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Neurodevelopmental and Behavioral Pediatrics - Publications


 

Cordeiro L, Tartaglia N. Sex chromosome aneuploidy: XXYY. In: Maloy S, Hughes K, editors. Brennen's encyclopedia of genetics. 2nd ed. Amsterdam: Elsevier/Academic Press; 2013.

Johnson K. Leaky gut syndrome. In: Volkmar FR, editor. Encyclopedia of autism spectrum disorders. 5 volumes. New York: Springer; 2013.

2012

Adkins KW, Molloy C, Weiss SK, Reynolds A, Goldman SE, Burnette C, Clemons T, Fawkes D, Malow BA. Effects of a standardized pamphlet on insomnia in children with autism spectrum disorders. Pediatrics. 2012 Nov;130 Suppl 2:S139-44. [PMID: 23118244]

Angkustsiri K, Leckliter I, Tartaglia N, Beaton EA, Enriquez J, Simon TJ. An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome. J Dev Behav Pediatr. 2012 Nov-2012 Dec 31;33(9):713-20. [PMID: 23117596]

Austin H, Katz T, Shick E. Online pamphlet: ATN/AIR-P dental professionals' tool kit. Autism Speaks/Autism Treatment Network; 2012. http://www.autismspeaks.org/science/resources-programs/autism-treatment-network/tools-you-can-use/dental

Boada R, Hutaff-Lee C, Schrader A, Weitzenkamp D, Benke TA, Goldson EJ, Costa AC. Antagonism of NMDA receptors as a potential treatment for Down syndrome: a pilot randomized controlled trial. Transl Psychiatry. 2012;2:e141. [PMID: 22806212]

Carelli D, Hepburn S, Katz, T, LaVesser P, Srivorakiat L, Santanello A. Online pamphlet: ATN/AIR-P parent's guide to toilet training in autism. Autism Speaks/Autism Treatment Network; 2012. http://www.autismspeaks.org/science/resources-programs/autism-treatment-network/atn-air-p-toilet-training

Cordeiro L, Tartaglia N, Roeltgen D, Ross J. Social deficits in male children and adolescents with sex chromosome aneuploidy: a comparison of XXY, XYY, and XXYY syndromes. Res Dev Disabil. 2012 Jul-2012 Aug 31;33(4):1254-63. [PMID: 22502852]

Coury DL, Anagnostou E, Manning-Courtney P, Reynolds A, Cole L, McCoy R, Whitaker A, Perrin JM. Use of psychotropic medication in children and adolescents with autism spectrum disorders. Pediatrics. 2012 Nov;130 Suppl 2:S69-76. [PMID: 23118256]

Friedman S, Crocker A, Helm D, Osborne P, Sezun S. Answers to parents' questions on mental retardation. Institute for Community Inclusion Intellectual Disability Information booklet. Boston: Institute for Community Inclusion; 2012. http://www.communityinclusion.org/pdf/res9.pdf

Friedman SL, Griffith EM, Katz TK. Awareness of autism spectrum disorders increases. CAFP Magazine. 2012 Spring; 2nd Quarter:21-22. http://coloradoafp.org/pdf/coafp.ed31-final.pdf

Friedman SL, Helm DT, Woodman AC. Unique and universal barriers: hospice care for aging adults with intellectual disability. Am J Intellect Dev Disabil. 2012 Nov;117(6):509-32. [PMID: 23167489]

Goldson E, Reynolds A. Child development and behavior. In: Hay Jr. WW, Levin MJ, Deterding RR, Abzug MJ, Sondheimer JM, editors. Current diagnosis and treatment pediatrics. 21st ed. New York: McGraw Hill; 2012.

Hager K, Jennings K, Hosono S, Howell S, Gruen JR, Rivkees SA, Tartaglia NR, Rinder HM. Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidies. Int J Pediatr Endocrinol. 2012;2012(1):8. [PMID: 22524164]

Hyman SL, Stewart PA, Schmidt B, Cain U, Lemcke N, Foley JT, Peck R, Clemons T, Reynolds A, Johnson C, Handen B, James SJ, Courtney PM, Molloy C, Ng PK. Nutrient intake from food in children with autism. Pediatrics. 2012 Nov;130 Suppl 2:S145-53. [PMID: 23118245]

Katz T, Reynolds A. Behavioral treatments for sleep problems in individuals with DS-ASD. In: Froehlke M, Zaborek R, editors. When down syndrome and autism intersect: a guide to DS-ASD for parents and professionals. Bethesda, Maryland: Woodbine House; 2012.

