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Health Supervision for Children and Adolescents With Down Syndrome.
Bull MJ, Trotter T, Santoro SL, Christensen C, Grout RW; COUNCIL ON GENETICS; Burke LW, Berry SA, Geleske TA, Holm I, Hopkin RJ, Introne WJ, Lyons MJ, Monteil DC, Scheuerle A, Stoler JM, Vergano SA, Chen E, Hamid R, Downs SM, Grout RW, Cunniff C, Parisi MA, Ralston SJ, Scott JA, Shapira SK, Spire P. Bull MJ, et al. Among authors: parisi ma. Pediatrics. 2022 May 1;149(5):e2022057010. doi: 10.1542/peds.2022-057010. Pediatrics. 2022. PMID: 35490285 No abstract available.
Molecular genetics in pediatric dermatology.
Parisi MA, Sybert VP. Parisi MA, et al. Curr Opin Pediatr. 2000 Aug;12(4):347-53. doi: 10.1097/00008480-200008000-00012. Curr Opin Pediatr. 2000. PMID: 10943815 Review.
Healthcare recommendations for Joubert syndrome.
Bachmann-Gagescu R, Dempsey JC, Bulgheroni S, Chen ML, D'Arrigo S, Glass IA, Heller T, Héon E, Hildebrandt F, Joshi N, Knutzen D, Kroes HY, Mack SH, Nuovo S, Parisi MA, Snow J, Summers AC, Symons JM, Zein WM, Boltshauser E, Sayer JA, Gunay-Aygun M, Valente EM, Doherty D. Bachmann-Gagescu R, et al. Among authors: parisi ma. Am J Med Genet A. 2020 Jan;182(1):229-249. doi: 10.1002/ajmg.a.61399. Epub 2019 Nov 11. Am J Med Genet A. 2020. PMID: 31710777 Free PMC article. Review.
Genetics of Hirschsprung disease.
Parisi MA, Kapur RP. Parisi MA, et al. Curr Opin Pediatr. 2000 Dec;12(6):610-7. doi: 10.1097/00008480-200012000-00017. Curr Opin Pediatr. 2000. PMID: 11106284 Review.
MKS3-related ciliopathy with features of autosomal recessive polycystic kidney disease, nephronophthisis, and Joubert Syndrome.
Gunay-Aygun M, Parisi MA, Doherty D, Tuchman M, Tsilou E, Kleiner DE, Huizing M, Turkbey B, Choyke P, Guay-Woodford L, Heller T, Szymanska K, Johnson CA, Glass I, Gahl WA. Gunay-Aygun M, et al. Among authors: parisi ma. J Pediatr. 2009 Sep;155(3):386-92.e1. doi: 10.1016/j.jpeds.2009.03.045. Epub 2009 Jun 21. J Pediatr. 2009. PMID: 19540516 Free PMC article. Clinical Trial.
A Gender Assessment Team: experience with 250 patients over a period of 25 years.
Parisi MA, Ramsdell LA, Burns MW, Carr MC, Grady RE, Gunther DF, Kletter GB, McCauley E, Mitchell ME, Opheim KE, Pihoker C, Richards GE, Soules MR, Pagon RA. Parisi MA, et al. Genet Med. 2007 Jun;9(6):348-57. doi: 10.1097/gim.0b013e3180653c47. Genet Med. 2007. PMID: 17575501 Free article.
Ambiguous genitalia: what prenatal genetic testing is practical?
Adam MP, Fechner PY, Ramsdell LA, Badaru A, Grady RE, Pagon RA, McCauley E, Cheng EY, Parisi MA, Shnorhavorian M. Adam MP, et al. Among authors: parisi ma. Am J Med Genet A. 2012 Jun;158A(6):1337-43. doi: 10.1002/ajmg.a.35338. Epub 2012 May 11. Am J Med Genet A. 2012. PMID: 22581420
89 results