Search Results

Display Settings
Results per page: 10
Sort By: Relevance
Filter
  • 1-10 of  26 results for ""Receptor, Notch3""

Your Filters

Publisher : saunders
Reset filters
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Report

A Novel Mutation Outside of the EGFr Encoding Exons of NOTCH3 Gene in a Chinese with CADASIL.

  • Authors : Wang W; Department of Neurology, People's Hospital of Zhengzhou University, Zhengzhou, Henan, China.; Ren Z

Subjects: Exons* ; Mutation, Missense*; CADASIL/CADASIL/CADASIL/*genetics

  • Source: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2020 Dec; Vol. 29 (12), pp. 105410. Date of Electronic Publisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

A Chinese CADASIL Family with a Novel Mutation on Exon 10 of Notch3 Gene.

  • Authors : Liu Y; Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China; Department of Neurology, Suzhou Ninth People's Hospital, Suzhou 215200, China.

Subjects: Mutation, Missense*; CADASIL/CADASIL/CADASIL/*genetics ; Receptor, Notch3/Receptor, Notch3/Receptor, Notch3/*genetics

  • Source: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2021 Aug; Vol. 30 (8), pp. 105674. Date of Electronic Publisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.

  • Authors : Algahtani H; King Abdulaziz Medical City / King Saud bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia. Electronic address: .; Shirah B

Subjects: Mutation, Missense*; CADASIL/CADASIL/CADASIL/*genetics ; Receptor, Notch3/Receptor, Notch3/Receptor, Notch3/*genetics

  • Source: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2020 Jul; Vol. 29 (7), pp. 104832. Date of Electronic Publisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Report

Not Described Variant of Notch3 Gen for Cadasil Disease.

  • Authors : Mellinger S; Neurology Service, Hospital Señor del Milagro, Salta Capital, Argentina. Electronic address: .; Romero D

Subjects: Mutation*; CADASIL/CADASIL/CADASIL/*genetics ; Receptor, Notch3/Receptor, Notch3/Receptor, Notch3/*genetics

  • Source: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2020 Jul; Vol. 29 (7), pp. 104803. Date of Electronic Publisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

NOTCH3 Gene Mutation in a Chilean Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Family.

  • Authors : Gallardo A; Department of Neurological Sciences, Faculty of Medicine, University of Chile, Santiago, Chile. Electronic address: .; Latapiat V

Subjects: Mutation*; CADASIL/CADASIL/CADASIL/*genetics ; Receptor, Notch3/Receptor, Notch3/Receptor, Notch3/*genetics

  • Source: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2020 Feb; Vol. 29 (2), pp. 104530. Date of Electronic Publisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Report

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Associated With a Novel In-Frame Mutation in the NOTCH3 Gene in a Japanese Patient.

  • Authors : Takeshi Y; Department of Neurology, Nippon Medical School, Tokyo, Japan.; Suda S

Subjects: Mutation*; CADASIL/CADASIL/CADASIL/*genetics ; Receptor, Notch3/Receptor, Notch3/Receptor, Notch3/*genetics

  • Source: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2020 Jan; Vol. 29 (1), pp. 104482. Date of Electronic Publisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

The CADASIL Scale-J, A Modified Scale to Prioritize Access to Genetic Testing for Japanese CADASIL-Suspected Patients.

  • Authors : Koizumi T; Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.; Mizuta I

Subjects: DNA Mutational Analysis* ; Decision Support Techniques* ; Health Services Accessibility*

  • Source: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2019 Jun; Vol. 28 (6), pp. 1431-1439. Date of ElectronicPublisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

A Novel NOTCH3 Gene Mutation in a Polish CADASIL Family.

Subjects: Mutation*; CADASIL/CADASIL/CADASIL/*genetics ; Receptor, Notch3/Receptor, Notch3/Receptor, Notch3/*genetics

  • Source: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2019 Mar; Vol. 28 (3), pp. 574-576. Date of Electronic Publisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

Recognition of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) in Two Oligosymptomatic Sisters with Low CADASIL Scale Scores and a Venous Dysplasia: Report of a Novel Greek Family.

  • Authors : Paraskevas GP; Cognitive and Movement Disorders Clinic, Eginition Hospital, 1st Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.; Constantinides VC

Subjects: Magnetic Resonance Imaging* ; Mutation* ; Siblings*

  • Source: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2018 Sep; Vol. 27 (9), pp. e191-e195. Date of ElectronicPublisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

First Report of Arg587Cys Mutation of Notch3 Gene in Two Chinese Families with CADASIL.

  • Authors : You J; Department of Neurology, The Second Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, People's Republic of China. Electronic address: .; Liao S

Subjects: Mutation, Missense*; CADASIL/CADASIL/CADASIL/*genetics ; Receptor, Notch3/Receptor, Notch3/Receptor, Notch3/*genetics

  • Source: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2017 Jan; Vol. 26 (1), pp. e1-e4. Date of Electronic Publisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
  • 1-10 of  26 results for ""Receptor, Notch3""