X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (29) 29
female (23) 23
male (19) 19
index medicus (12) 12
adult (9) 9
magnetic resonance imaging (9) 9
adolescent (7) 7
clinical neurology (7) 7
middle aged (7) 7
mutation (7) 7
aged (6) 6
dna mutational analysis (6) 6
genetics (6) 6
infant (6) 6
tomography, x-ray computed (6) 6
treatment outcome (6) 6
child (5) 5
children (5) 5
genetics & heredity (5) 5
pedigree (5) 5
animals (4) 4
care and treatment (4) 4
consanguinity (4) 4
immunology (4) 4
infant, newborn (4) 4
mice (4) 4
pediatrics (4) 4
proteins (4) 4
time factors (4) 4
aged, 80 and over (3) 3
brain (3) 3
cancer (3) 3
child, preschool (3) 3
diagnosis, differential (3) 3
dilated cardiomyopathy (3) 3
follow-up studies (3) 3
further section (3) 3
homozygote (3) 3
human genetics (3) 3
inflammation (3) 3
medicine, general & internal (3) 3
mitochondrial dna (3) 3
mitochondrial proteins - genetics (3) 3
mri (3) 3
neurosciences (3) 3
oncology (3) 3
surgery (3) 3
syndrome (3) 3
[ sdv.imm ] life sciences [q-bio]/immunology (2) 2
amino acid sequence (2) 2
article (2) 2
artifact (2) 2
biomedicine (2) 2
biopsy (2) 2
brain - pathology (2) 2
cardiovascular system (2) 2
case-control studies (2) 2
cell proliferation (2) 2
cells, cultured (2) 2
cerebrovascular circulation (2) 2
chromosome mapping (2) 2
corrigendum (2) 2
craniofacial (2) 2
degeneration (2) 2
dentistry (2) 2
deoxyribonucleic acid--dna (2) 2
disease (2) 2
encephalopathy (2) 2
fatal outcome (2) 2
fixed retainer (2) 2
gene (2) 2
gene function (2) 2
genes, recessive (2) 2
genetic aspects (2) 2
genetic association studies (2) 2
genetics, gene therapy & genetic disease (2) 2
genotype & phenotype (2) 2
hearing loss, sensorineural - diagnosis (2) 2
heart septal defects, atrial - complications (2) 2
identification (2) 2
in-vivo (2) 2
infants (2) 2
life sciences (2) 2
lung neoplasms (2) 2
medicine, research & experimental (2) 2
melanoma (2) 2
mesh : animals (2) 2
mesh : female (2) 2
mesh : mice (2) 2
metabolic diseases (2) 2
metabolic disorders (2) 2
metabolism, inborn errors - genetics (2) 2
microsatellite repeats (2) 2
middle cerebral artery (2) 2
middle cerebral artery - diagnostic imaging (2) 2
mitochondrial (2) 2
molecular medicine (2) 2
mutations (2) 2
myocarditis (2) 2
nervous system (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 6/2007, Volume 104, Issue 24, pp. 10152 - 10157
Journal Article
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 8, pp. 1019 - 1025
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2008, Volume 83, Issue 1, pp. 30 - 42
Hypomyelinating leukodystrophies (HMLs) are disorders involving aberrant myelin formation. The prototype of primary HMLs is the X-linked Pelizaeus-Merzbacher... 
CHAIN | GENE | HEREDITARY SPASTIC PARAPLEGIA | MOLECULAR CHAPERONES | HEAT-SHOCK-PROTEIN-60 | IN-VIVO | ESCHERICHIA-COLI | GENETICS & HEREDITY | PELIZAEUS-MERZBACHER-DISEASE | PROTEIN HSP60 | GJA12 MUTATIONS | Humans | Molecular Sequence Data | Neurodegenerative Diseases - diagnosis | Infant | Male | Hereditary Central Nervous System Demyelinating Diseases - physiopathology | Mitochondrial Proteins - genetics | Case-Control Studies | Chromosomes, Human, Pair 2 | Genes, Lethal | DNA Mutational Analysis | Conserved Sequence | Hereditary Central Nervous System Demyelinating Diseases - diagnosis | Female | Chaperonin 60 - metabolism | Microsatellite Repeats | Neurodegenerative Diseases - diagnostic imaging | Genetic Linkage | Hereditary Central Nervous System Demyelinating Diseases - genetics | Amino Acid Sequence | Chaperonin 60 - chemistry | Chaperonin 60 - genetics | Neurodegenerative Diseases - pathology | Physical Chromosome Mapping | Escherichia coli Proteins - metabolism | Neurodegenerative Diseases - genetics | Genetic Markers | Genes, Recessive | Radiography | Sequence Homology, Amino Acid | Hereditary Central Nervous System Demyelinating Diseases - pathology | Hereditary Central Nervous System Demyelinating Diseases - diagnostic imaging | Neurodegenerative Diseases - physiopathology | Polymorphism, Restriction Fragment Length | Pedigree | Escherichia coli Proteins - genetics | Consanguinity | Chaperonin 60 - analysis | Mutation | Heat shock proteins | Causes of | Nervous system | Myelination | Degeneration | Health aspects
Journal Article
Journal of Craniofacial Surgery, ISSN 1049-2275, 11/2012, Volume 23, Issue 6, pp. e654 - e657
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 09/2013, Volume 161, Issue 9, pp. 2204 - 2215
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2005, Volume 77, Issue 2, pp. 242 - 251
Journal Article
Journal of Therapeutic Ultrasound, ISSN 2050-5736, 12/2015, Volume 3, Issue S1
Journal Article
JOURNAL OF CRANIOFACIAL SURGERY, ISSN 1049-2275, 11/2012, Volume 23, Issue 6, pp. E654 - E657
Magnetic resonance imaging (MRI) is one of the most powerful tools in diagnostic imaging. With the growing rates of orthodontic treatment, there are increasing... 
SURGERY | orthodontic | MRI | ANXIETY | RETENTION | craniofacial | APPLIANCES | DENTAL MATERIALS | artifact | fixed retainer | TEMPOROMANDIBULAR-JOINT | ARTIFACTS | MR-IMAGES | Gold | Magnetic Resonance Imaging | Orthodontic Wires | Neurofibromatoses - diagnosis | Orthodontic Retainers | Humans | Adolescent | Craniocerebral Trauma - diagnosis | Female | Headache - diagnosis | Accidents, Traffic
Journal Article