Prader-Willi Syndrome
This graph shows the total number of publications written about "Prader-Willi Syndrome" by people in the URMC Research Network by year, and whether "Prader-Willi Syndrome" was a major or minor topic of these publication.
Below are the most recent publications written about "Prader-Willi Syndrome" by people in Profiles.
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Ingraham CA, Wertalik L, Schor NF. Necdin and neurotrophin receptors: interactors of relevance for neuronal resistance to oxidant stress. Pediatr Res. 2011 Apr; 69(4):279-84.
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Napolitano DA, Zarcone J, Nielsen S, Wang H, Caliendo JM. Perceptions of body image by persons with Prader-Willi syndrome and their parents. Am J Intellect Dev Disabil. 2010 Jan; 115(1):43-53.
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Zarcone J, Napolitano D, Peterson C, Breidbord J, Ferraioli S, Caruso-Anderson M, Holsen L, Butler MG, Thompson T. The relationship between compulsive behaviour and academic achievement across the three genetic subtypes of Prader-Willi syndrome. J Intellect Disabil Res. 2007 Jun; 51(Pt. 6):478-87.
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Ishmael HA, Pasztor LM, Rothberg PG, Butler MG, Pfotenhauer J, Hannig V, Summar M. Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancy. J Pediatr. 2000 Jan; 136(1):135-6.
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Iqbal MA, Ulmer C, Sakati N. Use of FISH technique in the diagnosis of chromosomal syndromes. East Mediterr Health J. 1999 Nov; 5(6):1218-24.
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Dykens EM, Kasari C. Maladaptive behavior in children with Prader-Willi syndrome, Down syndrome, and nonspecific mental retardation. Am J Ment Retard. 1997 Nov; 102(3):228-37.
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Fong CT. Clinical diagnosis of genetic diseases. Pediatr Ann. 1993 May; 22(5):277-81.
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