Perkins EA, Friedman SL. Introduction to the special issue on aging and end of life. Am J Intellect Dev Disabil. 2012 Nov;117(6):439-41. [PMID: 23167483]

Perrin JM, Coury DL, Hyman SL, Cole L, Reynolds AM, Clemons T. Complementary and alternative medicine use in a large pediatric autism sample. Pediatrics. 2012 Nov ;130 Suppl 2:S77-82. [PMID: 23118257]

Reaven J, Blakeley-Smith A, Leuthe E, Moody E, Hepburn S. Facing your fears in adolescence: cognitive-behavioral therapy for high-functioning autism spectrum disorders and anxiety. Autism Res Treat. 2012;2012:423905. [PMID: 23091719]

Reynolds A, Krebs NF, Stewart PA, Austin H, Johnson SL, Withrow N, Molloy C, James SJ, Johnson C, Clemons T, Schmidt B, Hyman SL. Iron status in children with autism spectrum disorder. Pediatrics . 2012 Nov;130 Suppl 2:S154-9. [PMID: 23118246]

Ross JL, Roeltgen DP, Kushner H, Zinn AR, Reiss A, Bardsley MZ, McCauley E, Tartaglia N. Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome. Pediatrics. 2012 Apr;129(4):769-78. [PMID: 22412026]

Schaaf CP, Boone PM, Sampath S, Williams C, Bader PI, Mueller JM, Shchelochkov OA, Brown CW, Crawford HP, Phalen JA, Tartaglia NR, Evans P, Campbell WM, Tsai AC, Parsley L, Grayson SW, Scheuerle A, Luzzi CD, Thomas SK, Eng PA, Kang SH, Patel A, Stankiewicz P, Cheung SW. Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions. Eur J Hum Genet. 2012 Dec;20(12):1240-7. [PMID: 22617343]

Schendel DE, Diguiseppi C, Croen LA, Fallin MD, Reed PL, Schieve LA, Wiggins LD, Daniels J, Grether J, Levy SE, Miller L, Newschaffer C, Pinto-Martin J, Robinson C, Windham GC, Alexander A, Aylsworth AS, Bernal P, Bonner JD, Blaskey L, Bradley C, Collins J, Ferretti CJ, Farzadegan H, Giarelli E, Harvey M, Hepburn S, Herr M, Kaparich K, Landa R, Lee LC, Levenseller B, Meyerer S, Rahbar MH, Ratchford A, Reynolds A, Rosenberg S, Rusyniak J, Shapira SK, Smith K, Souders M, Thompson PA, Young L, Yeargin-Allsopp M. The Study to Explore Early Development (SEED): a multisite epidemiologic study of autism by the Centers for Autism and Developmental Disabilities Research and Epidemiology (CADDRE) network. J Autism Dev Disord. 2012 Oct;42(10):2121-40. [PMID: 22350336]

Sikora DM, Johnson K, Clemons T, Katz T. The relationship between sleep problems and daytime behavior in children of different ages with autism spectrum disorders. Pediatrics. 2012 Nov;130 Suppl 2:S83-90. [PMID: 23118258]

Tartaglia NR, Ayari N, Hutaff-Lee C, Boada R. Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYY. J Dev Behav Pediatr. 2012 May;33(4):309-18. [PMID: 22333574]


2011

Campbell W. Autism spectrum disorders. In: Bajaj L, Hambidge S, Nyquist A-C, Kerby G, editors. Berman's pediatric decision making. 5th ed. Philadelphia: Elsevier Mosby; 2011.

Campbell W. Development delay in children younger than 6 years. In: Bajaj L, Hambidge S, Nyquist A-C, Kerby G, editors. Berman's pediatric decision making. 5th ed. Philadelphia: Elsevier Mosby; 2011.

Campbell W. School learning problems. In: Bajaj L, Hambidge S, Nyquist A-C, Kerby G, editors. Berman's pediatric decision making. 5th ed. Philadelphia: Elsevier Mosby; 2011.

Griffith E, Katz T, Friedman S. Practice Update Newsletter: Autism spectrum disorders. Children's Hospital Colorado. Fall 2011.

Pickler L, Kellar-Guenther Y, Goldson E. Barriers to transition to adult care for youth with intellectual disabilities. International Journal of Child and Adolescent Health. 2011;3(3):575-584.

Reynolds AM, Malow BA. Sleep and autism spectrum disorders. Pediatr Clin North Am. 2011 Jun;58(3):685-98. [PMID: 21600349]

Tartaglia N, Ayari N, Howell S, D'Epagnier C, Zeitler P. 48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome. Acta Paediatr. 2011 Jun;100(6):851-60. [PMID: 21342258]

2010

Ching MSL, Shen Y, Tan W-H, Shafali SJ, Morrow EM, Chen X, Mukaddes NM, Yoo S-Y, Hanson E, Hundley R, Austin C, Becker, RE, Berry GT, Driscoll, K, Engle, EC, Friedman S, Gusella JF, Hisama FM, Irons MB, Lafiosca T, LeClair E, Miller DT, Neessen M, Picker JD, Rappaport, L, Rooney CM, Sarco DP, Stoler JM, Walsh CA, Wolff RR, Zhang T, Nasir RH, Wu B-L. Deletions of NRXN1 (neurexin-1) predisposes to a wide spectrum of developmental disorders. Amer J Med Genetics. 2010 June;153B(4):937-947.

Friedman SL. Complex Medical problems affecting life and lifespan in children. In: Friedman SL, Helm DT, editors. End-of-life care for children and adults with intellectual and developmental disabilities. 1st ed. Washington DC: AAIDD Press; 2010. p. 53-74.

Friedman SL, Helm DT. End-of-life care for children and adults with intellectual and developmental disabilities. 1st ed. Washington DC: AAIDD Press; 2010. 392 p.

Friedman SL, Helm DT. Postscript. In: Friedman SL, Helm DT, editors. End-of-life care for children and adults with intellectual and developmental disabilities. 1st ed. Washington DC: AAIDD Press; 2010. p. 353-356.

Goldson E, Reynolds A. Child development and behavior. In: Hay WW Jr, Levin MJ, Sondheimer JM, Deterding RR, editors. Current pediatric diagnosis and treatment. 20th ed. New York: McGraw-Hill; 2010.

Helm DT, Friedman SL. Constructing a "good death:" historical and social frameworks. In: Friedman SL, Helm DT, editors. End-of-life care for children and adults with intellectual and developmental disabilities. 1st ed. Washington DC: AAIDD Press; 2010. p. 3-12.

Ottesen AM, Aksglaede L, Garn I, Tartaglia N, Tassone F, Gravholt CH, Bojesen A, Sorensen K, Jorgensen N, Rajpert-De Meyts E, Gerdes T, Lind AM, Kjaergaard S, Juul A. Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy. Am J Med Genet A. 2010 May;152A(5):1206-12. [PMID: 20425825]

Reynolds A, Fussell J. Cognitive Development. In: Voigt RG, Macias MM, Myers SM, editors. Developmental and Behavioral Pediatrics, 1st edition. USA: AAP; 2010. ch. 10.

Shen Y, Dies KA, Holm IA, Bridgemohan C, Sobeih MM, Caronna EB, Miller KJ, Frazier JA, Silverstein I, Picker J, Weissman L, Raffalli P, Jeste S, Demmer LA, Peters HK, Brewster SJ, Kowalczyk SJ, Rosen-Sheidley B, McGowan C, Duda AW, Lincoln SA, Lowe KR, Schonwald A, Robbins A, Robbins M, Hisama F, Wolff R, Becker R, Nasir R, Urion DK, Milunksy JM, Rappaport L, Gusella JF, Walsh CA, Wi B-L, Miller DR on behalf of the Autism Consortium Clinical Genetics/DNA Diagnostics Collaboration. Clinical genetic testing for patients with autism spectrum disorders. Pediatrics. 2010 Apr 4;125(4);e727-e735.

Tracy S, Estroff J, Valim C, Friedman S, Chen C. Abnormal neuroimaging and neurodevelopmental findings in a cohort of antenatally diagnosed congenital diaphragmatic hernia survivors. J Pediatr Surg. 2010 May;45(5):958-65. [PMID: 20438935]

Wilson R, Bennett E, Howell SE, Tartaglia N. Sex chromosome aneuploidies. In: Davis A, editor. Handbook of pediatric neuropsychology. New York: Springer; 2010. p. 805-820.


2009

No 2009 Publications Listed

2008

Ben-Shachar S, Ou Z, Shaw CA, Belmont JW, Patel MS, Hummel M, Amato S, Tartaglia N, Berg J, Sutton VR, Lalani SR, Chinault AC, Cheung SW, Lupski JR, Patel A. 22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome. Am J Hum Genet. 2008 Jan;82(1):214-21. [PMID: 18179902]

Brega AG, Goodrich G, Bennett RE, Hessl D, Engle K, Leehey MA, Bounds LS, Paulich MJ, Hagerman RJ, Hagerman PJ, Cogswell JB, Tassone F, Reynolds A, Kooken R, Kenny M, Grigsby J. The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome. J Clin Exp Neuropsychol. 2008 Feb;1-17. [PMID: 18608667]

