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CADASIL

  • CADASIL
  • Medical condition

    CADASIL or CADASIL syndrome, involving cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, is the most common form

    CADASIL

    CADASIL

    CADASIL

  • Cerebrovascular disease
  • Condition that affects the arteries that supply the brain

    disease, including those that are congenital or idiopathic and include CADASIL, aneurysms, amyloid angiopathy, arteriovenous malformations, fistulas,

    Cerebrovascular disease

    Cerebrovascular disease

    Cerebrovascular_disease

  • Leukoencephalopathy
  • Term to describe all brain white-matter diseases

    and traumatic. This classification is diffuse sometimes. For example CADASIL syndrome is at the same time hereditary and hypoxic. Lyon, G.; Fattal-Valevski

    Leukoencephalopathy

    Leukoencephalopathy

    Leukoencephalopathy

  • James Dewar (musician)
  • Scottish singer and bassist (1942–2002)

    stroke after years of disability resulting from a rare medical condition, CADASIL, which caused a series of strokes. His funeral was held at Paisley's Woodside

    James Dewar (musician)

    James Dewar (musician)

    James_Dewar_(musician)

  • NOTCH3
  • Protein-coding gene in humans

    dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Mutations in NOTCH3 have also been identified in families with Alzheimer's

    NOTCH3

    NOTCH3

    NOTCH3

  • Migraine
  • Disorder resulting in recurrent moderate–severe headaches

    SCN1A. Another genetic disorder that has been associated with migraine is CADASIL syndrome or cerebral autosomal dominant arteriopathy with subcortical infarcts

    Migraine

    Migraine

    Migraine

  • Friedrich Nietzsche
  • German philosopher (1844–1900)

    while other researchers have proposed a hereditary stroke disorder called CADASIL. Poisoning by mercury, a treatment for syphilis at the time of Nietzsche's

    Friedrich Nietzsche

    Friedrich Nietzsche

    Friedrich_Nietzsche

  • Stroke
  • Death of a region of brain cells due to poor blood flow

    reduction in case fatality at six months. Anoxic depolarization in the brain CADASIL Cerebrovascular disease Cerebral palsy Dejerine–Roussy syndrome Functional

    Stroke

    Stroke

    Stroke

  • Aura (symptom)
  • Symptom of epilepsy and migraine

    Synesthesia – Neurological condition involving the crossing of senses CADASIL Retinal migraine – Medical condition of the eye Photopsia – Presence of

    Aura (symptom)

    Aura (symptom)

    Aura_(symptom)

  • The Fall of the House of Usher (miniseries)
  • 2023 American television miniseries

    from the facility's tanks to signal an orgy. Roderick, suffering from CADASIL, pins hope on Victorine's experimental heart mesh, while Madeline, now

    The Fall of the House of Usher (miniseries)

    The_Fall_of_the_House_of_Usher_(miniseries)

  • The Sea Inside
  • 2004 Spanish drama film

    explores Ramón's relationships with two women: Julia, a lawyer suffering from Cadasil syndrome who supports his cause, and Rosa, a local woman who wants to convince

    The Sea Inside

    The_Sea_Inside

  • CARASIL
  • Medical condition

    frequently used for differential diagnoses include Binswanger's disease, CADASIL, Nasu-Hakola disease, and chronic progressive multiple sclerosis. There

    CARASIL

    CARASIL

    CARASIL

  • Dianna Agron
  • American actress and singer (born 1986)

    When she was a teenager, her father became ill with the stroke disorder CADASIL. The family thought it was multiple sclerosis after tests proved indefinitive;

    Dianna Agron

    Dianna Agron

    Dianna_Agron

  • Notch signaling pathway
  • Series of molecular signals

    autosomal-dominant arteriopathy with sub-cortical infarcts and leukoencephalopathy (CADASIL), multiple sclerosis, Tetralogy of Fallot, and Alagille syndrome. Inhibition

