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A review of trisomy X (47,XXX)Tartaglia, Nicole R ; Howell, Susan ; Sutherland, Ashley ; Wilson, Rebecca ; Wilson, LennieOrphanet journal of rare diseases, 2010-05, Vol.5 (1), p.8-8, Article 8 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordanceHowell, Susan ; Davis, Shanlee M. ; Thompson, Talia ; Brown, Mariah ; Tanda, Tanea ; Kowal, Karen ; Alston, Amanda ; Ross, Judith ; Tartaglia, Nicole R.Journal of genetic counseling, 2023-02, Vol.32 (1), p.250-259 [Periódico revisado por pares]United States: Blackwell Publishing LtdTexto completo disponível |
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Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYYTartaglia, Nicole R ; Wilson, Rebecca ; Miller, Judith S ; Rafalko, Jessica ; Cordeiro, Lisa ; Davis, Shanlee ; Hessl, David ; Ross, JudithJournal of developmental and behavioral pediatrics, 2017-04, Vol.38 (3), p.197-207 [Periódico revisado por pares]United States: Lippincott Williams & Wilkins Ovid TechnologiesTexto completo disponível |
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Material Type: Artigo
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47,XYY Syndrome: Clinical Phenotype and Timing of AscertainmentBardsley, Martha Zeger, MD ; Kowal, Karen, PAC ; Levy, Carly, MD ; Gosek, Ania, BA ; Ayari, Natalie, BA ; Tartaglia, Nicole, MD ; Lahlou, Najiba, MD ; Winder, Breanna, PhD ; Grimes, Shannon, BA ; Ross, Judith L., MDThe Journal of pediatrics, 2013-10, Vol.163 (4), p.1085-1094 [Periódico revisado por pares]United States: Mosby, IncTexto completo disponível |
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Material Type: Artigo
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Attention-Deficit Hyperactivity Disorder Symptoms in Children and Adolescents with Sex Chromosome Aneuploidy: XXY, XXX, XYY, and XXYYTARTAGLIA, Nicole R ; AYARI, Natalie ; HUTAFF-LEE, Christa ; BOADA, RichardJournal of developmental and behavioral pediatrics, 2012-05, Vol.33 (4), p.309-318 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
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Material Type: Artigo
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Advances in the Treatment of Fragile X SyndromeHagerman, Randi J ; Berry-Kravis, Elizabeth ; Kaufmann, Walter E ; Ono, Michele Y ; Tartaglia, Nicole ; Lachiewicz, Ave ; Kronk, Rebecca ; Delahunty, Carol ; Hessl, David ; Visootsak, Jeannie ; Picker, Jonathan ; Gane, Louise ; Tranfaglia, MichaelPediatrics (Evanston), 2009-01, Vol.123 (1), p.378-390 [Periódico revisado por pares]Elk Grove Village, IL: Am Acad PediatricsTexto completo disponível |
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Material Type: Artigo
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Androgen Treatment Effects on Motor Function, Cognition, and Behavior in Boys with Klinefelter SyndromeRoss, Judith L., MD ; Kushner, Harvey, PhD ; Kowal, Karen, PA ; Bardsley, Martha, MD ; Davis, Shanlee, MD ; Reiss, Allan L., MD ; Tartaglia, Nicole, MD ; Roeltgen, David, MDThe Journal of pediatrics, 2017-06, Vol.185, p.193-199.e4 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Gaboxadol in Fragile X Syndrome: A 12-Week Randomized, Double-Blind, Parallel-Group, Phase 2a StudyBudimirovic, Dejan B ; Dominick, Kelli C ; Gabis, Lidia V ; Adams, Maxwell ; Adera, Mathews ; Huang, Linda ; Ventola, Pamela ; Tartaglia, Nicole R ; Berry-Kravis, ElizabethFrontiers in pharmacology, 2021-10, Vol.12, p.757825-757825 [Periódico revisado por pares]Switzerland: Frontiers Media S.ATexto completo disponível |
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Material Type: Artigo
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Diminished Ovarian Reserve in Girls and Adolescents with Trisomy X SyndromeDavis, Shanlee M. ; Soares, Katelyn ; Howell, Susan ; Cree-Green, Melanie ; Buyers, Eliza ; Johnson, Joshua ; Tartaglia, Nicole R.Reproductive sciences (Thousand Oaks, Calif.), 2020-11, Vol.27 (11), p.1985-1991 [Periódico revisado por pares]Cham: Springer International PublishingTexto completo disponível |
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Material Type: Artigo
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High prevalence of cardiometabolic risk features in adolescents with 47,XXY/Klinefelter syndromeDavis, Shanlee M. ; DeKlotz, Sophia ; Nadeau, Kristen J. ; Kelsey, Megan M. ; Zeitler, Philip S. ; Tartaglia, Nicole R.American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.327-333Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |