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Fragile X Syndrome - Bibliography
Alanay Y, Unal F, Turanli G, Alikaşifoğlu M, Alehan D, Akyol U, Belgin E, Sener C, Aktaş D, Boduroğlu K, Utine E, Volkan-Salanci
B, Ozusta S, Genç A, Başar F, Sevinç S, Tunçbilek E.
A multidisciplinary approach to the management of individuals with fragile X syndrome.
J Intellect Disabil Res.
2007;51(Pt 2):151-61.
PubMed abstract
American Academy of Pediatrics Committee on Genetics.
Health supervision for children with fragile X syndrome.
Pediatrics.
1996;98(2 Pt 1):297-300.
PubMed abstract / Full Text
Guidelines reaffirmed in 2007 by the AAP.
American Psychiatric Association.
DSM-IV-TR Diagnostic and Statistical Manual of Mental Disorders.
Fourth Edition ed. Washington, D.C.: American Psychiatric Association;
2000.
Bailey, DB, Skinner, D, Sparkman, K, .
Delayed diagnosis of fragile X syndrome: United States 1990-1999.
(2002)
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5133a3.htm.
CDC.
Delayed diagnosis of fragile X syndrome--United States, 1990-1999.
MMWR Morb Mortal Wkly Rep.
2002;51(33):740-2.
PubMed abstract
Crawford, DC.
FMR1 and the Fragile X Syndrome.
CDC: National Office of Public Health Genomics; HuGENet: Fact Sheets; (2001)
http://www.cdc.gov/genomics/hugenet/factsheets/FS_FragileX.htm. Accessed on 1/3/2009.
Hagerman PJ, Hagerman RJ.
The fragile-X premutation: a maturing perspective.
Am J Hum Genet.
2004;74(5):805-16.
PubMed abstract / Full Text
Hagerman RJ, Berry-Kravis E, Kaufmann WE, Ono MY, Tartaglia N, Lachiewicz A, Kronk R, Delahunty C, Hessl D, Visootsak J, Picker
J, Gane L, Tranfaglia M.
Advances in the treatment of fragile X syndrome.
Pediatrics.
2009;123(1):378-90.
PubMed abstract
Hatton DD, Hooper SR, Bailey DB, Skinner ML, Sullivan KM, Wheeler A.
Problem behavior in boys with fragile X syndrome.
Am J Med Genet.
2002;108(2):105-16.
PubMed abstract
Hersh, JH, Saul, RA, and Committee on Genetics.
Health supervision for children with fragile x syndrome.
Pediatrics.
2011;127(5):994-1006.
PubMed abstract / Full Text
Moeschler JB.
Genetic evaluation of intellectual disabilities.
Semin Pediatr Neurol.
2008;15(1):2-9.
PubMed abstract
Moeschler JB, Shevell M.
Clinical genetic evaluation of the child with mental retardation or developmental delays.
Pediatrics.
2006;117(6):2304-16.
PubMed abstract / Full Text
This report describes the "optimal clinical genetics evaluation" for children with developmental delay or mental retardation
for medical home providers.
Moro F, Pisano T, Bernardina BD, Polli R, Murgia A, Zoccante L, Darra F, Battaglia A, Pramparo T, Zuffardi O, Guerrini R.
Periventricular heterotopia in fragile X syndrome.
Neurology.
2006;67(4):713-5.
PubMed abstract
Reiss AL, Hall SS.
Fragile X syndrome: assessment and treatment implications.
Child Adolesc Psychiatr Clin N Am.
2007;16(3):663-75.
PubMed abstract
Shevell M, Ashwal S, Donley D, Flint J, Gingold M, Hirtz D, Majnemer A, Noetzel M, Sheth RD.
Practice parameter: evaluation of the child with global developmental delay: report of the Quality Standards Subcommittee
of the American Academy of Neurology and The Practice Committee of the Child Neurology Society.
Neurology.
2003;60(3):367-80.
PubMed abstract / Full Text
Wiesner GL, Cassidy SB, Grimes SJ, Matthews AL, Acheson LS.
Clinical consult: developmental delay/fragile X syndrome.
Prim Care.
2004;31(3):621-5, x.
PubMed abstract
Information for the primary care provider regarding children with fragile X syndrome.
