Detalhe da pesquisa
1.
An online survey to understand the needs of caregivers of family members with 22q11 deletion syndrome.
J Intellect Disabil Res
; 67(9): 860-868, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37449408
2.
The COVID-19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregivers.
J Intellect Disabil Res
; 66(4): 313-322, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35191118
3.
Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia.
Psychol Med
; 49(6): 1047-1054, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30064532
4.
A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium.
Mol Psychiatry
; 22(12): 1664-1672, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28761081
5.
Cerebral dopamine deficiency, plasma monoamine alterations and neurocognitive deficits in adults with phenylketonuria.
Psychol Med
; 47(16): 2854-2865, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28552082
6.
Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.
Ultrasound Obstet Gynecol
; 47(2): 177-83, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26396068
7.
Pharmacological treatment of 22q11.2 deletion syndrome-related psychoses.
Pharmacopsychiatry
; 48(6): 219-20, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26091278
8.
Perceived burden and neuropsychiatric morbidities in adults with 22q11.2 deletion syndrome.
J Intellect Disabil Res
; 58(2): 198-210, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23106770
9.
The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43.
Clin Genet
; 83(4): 321-31, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22725725
10.
Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome.
J Intellect Disabil Res
; 56(6): 641-51, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22142442
11.
Neuropathologic features in adults with 22q11.2 deletion syndrome.
Cereb Cortex
; 19(1): 153-64, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18483005
12.
Premature death in adults with 22q11.2 deletion syndrome.
J Med Genet
; 46(5): 324-30, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19246480
13.
Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22.
Science
; 288(5466): 678-82, 2000 Apr 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-10784452
14.
Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study.
Schizophr Res
; 188: 59-62, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28119035
15.
The New York High-Risk Project. Psychoses and cluster A personality disorders in offspring of schizophrenic parents at 23 years of follow-up.
Arch Gen Psychiatry
; 52(10): 857-65, 1995 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-7575106
16.
The New York High-Risk Project. Prevalence and comorbidity of axis I disorders in offspring of schizophrenic parents at 25-year follow-up.
Arch Gen Psychiatry
; 54(12): 1096-102, 1997 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-9400345
17.
22q11 deletion syndrome: a genetic subtype of schizophrenia.
Biol Psychiatry
; 46(7): 882-91, 1999 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-10509171
18.
Temporal lobe abnormalities in multigenerational families with schizophrenia.
Biol Psychiatry
; 36(11): 737-43, 1994 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-7858069
19.
Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia.
Biol Psychiatry
; 46(10): 1436-42, 1999 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-10578458
20.
Impaired olfactory identification in relatives of patients with familial schizophrenia.
Am J Psychiatry
; 158(8): 1286-90, 2001 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-11481164