    Notch signaling pathway

    Notch signaling pathway

    Notch_signaling_pathway

  • Donepezil
  • Medication used for dementia

    cognitive impairment, cognitive impairment associated with multiple sclerosis, CADASIL syndrome, and Down syndrome. A three-year National Institutes of Health

    Donepezil

    Donepezil

  • Anne Joutel
  • French neurologist and medical geneticist

    vessel diseases (SVD) of the brain. She has a long-standing interest in CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and

    Anne Joutel

    Anne_Joutel

  • Apathy
  • State of indifference, or the suppression of emotions

    conditions, more prominently recognized in the elderly, some of which are: CADASIL syndrome, depression, Alzheimer's disease, Chagas disease, Creutzfeldt–Jakob

    Apathy

    Apathy

    Apathy

  • Nocturne in Black and Gold – The Falling Rocket
  • 1875 painting by James Abbott McNeil Whistler

    perceived as a delight. It has been suggested John Ruskin suffered from CADASIL syndrome and the visual disturbances this condition caused him might have

    Nocturne in Black and Gold – The Falling Rocket

    Nocturne in Black and Gold – The Falling Rocket

    Nocturne_in_Black_and_Gold_–_The_Falling_Rocket

  • Perivascular space
  • Space surrounding blood vessels

    characteristic of diseases or disorders of vascular pathologies, including CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and

    Perivascular space

    Perivascular space

    Perivascular_space

  • Transient global amnesia
  • Temporary disruption of short-term memory

    anterior circulation infarct Partial anterior circulation infarct Other CADASIL Binswanger's disease Transient global amnesia Haemorrhagic stroke Extra-axial

    Transient global amnesia

    Transient global amnesia

    Transient_global_amnesia

  • Marie-Germaine Bousser
  • French neuroscientist (born 1943)

    French neuroscientist. She won the Brain Prize in 2019 for her work on CADASIL. Bousser graduated from Paris-Sorbonne University in neuro-psychiatry in

    Marie-Germaine Bousser

    Marie-Germaine Bousser

    Marie-Germaine_Bousser

  • Proteinopathy
  • Diseases caused by abnormal protein structure

    3389/fneur.2013.00076. PMC 3687200. PMID 23801983. Spinner NB (March 2000). "CADASIL: Notch signaling defect or protein accumulation problem?". The Journal

    Proteinopathy

    Proteinopathy

    Proteinopathy

  • Leukoaraiosis
  • Type of white matter abnormality near the lateral ventricles

    Radial Peripapillary Capillary Network Density Reduction and Leukoaraiosis CADASIL is a hereditary cerebrovascular disorder associated with T2-hyperintense

    Leukoaraiosis

    Leukoaraiosis

    Leukoaraiosis

  • List of skin conditions
  • arteriopathy with subcortical infarcts and leukoencephalopathy syndrome (CADASIL syndrome) Cerebrotendinous xanthomatosis Citrullinemia Congenital erythropoietic

    List of skin conditions

    List of skin conditions

    List_of_skin_conditions

  • HACL2
  • Protein-coding gene in the species Homo sapiens

    lyase). Human ILVBL gene has 17 exons resides on chromosome 19 at q13.1. CADASIL, an identified autosomal dominant condition characterized by the recurrence

    HACL2

    HACL2

    HACL2

  • Human, All Too Human
  • Book by Friedrich Nietzsche

    health (possibly the early effects of a brain tumor, or on another theory, CADASIL) compelled him to request a leave of absence from his academic duties at

    Human, All Too Human

    Human, All Too Human

    Human,_All_Too_Human

  • List of genetic disorders
  • Brody myopathy ATP2A1 1:10,000,000 Brunner syndrome MAOA 1:500,000,000 CADASIL syndrome NOTCH3 P 1:156,000,000 Cat eye syndrome 22 1:74,000 CATSHL syndrome

    List of genetic disorders

    List_of_genetic_disorders

  • List of abbreviations for diseases and disorders
  • hypomyelination (see vanishing white matter disease) CAD Coronary artery disease CADASIL Cerebral autosomal dominant arteriopathy with subcortical infarcts and

    List of abbreviations for diseases and disorders

    List_of_abbreviations_for_diseases_and_disorders

  • List of genes mutated in cutaneous conditions
  • Neurofibromatosis type 1 NOD2 Blau syndrome, Early-onset sarcoidosis NOTCH3 CADASIL syndrome NSDHL 3-beta-hydroxysteroid dehydrogenase CHILD syndrome OCA2

    List of genes mutated in cutaneous conditions

    List_of_genes_mutated_in_cutaneous_conditions

  • Binswanger's disease
  • Medical condition

    process. There are many diseases similar to Binswanger's disease including CADASIL syndrome and Alzheimer's disease, which makes this specific type of white

    Binswanger's disease

    Binswanger's disease

    Binswanger's_disease

  • List of syndromes
  • Syndromes

    Burnside–Butler syndrome Buschke–Ollendorff syndrome CACNA1C-related disorders CADASIL Camera-Marugo-Cohen syndrome CAMFAK syndrome Camptodactyly-arthropathy-coxa

    List of syndromes

    List_of_syndromes

  • Early onset dementia
  • Cognitive disorder

    dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) (which has the disease specific symptom of migraine with aura and mood

    Early onset dementia

    Early onset dementia

    Early_onset_dementia

  • Stroke in China
  • Health issue in China

    epidemiology, brain ischemia/reperfusion exploring, leukoencephalopathy (CADASIL), neural stem cell and stroke, neuroprotective treatment for stroke, clinical

    Stroke in China

    Stroke_in_China

  • List of medical abbreviations: C
  • "cabbage") CABP coronary artery bypass procedure CAD coronary artery disease CADASIL cerebral autosomal dominant arteriopathy with subcortical infarcts and

    List of medical abbreviations: C

    List_of_medical_abbreviations:_C

  • Leukoencephalopathy with vanishing white matter
  • Neurological disease

    hypomyelination (CACH) is another commonly accepted name. The Stennis Foundation CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and

    Leukoencephalopathy with vanishing white matter

    Leukoencephalopathy with vanishing white matter

    Leukoencephalopathy_with_vanishing_white_matter

  • List of MeSH codes (C16)
  • The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM)

    List of MeSH codes (C16)

    List_of_MeSH_codes_(C16)

  • Amaurosis fugax
  • Medical condition

    anterior circulation infarct Partial anterior circulation infarct Other CADASIL Binswanger's disease Transient global amnesia Haemorrhagic stroke Extra-axial

    Amaurosis fugax

    Amaurosis fugax

    Amaurosis_fugax

  • Night in paintings (Western art)
  • Overview of nighttime themes in European art

    of the case bankrupted him. It has been suggested John Ruskin had had CADASIL and the visual disturbances this condition caused him might have been a

    Night in paintings (Western art)

    Night in paintings (Western art)

    Night_in_paintings_(Western_art)

  • Innovations in International Health
  • 2012-04-18. "Experimental Approach to Genotype-Phenotype Relationships in CADASIL Pathogenesis" (PDF). Archived from the original (PDF) on 2010-06-27. Retrieved

    Innovations in International Health

    Innovations_in_International_Health

  • International Classification of Headache Disorders
  • Detailed hierarchical classification

    thrombosis (CVT) Headache attributed to other intracranial vascular disorder CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and

    International Classification of Headache Disorders

    International_Classification_of_Headache_Disorders

  • CARASAL
  • Medical condition

    unaffected person. CARASAL was described in 5 French patients by Herve et al. CADASIL (Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And

    CARASAL

    CARASAL

    CARASAL

  • Delta-like 1
  • Protein found in humans

    H, Beatus P, Dannaeus K, Chapman G, Lendahl U, Lundkvist J (2003). "A CADASIL-mutated Notch 3 receptor exhibits impaired intracellular trafficking and

