*  Nursing Care for Neurological Patients
Suspected causes include genetic factors, viruses, chemical toxicity, encephalitis, and cerebrovascular disease.. b. Signs and ... 1) Primary degenerative changes of the basal ganglia and their connections prevent motor transmission of automatic movements ( ... PARKINSON'S DISEASE a. Definition. Parkinson's disease is a progressive neurological disorder affecting the brain centers that ... 6) Inform patient about American Parkinson's Disease Foundation for patient education and group support.. ...
  http://www.free-ed.net/sweethaven/MedTech/NurseCare/NeuroNurse01.asp?iNum=35
*  Assessment of Social-emotional Functioning in Neurological Diseases - Full Text View - ClinicalTrials.gov
Nervous System Diseases. Vascular Diseases. Cardiovascular Diseases. Parkinsonian Disorders. Basal Ganglia Diseases. Movement ... Alzheimer Disease. Dementia. Huntington Disease. Lewy Body Disease. Cerebrovascular Disorders. Brain Diseases. Central Nervous ... Genetic and Rare Diseases Information Center resources: Familial Alzheimer Disease Primary Progressive Aphasia Frontotemporal ... Condition or disease Intervention/treatment Alzheimer Disease Stroke Parkinson's Disease Lewy Body Dementia Huntington Disease ...
  https://clinicaltrials.gov/ct2/show/NCT01339130?recr=Open&cond=%22Huntington+Disease%22&rank=20
*  Research - Medical Neurobiology - University of Rochester Medical Center
Haber Lab - Basal Ganglia and Degenerative Diseases. *Halterman Stroke Lab - Targeted Therapeutics for Cerebrovascular Diseases ... Neurobiology of Disease. Fundamental pathologic, translational, and clinical processes and genetic predispositions that afflict ... Haber Lab - Basal Ganglia and Degenerative Diseases. *Huxlin Lab - Behavioral Studies and Functional Imaging of Visual Function ... Halterman Stroke Lab - Targeted Therapeutics for Cerebrovascular Diseases. *Holt Lab - Synaptic Pharmacology of the Vestibular ...
  https://www.urmc.rochester.edu/education/graduate/masters/medical-neurobiology/research.aspx
*  Cerebrovascular Disease - Radiology Notes
... to basal ganglia and insula. Lateral lenticulostriate branches (supply most basal ganglia: putamen, lateral globus pallidus, ... Moyamoya Disease. Idiopathic, linked to genetic defect, ?epiphenomenon of other proximal stenosis vasculopathies (NF with ICA ... Multiple basal ganglia, cortical and subcortical infarcts, basal ganglia haemorrhage, SAH, atrophy. ... low attenuation in basal ganglia, poor definition of the insula.. Assessment of Cerebrovascular Reserve. Proximal stenoses may ...
  http://radnotes.co.nz/neuroimaging/cerebrovascular_disease/
*  Books - Lane Medical Library - Stanford University School of Medicine
Basal ganglia -- Olfactory and limbic systems -- Cerebrovascular disease. ... Genetic and acquired bullous diseases -- Neutrophil-mediated diseases -- The acutely ill and hospitalized patient -- Benign ... Metabolic Disease -- Immunologic Disease -- Infectious Disease -- Gastrointestinal Disease -- Respiratory Tract Disease -- ... Immunologic disease -- Infectious disease -- Gastrointestinal disease -- Respiratory disease -- Cardiovascular disease -- Renal ...
  http://lane.stanford.edu/biomed-resources/eb.html?a=f&page=2&proxy-links=false
*  Neurological disorder - Wikipedia
... cerebrovascular attack) Tumors of the nervous system (e.g. cancer) Multiple sclerosis and other demyelinating diseases ... brain areas such as basal ganglia, cerebellum, brainstem): Frontal lobe damage Parietal lobe damage Temporal lobe damage ... The specific causes of neurological problems vary, but can include genetic disorders, congenital abnormalities or disorders, ... Huntington's disease, Alzheimer's disease, multiple sclerosis and organic psychosis.) Many of the diseases and disorders listed ...