Coffey SM, Cook K, Tartaglia N, Tassone F, Nguyen DV, Pan R, Bronsky HE, Yuhas J, Borodyanskaya M, Grigsby J, Doerflinger M, Hagerman PJ, Hagerman RJ. Expanded clinical phenotype of women with the FMR1 premutation. Am J Med Genet A. 2008 Apr;146A(8):1009-16. [PMID: 18348275]

Gabriels RL, Agnew JA, Miller LJ, Gralla J, Pan Z, Goldson E, Ledbetter JC, Dinkens JP, Hooks E. Is there a relationship between restricted, repetitive, stereotyped behaviors and interests and abnormal sensory response in children with autism spectrum disorders? Res Autism Spectr Disord. 2008;2:660-70.

Garcia-Nonell C, Ratera ER, Harris S, Hessl D, Ono MY, Tartaglia N, Marvin E, Tassone F, Hagerman RJ. Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder. Am J Med Genet A. 2008 Aug;146A(15):1911-6. [PMID: 18627038]

Goldson E, Bonner BL. Child maltreatment: developmental consequences. In: Wolraich ML, Drotar DD, Dworkin PH, Perrin EC, editors. Developmental-behavioral pediatrics: evidence and practice. Philadelphia: Mosby; 2008.

Goldson E, Gardner SL. The effects of adverse neonatal factors and prematurity. In: Wolraich ML, Drotar DD, Dworkin PH, Perrin EC, editors. Developmental-behavioral pediatrics: evidence and practice. Philadelphia: Mosby; 2008.

Goldson E, Reynolds A. Child development and behavior. In: Hay WW Jr, Levin MJ, Sondheimer JM, Deterding RR, editors. Current pediatric diagnosis and treatment. 19th ed. New York: McGraw Hill; 2009.

Greco CM, Tassone F, Garcia-Arocena D, Tartaglia N, Coffey SM, Vartanian TK, Brunberg JA, Hagerman PJ, Hagerman RJ. Clinical and neuropathologic findings in a woman with the FMR1 premutation and multiple sclerosis. Arch Neurol. 2008 Aug;65(8):1114-6. [PMID: 18695063]

Grigsby J, Brega AG, Engle K, Leehey MA, Hagerman RJ, Tassone F, Hessl D, Hagerman PJ, Cogswell JB, Bennett RE, Cook K, Hall DA, Bounds LS, Paulich MJ, Reynolds A. Cognitive profile of fragile X premutation carriers with and without fragile X-associated tremor/ataxia syndrome. Neuropsychology. 2008 Jan;22(1):48-60. [PMID: 18211155]

Leehey MA, Berry-Kravis E, Goetz CG, Zhang L, Hall DA, Li L, Rice CD, Lara R, Cogswell J, Reynolds A, Gane L, Jacquemont S, Tassone F, Grigsby J, Hagerman RJ, Hagerman PJ. FMR1 CGG repeat length predicts motor dysfunction in premutation carriers. Neurology. 2008;70(16 Pt2):1397-402. [PMID: 18057320]

Murphy M. Developmental management of toddlers and preschoolers. In: Burns C, Brady M, Dunn A, Starr N, editors. Pediatric primary care. 4th ed. Philadelphia: Saunders/Elsevier; 2008.

Tartaglia N, Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J, Hansen R, Hagerman R. A new look at XXYY syndrome: medical and psychological features. Am J Med Genet A. 2008 Jun;146A(12):1509-22. [PMID: 18481271]


2007

Berry-Kravis E, Goetz CG, Leehey MA, Hagerman RJ, Zhang L, Li L, Nguyen D, Hall DA, Tartaglia N, Cogswell J, Tassone F, Hagerman PJ. Neuropathic features in fragile X premutation carriers. Am J Med Genet A. 2007 Jan;143(1):19-26. [PMID: 17152065]

Bross DC, Goldson E. The reality and the issues of child abuse and neglect in the United States. In: Etsuko F, editor. Change of family and violence. Tokyo: Akashi; 2007.

Goldson E, Bauman M. Medical health assessment and treatment issues in autism. In: Gabriels RL, Hill DE, editors. Growing up with autism: working with school-age children and adolescents. New York: Guilford Press; 2007.

Goldson E, Reynolds A. Child development and behavior. In: Hay WW Jr, Levin MJ, Sondheimer JM, Deterding RR, editors. Current pediatric diagnosis and treatment. 18th ed. New York: McGraw Hill; 2007.

