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Cerebral Vasospasms -- 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)
  1
 

Cerebral Veins -- See Also Cerebral Angiography


Radiography of the vascular system of the brain after injection of a contrast medium
  1
Cerebral veins. : Cerebral venous system in acute and chronic brain injuries / Min Lou, Jianmin Zhang, Yilong Wang, Yan Qu, Wuwei Feng, Xunming Ji, John H. Zhang, editors  2019 1
Cerebral Veins -- diagnostic imaging : Neurosonological evaluation of cerebral venous outflow : an ultrasound atlas / by Giovanni Malferrari, Marialuisa Zedde, Patrizio Prati  2014 1
Cerebral Ventricles   2
Cerebral Ventricles -- cytology : Mammalian subventricular zones : their roles in brain development, cell replacement, and disease / edited by Steven W. Levison  2006 1
  Cerebral Ventriculitis -- 2 Related Subjects   2
 

Cerebral Ventriculomegalies -- See Hydrocephalus


Excessive accumulation of cerebrospinal fluid within the cranium which may be associated with dilation of cerebral ventricles, INTRACRANIAL HYPERTENSION; HEADACHE; lethargy; URINARY INCONTINENCE; and ATAXIA
  1
 

Cerebral Ventriculomegalies, Fetal -- See Hydrocephalus


Excessive accumulation of cerebrospinal fluid within the cranium which may be associated with dilation of cerebral ventricles, INTRACRANIAL HYPERTENSION; HEADACHE; lethargy; URINARY INCONTINENCE; and ATAXIA
  1
 

Cerebral Ventriculomegaly -- See Hydrocephalus


Excessive accumulation of cerebrospinal fluid within the cranium which may be associated with dilation of cerebral ventricles, INTRACRANIAL HYPERTENSION; HEADACHE; lethargy; URINARY INCONTINENCE; and ATAXIA
  1
 

Cerebral Ventriculomegaly, Fetal -- See Hydrocephalus


Excessive accumulation of cerebrospinal fluid within the cranium which may be associated with dilation of cerebral ventricles, INTRACRANIAL HYPERTENSION; HEADACHE; lethargy; URINARY INCONTINENCE; and ATAXIA
  1
Cerebrale Bewegungsstörung : Movement disorder surgery / volume editor, A.M. Lozano  2000 1
Cerebrale Kinderlähmung : Improving hand function in cerebral palsy : theory, evidence and intervention / edited by Ann-Christin Eliasson and Patricia A. Burtner  2008 1
Cerebrale stoornissen.   7
Cerebrale verlamming.   2
 

Cerebri, Cortex -- See Cerebral Cortex


The thin layer of GRAY MATTER on the surface of the CEREBRAL HEMISPHERES that develops from the TELENCEPHALON and folds into gyri and sulchi. It reaches its highest development in humans and is responsible for intellectual faculties and higher mental functions
  1
 

Cerebri, Falx -- 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-
  1
 

Cerebri, Hypophysis -- See Pituitary Gland


A small, unpaired gland situated in the SELLA TURCICA. It is connected to the HYPOTHALAMUS by a short stalk which is called the INFUNDIBULUM

--consider also terms at HYPOPHYS-
  1
Cérebro. : Nutrition and brain / John D. Fernstrom, Ricardo Uauy, Pedro Arroyo, [editors]  2001 1
Cerebro -- Imágenes por resonancia magnética -- Modelos matemáticos : Mathematical modeling of the human brain : from magnetic resonance images to finite element simulation / Kent-André Mardal, Marie E. Rognes, Travis B. Thompson, Lars Magnus Valnes  2022 1
 

Cerebro Spinal Fluid -- See Cerebrospinal Fluid


A watery fluid that is continuously produced in the CHOROID PLEXUS and circulates around the surface of the BRAIN; SPINAL CORD; and in the CEREBRAL VENTRICLES
  1
 

Cerebro Spinal Fluids -- See Cerebrospinal Fluid


A watery fluid that is continuously produced in the CHOROID PLEXUS and circulates around the surface of the BRAIN; SPINAL CORD; and in the CEREBRAL VENTRICLES
  1
 

Cerebroatrophic Hyperammonemia -- See Rett Syndrome


An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199)
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Cerebroatrophic Hyperammonemias -- See Rett Syndrome


An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199)
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Cerebrocuprein -- See Superoxide dismutase


  1
 

Cerebrorachidian fluid -- See Cerebrospinal fluid


  1
 

Cerebroretinal Degeneration, Juvenile -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
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Cerebroretinal Degenerations, Juvenile -- See Neuronal Ceroid-Lipofuscinoses


A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure
  1
 

Cerebroside Lipidoses, Glucosyl -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Cerebroside lipidosis -- See Gaucher disease


  1
 

Cerebroside Lipidosis, Glucosyl -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Cerebroside Lipidosis Syndrome -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Cerebroside Lipidosis Syndromes -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Cerebrosides Metabolism Disorders -- See Also the narrower term Gaucher disease


  1
 

Cerebrospinal Axi -- See Central Nervous System


The main information-processing organs of the nervous system, consisting of the brain, spinal cord, and meninges
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Cerebrospinal Axis -- See Central Nervous System


The main information-processing organs of the nervous system, consisting of the brain, spinal cord, and meninges
  1
 

Cerebrospinal cysticercosis -- See Neurocysticercosis


  1
 

Cerebrospinal fever -- See Meningitis, Cerebrospinal


  1
  Cerebrospinal fluid -- 4 Related Subjects   4
Cerebrospinal fluid.   16
Cerebrospinal fluid -- Analysis : Diagnostic lumbar puncture in adults : animated demonstration  2020 1
Cerebrospinal fluid -- Atlases. : Atlas der praktischen Liquorzytologie. English  2007 1
cerebrospinal fluid Central Nervous System Diseases : Cerebrospinal fluid in clinical practice / [edited by] David N. Irani  2009 1
Cerebrospinal Fluid -- cytology.   2
Cerebrospinal fluid -- Diseases : Cerebrospinal fluid rhinorrhea : comprehensive guide to evaluation and management / [edited by] Raj Sindwani, Christopher Roxbury  2024 1
Cerebrospinal fluid -- Examination.   6
Cerebrospinal fluid -- Laboratory manuals : Cerebrospinal fluid (CSF) proteomics : methods and protocols / edited by Enrique Santamaría and Joaquín Fernández-Irigoyen  2019 1
Cerebrospinal Fluid -- metabolism : Molecular Physiology and Metabolism of the Nervous System : a Clinical Perspective  2012 1
cerebrospinal fluid Nervous System Diseases : Cerebrospinal fluid in clinical neurology / Florian Deisenhammer, Finn Sellebjerg, Charlotte E Teunissen, Hayrettin Tumani, editors  2015 1
Cerebrospinal fluid -- Periodicals : Fluids and barriers of the CNS  2011- 1
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