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Items: 1 to 20 of 75

1.

Cytogenetic abnormalities in attention-deficit/hyperactivity disorder.

Bastain TM, Lewczyk CM, Sharp WS, James RS, Long RT, Eagen PB, Ebens CL, Meck JM, Chan WY, Sidransky E, Rapoport JL, Castellanos FX.

J Am Acad Child Adolesc Psychiatry. 2002 Jul;41(7):806-10.

PMID:
12108805
2.

Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation.

Farzin F, Perry H, Hessl D, Loesch D, Cohen J, Bacalman S, Gane L, Tassone F, Hagerman P, Hagerman R.

J Dev Behav Pediatr. 2006 Apr;27(2 Suppl):S137-44.

PMID:
16685180
3.

Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome.

Gothelf D, Presburger G, Levy D, Nahmani A, Burg M, Berant M, Blieden LC, Finkelstein Y, Frisch A, Apter A, Weizman A.

Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 1;126B(1):116-21.

PMID:
15048660
4.

Methylphenidate treatment for attention-deficit/hyperactivity disorder in children and adolescents with velocardiofacial syndrome: an open-label study.

Gothelf D, Gruber R, Presburger G, Dotan I, Brand-Gothelf A, Burg M, Inbar D, Steinberg T, Frisch A, Apter A, Weizman A.

J Clin Psychiatry. 2003 Oct;64(10):1163-9.

PMID:
14658963
5.

Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.

Niklasson L, Rasmussen P, Oskarsdóttir S, Gillberg C.

Dev Med Child Neurol. 2002 Jan;44(1):44-50.

6.

The neuropsychology of 22q11 deletion syndrome. A neuropsychiatric study of 100 individuals.

Niklasson L, Gillberg C.

Res Dev Disabil. 2010 Jan-Feb;31(1):185-94. doi: 10.1016/j.ridd.2009.09.001. Epub 2009 Oct 7.

PMID:
19815377
7.
8.
9.

Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing.

Hagerman RJ, Wilson P, Staley LW, Lang KA, Fan T, Uhlhorn C, Jewell-Smart S, Hull C, Drisko J, Flom K, et al.

Am J Med Genet. 1994 Jul 15;51(4):474-81.

PMID:
7943023
10.
11.

Is attention deficit hyperactivity disorder a valid diagnosis in the presence of high IQ? Results from the MGH Longitudinal Family Studies of ADHD.

Antshel KM, Faraone SV, Stallone K, Nave A, Kaufmann FA, Doyle A, Fried R, Seidman L, Biederman J.

J Child Psychol Psychiatry. 2007 Jul;48(7):687-94.

PMID:
17593149
12.

Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.

Carlson C, Papolos D, Pandita RK, Faedda GL, Veit S, Goldberg R, Shprintzen R, Kucherlapati R, Morrow B.

Am J Hum Genet. 1997 Apr;60(4):851-9.

13.

Screening for fragile X syndrome.

Murray J, Cuckle H, Taylor G, Hewison J.

Health Technol Assess. 1997;1(4):i-iv, 1-71. Review.

14.

Two cases of generalized seizures and the Velocardiofacial syndrome -- a clinically significant association?

El Tahir MO, Kerr M, Jones RG.

J Intellect Disabil Res. 2004 Oct;48(Pt 7):695-8.

PMID:
15357690
15.

Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development.

Freedenberg DL, Gane LW, Richards CS, Lampe M, Hills J, O'Connor R, Manchester D, Taylor A, Tassone F, Hulseberg D, Hagerman RJ, Patil SR.

Am J Med Genet. 1999 Jul 30;85(3):197-201.

PMID:
10398226
16.

Morphometry of the head of the caudate nucleus in patients with velocardiofacial syndrome (del 22q11.2).

Sugama S, Bingham PM, Wang PP, Moss EM, Kobayashi H, Eto Y.

Acta Paediatr. 2000 May;89(5):546-9.

PMID:
10852189
17.

Further studies on periodic limb movement disorder and restless legs syndrome in children with attention-deficit hyperactivity disorder.

Picchietti DL, Underwood DJ, Farris WA, Walters AS, Shah MM, Dahl RE, Trubnick LJ, Bertocci MA, Wagner M, Hening WA.

Mov Disord. 1999 Nov;14(6):1000-7.

PMID:
10584676
18.

The frequency of chromosomal abnormalities in patients referred for fragile X analysis.

Mark HF, Bier JA, Scola P.

Ann Clin Lab Sci. 1996 Jul-Aug;26(4):323-8.

PMID:
8800432
19.

22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

Portnoï MF, Lebas F, Gruchy N, Ardalan A, Biran-Mucignat V, Malan V, Finkel L, Roger G, Ducrocq S, Gold F, Taillemite JL, Marlin S.

Am J Med Genet A. 2005 Aug 15;137(1):47-51. Review.

PMID:
16007629
20.

A case of ADHD and a major Y chromosome abnormality.

Mulligan A, Gill M, Fitzgerald M.

J Atten Disord. 2008 Jul;12(1):103-5. doi: 10.1177/1087054707311220. Epub 2008 Jan 11.

PMID:
18192621

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