Modahl C - Search Results

1

Mitochondrial dysfunction in autistic patients with 15q inverted duplication.

Filipek PA, Juranek J, Smith M, Mays LZ, Ramos ER, Bocian M, Masser-Frye D, Laulhere TM, Modahl C, Spence MA, Gargus JJ. Filipek PA, et al. Among authors: modahl c. Ann Neurol. 2003 Jun;53(6):801-4. doi: 10.1002/ana.10596. Ann Neurol. 2003. PMID: 12783428 Free article.

2

Association between amygdala volume and anxiety level: magnetic resonance imaging (MRI) study in autistic children.

Juranek J, Filipek PA, Berenji GR, Modahl C, Osann K, Spence MA. Juranek J, et al. Among authors: modahl c. J Child Neurol. 2006 Dec;21(12):1051-8. doi: 10.1177/7010.2006.00237. J Child Neurol. 2006. PMID: 17156697

3

Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13.

Smith M, Filipek PA, Wu C, Bocian M, Hakim S, Modahl C, Spence MA. Smith M, et al. Among authors: modahl c. Am J Med Genet. 2000 Dec 4;96(6):765-70. doi: 10.1002/1096-8628(20001204)96:6<765::aid-ajmg13>3.0.co;2-l. Am J Med Genet. 2000. PMID: 11121177 Free article.

4

A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R.

Ramanathan S, Woodroffe A, Flodman PL, Mays LZ, Hanouni M, Modahl CB, Steinberg-Epstein R, Bocian ME, Spence MA, Smith M. Ramanathan S, et al. BMC Med Genet. 2004 Apr 16;5:10. doi: 10.1186/1471-2350-5-10. BMC Med Genet. 2004. PMID: 15090072 Free PMC article.

5

Language and other regression: assessment and timing.

Goldberg WA, Osann K, Filipek PA, Laulhere T, Jarvis K, Modahl C, Flodman P, Spence MA. Goldberg WA, et al. Among authors: modahl c. J Autism Dev Disord. 2003 Dec;33(6):607-16. doi: 10.1023/b:jadd.0000005998.47370.ef. J Autism Dev Disord. 2003. PMID: 14714930

6

Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.

Smith M, Escamilla JR, Filipek P, Bocian ME, Modahl C, Flodman P, Spence MA. Smith M, et al. Among authors: modahl c. Cytogenet Cell Genet. 2001;94(1-2):15-22. doi: 10.1159/000048775. Cytogenet Cell Genet. 2001. PMID: 11701947 Free article.

7

Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits.

Smith M, Woodroffe A, Smith R, Holguin S, Martinez J, Filipek PA, Modahl C, Moore B, Bocian ME, Mays L, Laulhere T, Flodman P, Spence MA. Smith M, et al. Among authors: modahl c. Cytogenet Genome Res. 2002;98(4):233-9. doi: 10.1159/000071040. Cytogenet Genome Res. 2002. PMID: 12826745 Free article.

8

Multisite, double-blind, placebo-controlled trial of porcine secretin in autism.

Owley T, McMahon W, Cook EH, Laulhere T, South M, Mays LZ, Shernoff ES, Lainhart J, Modahl CB, Corsello C, Ozonoff S, Risi S, Lord C, Leventhal BL, Filipek PA. Owley T, et al. Among authors: modahl cb. J Am Acad Child Adolesc Psychiatry. 2001 Nov;40(11):1293-9. doi: 10.1097/00004583-200111000-00009. J Am Acad Child Adolesc Psychiatry. 2001. PMID: 11699803 Clinical Trial.

9

Oxytocin and autistic disorder: alterations in peptide forms.

Green L, Fein D, Modahl C, Feinstein C, Waterhouse L, Morris M. Green L, et al. Among authors: modahl c. Biol Psychiatry. 2001 Oct 15;50(8):609-13. doi: 10.1016/s0006-3223(01)01139-8. Biol Psychiatry. 2001. PMID: 11690596

10

Does oxytocin deficiency mediate social deficits in autism?

Modahl C, Fein D, Waterhouse L, Newton N. Modahl C, et al. J Autism Dev Disord. 1992 Sep;22(3):449-51. doi: 10.1007/BF01048246. J Autism Dev Disord. 1992. PMID: 1400106 No abstract available.

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