نتائج البحث

Most common NOTCH3 mutations causing CADASIL or CADASIL-like cerebral small vessel disease: A systematic review

• Authors : Georgina Boston; Dan Jobson; Toshiki Mizuno

Subjects: CADASIL; Dementia; NOTCH3

• Source: Cerebral Circulation - Cognition and Behavior, Vol 6, Iss , Pp 100227- (2024)

تفاصيل العنوان

TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients

• Authors : Foddis, Marco; Foddis, Marco; Blumenau, Sonja

Subjects: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL); Early-onset stroke; Exome sequencing

• Source: Neurobiology of Aging

تفاصيل العنوان

A novel heterozygous HTRA1 mutation in an Asian family with CADASIL‐like disease.

• Authors : Cao, Hua¹ (AUTHOR); Liu, Jiahui¹ (AUTHOR); Tian, Wen¹ (AUTHOR)

• Source: Journal of Clinical Laboratory Analysis. Feb2022, Vol. 36 Issue 2, p1-4. 4p.

تفاصيل العنوان

Heterozygous HTRA1 missense mutation in CADASIL-like family disease

• Authors : Xiaowei Wu; Changxin Li; Jinming Mao

Subjects: HTRA1; CADASIL-like; SNP

• Source: Brazilian Journal of Medical and Biological Research, Vol 51, Iss 5 (2018)

تفاصيل العنوان

CADASIL‐like leukodystrophy and symptomatic cerebral infarction in myotonic dystrophy type 1.

• Authors : Liu, Bin^1,2 (AUTHOR); Yang, Chun‐Lin^1,2 (AUTHOR); Li, Xiao‐Li^1,2 (AUTHOR)

• Source: CNS Neuroscience & Therapeutics. Oct2022, Vol. 28 Issue 10, p1655-1657. 3p.

تفاصيل العنوان

Heterozygous HTRA1 missense mutation in CADASIL-like family disease

• Authors : Wu, Xiaowei; Li, Changxin; Mao, Jinming

Subjects: HTRA1; CADASIL-like; SNP

• Source: Brazilian Journal of Medical and Biological Research. January 2018 51(5)

تفاصيل العنوان

Clinical, familial, and neuroimaging features of CADASIL-like patients.

• Authors : Nannucci, S.¹; Pescini, F.²; Bertaccini, B.³

• Source: Acta Neurologica Scandinavica. Jan2015, Vol. 131 Issue 1, p30-36. 7p.

تفاصيل العنوان

A CADASIL-Like Case with a Novel Noncysteine Mutation of the NOTCH3 Gene and Granular Deposits in the Renal Arterioles.

• Authors : Nakamura, Kuniyuki^1,2 ; Ago, Tetsuro¹ ; Tsuchimoto, Akihiro¹

• Source: Case Reports in Neurological Medicine. 3/9/2015, Vol. 2015, p1-6. 6p.

تفاصيل العنوان

Heterozygous HTRA1 missense mutation in CADASIL-like family disease

• Authors : Changxin Li; Jinming Mao; Yan Liu

Subjects: 0301 basic medicine; Adult; Male

• Source: Brazilian Journal of Medical and Biological ResearchBrazilian Journal of Medical and Biological Research, Volume: 51, Issue: 5, Article number: e6632, Published: 15 MAR 2018Brazilian

تفاصيل العنوان

Mitochondrial encephalopathy with CADASIL-Like MRI

• Authors : Akhvlediani, Tamar; Sandor, Peter S; Henning, Anke

Subjects: Institute of Biomedical Engineering; 170 Ethics; 610 Medicine & health

• Source: Akhvlediani, Tamar; Sandor, Peter S; Henning, Anke; Schaller, André; Jauslin, Marco; Gallati, Sabina; Boesiger, Peter; Jung, Hans H (2007). Mitochondrial encephalopathy with

تفاصيل العنوان