  https://en.wikipedia.org/wiki/Neurological_disorder
*  Moyamoya Disease
... progressive cerebrovascular disorder caused by blocked arteries at the base of the brain in an area called the basal ganglia. ... Because it tends to run in families, researchers think that Moyamoya disease is the result of inherited genetic abnormalities. ... Moyamoya Disease What is Moyamoya Disease?. Moyamoya disease is a rare, ... The disease primarily affects children, but it can also occur in adults. In children, the first symptom of Moyamoya disease is ...
  http://neurologycolorado.com/moyamoya.htm
*  Risk factors for dementia | BJPsych Advances
In the search for genetic risk factors for both Alzheimer's disease and vascular dementia, generalised vascular disease genetic ... basal ganglia and angular gyrus (14%). ... cerebrovascular disease; and (c) a temporal relation between ... Genetic factors. Several rare genetic diseases have been associated with stroke and subsequent vascular dementia. These include ... Genetic risk factors for dementia. Alzheimer's disease is the most common form of dementia, and the fact that the vast majority ...
  http://apt.rcpsych.org/content/7/1/24.full
*  Update on Parkinson's Disease - American Family Physician
... or by cerebrovascular disease (e.g., multiple lacunar strokes). The disease can usually be diagnosed based on the history and ... Idiopathic Parkinson's disease is caused by the progressive loss of dopaminergic neurons in the substantia nigra and ... Dopamine replacement is still considered the most efficacious treatment for Parkinson's disease, but dopamine agonists, ... nutritional counseling and techniques to help patients manage emotional and cognitive changes related to the disease. ...
  https://www.aafp.org/afp/1999/0415/p2155.html
*  Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy - Wikipedia
Further genetic testing can be used to confirm the presence of the disease. There is currently no treatment or cure for CARASIL ... Diffuse white matter changes (leukoencephalopathy) and multiple lacunar infarcts in basal ganglia of thalamus are usually ... Journal of Stroke and Cerebrovascular Diseases, 20(2), 85-86,87,88,89,90,91.. ... The disease is rare and has only been diagnosed in about 50 patients, mostly of Japanese descent but few of Chinese and Spanish ...
  https://en.wikipedia.org/wiki/Cerebral_autosomal_recessive_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy
*  Belgian Fabry Study | Stroke
... findings suggest that atypical variants of Fabry disease with late-onset cerebrovascular disease exist and that their genetic ... The location of intracerebral hemorrhage was lobar in 13 patients (39.4%), involved basal ganglia in 11 (33.3%), brain stem in ... Prevalence of Fabry Disease in a Cohort of 1000 Young Patients With Cerebrovascular Disease. Raf Brouns, Vincent Thijs, ... Our results suggest that Fabry disease may play a role in up to 1% of young patients presenting with cerebrovascular disease. ...
  http://stroke.ahajournals.org/content/41/5/863
*  Neurofibromatosis type 1 - ONA
What causes this disease and how frequent is it?. NF1 is an autosomal dominant genetic disease without specific racial or ... They most commonly occur in the cerebellum, brainstem, basal ganglia and subcortical white matter. UBOs may represent areas of ... Cerebrovascular abnormalities are also seen, particularly stenosis or occlusion of the internal carotid arteries or the ... Genetic mosaicism can occur.. How do these pathogens/genes/exposures cause the disease?. Mutations in the NF1 gene result in ...
  http://www.oncologynurseadvisor.com/pediatrics/neurofibromatosis-type-1/article/624336/
*  Atomoxetine and Huntington's Disease - Full Text View - ClinicalTrials.gov
Huntington Disease. Basal Ganglia Diseases. Brain Diseases. Central Nervous System Diseases. Nervous System Diseases. Movement ... Neurodegenerative Diseases. Genetic Diseases, Inborn. Cognition Disorders. Neurocognitive Disorders. Mental Disorders. Chorea. ... Cardiovascular or cerebrovascular disease. *History of a loss of consciousness for greater than (or equal to) 5 minutes ... Clinical markers of early disease in persons near onset of Huntington's disease. Neurology. 2001 Aug 28;57(4):658-62. ...
