Perspectives on Craniosynostosis.

Understanding craniosynostosis as a growth disorder. Wiley Interdiscip Rev Dev Biol (2016) 0.79

Silicon membrane interpositioning for the prevention of skull deformity following experimental craniosynostosis. Childs Nerv Syst (1993) 0.75

Immediate correction of sagittal synostosis. J Neurosurg (1978) 1.95

Lateral canthal advancement of the supraorbital margin. A new corrective technique in the treatment of coronal synostosis. J Neurosurg (1976) 1.87

The definitive plastic surgical treatment of the severe facial deformities of craniofacial dysostosis. Crouzon's and Apert's diseases. Plast Reconstr Surg (1971) 1.87

[Total facial osteotomy. Crouzon's syndrome, Apert's syndrome: oxycephaly, scaphocephaly, turricephaly]. Ann Chir Plast (1967) 1.82

Craniosynostosis and syndromes with craniosynostosis: incidence, genetics, penetrance, variability, and new syndrome updating. Birth Defects Orig Artic Ser (1979) 1.67

An etiologic and nosologic overview of craniosynostosis syndromes. Birth Defects Orig Artic Ser (1975) 1.62

Relationship of craniostenoses to craniofacial dysostoses, and to faciostenoses: a study with therapeutic implications. Plast Reconstr Surg (1971) 1.45

Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly. Teratology (1977) 1.33

Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s). Teratology (1976) 1.33

The prognosis of occipital encephalocele. Dev Med Child Neurol (1967) 1.29

The pathogenesis of premature cranial synostosis in man. Acta Anat (Basel) (1959) 1.25

Genetic perspectives on craniosynostosis and syndromes with craniosynostosis. J Neurosurg (1977) 1.19

Surgical management of unilateral and bilateral coronal craniosynostosis: 21 years of experience. Neurosurgery (1979) 1.18

Craniofacial growth following experimental craniosynostosis and craniectomy in rabbits. J Neurosurg (1979) 1.18

Premature craniosynostosis-a complication of thyroid replacement therapy. J Pediatr (1975) 1.05

Cranial synostosis in Job's syndrome. Lancet (1978) 1.04

Early skeletal release in the infant with craniofacial dysostosis: the role of the sphenozygomatic suture. Plast Reconstr Surg (1978) 1.04

CRANIOSYNOSTOSIS IN THE RACHITIC SPECTRUM. J Pediatr (1964) 1.01

Ataxia-telangiectasia presenting with craniostenosis. Arch Dis Child (1962) 1.00

Craniosynostosis secondary o ventriculoatrial shunt. Am J Dis Child (1968) 0.91

The premature synostosis of the cranial sutures. Acta Ophthalmol Suppl (1958) 0.91

Sagittal craniostenosis: fetal head constraint as one possible cause. J Pediatr (1979) 0.88

Progressive synosteosis in Apert's syndrome (acrocephalosyndactyly), with a description of roentgenographic changes in the feet. Am J Roentgenol Radium Ther Nucl Med (1966) 0.87

New surgical concepts resulting from cranio-orbito-facial surgery. Ann Surg (1975) 0.86

Immune-complex-mediated glomerulonephritis and pulmonary hemorrhage simulating Goodpasture syndrome. J Pediatr (1978) 0.86

Evaluation of craniofacial surgery in the treatment of facial deformities. Ann Surg (1975) 0.81

Premature craniosynostosis associated with hyperthyroidism in 4 children with reference to 5 further cases in the literature. Monatsschr Kinderheilkd (1972) 0.80

The pathogenesis of premature craniosynostosis in acrocephalosyndactyly (Apert's syndrome). A reconsideration. Plast Reconstr Surg (1977) 0.79

Reconstructive surgery for major craniofacial deformities. Surg Clin North Am (1976) 0.77

Craniosynostosis: correlation of bone scans, radiographs, and surgical findings. Radiology (1979) 0.77

Characteristics of the BGM line of cells from African green monkey kidney. Brief report. Arch Gesamte Virusforsch (1970) 6.50

Mortality and reoperation after open and transurethral resection of the prostate for benign prostatic hyperplasia. N Engl J Med (1989) 3.97

Syndromes with cleft lip and cleft palate. Cleft Palate J (1978) 3.84

The airway: problems and predictions in 18,500 patients. Can J Anaesth (1994) 3.46

Registries and administrative data: organization and accuracy. Med Care (1993) 3.44

Reliability of the timeline follow-back sexual behavior interview. Ann Behav Med (1998) 3.15

Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation. Am J Med Genet (1999) 3.02

The Proteus syndrome: the Elephant Man diagnosed. Br Med J (Clin Res Ed) (1986) 2.73

Establishment in continuous culture of a new type of lymphocyte from a "Burkitt like" malignant lymphoma (line D.G.-75). Int J Cancer (1977) 2.66

