scholarly article | Q13442814 |
P50 | author | Mirjam Langeveld | Q55948686 |
Ans van der Ploeg | Q88008512 | ||
Esmee Oussoren | Q88499253 | ||
George J G Ruijter | Q130279286 | ||
P2093 | author name string | Irene M J Mathijssen | |
Jan C van der Meijden | |||
Margreet Wagenmakers | |||
Rob M Verdijk | |||
Hansje H Bredero-Boelhouwer | |||
Marie-Lise C van Veelen-Vincent | |||
Johanna M P van den Hout | |||
P2860 | cites work | Evidence-Based Medicine: Nonsyndromic Craniosynostosis | Q48222386 |
Mucopolysaccharidosis type I with craniosynostosis. | Q50575918 | ||
Brain and spine MRI features of Hunter disease: frequency, natural evolution and response to therapy. | Q51873956 | ||
A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003. | Q51961876 | ||
Tracing craniosynostosis to its developmental stage through bone center displacement. | Q52175646 | ||
Mucopolysaccharidosis type I and craniosynostosis. | Q53099264 | ||
Craniosynostosis in Western Australia, 1980-1994: a population-based study | Q56379512 | ||
A population-based study of craniosynostosis | Q56396444 | ||
Optic nerve head swelling and optic atrophy in the systemic mucopolysaccharidoses | Q68369003 | ||
New insights into craniofacial malformations | Q28088384 | ||
The timing of physiologic closure of the metopic suture: a review of 159 patients using reconstructed 3D CT scans of the craniofacial region | Q28205803 | ||
Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on Craniosynostosis | Q28607705 | ||
Virchow and the pathogenesis of craniosynostosis: a translation of his original work | Q30459823 | ||
Report of a mucopolysaccharidosis occurring in Australian aborigines | Q33588412 | ||
Disc oedema in association with Hunter's syndrome: ocular histopathological findings | Q33643474 | ||
Slit ventricle syndrome and early-onset secondary craniosynostosis in an infant | Q33769372 | ||
Mucopolysaccharidosis VI. | Q33863356 | ||
Single-suture craniosynostosis: a review of neurobehavioral research and theory | Q34359996 | ||
Overcoming the barriers to diagnosis of Morquio A syndrome | Q34789123 | ||
Long-term functional outcome in 167 patients with syndromic craniosynostosis; defining a syndrome-specific risk profile | Q35012869 | ||
Sinus pericranii involving the torcular sinus in a patient with Hunter's syndrome and trigonocephaly: case report and review of the literature | Q35864916 | ||
Hydrocephalus and mucopolysaccharidoses: what do we know and what do we not know? | Q36395552 | ||
Long-term cognitive follow-up in children treated for Maroteaux-Lamy syndrome | Q36582221 | ||
Normocephalic pancraniosynostosis resulting in late presentation of elevated intracranial pressures | Q37741736 | ||
Altered FGF signalling in congenital craniofacial and skeletal disorders | Q38674265 | ||
Craniosynostosis update 1987. | Q39607907 | ||
Sutural biology and the correlates of craniosynostosis | Q40793420 | ||
The incidence of isolated craniosynostosis in the newborn infant. | Q44958828 | ||
Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome | Q46898196 | ||
Developmental and behavioral aspects of mucopolysaccharidoses with brain manifestations - Neurological signs and symptoms. | Q47668549 | ||
Surgical management of neurological manifestations of mucopolysaccharidosis disorders | Q47962754 | ||
P433 | issue | 6 | |
P921 | main subject | craniosynostosis | Q378183 |
P304 | page(s) | 1247-1258 | |
P577 | publication date | 2018-08-06 | |
P1433 | published in | Journal of Inherited Metabolic Disease | Q6295359 |
P1476 | title | Craniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure | |
P478 | volume | 41 |
Q89503466 | Posterior fossa horns; a new calvarial finding of mucopolysaccharidoses with well-known cranial MRI features | cites work | P2860 |
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