Alstrom, C. H., Hallgren, B., Nilsson, L. B., Asander, H. Retinal degeneration combined with obesity, diabetes mellitus and neurogenous deafness: a specific syndrome (not hitherto described) distinct from the Laurence-Moon-Biedl syndrome. A clinical endocrinological and genetic examination based on a large pedigree. Acta Psychiat. Neurol. Scand. 34 (suppl. 129): 1-35, 1959.
Alter, C. A., Moshang, T., Jr. Growth hormone deficiency in two siblings with Alstrom syndrome. Am. J. Dis. Child. 147: 97-99, 1993.
Collin, G. B., Marshall, J. D., Ikeda, et al.:  Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alstrom syndrome. Nature Genet. 31: 74-78, 2002.
Connolly, M. B., Jan, J. E., Couch, R. M., Wong, L. T. K., Dimmick, J. E., Rigg, J. M. Hepatic dysfunction in Alstrom disease. Am. J. Med. Genet. 40: 421-424, 1991.
Goldstein, J. L., Fialkow, P. J. The Alstrom syndrome: report of three cases with further delineation of the clinical, pathophysiological, and genetic aspects of the disorder. Medicine 52: 53-71, 1973. 
Marshal JD, Paisey RB, Carey C, Macdermott S. In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2014.                                                                                                                                                  
Michaud, J. L., Heon, E., Guilbert, F., et al.: Natural history of Alstrom syndrome in early childhood: onset with dilated cardiomyopathy. J. Pediat. 128: 225-229, 1996.     
Taskesen, M., Collin, G. B., Evsikov, A. V., Guzel, A., Ozgul, R. K., Marshall, J. D., Naggert, J. K. Novel Alu retrotransposon insertion leading to Alstrom syndrome. Hum. Genet. 131: 407-413, 2012