Leehey MA, Berry-Kravis E, Min SJ, Hall DA, Rice CD, Zhang L, Grigsby J, Greco CM, Reynolds A, Lara R, Cogswell J, Jacquemont S, Hessl DR, Tassone F, Hagerman R, Hagerman PJ. Progression of tremor and ataxia in male carriers of the FMR1 premutation. Mov Disord. 2007 Jan;22(2):203-6. [PMID: 17133502]

Newschaffer CJ, Croen LA, Daniels J, Giarelli E, Grether JK, Levy SE, Mandell DS, Miller LA, Pinto-Martin J, Reaven J, Reynolds AM, Rice CE, Schendel D, Windham GC. The epidemiology of autism spectrum disorders. Annu Rev Public Health. 2007;28:235-58. Review. [PMID: 17367287]

Tartaglia N, Hansen R, Hagerman R. Advances in genetics. In: Odom S, Horner RH, Snell ME, Blacher JB, editors. Handbook of developmental disabilities. New York: Guilford Press; 2007.

Visootsak J, Rosner B, Dykens E, Tartaglia N, Graham JM Jr. Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY. Am J Med Genet A. 2007 Jun;143A(11):1198-203. [PMID: 17497714]

2006

Federico SG, Zachar PA, Oravec CM, Mandler T, Goldson E, Brown J. A successful international child health elective: the University of Colorado Department of Pediatrics' experience. Arch Pediatr Adolesc Med. 2006 Feb;160(2):191-6. [PMID: 16461877]

Gardner S, Goldson E. The Neonate and the environment: impact on development. In: Merenstein GB, Gardner S, editors. Handbook of neonatal intensive care. 6th ed. Philadelphia: Elsevier Science; 2006.

Goldson E. Behavioral issues in the care of children with special health care needs. In: Greydanus DE, Patel DR, Pratt HD, editors. Behavioral pediatrics. 2nd ed. New York: iUniverse Inc; 2006.

Goldson E, Louch G, Washington K, Scheu H. Guidelines for the care of the child with special health care needs. Adv Pediatr. 2006;53:165-82. [PMID: 17089866]


2005

Browne JV, Talmi A. Family-based intervention to enhance infant-parent relationships in the neonatal intensive care unit. J Pediatr Psychol. 2005 Dec;30(8):667-77. [PMID: 16260436]

Chapieski L, Brewer V, Evankovich K, Culhane-Shelburne K, Zelman K, Alexander A. Adaptive functioning in children with seizures: impact of maternal anxiety about epilepsy. Epilepsy Behav. 2005 Sep;7(2):246-52. [PMID: 15996525]

Fidler DJ, Hepburn SL, Mankin G, Rogers SJ. Praxis skills in young children with down syndrome, other developmental disabilities, and typically developing children. Am J Occup Ther. 2005 Mar-Apr;59(2):129-38. [PMID: 15830612]

Fidler DJ, Philofsky A, Hepburn SL, Rogers SJ. Nonverbal requesting and problem-solving by toddlers with down syndrome. Am J Ment Retard. 2005 Jul;110(4):312-22. [PMID: 15941367]

Gabriels RL, Cuccaro ML, Hill DE, Ivers BJ, Goldson E. Repetitive behaviors in autism: relationships with associated clinical features. Res Dev Disabil. 2005 Mar-Apr;26(2):169-81. [PMID: 15590247]

Goldson E, Reynolds A. Child development and behavior. In: Hay WW Jr., Levin MJ, Sondheimer JM, Deterding RR, editors. Current pediatric diagnosis and treatment. 17th ed. New York: McGraw-Hill; 2005.

Goldson E, Sirotnak A. Neglect. In: Alexander R, Giardino AP, editors. Child maltreatment: a comprehensive photographic reference identifying potential child abuse. 3rd ed. St. Louis: G.W. Medical Publishing; 2005.

Hepburn SL, Philofsky A, John A, Fidler D. A case study of early development in Williams syndrome: implications for early intervention. Infants Young Child. 2005;18(3):234-44.

Hertzberg DL, Krajicek MJ. Preschool and early childhood. In: Nehring WM, editor. Core curriculum for specializing in intellectual and developmental disability: a resource for nurses and other health care professionals. Sudbury, MA: Jones and Bartlett; 2005.

Krajicek MJ, Thomas DT, Hertzberg DL. Sexuality. In: Nehring WM, editor. Core curriculum for specializing in intellectual and developmental disability: a resource for nurses and other health care professionals. Sudbury, MA: Jones and Bartlett; 2005.

Phalen JA. Fragile X syndrome. Pediatr Rev. 2005 May;26(5):181-2. [PMID: 16562360]

Phalen JA. Index of suspicion. Pediatr Rev. 2005 Jun;26(6):218-25. [PMID: 15930329]