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Items: 15


Complex Neurological Phenotype in Female Carriers of NHE6 Mutations.

Pescosolido MF, Kavanaugh BC, Pochet N, Schmidt M, Jerskey BA, Rogg JM, De Jager PL, Young-Pearse TL, Liu JS, Morrow EM.

Mol Neuropsychiatry. 2019 Apr;5(2):98-108. doi: 10.1159/000496341. Epub 2019 Mar 6.


Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome.

Xu M, Ouyang Q, Gong J, Pescosolido MF, Pruett BS, Mishra S, Schmidt M, Jones RN, Gamsiz Uzun ED, Lizarraga SB, Morrow EM.

eNeuro. 2018 Jan 17;4(6). pii: ENEURO.0388-17.2017. doi: 10.1523/ENEURO.0388-17.2017. eCollection 2017 Nov-Dec.


Christianson Syndrome.

Morrow EM, Pescosolido MF.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020.
2018 Jan 11.


Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms.

Gamsiz ED, Sciarra LN, Maguire AM, Pescosolido MF, van Dyck LI, Morrow EM.

Neurotherapeutics. 2015 Jul;12(3):553-71. doi: 10.1007/s13311-015-0363-9. Review.


Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein.

Pescosolido MF, Schwede M, Johnson Harrison A, Schmidt M, Gamsiz ED, Chen WS, Donahue JP, Shur N, Jerskey BA, Phornphutkul C, Morrow EM.

J Med Genet. 2014 Sep;51(9):587-9. doi: 10.1136/jmedgenet-2014-102444. Epub 2014 Jul 23. No abstract available.


Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome.

Pescosolido MF, Stein DM, Schmidt M, El Achkar CM, Sabbagh M, Rogg JM, Tantravahi U, McLean RL, Liu JS, Poduri A, Morrow EM.

Ann Neurol. 2014 Oct;76(4):581-93. doi: 10.1002/ana.24225. Epub 2014 Sep 19.


Clinical characteristics of children with autism spectrum disorder and co-occurring epilepsy.

Viscidi EW, Triche EW, Pescosolido MF, McLean RL, Joseph RM, Spence SJ, Morrow EM.

PLoS One. 2013 Jul 4;8(7):e67797. doi: 10.1371/journal.pone.0067797. Print 2013.


Family functioning deficits in bipolar disorder and ADHD in youth.

Young ME, Galvan T, Reidy BL, Pescosolido MF, Kim KL, Seymour K, Dickstein DP.

J Affect Disord. 2013 Sep 25;150(3):1096-102. doi: 10.1016/j.jad.2013.04.027. Epub 2013 May 22.


Emotional face identification in youths with primary bipolar disorder or primary attention-deficit/hyperactivity disorder.

Seymour KE, Pescosolido MF, Reidy BL, Galvan T, Kim KL, Young M, Dickstein DP.

J Am Acad Child Adolesc Psychiatry. 2013 May;52(5):537-546.e3. doi: 10.1016/j.jaac.2013.03.011.


Distribution of disease-associated copy number variants across distinct disorders of cognitive development.

Pescosolido MF, Gamsiz ED, Nagpal S, Morrow EM.

J Am Acad Child Adolesc Psychiatry. 2013 Apr;52(4):414-430.e14. doi: 10.1016/j.jaac.2013.01.003. Review.


An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma.

Minhas HM, Pescosolido MF, Schwede M, Piasecka J, Gaitanis J, Tantravahi U, Morrow EM.

Am J Med Genet A. 2013 Apr;161A(4):787-91. doi: 10.1002/ajmg.a.35841. Epub 2013 Mar 12.


Developmental meta-analysis of the functional neural correlates of autism spectrum disorders.

Dickstein DP, Pescosolido MF, Reidy BL, Galvan T, Kim KL, Seymour KE, Laird AR, Di Martino A, Barrett RP.

J Am Acad Child Adolesc Psychiatry. 2013 Mar;52(3):279-289.e16. doi: 10.1016/j.jaac.2012.12.012.


Lighting a path: genetic studies pinpoint neurodevelopmental mechanisms in autism and related disorders.

Pescosolido MF, Yang U, Sabbagh M, Morrow EM.

Dialogues Clin Neurosci. 2012 Sep;14(3):239-52. Review.


Translational neuroscience in pediatric bipolar disorder.

Dickstein DP, Reidy BL, Pescosolido MF, Galvan T, Kim KL.

Expert Rev Neurother. 2011 Dec;11(12):1699-701. doi: 10.1586/ern.11.157.


A novel familial 11p15.4 microduplication associated with intellectual disability, dysmorphic features, and obesity with involvement of the ZNF214 gene.

Sofos E, Pescosolido MF, Quintos JB, Abuelo D, Gunn S, Hovanes K, Morrow EM, Shur N.

Am J Med Genet A. 2012 Jan;158A(1):50-8. doi: 10.1002/ajmg.a.34290. Epub 2011 Nov 3.


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