Pages that link to "Q52081305"
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The following pages link to Hydrocephalus and mental retardation in craniosynostosis (Q52081305):
Displaying 29 items.
- The prehistory of compassion (Q24655555) (← links)
- Craniosynostosis in Growing Children : Pathophysiological Changes and Neurosurgical Problems (Q26745868) (← links)
- Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on Craniosynostosis (Q28607705) (← links)
- Hydrocephalus in craniosynostosis: a review (Q30988664) (← links)
- Thrombophilia and first arterial ischaemic stroke: a systematic review (Q35283067) (← links)
- Pre- and postoperative developmental attainment in sagittal synostosis (Q35283080) (← links)
- Multicenter study of neurodevelopment in 3-year-old children with and without single-suture craniosynostosis (Q36123937) (← links)
- Diagnostic imaging in the management of craniosynostoses (Q36676132) (← links)
- Agenesis of the corpus callosum. Its associated anomalies and syndromes with special reference to the Apert syndrome. (Q37062973) (← links)
- A review and dental management of persons with craniosynostosis anomalies (Q37167689) (← links)
- Crouzon syndrome: A case report and review of literature (Q38057303) (← links)
- Contemporary occurrence of hydrocephalus and Chiari I malformation in sagittal craniosynostosis. Case report and review of the literature (Q38905503) (← links)
- Brain phenotypes in two FGFR2 mouse models for Apert syndrome (Q39326391) (← links)
- Presurgical and Postsurgical Mental and Psychomotor Development of Infants with Sagittal Synostosis (Q39455000) (← links)
- Premature craniosynostosis in a rare genetic disease- a case report (Q39769043) (← links)
- The calvarium (Q40606675) (← links)
- Growth hormone deficiency in a case of crouzon syndrome with hydrocephalus (Q40818219) (← links)
- Hydrocephalus and craniosynostosis (Q41695090) (← links)
- Apert syndrome: magnetic resonance imaging (MRI) of associated intracranial anomalies. (Q47568337) (← links)
- Pattern of Closure of Skull Base Synchondroses in Crouzon Syndrome. (Q47612142) (← links)
- History of the Kleeblattschädel deformity: origin of concepts and evolution of management in the past 50 years (Q48739739) (← links)
- Apert syndrome: factors involved in the cognitive development (Q51922516) (← links)
- Skull base morphology in fibroblast growth factor receptor type 2-related faciocraniosynostosis: a descriptive analysis. (Q53014589) (← links)
- The growth of the foramen magnum in Crouzon syndrome. (Q53148325) (← links)
- Morphology of the foramen magnum in syndromic and non-syndromic brachycephaly: letter to the editor (Q56266793) (← links)
- Pfeiffer syndrome, type II (Q56366828) (← links)
- Crouzon disease associated with sinus pericranii: a report on identical twin sisters (Q56392887) (← links)
- Hydrocephalus in craniosynostosis (Q56401219) (← links)
- Hydrocephalus in Crouzon's syndrome (Q69676041) (← links)