X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (979) 979
Book Review (145) 145
Publication (53) 53
Book Chapter (4) 4
Conference Proceeding (4) 4
Book / eBook (2) 2
Dissertation (2) 2
Magazine Article (1) 1
Newspaper Article (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (652) 652
index medicus (645) 645
crouzon-syndrome (405) 405
craniosynostosis (386) 386
crouzon syndrome (377) 377
female (350) 350
male (342) 342
surgery (308) 308
mutation (221) 221
genetics & heredity (188) 188
infant (182) 182
dentistry (181) 181
child (180) 180
animals (170) 170
receptors, fibroblast growth factor - genetics (168) 168
mutations (166) 166
apert syndrome (163) 163
craniosynostoses - genetics (151) 151
child, preschool (149) 149
fgfr2 (127) 127
adolescent (126) 126
syndrome (122) 122
crouzon (119) 119
adult (115) 115
growth-factor receptor-2 (109) 109
pediatrics (107) 107
pfeiffer-syndrome (106) 106
phenotype (105) 105
mice (101) 101
gene (97) 97
apert-syndrome (95) 95
acrocephalosyndactylia - genetics (94) 94
craniofacial dysostosis - genetics (91) 91
receptor, fibroblast growth factor, type 2 (91) 91
receptor protein-tyrosine kinases - genetics (90) 90
receptor, fibroblast growth factor, type 2 - genetics (87) 87
clinical neurology (85) 85
infant, newborn (85) 85
dentistry, oral surgery & medicine (82) 82
acanthosis nigricans (80) 80
biochemistry & molecular biology (77) 77
craniofacial dysostosis - surgery (76) 76
gene cause (74) 74
craniofacial dysostosis (73) 73
point mutation (72) 72
children (71) 71
pfeiffer syndrome (71) 71
apert (67) 67
craniosynostoses - surgery (64) 64
abridged index medicus (62) 62
growth (61) 61
pfeiffer (61) 61
craniosynostoses - pathology (60) 60
tomography, x-ray computed (60) 60
craniofacial dysostosis - complications (59) 59
developmental biology (58) 58
dna mutational analysis (58) 58
fgfr2 mutations (56) 56
fibroblast growth factors (56) 56
genetic aspects (56) 56
jackson-weiss-syndrome (56) 56
achondroplasia (55) 55
retrospective studies (55) 55
molecular sequence data (54) 54
radiography (53) 53
crouzon's syndrome (51) 51
research (49) 49
cephalometry (48) 48
saethre-chotzen-syndrome (48) 48
growth-factor receptor-3 (47) 47
amino acid sequence (46) 46
craniosynostoses - complications (46) 46
distraction osteogenesis (46) 46
autosomal-dominant craniosynostosis (45) 45
pedigree (45) 45
acrocephalosyndactylia - pathology (44) 44
cell biology (44) 44
craniofacial dysostosis - pathology (44) 44
follow-up studies (44) 44
signal transduction (44) 44
thanatophoric dysplasia (43) 43
advancement (42) 42
saethre-chotzen syndrome (42) 42
mutation - genetics (41) 41
treatment outcome (41) 41
craniofacial dysostosis - diagnosis (40) 40
musculoskeletal diseases (40) 40
polymerase chain reaction (40) 40
acrocephalosyndactylia - surgery (39) 39
craniosynostoses - diagnosis (39) 39
diagnosis (39) 39
care and treatment (38) 38
expression (38) 38
fibroblast growth factor receptor (38) 38
osteogenesis (38) 38
base sequence (37) 37
craniosynostoses - diagnostic imaging (37) 37
genetics (37) 37
receptor, fibroblast growth factor, type 3 - genetics (37) 37
abnormalities, multiple - genetics (36) 36
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (944) 944
French (10) 10
Spanish (9) 9
German (8) 8
Japanese (6) 6
Portuguese (4) 4
Italian (3) 3
Turkish (3) 3
Chinese (2) 2
Hungarian (1) 1
Indonesian (1) 1
Persian (1) 1
Polish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Cranio-Maxillo-Facial Surgery, ISSN 1010-5182, 10/2016, Volume 44, Issue 10, pp. 1567 - 1575
Journal Article
Human Mutation, ISSN 1059-7794, 1999, Volume 14, Issue 2, pp. 115 - 125
Journal Article
Journal of Glaucoma, ISSN 1057-0829, 03/2018, Volume 27, Issue 6, pp. e110 - e112
BACKGROUND:Crouzon syndrome is the most common form of craniosynostosis, and mutations in the fibroblast growth factor receptor 2 and 3 (FGFR2 and FGFR3) genes... 
