Meticulous and Early Understanding of Congenital Cranial Defects Can Save Lives
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[1] Syndromic Hydrocephalus. , 2022, Neurosurgery clinics of North America.
[2] Janice S. Lee,et al. Loeys-Dietz and Shprintzen-Goldberg syndromes: analysis of TGF-β-opathies with craniofacial manifestations using an innovative multimodality method , 2021, Journal of Medical Genetics.
[3] M. Krimmel,et al. Three-Dimensional Quantification of Facial Asymmetry in Children with Positional Cranial Deformity , 2021, Plastic and reconstructive surgery.
[4] R. R. van der Hulst,et al. Demographics of Positional Plagiocephaly and Brachycephaly; Risk Factors and Treatment , 2021, The Journal of craniofacial surgery.
[5] R. George,et al. Mutations in SKI in Shprintzen–Goldberg syndrome lead to attenuated TGF-β responses through SKI stabilization , 2021, eLife.
[6] Joshua C. Demke,et al. Syndromic Craniosynostosis. , 2019, Facial plastic surgery clinics of North America.
[7] S. Bartlett,et al. Onset and resolution of Chiari malformations and hydrocephalus in syndromic craniosynostosis following posterior vault distraction. , 2019, Plastic and reconstructive surgery.
[8] G. Pennisi,et al. The growth of the neurocranium: literature review and implications in cranial repair , 2019, Child's Nervous System.
[9] F. Grill,et al. Craniosynostosis, Scheuermann's disease, and intellectual disability resembling Shprintzen–Goldberg syndrome: a report on a family over 4 generations , 2017, Medicine.
[10] J. Riva-Cambrin,et al. Risk factors and rates of bone flap resorption in pediatric patients after decompressive craniectomy for traumatic brain injury. , 2013, Journal of neurosurgery. Pediatrics.
[11] Seneca L. Bessling,et al. Mutations in the TGF-β Repressor SKI Cause Shprintzen-Goldberg Syndrome with Aortic Aneurysm , 2012, Nature Genetics.
[12] L. Amaral,et al. Neuroimaging of Dandy-Walker Malformation: New Concepts , 2011, Topics in magnetic resonance imaging : TMRI.
[13] J. Visootsak,et al. Developmental outcomes of Down syndrome and Dandy-Walker malformation , 2011, Journal of Pediatric Neurology.
[14] J. Rhodes,et al. Pfeiffer Syndrome: A Treatment Evaluation , 2009, Plastic and reconstructive surgery.
[15] Wolfram Kress,et al. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 , 2005, Nature Genetics.
[16] Gillian M Morriss-Kay,et al. Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies , 2005, Journal of anatomy.
[17] L A Opperman,et al. Cranial sutures as intramembranous bone growth sites , 2000, Developmental dynamics : an official publication of the American Association of Anatomists.
[18] M. Giordano. Principles and practice of pediatric neurosurgery , 1999, Child's Nervous System.
[19] F. Brunelle,et al. Hydrocephalus and craniosynostosis. , 1997, Journal of neurosurgery.
[20] E. Haan,et al. Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome. , 1995, American journal of medical genetics.
[21] S. Braddock,et al. Sagittal craniosynostosis, Dandy-Walker malformation, and hydrocephalus: a unique multiple malformation syndrome. , 1993, American journal of medical genetics.
[22] A. Hockley,et al. Craniosynostosis , 1993, The Lancet.
[23] D. David,et al. Hydrocephalus in Crouzon's syndrome , 1989, Child's Nervous System.
[24] N. Sörensen,et al. Hydrocephalus in craniosynostosis , 1988, Child's Nervous System.
[25] J. Fryns,et al. X-linked mental retardation with marfanoid habitus. , 1987, American journal of medical genetics.
[26] M. Thong,et al. Crouzon syndrome: Genetic and intervention review. , 2019, Journal of oral biology and craniofacial research.
[27] E. Wolvius,et al. [Genetics of craniofacial development]. , 2008, Nederlands tijdschrift voor tandheelkunde.
[28] H. Lubs,et al. A form of X-linked mental retardation with marfanoid habitus. , 1984, American journal of medical genetics.
[29] R. Shprintzen,et al. A recurrent pattern syndrome of craniosynostosis associated with arachnodactyly and abdominal hernias. , 1982, Journal of craniofacial genetics and developmental biology.