X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (19) 19
female (10) 10
genetics & heredity (10) 10
non-jewish patients (10) 10
male (8) 8
population (7) 7
canavan disease - genetics (6) 6
adolescent (5) 5
adult (5) 5
ashkenazi jews (5) 5
aspartoacylase deficiency (5) 5
clinical neurology (5) 5
index medicus (5) 5
jews (5) 5
jews - genetics (5) 5
non-jewish family (5) 5
phenotype (5) 5
amidohydrolases - genetics (4) 4
canavan disease (4) 4
child, preschool (4) 4
dna mutational analysis (4) 4
dystonia musculorum deformans - genetics (4) 4
gene (4) 4
identification (4) 4
middle aged (4) 4
missense mutation (4) 4
mutation (4) 4
neurosciences (4) 4
non-jewish americans (4) 4
pedigree (4) 4
9q34 (3) 3
age of onset (3) 3
amidohydrolases - deficiency (3) 3
animals (3) 3
biochemistry & molecular biology (3) 3
child (3) 3
chromosomes, human, pair 9 (3) 3
demography (3) 3
disease models, animal (3) 3
dyt1 locus (3) 3
educational psychology (3) 3
exclusion (3) 3
gaucher disease - genetics (3) 3
genetic linkage (3) 3
genetic markers (3) 3
genetics, population (3) 3
glucosylceramidase - genetics (3) 3
idiopathic torsion dystonia (3) 3
inheritance (3) 3
k rt clinical neurology (3) 3
mutation, missense - genetics (3) 3
research (3) 3
acid beta-glucosidase (2) 2
african-americans (2) 2
aged (2) 2
alleles (2) 2
analysis (2) 2
ancestry (2) 2
anthropology (2) 2
biology (2) 2
brain - pathology (2) 2
canavan disease - diagnosis (2) 2
canavan disease - therapy (2) 2
causes of (2) 2
chromosomes, human, pair 8 (2) 2
congenital, hereditary, and neonatal diseases and abnormalities (2) 2
dystonia musculorum deformans - ethnology (2) 2
dystonia musculorum deformans - physiopathology (2) 2
enzymes (2) 2
ethnic groups (2) 2
gaucher disease (2) 2
gaucher disease - enzymology (2) 2
gaucher disease - physiopathology (2) 2
genetic aspects (2) 2
genetic testing (2) 2
genetics (2) 2
genotype (2) 2
genotype/phenotype correlations (2) 2
glucocerebrosidase (2) 2
haplotypes (2) 2
heterogeneity (2) 2
heterologous expression (2) 2
human genetics (2) 2
infant (2) 2
infant, newborn (2) 2
italy (2) 2
jewish americans (2) 2
jewish-non-jewish relations (2) 2
judaism (2) 2
lysosomal storage disorder (2) 2
medicine, research & experimental (2) 2
minority & ethnic groups (2) 2
mutation - genetics (2) 2
n-acetylaspartic acid (2) 2
native americans (2) 2
polymorphism, genetic (2) 2
population-structure (2) 2
prevalence (2) 2
psychology, educational (2) 2
religious studies (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Contemporary Jewry, ISSN 0147-1694, 7/2014, Volume 34, Issue 2, pp. 75 - 91
In the first part of his article, by tracing the different stages of his academic training, the author outlines the analytic and methodological premises and... 
Demography | Narratives | Intermarriage | Jewish peoples | Narrative modes | Jewish diaspora | Jewish culture | Judaism | Jewish history | Jewish Americans | Religious Studies | US Jewry | Comparative research | Anthropology | Social Sciences, general | Humanities, general | Jewish/non-Jewish dichotomy | Humanities / Arts | Population estimates | Policy options | Sociology, general | Jews
Journal Article
Journal Article
Journal Article
Neurology, ISSN 0028-3878, 06/1997, Volume 48, Issue 6, pp. 1571 - 1577
Early-onset (<28 years) primary dystonia in most Ashkenazi Jews is due to a single founder mutation in the DYT1 gene on chromosome 9q34, as determined by very... 
POPULATION | EXCLUSION | 9Q34 | IDIOPATHIC TORSION DYSTONIA | DELAYED-ONSET DYSTONIA | ASHKENAZI JEWS | NON-JEWISH FAMILY | INHERITANCE | MAP | K RT CLINICAL NEUROLOGY | CLINICAL NEUROLOGY | Haplotypes | Humans | Middle Aged | Male | Chromosomes, Human, Pair 9 | Genetic Markers | Mutation - genetics | Jews - genetics | Dystonia - genetics | Phenotype | Adolescent | Age of Onset | Alleles | Adult | Female | Aged | Dystonia - etiology | Child | Genetic Linkage
Journal Article
Obstetrics and Gynecology Clinics of North America, ISSN 0889-8545, 2002, Volume 29, Issue 2, pp. 297 - 304
Canavan disease is a severe leukodystrophy more common among Ashkenazi Jews. The enzyme defect, apartoacylase, has been identified, and the gene cloned. Only... 
MUTATIONS | ASPARTOACYLASE DEFICIENCY | NON-JEWISH PATIENTS | OBSTETRICS & GYNECOLOGY | Pregnancy | Canavan Disease - diagnosis | Risk Assessment | United States | Canavan Disease - genetics | Humans | Sensitivity and Specificity | Genetic Counseling - methods | Female | Prenatal Diagnosis - methods | Genetic Testing - methods
Journal Article