congenital glaucoma | anterior segment dysgenesis | glaucoma | Crouzon syndrome | ANTERIOR-CHAMBER DYSGENESIS | MUTATION | OPHTHALMOLOGY | CRANIOSYNOSTOSIS | Glaucoma | Complications and side effects | Risk factors | Craniofacial dysostosis
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 04/2019, Volume 179, Issue 4, pp. 668 - 673
In 2011, biallelic loss‐of‐function variants in the interleukin receptor 11 alpha gene IL11RA were found to be associated with a Crouzon‐like craniosynostosis... 
conductive hearing loss | interleukin 11 receptor alpha | dentition | craniosynostosis | malocclusion | Crouzon syndrome | GENETICS & HEREDITY | MUTATIONS | Phenotypes | Gene frequency | Craniosynostosis | Interleukin 1 | Diagnosis | Middle ear | Minority & ethnic groups | Hearing loss
Journal Article
Pediatric pharmacology, ISSN 1727-5776, 04/2019, Volume 16, Issue 1, pp. 36 - 43
Relevance. Crouzon syndrome is a craniostenosis due to combination of cranial bones hypoplasia and premature ectocranial sutures fusion resulting in... 
eyeball dislocation | distance osteogenesis | osteotomy | clinical case | blepharorrhaphy | Crouzon syndrome
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 05/2013, Volume 161, Issue 5, pp. 1132 - 1136
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 04/2017, Volume 32, Issue 4, pp. 757 - 769
In 1985, we briefly characterized “congenital sclerosing osteomalacia with cerebral calcification” (CSOCC) in infant sisters. Later, Raine syndrome (RNS)... 
CRANIOFACIAL DYSOSTOSIS | OSTEOMALACIA | RICKETS | DENTIN MATRIX PROTEIN | KINASE | PHOSPHOPROTEOME | CROUZON SYNDROME | CRANIOSYNOSTOSIS | HYPOPHOSPHATEMIA | SIBLING PROTEINS | OSTEOPONTIN | METOPIC SUTURE | MINERALIZATION | OSTEOSCLEROSIS | OSTEOPETROSIS | TRIGONOCEPHALY | AUTOSOMAL RECESSIVE SYNDROME | INTRACRANIAL CALCIFICATION | HYPOPLASTIC NOSE | SECRETED PROTEINS | ENDOCRINOLOGY & METABOLISM | OSTEOSCLEROTIC BONE DYSPLASIA | ANHYDRASE-II DEFICIENCY | CASEIN KINASE | RENAL TUBULAR-ACIDOSIS | Abnormalities, Multiple - metabolism | Calcinosis - genetics | Microcephaly - genetics | Cerebrum - diagnostic imaging | Casein Kinase I - genetics | Osteomalacia - diagnostic imaging | Humans | Calcinosis - diagnostic imaging | Male | Cleft Palate - genetics | Exophthalmos - genetics | Osteosclerosis - metabolism | Adult | Cerebrum - metabolism | Female | Osteomalacia - metabolism | Osteosclerosis - genetics | Calcinosis - metabolism | Cleft Palate - diagnostic imaging | Cerebrum - pathology | Osteosclerosis - diagnostic imaging | Abnormalities, Multiple - genetics | Extracellular Matrix Proteins - metabolism | Infant, Newborn | Extracellular Matrix Proteins - genetics | Microcephaly - metabolism | Abnormalities, Multiple - diagnostic imaging | Exophthalmos - diagnostic imaging | Microcephaly - diagnostic imaging | Osteomalacia - genetics | Exophthalmos - metabolism | Casein Kinase I - metabolism | Cleft Palate - metabolism | Medical research | Dysplasia | Genetic disorders | Calcification | Medicine, Experimental | Genetics | Genetic aspects | Histochemistry | Index Medicus
Journal Article
Journal of Craniofacial Surgery, ISSN 1049-2275, 07/2016, Volume 27, Issue 5, pp. 1125 - 1134
Journal Article
Surgical and Radiologic Anatomy, ISSN 0930-1038, 07/2019, pp. 1 - 3
This article describes a retrospective diagnosis through an artistic representation of a pre-Columbian Central America bowl figuring a child with clinical... 
