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Adult-onset Alexander disease among patients of Jewish Syrian descent
Saar Anis
, Tsvia Fay-Karmon
, Simon Lassman
, Fadi Shbat
, Orit Lesman-Segev
, Nofar Mor
, Ortal Barel
,
Dan Dominissini
,
Odelia Chorin
,
Elon Pras
,
Lior Greenbaum
,
Sharon Hassin-Baer
*
*
Corresponding author for this work
School of Continuing Medical Education
Human Molecular Genetics & Biochem
Pediatrics
Internal Medicine
Neurology
Sheba Medical Center at Tel Hashomer
Tel Aviv University
University of London
Tel Hashomer Hospital
The Gertner Institute
Research output
:
Contribution to journal
›
Article
›
peer-review
5
Scopus citations
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Keyphrases
Adult-onset Alexander Disease
100%
Adulthood
16%
Age of Onset
33%
Alexander Disease
16%
Autosomal Dominant Leukodystrophy
16%
Brainstem-spinal Cord
16%
Bulbar
33%
Cerebellar Degeneration
16%
Cervical Spinal Cord
33%
Chronic Conditions
16%
Clinical Characteristics
16%
Clinical Signs
16%
Clinical Symptoms
16%
Cognitive Decline
16%
Differential Diagnosis
16%
Diverse Populations
16%
Dysautonomia
16%
Family Members
16%
Family Planning
16%
Gait Disturbance
16%
Genetic Counseling
16%
Glial Fibrillary Acidic Protein
33%
Heterozygous mutation
16%
Imaging Findings
16%
Infratentorial
16%
Israel
16%
Jewish
100%
Jews
16%
Neuroradiological Findings
16%
Progressive Conditions
16%
Protein-coding Genes
16%
Radiological Manifestations
16%
Spinal Atrophy
16%
Syrian
100%
Variable Clinical Manifestation
16%
White Matter Hyperintensities
16%
Medicine and Dentistry
Acid Protein
28%
Alexander Disease
100%
Autosomal Dominant Inheritance
14%
Brainstem
14%
Cervical Spinal Cord
14%
Differential Diagnosis
14%
Diseases
14%
Dysautonomia
14%
Family Planning
14%
Genetic Counseling
14%
Infancy
14%
Leukodystrophy
14%
Physical Disease by Body Function
14%
Neuroscience
Acid Protein
28%
Alexander Disease
100%
Brainstem
14%
Differential Diagnosis
14%
Dysautonomia
14%
Leukodystrophy
14%