    Delta-like 1

    Delta-like 1

    Delta-like_1

  • Chromosome 19
  • Human chromosome

    chromosome 19: Alternating hemiplegia of childhood Alzheimer's disease CADASIL Centronuclear myopathy autosomal dominant form Charcot–Marie–Tooth disease

    Chromosome 19

    Chromosome 19

    Chromosome_19

  • Sudden (TV series)
  • 2013 Singaporean TV series or program

    Chen Yirou 陈以柔 Cheng Chuning's mother Cheng Gaofeng's wife Suffers from CADASIL and left her family because of it Lives in a nursing home Li Wenhai Guo

    Sudden (TV series)

    Sudden_(TV_series)

  • Baló concentric sclerosis
  • Medical condition

    also associated to standard multiple sclerosis, neuromyelitis optica, CADASIL and progressive multifocal leukoencephalopathy. There is an overlap between

    Baló concentric sclerosis

    Baló concentric sclerosis

    Baló_concentric_sclerosis

  • The Luvvers
  • Scottish rock group

    found success as a member of the Robin Trower Band, died in 2002 from Cadasil hereditary stroke disorder. With Lulu: Singles (all on the Decca label)

    The Luvvers

    The_Luvvers

  • Genetics of migraine
  • exocytosis complex. Another genetic disorder associated with migraine is CADASIL syndrome or cerebral autosomal dominant arteriopathy with subcortical infarcts

    Genetics of migraine

    Genetics_of_migraine

  • Arterial spin labelling
  • Magnetic resonance imaging technique

    DP-pCASL in cerebrovascular diseases, including acute ischemic stroke, CADASIL, hereditary cerebral small vessel disease as well as in animal models.

    Arterial spin labelling

    Arterial_spin_labelling

  • List of MeSH codes (C10)
  • MeSH C10.228.140.300.400 – dementia, vascular MeSH C10.228.140.300.400.203 – cadasil MeSH C10.228.140.300.400.408 – dementia, multi-infarct MeSH C10.228.140

    List of MeSH codes (C10)

    List_of_MeSH_codes_(C10)

  • The Brain Prize
  • Award

    understanding and diagnosing the most common inherited form of stroke, CADASIL" Hugues Chabriat Anne Joutel Elisabeth Tournier-Lasserve 2020 Sir Adrian

    The Brain Prize

    The_Brain_Prize

  • Ankyrin repeat
  • Protein domain

    of cell signalling pathways) which can cause the neurological disorder CADASIL when the repeat domain is disrupted by mutations. A specialized family

    Ankyrin repeat

    Ankyrin repeat

    Ankyrin_repeat

  • Familial hemiplegic migraine
  • Medical condition

    SPECT, are used to look for signs of other familial conditions such as CADASIL or mitochondrial disease, and for evidence of cerebellar degeneration.

    Familial hemiplegic migraine

    Familial_hemiplegic_migraine

  • Elisabeth Tournier-Lasserve
  • French neurologist, medical geneticist and university professor

    Marie-Germaine Bousser, she discovered a genetic disease, designated by the acronym CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and

    Elisabeth Tournier-Lasserve

    Elisabeth_Tournier-Lasserve

  • Autosomal dominant porencephaly type I
  • Medical condition

    including brain small vessel disease with hemorrhage and HANAC syndrome. CADASIL syndrome is caused by a mutation in a different gene, but may cause similar

    Autosomal dominant porencephaly type I

    Autosomal dominant porencephaly type I

    Autosomal_dominant_porencephaly_type_I

  • List of MeSH codes (C14)
  • MeSH C14.907.253.337 – cerebral arterial diseases MeSH C14.907.253.337.187 – cadasil MeSH C14.907.253.337.375 – infarction, anterior cerebral artery MeSH C14

    List of MeSH codes (C14)

    List_of_MeSH_codes_(C14)

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