Pages that link to "Q48579417"
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The following pages link to Hereditary endotheliopathy with retinopathy, nephropathy, and stroke(HERNS) (Q48579417):
Displaying 50 items.
- Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome (Q24323565) (← links)
- Neuropathological diagnosis of vascular cognitive impairment and vascular dementia with implications for Alzheimer's disease (Q26750515) (← links)
- Cerebral small vessel disease: Capillary pathways to stroke and cognitive decline (Q26776375) (← links)
- Microvascular pathology and morphometrics of sporadic and hereditary small vessel diseases of the brain (Q26824027) (← links)
- Ischemic stroke in young adults: an overview of etiological aspects (Q26824314) (← links)
- Genetic Risk Factors for Ischemic and Hemorrhagic Stroke (Q28079249) (← links)
- Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3 (Q28343561) (← links)
- Neuroimaging of cerebral small vessel disease (Q30861858) (← links)
- HERNS. A rare, hereditary, multisystemic disease with cerebral microangiopathy (Q30988241) (← links)
- Neuropsychiatric manifestations in CADASIL. (Q31122866) (← links)
- New roles for the major human 3'-5' exonuclease TREX1 in human disease (Q33671295) (← links)
- Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL): From Discovery to Gene Identification (Q33788625) (← links)
- Molecular genetics of migraine headaches: a review (Q33922114) (← links)
- Hereditary vascular dementia linked to notch 3 mutations. CADASIL in British families (Q33922717) (← links)
- The genetics of white matter lesions (Q34032512) (← links)
- Advances in molecular genetics and pathology of cerebrovascular disorders (Q34284883) (← links)
- Genetics of cerebral small vessel disease (Q35076464) (← links)
- Molecular disorganization of axons adjacent to human lacunar infarcts (Q35119429) (← links)
- Migraine: an ophthalmologist's perspective (Q35582787) (← links)
- Genetics of cerebrovascular disorders (Q36018306) (← links)
- Retinal vascular image analysis as a potential screening tool for cerebrovascular disease: a rationale based on homology between cerebral and retinal microvasculatures. (Q36091834) (← links)
- Hereditary endotheliopathy with retinopathy and encephalopathy: pathological and genetic studies of a family (Q36095171) (← links)
- Single gene disorders causing ischaemic stroke (Q36522909) (← links)
- Genetics of ischaemic stroke (Q36713912) (← links)
- Destruction of tissue, cells and organelles in type 1 diabetic rats presented at macromolecular resolution (Q36824567) (← links)
- Monogenic vessel diseases related to ischemic stroke: a clinical approach (Q36853643) (← links)
- Genetics of ischaemic stroke; single gene disorders (Q37244585) (← links)
- Migraine and stroke: current perspectives (Q37282908) (← links)
- Nogo receptor blockade overcomes remyelination failure after white matter stroke and stimulates functional recovery in aged mice (Q37549901) (← links)
- Migraine and genetic and acquired vasculopathies (Q37581975) (← links)
- Review: molecular genetics and pathology of hereditary small vessel diseases of the brain. (Q37808273) (← links)
- Neurological features of Fabry disease: clinical, pathophysiological aspects and therapy. (Q37994740) (← links)
- Tumefactive demyelination: an approach to diagnosis and management (Q38075462) (← links)
- Migraine and neurogenetic disorders (Q38125646) (← links)
- Migraine genetics: Part II. (Q38126970) (← links)
- Neuropathology and genetics of cerebroretinal vasculopathies (Q38260913) (← links)
- Dissecting the association between migraine and stroke (Q38344344) (← links)
- Human disease phenotypes associated with mutations in TREX1. (Q38366756) (← links)
- Genetic factors in cerebral small vessel disease and their impact on stroke and dementia (Q38433566) (← links)
- Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (Q38823604) (← links)
- TREX1 C-terminal frameshift mutations in the systemic variant of retinal vasculopathy with cerebral leukodystrophy (Q38957343) (← links)
- Migraine genetics: current findings and future lines of research (Q39077188) (← links)
- C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy (Q40101085) (← links)
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and CADASIL-like disorders in Japan (Q40615837) (← links)
- A 44-year-old man with eye, kidney, and brain dysfunction (Q41070317) (← links)
- Molecular basis of genetic heterogeneity: role of the clinical neurologist (Q41735698) (← links)
- Retinal findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (cadasil). (Q42501845) (← links)
- Dolichoectasia and multifocal simultaneous intracranial haemorrhages (Q42584875) (← links)
- The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine (Q43601875) (← links)
- Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseases. (Q44494580) (← links)