  https://clinicaltrials.gov/ct2/show/NCT00368849?term=Leigh
*  Browse School of Medicine | Stanford Medicine Profiles
With these we are measuring local field potentials in basal ganglia nuclei in patients with Parkinson's disease and dystonian ... Current Research and Scholarly Interests Our group 's research focus is the acute treatment and prevention of cerebrovascular ... He spent 3 years of integrated PhD research at Columbia University Medical Center to study genetic predictors of vascular ... Our overall goal is to understand the role of the basal ganglia electrical activity in the pathogenesis of movement disorders. ...
  https://med.stanford.edu/profiles/browse?org=school-of-medicine/neurosurgery&affiliations=capFaculty
*  Orphanet: Bilateral striopallidodentate calcinosis
The portal for rare diseases and orphan drugs ... Cerebrovascular ferrocalcinosis. *Idiopathic basal ganglia ... Calcium is the major element deposited on the basal ganglia and accounts for the radiologic appearance of the disease. It is ... Genetic counseling It can be familial or sporadic. Over 30 families with the familial form have been reported. The familial ... Single proton emission computed tomography (SPECT) reveals markedly decreased perfusion to the basal ganglia bilaterally with ...
  http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=1980
*  Thalamus - Wikipedia
Ventricles of brain and basal ganglia. Superior view. Horizontal section. Deep dissection Ventricles of brain and basal ganglia ... A cerebrovascular accident (stroke) can lead to the thalamic syndrome, which involves a one-sided burning or aching sensation ... In humans, a common genetic variation in the promotor region of the serotonin transporter (the SERT-long and -short allele: 5- ... Fatal familial insomnia is a hereditary prion disease in which degeneration of the thalamus occurs, causing the patient to ...
  https://en.wikipedia.org/wiki/Thalamus
*  Superficial temporal artery-to-middle cerebral artery bypass surgery for middle cerebral artery stenosis in a patient with...
3a, b). Some cerebral microbleeds (CMBs) were also present in both the basal ganglia and the subcortical areas. The patient was ... Three years previously, he had been diagnosed with CADASIL by genetic testing for mutation in the Notch 3 gene. At the time of ... Cerebrovascular events such as TIA, infarction and hemorrhage have not appeared. Follow up MRI 14 months after surgery showed ... monogenic small-vessel disease caused by mutations in the Notch3 gene on chromosome 19 (Chabriat et al. 2009; Joutel et al. ...
  https://springerplus.springeropen.com/articles/10.1186/s40064-015-1407-7
*  Safety and Tolerability of Etanercept in Alzheimer's Disease - Full Text View - ClinicalTrials.gov
... more than 1 lacune within basal ganglia, more than 2 lacunes in white matter) ... Signs of major cerebrovascular disease on MRI or CT scan, if performed prior to entry into study (i.e. presence of infarction ... Genetic and Rare Diseases Information Center resources: Familial Alzheimer Disease U.S. FDA Resources ... Alzheimer Disease. Dementia. Brain Diseases. Central Nervous System Diseases. Nervous System Diseases. Tauopathies. ...
  https://clinicaltrials.gov/ct2/show/study/NCT01068353?view=results
*  PETDE10] Imaging of PDE10A Enzyme Levels in Huntington's Disease Gene Expansion Carriers and Healthy Controls With PET. -...
Huntington Disease. Basal Ganglia Diseases. Brain Diseases. Central Nervous System Diseases. Nervous System Diseases. Dementia ... Neurodegenerative Diseases. Genetic Diseases, Inborn. Cognition Disorders. Neurocognitive Disorders. Mental Disorders. ... s disease, brain surgery, intracranial haematoma, stroke/cerebrovascular disorders, epilepsy) or psychiatric conditions ... Huntington's Disease Radiation: PET Imaging with [18F]MNI-659 Early Phase 1 ...
