Cerebello-Retinal 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
  1
 

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)
  1
 

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)
  1
Cerebellopontile angle -- Surgery.   2
 

Cerebellopontine angle -- See Cerebellopontile angle


  1
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
  1
 

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
  1
  Cerebellum -- 2 Related Subjects   2
Cerebellum.   10
 

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


  1
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


  1
 

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
  1
  Cerebellum Diseases -- 2 Related Subjects   2
Cerebellum -- Diseases.   9
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 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
  1
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