Freund LS - Search Results

1

Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome.

Tierney E, Nwokoro NA, Porter FD, Freund LS, Ghuman JK, Kelley RI. Tierney E, et al. Among authors: freund ls. Am J Med Genet. 2001 Jan 15;98(2):191-200. doi: 10.1002/1096-8628(20010115)98:2<191::aid-ajmg1030>3.0.co;2-m. Am J Med Genet. 2001. PMID: 11223857

2

Early detection of social interaction problems: development of a social interaction instrument in young children.

Ghuman JK, Freund L, Reiss A, Serwint J, Folstein S. Ghuman JK, et al. J Dev Behav Pediatr. 1998 Dec;19(6):411-9. doi: 10.1097/00004703-199812000-00004. J Dev Behav Pediatr. 1998. PMID: 9866088

3

Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children.

Reiss AL, Freund L. Reiss AL, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):35-46. doi: 10.1002/ajmg.1320430106. Am J Med Genet. 1992. PMID: 1605210

4

Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressing FRAXE.

Abrams MT, Doheny KF, Mazzocco MM, Knight SJ, Baumgardner TL, Freund LS, Davies KE, Reiss AL. Abrams MT, et al. Among authors: freund ls. Am J Med Genet. 1997 Feb 21;74(1):73-81. doi: 10.1002/(sici)1096-8628(19970221)74:1<73::aid-ajmg16>3.0.co;2-o. Am J Med Genet. 1997. PMID: 9034011

5

Molecular-neurobehavioral associations in females with the fragile X full mutation.

Abrams MT, Reiss AL, Freund LS, Baumgardner TL, Chase GA, Denckla MB. Abrams MT, et al. Among authors: freund ls. Am J Med Genet. 1994 Jul 15;51(4):317-27. doi: 10.1002/ajmg.1320510407. Am J Med Genet. 1994. PMID: 7942994

6

Specification of the neurobehavioral phenotype in males with fragile X syndrome.

Baumgardner TL, Reiss AL, Freund LS, Abrams MT. Baumgardner TL, et al. Among authors: freund ls. Pediatrics. 1995 May;95(5):744-52. Pediatrics. 1995. PMID: 7724315

7

Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes.

Collins FA, Murphy DL, Reiss AL, Sims KB, Lewis JG, Freund L, Karoum F, Zhu D, Maumenee IH, Antonarakis SE. Collins FA, et al. Am J Med Genet. 1992 Jan 1;42(1):127-34. doi: 10.1002/ajmg.1320420126. Am J Med Genet. 1992. PMID: 1308352

8

Preliminary communication: neuroanatomical variations of the posterior fossa in men with the fragile X (Martin-Bell) syndrome.

Reiss AL, Patel S, Kumar AJ, Freund L. Reiss AL, et al. Am J Med Genet. 1988 Oct;31(2):407-14. doi: 10.1002/ajmg.1320310220. Am J Med Genet. 1988. PMID: 3232704

9

Early behavior signs of psychiatric phenotypes in fragile X syndrome.

Kau AS, Reider EE, Payne L, Meyer WA, Freund L. Kau AS, et al. Am J Ment Retard. 2000 Jul;105(4):286-99. doi: 10.1352/0895-8017(2000)105<0286:EBSOPP>2.0.CO;2. Am J Ment Retard. 2000. PMID: 10934570

10

Autistic behaviors among girls with fragile X syndrome.

Mazzocco MM, Kates WR, Baumgardner TL, Freund LS, Reiss AL. Mazzocco MM, et al. Among authors: freund ls. J Autism Dev Disord. 1997 Aug;27(4):415-35. doi: 10.1023/a:1025857422026. J Autism Dev Disord. 1997. PMID: 9261667

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