Spectrum of Leukodystrophy and Genetic Leukoencephalopathy in Indian Population Diagnosed by Clinical Exome Sequencing and Clinical Utility-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Spectrum of Leukodystrophy and Genetic Leukoencephalopathy in Indian Population Diagnosed by Clinical Exome Sequencing and Clinical Utility

Published:2024-10 Issue:5 Volume:10 Page:
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Manisha Karamala Yalapalli¹,Fasaludeen Alfiya¹,Poulose Prashanth¹,Menon Ramshekhar¹,Thomas Bejoy¹^ORCID,Nair Sruthi S.¹,Cherian Ajith¹,Divya Kalikavil Puthanveedu¹^ORCID,Sundaram Soumya¹^ORCID

Affiliation:

1. From the Department of Neurology (K.Y.M., A.F., P.P., S.S.N., A.C., K.P.D.); Pediatric Neurology and Neurodevelopmental Disorders (R.M., S.S.); and Department of Imaging Sciences and Intervention Radiology (B.T.), Sree Chitra Tirunal Institute for Medical Sciences and Technology (SCTIMST), Thiruvananthapuram, Kerala, India.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Link

https://www.neurology.org/doi/pdfdirect/10.1212/NXG.0000000000200190

Reference31 articles.

1. Case definition and classification of leukodystrophies and leukoencephalopathies

2. A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies

3. Leukodystrophies: a proposed classification system based on pathological changes and pathogenetic mechanisms

4. Invited Article: An MRI-based approach to the diagnosis of white matter disorders

5. Diagnosis, prognosis, and treatment of leukodystrophies

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP