Detalhe da pesquisa
1.
Trial Readiness of Cavernous Malformations With Symptomatic Hemorrhage, Part I: Event Rates and Clinical Outcome.
Stroke
; 55(1): 22-30, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38134268
2.
Trial Readiness of Cavernous Malformations With Symptomatic Hemorrhage, Part II: Biomarkers and Trial Modeling.
Stroke
; 55(1): 31-39, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38134265
3.
Endothelial TLR4 and the microbiome drive cerebral cavernous malformations.
Nature
; 545(7654): 305-310, 2017 05 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-28489816
4.
Cutaneous findings of familial cerebral cavernous malformation syndrome due to the common Hispanic mutation.
Am J Med Genet A
; 182(5): 1066-1072, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32100472
5.
Vertebral Intraosseous Vascular Malformations in a Familial Cerebral Cavernous Malformation Population: Prevalence, Histologic Features, and Associations With CNS Disease.
AJR Am J Roentgenol
; 214(2): 428-436, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31825263
6.
Familial Cerebral Cavernous Malformations Are Associated with Adrenal Calcifications on CT Scans: An Imaging Biomarker for a Hereditary Cerebrovascular Condition.
Radiology
; 284(2): 443-450, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28318403
7.
Automated algorithm for counting microbleeds in patients with familial cerebral cavernous malformations.
Neuroradiology
; 59(7): 685-690, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28534135
8.
Occurrence of DNET and other brain tumors in Noonan syndrome warrants caution with growth hormone therapy.
Am J Med Genet A
; 170A(1): 195-201, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26377682
9.
Familial Cerebral Cavernous Malformations.
Stroke
; 50(5): 1294-1301, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30909834
10.
Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation.
Cerebrovasc Dis
; 37(1): 57-63, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24401931
11.
Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity.
Cerebrovasc Dis
; 38(6): 433-40, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25472749
12.
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
Nat Genet
; 35(4): 318-21, 2003 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-14595441
13.
Intracranial Hemorrhage Rate and Lesion Burden in Patients With Familial Cerebral Cavernous Malformation.
J Am Heart Assoc
; 12(3): e027572, 2023 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36695309
14.
Cavernous Angioma Symptomatic Hemorrhage (CASH) Trial Readiness II: Imaging Biomarkers and Trial Modeling.
medRxiv
; 2023 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37333396
15.
Systemic and CNS manifestations of inherited cerebrovascular malformations.
Clin Imaging
; 75: 55-66, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33493737
16.
Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation.
Mol Genet Genomic Med
; 9(10): e1794, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34491620
17.
Seizure Incidence Rates in Children and Adults With Familial Cerebral Cavernous Malformations.
Neurology
; 2021 Aug 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34389651
18.
Somatosensory responses in normal aging, mild cognitive impairment, and Alzheimer's disease.
J Neural Transm (Vienna)
; 117(2): 217-25, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20013008
19.
Clinical Imaging of Cerebral Cavernous Malformations: Computed Tomography and Magnetic Resonance Imaging.
Methods Mol Biol
; 2152: 85-96, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32524546
20.
Subjective Cognitive Concerns and Attitudes toward Genetic Testing Are Associated with Depressive Symptoms and Quality of Life after Genetic Testing for the Cerebral Cavernous Malformation Common Hispanic Mutation (CCM1).
J Behav Brain Sci
; 10(2): 118-127, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32467778