  https://clinicaltrials.gov/ct2/show/NCT02061722?recr=Open&cond=%22Chorea%22&rank=12
*  Citalopram to Enhance Cognition in HD - Full Text View - ClinicalTrials.gov
Huntington Disease. Basal Ganglia Diseases. Brain Diseases. Central Nervous System Diseases. Nervous System Diseases. Movement ... Neurodegenerative Diseases. Genetic Diseases, Inborn. Cognition Disorders. Neurocognitive Disorders. Mental Disorders. Chorea. ... Other serious medical conditions such as cardiovascular or cerebrovascular disease; head injury deemed clinically significant ... Huntington Disease Chorea Executive Dysfunction Drug: 20mg daily citalopram Drug: Placebo Phase 2 ...
  https://clinicaltrials.gov/ct2/show/NCT00271596?term=Leigh
*  appde.eu
The severity of nigra (part of the basal ganglia) leads to a decreased the disease is often classified according to the Hoehn ... genetic factors18 seem to play a role in lation of 55 years and older.22 In the Netherlands the cause of the disease.. the ... The MRI-scan If no clinically relevant effect was demonstrated in shows, among other things, cerebro-vascular lesions. the ... Parkinson's disease: dysfunction of the basal ganglia, caused by degeneration of dopamine-producing cells in the substantia ...
  http://gotomydoctor.com/a/appde.eu1.html
*  Is Breakdown of the Blood-Brain Barrier Responsible for Lacunar Stroke, Leukoaraiosis, and Dementia? | Stroke
... lesions elsewhere in the white matter and basal ganglia. Diffuse white matter disease, or leukoaraiosis, originated from the ... Angiotensin-converting enzyme insertion deletion polymorphism and cerebrovascular disease. Stroke. 1996; 27: 435-440. ... 61 Abnormalities in the nitric oxide synthase gene62 or other genetic factors (for example, the Notch 3 gene mutation ... vascular diseases. The brain may have a limited repertoire of pathological responses to different disease triggers, even though ...
  http://stroke.ahajournals.org/content/34/3/806
*  PET Imaging Study of Neurochemical and Autonomic Disorders in Multiple System Atrophy (MSA) - Full Text View - ClinicalTrials...
Nervous System Diseases. Basal Ganglia Diseases. Brain Diseases. Central Nervous System Diseases. Movement Disorders. ... Subjects will have whole blood drawn sample for DNA banking to support genetic research of human disease and human genetic ... severe cerebrovascular accidents (causing symptoms such as hemiplegia, aphasia and non-dominant parietal lobe syndrome), and ... By pooling these results from many MSA patients, and comparing with other diseases (such as Parkinson's disease) we hope to ...
  https://clinicaltrials.gov/ct2/show/NCT02035761?term=Cerebellar+Degeneration&rank=12
*  PET Imaging Study of Neurochemical and Autonomic Disorders in Multiple System Atrophy (MSA) - Full Text View - ClinicalTrials...
Basal Ganglia Diseases. Brain Diseases. Movement Disorders. Neurodegenerative Diseases. Hypotension. Vascular Diseases. ... Subjects will have whole blood drawn sample for DNA banking to support genetic research of human disease and human genetic ... severe cerebrovascular accidents (causing symptoms such as hemiplegia, aphasia and non-dominant parietal lobe syndrome), and ... Autonomic Nervous System Diseases. Nervous System Diseases. Central Nervous System Diseases. Primary Dysautonomias. ...
  https://clinicaltrials.gov/ct2/show/NCT02035761?term=Multiple+System+Atrophy&rank=4
*  Zantac 150 mg, 300 mg. Discount online Zantac
MOTOR PRODUCE Brainstem, spinal rope CEREBRAL CORTEX BASAL GANGLIA Dopamine Thalamus GABA Glutamate Direct Crooked Glutamate ... There are two main types limited disease (CREST syndrome) and diffuse disease. ... Most researchers agree that development of IBD requires four part components: the input of multiple genetic variations, ... Put to use cautiously in patients with prolonged QT lacuna, cerebrovascular condition, dehydration, hypovolemia, account of ...
  http://www.bonetumor.org/learning/resourses/case21/vol.1/index.html