“Macrodactyly, hemihypertrophy, and connective tissue nevi: Report of a new syndrome and review of the literature”. The Journal of Pediatrics89 (6): 924–927. (December 1976). doi:10.1016/S0022-3476(76)80597-5. PMID993918.
“Hamartoma Syndromes, Exome Sequencing, and a Protean Puzzle”. The New England Journal of Medicine365 (7): 661–3. (July 27, 2011). doi:10.1056/NEJMe1107384. PMID21793737.
“Reassessment of the Proteus syndrome literature: application of diagnostic criteria to published cases”. American Journal of Medical Genetics130A (2): 111–122. (Oct 1, 2004). doi:10.1002/ajmg.a.30327. PMID15372514.
Bastos, Halisson; da Silva, Paula Fabiana Sobral; de Albuquerque, Marco Antônio Veloso; Mattos, Adriana; Riesgo, Rudimar Santos; Ohlweiler, Lygia; Winckler, Maria Isabel Bragatti; Bragatti, José Augusto et al. (June 2008). “Proteus syndrome associated with hemimegalencephaly and Ohtahara syndrome: Report of two cases”. Seizure17 (4): 378–382. doi:10.1016/j.seizure.2007.11.001. PMID18082431.
“Mutation analysis of the tumor suppressor PTEN and the glypican 3 (GPC3) gene in patients diagnosed with Proteus syndrome”. Am. J. Med. Genet. A130A (2): 123–7. (October 2004). doi:10.1002/ajmg.a.30335. PMID15372512.
“Rapamycin treatment for a child with germline PTEN mutation”. Nature Clinical Practice Oncology5 (6): 357–361. (April 22, 2008). doi:10.1038/ncponc1112. PMID18431376.
“Proteus Syndrome: Misdiagnosis with PTEN Mutations”. American Journal of Medical Genetics122A (4): 323–324. (November 1, 2003). doi:10.1002/ajmg.a.20474. PMID14518070.
“Macrodactyly, hemihypertrophy, and connective tissue nevi: Report of a new syndrome and review of the literature”. The Journal of Pediatrics89 (6): 924–927. (December 1976). doi:10.1016/S0022-3476(76)80597-5. PMID993918.
“Hamartoma Syndromes, Exome Sequencing, and a Protean Puzzle”. The New England Journal of Medicine365 (7): 661–3. (July 27, 2011). doi:10.1056/NEJMe1107384. PMID21793737.
“Reassessment of the Proteus syndrome literature: application of diagnostic criteria to published cases”. American Journal of Medical Genetics130A (2): 111–122. (Oct 1, 2004). doi:10.1002/ajmg.a.30327. PMID15372514.
Bastos, Halisson; da Silva, Paula Fabiana Sobral; de Albuquerque, Marco Antônio Veloso; Mattos, Adriana; Riesgo, Rudimar Santos; Ohlweiler, Lygia; Winckler, Maria Isabel Bragatti; Bragatti, José Augusto et al. (June 2008). “Proteus syndrome associated with hemimegalencephaly and Ohtahara syndrome: Report of two cases”. Seizure17 (4): 378–382. doi:10.1016/j.seizure.2007.11.001. PMID18082431.
“Mutation analysis of the tumor suppressor PTEN and the glypican 3 (GPC3) gene in patients diagnosed with Proteus syndrome”. Am. J. Med. Genet. A130A (2): 123–7. (October 2004). doi:10.1002/ajmg.a.30335. PMID15372512.
“Rapamycin treatment for a child with germline PTEN mutation”. Nature Clinical Practice Oncology5 (6): 357–361. (April 22, 2008). doi:10.1038/ncponc1112. PMID18431376.
“Proteus Syndrome: Misdiagnosis with PTEN Mutations”. American Journal of Medical Genetics122A (4): 323–324. (November 1, 2003). doi:10.1002/ajmg.a.20474. PMID14518070.