Predicting difficult intubation: a multivariable analysis. Can J Anaesth (2000) 2.41

In vivo and in vitro chromosomal damage induced by LSD-25. N Engl J Med (1967) 2.39

Testing the raters: inter-rater reliability of standardized anaesthesia simulator performance. Can J Anaesth (1997) 2.37

Craniosynostoses: phenotypic/molecular correlations. Am J Med Genet (1995) 2.35

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. Am J Hum Genet (1997) 2.22

Colon and rectal anastomoses do not require routine drainage: a systematic review and meta-analysis. Ann Surg (1999) 2.20

Why is there no progress against cervical cancer? CMAJ (1996) 2.14

Is there a Baller-Gerold syndrome? Am J Med Genet (1996) 2.11

A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies. J Pediatr (1973) 1.98

Complementary therapies: have they become accepted in general practice? Med J Aust (2000) 1.98

The anesthetic record: accuracy and completeness. Can J Anaesth (1999) 1.96

Testing internal consistency and construct validity during evaluation of performance in a patient simulator. Anesth Analg (1998) 1.95

A newly recognized hamartomatous syndrome. Birth Defects Orig Artic Ser (1979) 1.89

Laparoscopic loop ileostomy for temporary fecal diversion. Dis Colon Rectum (1993) 1.88

Measuring patient satisfaction with anesthesia care: a review of current methodology. Anesth Analg (1998) 1.86

Analysis of phenotypic features and FGFR2 mutations in Apert syndrome. Am J Hum Genet (1995) 1.85

Comparing clinical information with claims data: some similarities and differences. J Clin Epidemiol (1991) 1.83

A survey of 112,000 anaesthetics at one teaching hospital (1975-83). Can Anaesth Soc J (1986) 1.81

The Saethre-Chotzen syndrome. Birth Defects Orig Artic Ser (1975) 1.72

Klippel-Trenaunay syndrome. Am J Med Genet (2000) 1.72

Bannayan-Riley-Ruvalcaba syndrome. Am J Med Genet (1992) 1.69

Craniosynostosis and syndromes with craniosynostosis: incidence, genetics, penetrance, variability, and new syndrome updating. Birth Defects Orig Artic Ser (1979) 1.67

The incidence of airway problems depends on the definition used. Can J Anaesth (1996) 1.65

Holoprosencephaly and cytogenetic findings: further information. Am J Med Genet (1989) 1.63

Frontonasal dysplasia. J Pediatr (1970) 1.62

An etiologic and nosologic overview of craniosynostosis syndromes. Birth Defects Orig Artic Ser (1975) 1.62

The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography. Ann Genet (1971) 1.61

Bayes factor of model selection validates FLMP. Psychon Bull Rev (2001) 1.55

Tests of auditory-visual integration efficiency within the framework of the fuzzy logical model of perception. J Acoust Soc Am (2000) 1.55

Chromosomal damage in human leukocytes induced by lysergic acid diethylamide. Science (1967) 1.54

Pericentric inversion in a group D chromosome (13-15) associated with amenorrhea and gonadal dysgenesis. Ann Hum Genet (1967) 1.51

Perception of asynchronous and conflicting visual and auditory speech. J Acoust Soc Am (1996) 1.51

The premature infant: anesthesia for cesarean delivery. Anesth Analg (1994) 1.50

Critical respiratory events in the postanesthesia care unit. Patient, surgical, and anesthetic factors. Anesthesiology (1994) 1.49

Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome. Nat Genet (1996) 1.49

Variations in hysterectomy rates in Ontario: does the indication matter? CMAJ (1994) 1.48

Two human X-autosome translocations identified by autoradiography and fluorescence. Am J Hum Genet (1972) 1.48

Planned and unplanned postoperative admissions to critical care for mechanical ventilation. Can J Anaesth (1996) 1.48

Presence of gallstones is a poor indicator of the cause of obstructive jaundice. Surg Gynecol Obstet (1980) 1.41

Caffeine-stimulated acid and pepsin secretion: dose-response studies. Scand J Gastroenterol (1971) 1.39

Stimulation of mucus and nonparietal cell secretion by the E2 prostaglandins. Am J Dig Dis (1978) 1.39

Craniosynostosis in the Ullrich-Turner syndrome. Am J Med Genet (1990) 1.39

Chorionic villus sampling: the University of Maryland experience. Md Med J (1992) 1.38

Wiedemann-Beckwith syndrome, imprinting, IGF2, and H19: implications for hemihyperplasia, associated neoplasms, and overgrowth. Am J Med Genet (1994) 1.38

Human dicentric Y chromosomes. Case report and review of the literature. J Med Genet (1973) 1.32

Fetal risk of anesthesia and surgery during pregnancy. Anesthesiology (1986) 1.31

