| scholarly article | Q13442814 |
| P2093 | author name string | Landgraf F | |
| Michel A | |||
| Rolland Y | |||
| Chabriat H | |||
| Tournier-Lasserve E | |||
| Vahedi K | |||
| Martinet JP | |||
| Vérin M | |||
| Bompais B | |||
| Lemaitre MH | |||
| P2860 | cites work | Hereditary multi-infarct dementia | Q69444701 |
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| Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian family | Q72641462 | ||
| A gene for familial hemiplegic migraine maps to chromosome 19 | Q28255425 | ||
| Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12 | Q28268718 | ||
| A second-generation linkage map of the human genome | Q33192755 | ||
| Progress in the genetics of cerebrovascular disease: inherited subcortical arteriopathies | Q40678672 | ||
| Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms | Q44016358 | ||
| Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease | Q48271434 | ||
| Hereditary multi-infarct dementia | Q48292907 | ||
| Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study | Q48365396 | ||
| A familial disorder with subcortical ischemic strokes, dementia, and leukoencephalopathy | Q48485739 | ||
| Slowly progressive familial dementia with recurrent strokes and white matter hypodensities on CT scan | Q48513269 | ||
| Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy | Q48642657 | ||
| Mania after brain injury: neuroradiological and metabolic findings | Q48956622 | ||
| Summary of the proceedings of the First International Workshop on CADASIL. Paris, May 19-21, 1993. | Q53384692 | ||
| Chronic familial vascular encephalopathy | Q66695594 | ||
| Familial subcortical dementia with arteriopathic leukoencephalopathy. A clinico-pathological case | Q67917328 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | phenotype | Q104053 |
| migraine | Q133823 | ||
| P304 | page(s) | 579-585 | |
| P577 | publication date | 1995-12-01 | |
| P1433 | published in | Journal of Neurology, Neurosurgery and Psychiatry | Q1599804 |
| P1476 | title | New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature | |
| P478 | volume | 59 |
| Q38828065 | Animal models of monogenic migraine |
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| Q36260158 | Diagnostic criteria for CADASIL in the International Classification of Headache Disorders (ICHD-II): are they appropriate? |
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| Q36961494 | Investigation of the NOTCH3 and TNFSF7 genes on C19p13 as candidates for migraine |
| Q37156443 | Migraine and ischemic stroke: a debated question |
| Q38125646 | Migraine and neurogenetic disorders |
| Q35396454 | Multimodal retinal vessel analysis in CADASIL patients |
| Q31122866 | Neuropsychiatric manifestations in CADASIL. |
| Q46502526 | Pathophysiology of migraine and clinical implications |
| Q55004438 | Polygenic risk score: use in migraine research. |
| Q35951724 | R54C Mutation of NOTCH3 Gene in the First Rungus Family with CADASIL. |
| Q43601875 | The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine |
| Q35172431 | The genetics of migraine |
| Q34424023 | The migraine-ischemic stroke relation in young adults |
| Q82010266 | Vascular dementia |
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