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Sturge-Weber syndrome: a review.
Thomas-Sohl KA, Vaslow DF, Maria BL. Thomas-Sohl KA, et al. Pediatr Neurol. 2004 May;30(5):303-10. doi: 10.1016/j.pediatrneurol.2003.12.015. Pediatr Neurol. 2004. PMID: 15165630 Review.
Epileptic Encephalopathies: Clinical Aspects, Molecular Features and Pathogenesis, Therapeutic Targets and Translational Opportunities, and Future Research Directions.
Germain B, Maria BL. Germain B, et al. Among authors: maria bl. J Child Neurol. 2018 Jan;33(1):7-40. doi: 10.1177/0883073817697846. Epub 2017 Mar 28. J Child Neurol. 2018. PMID: 28349773
Joubert syndrome is not a cause of classical autism.
Takahashi TN, Farmer JE, Deidrick KK, Hsu BS, Miles JH, Maria BL. Takahashi TN, et al. Am J Med Genet A. 2005 Feb 1;132A(4):347-51. doi: 10.1002/ajmg.a.30500. Am J Med Genet A. 2005. PMID: 15633174
Central nervous system structure and function in Sturge-Weber syndrome: evidence of neurologic and radiologic progression.
Maria BL, Neufeld JA, Rosainz LC, Drane WE, Quisling RG, Ben-David K, Hamed LM. Maria BL, et al. J Child Neurol. 1998 Dec;13(12):606-18. doi: 10.1177/088307389801301204. J Child Neurol. 1998. PMID: 9881531
High prevalence of bihemispheric structural and functional defects in Sturge-Weber syndrome.
Maria BL, Neufeld JA, Rosainz LC, Ben-David K, Drane WE, Quisling RG, Hamed LM. Maria BL, et al. J Child Neurol. 1998 Dec;13(12):595-605. doi: 10.1177/088307389801301203. J Child Neurol. 1998. PMID: 9881530
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