The quest for meaningful outcomes. Anesthesiology (1993) 1.30

DNA content measurements and an improved idiogram for the Indian muntjac. Cytometry (1993) 1.30

Accuracy of common hapatic duct size in the evaluation of extrahepatic biliary obstruction. Radiology (1980) 1.30

An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15. Ann Genet (1975) 1.28

Risk adjustment in claims-based research: the search for efficient approaches. J Clin Epidemiol (1989) 1.27

Sex-linked cleft palate. Report of a family and review of 77 kindreds. J Med Genet (1966) 1.26

Ascorbic acid nutrition in gastroduodenal disorders. Br Med J (1967) 1.24

The oral manifestations of Apert syndrome. J Craniofac Genet Dev Biol (1992) 1.23

An update on the holoprosencephalic disorders. J Pediatr (1982) 1.22

A prospective study of the risk of developing multiple sclerosis in uncomplicated optic neuritis. Neurology (1979) 1.22

A multivariable model for predicting the need for blood transfusion in patients undergoing first-time elective coronary bypass graft surgery. Transfusion (2001) 1.21

Clinical differentiation between Proteus syndrome and hemihyperplasia: description of a distinct form of hemihyperplasia. Am J Med Genet (1998) 1.21

Racial differences in the length of the human Y chromosome. Cytogenetics (1966) 1.19

Genetic perspectives on craniosynostosis and syndromes with craniosynostosis. J Neurosurg (1977) 1.19

Holt-Oram syndrome: clinical and genetic study of a large family. Am J Hum Genet (1966) 1.18

Holoprosencephaly and facial dysmorphia: nosology, etiology and pathogenesis. Birth Defects Orig Artic Ser (1971) 1.17

Langer-Giedion syndrome. Birth Defects Orig Artic Ser (1974) 1.17

Chromatin-positive Klinefelter's syndrome with undetectable peripheral FSH levels. Am J Med (1975) 1.16

Further delineation of Weaver syndrome. J Pediatr (1986) 1.15

Case report and delineation of the congenital hypothalamic hamartoblastoma syndrome (Pallister-Hall syndrome). Am J Med Genet (1989) 1.14

The prevalence of Campylobacter pylori gastritis among asymptomatic adults. CMAJ (1989) 1.14

Paresthesias and motor dysfunction after labor and delivery. Anesth Analg (1987) 1.13

The Canadian four-centre study of anaesthetic outcomes: III. Are anaesthetic complications predictable in day surgical practice? Can J Anaesth (1992) 1.13

Down's syndrome associated with a familial (21q-; 22q+) translocation. Cytogenetics (1967) 1.13

An autosomal-dominant form of juvenile periodontitis: its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc. J Craniofac Genet Dev Biol (1986) 1.12

Letter: The demise of the Marshall syndrome. J Pediatr (1974) 1.11

Effect of cigarette smoking on human gastric secretory responses. Gut (1971) 1.11

Robin sequences and complexes: causal heterogeneity and pathogenetic/phenotypic variability. Am J Med Genet (1999) 1.10

Craniofrontonasal syndrome: study of 41 patients. Am J Med Genet (1996) 1.10

Frontometaphyseal dysplasia. A new syndrome. Am J Dis Child (1969) 1.10

Saethre-Chotzen syndrome with familial translocation at chromosome 7p22. Am J Med Genet (1993) 1.09

PTEN mutations and proteus syndrome. Lancet (2001) 1.09

A comparison of outcome and cost of open vs. laparoscopic cholecystectomy. J Laparoendosc Surg (1992) 1.09

The validity of performance assessments using simulation. Anesthesiology (2001) 1.08

Genetic approaches to understanding brain development: holoprosencephaly as a model. Ment Retard Dev Disabil Res Rev (2000) 1.08

Protection against aspirin-induced antral and duodenal damage with enprostil. A double-blind endoscopic study. Gastroenterology (1985) 1.08

Craniosynostosis-radial aplasia: Baller-Gerold syndrome. Am J Dis Child (1979) 1.08

Treatment and mortality of perforated peptic ulcer: a survey of 852 cases. Can Med Assoc J (1971) 1.07

Holoprosencephaly survival and performance. Am J Med Genet (1999) 1.07

Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes. J Craniomaxillofac Surg (1993) 1.06

Cigarette smoking reduces human gastric luminal prostaglandin E2. Gut (1985) 1.05

Confirmation of an oroacral pattern of anomalies: a disruption? Am J Med Genet (1992) 1.05

Stimulation of non-parietal cell secretion in canine Heidenhain pouches by 16,16-dimethyl prostaglandin E2. Digestion (1978) 1.05

Beare-Stevenson cutis gyrata syndrome. Am J Med Genet (1992) 1.04

Macrocephaly in association with unusual cutaneous angiomatosis. J Pediatr (1975) 1.04