Mayan civilization | Diagnosis | Crouzon syndrome | Index Medicus
Journal Article
International Journal of Oral & Maxillofacial Surgery, ISSN 0901-5027, 03/2019, Volume 48, Issue 3, pp. 309 - 321
The facial malformations of Crouzon syndrome involve the entire cranio-orbito-zygomatic region. The detailed sequence of changes in orbit, zygoma, and maxilla... 
midface | zygoma | orbit | maxilla | Crouzon syndrome | SURGERY | APERT | DYSMORPHOLOGY | CRANIAL BASE | ADVANCEMENT | DISTRACTION OSTEOGENESIS | OSTEOTOMY | DENTISTRY, ORAL SURGERY & MEDICINE | FACIAL GROWTH | EXPANSION | Medical colleges | Surgery, Plastic | Analysis
Journal Article
Surgical and Radiologic Anatomy, ISSN 0930-1038, 08/2019, pp. 1 - 2
Journal Article
Child's Nervous System, ISSN 0256-7040, 03/2019, Volume 35, Issue 3, pp. 501 - 507
PurposeCranial lacunae (foci of attenuated calvarial bone) are CT equivalents of copper beating seen on plain skull radiographs in children with... 
3D morphometric | Apert | Crouzon | Intracranial pressure | SURGERY | PRESSURE | SCANS | SINGLE-SUTURE | PEDIATRICS | CRANIOSYNOSTOSIS | CLINICAL NEUROLOGY | Usage | Morphometrics (Biology) | Intracranial hypertension | Craniofacial dysostosis | Acrocephalosyndactylia | Reports | Analysis | Physiological aspects | Genetic aspects | Diagnosis | Children | Health aspects
Journal Article
JOURNAL OF CRANIOFACIAL SURGERY, ISSN 1049-2275, 03/2019, Volume 30, Issue 2, pp. 317 - 325
Complicated craniofacial malformations interfacing with multiple intracellular regulatory mechanisms, lead to ambiguous growth patterns in Apert syndrome. This... 
3-D cephalometries | SURGERY | development | Apert syndrome | ULTRASOUND | CRANIAL BASE | FACIAL GROWTH | GROWTH-FACTOR RECEPTOR-3 | craniofacial relationship | CROUZON-SYNDROMES | MUTATIONS | PRENATAL-DIAGNOSIS
Journal Article
British Journal of Oral & Maxillofacial Surgery, ISSN 0266-4356, 11/2018, Volume 56, Issue 9, pp. 864 - 869
Bony malformations of the orbit and alterations to the soft tissue in Apert syndrome contribute to ophthalmic dysfunction. Recognised structural malformation... 
malformation | development | Apert syndrome | orbit | SURGERY | DENTISTRY, ORAL SURGERY & MEDICINE | ADVANCEMENT | MONOBLOC | BIPARTITION | CROUZON-PFEIFFER | Medicine, Experimental | Medical research | Medical colleges | Surgery, Plastic | Multiple abnormalities
Journal Article