Detalhe da pesquisa
1.
Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and Seizures.
Am J Hum Genet
; 106(4): 467-483, 2020 04 02.
Artigo
Inglês
| MEDLINE | ID: mdl-32220291
2.
TrackUSF, a novel tool for automated ultrasonic vocalization analysis, reveals modified calls in a rat model of autism.
BMC Biol
; 20(1): 159, 2022 07 12.
Artigo
Inglês
| MEDLINE | ID: mdl-35820848
3.
Effect of Magnetic Resonance Imaging on Acute Surgical Treatment of Pregnant Patients: A Single Institution Study.
Isr Med Assoc J
; 25(6): 392-397, 2023 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-37381931
4.
De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder.
Genet Med
; 24(12): 2464-2474, 2022 12.
Artigo
Inglês
| MEDLINE | ID: mdl-36214804
5.
Realistic model of entanglement-enhanced sensing in optical fibers.
Opt Express
; 30(6): 8652-8666, 2022 Mar 14.
Artigo
Inglês
| MEDLINE | ID: mdl-35299312
6.
Weak thermal state quadrature-noise shadow imaging.
Opt Express
; 30(16): 29401-29408, 2022 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36299115
7.
Wave-front reconstruction via single-pixel homodyne imaging.
Opt Express
; 30(21): 37938-37945, 2022 Oct 10.
Artigo
Inglês
| MEDLINE | ID: mdl-36258372
8.
The Solubility Limit of Carbon in Alumina at 1,600°C.
Microsc Microanal
; : 1-11, 2022 Sep 08.
Artigo
Inglês
| MEDLINE | ID: mdl-36073062
9.
Patterns of alliance development in cognitive behavioral therapy versus attention bias modification for social anxiety disorder: Sawtooth patterns and sudden gains.
J Clin Psychol
; 78(2): 122-136, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34297850
10.
Efficient Simulation of Loop Quantum Gravity: A Scalable Linear-Optical Approach.
Phys Rev Lett
; 126(2): 020501, 2021 Jan 15.
Artigo
Inglês
| MEDLINE | ID: mdl-33512208
11.
The alliance mediates outcome in cognitive-behavioral therapy for social anxiety disorder, but not in attention bias modification.
Psychother Res
; 31(5): 589-603, 2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33112720
12.
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Genet Med
; 22(2): 389-397, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31388190
13.
Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Genet Med
; 22(3): 669, 2020 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-31844176
14.
Quantum-Limited Squeezed Light Detection with a Camera.
Phys Rev Lett
; 125(11): 113602, 2020 Sep 11.
Artigo
Inglês
| MEDLINE | ID: mdl-32975994
15.
De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures.
Brain
; 142(11): 3351-3359, 2019 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31504246
16.
De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive Dysmorphisms.
Am J Hum Genet
; 99(4): 934-941, 2016 Oct 06.
Artigo
Inglês
| MEDLINE | ID: mdl-27616479
17.
Thresholded Quantum LIDAR: Exploiting Photon-Number-Resolving Detection.
Phys Rev Lett
; 123(20): 203601, 2019 Nov 15.
Artigo
Inglês
| MEDLINE | ID: mdl-31809093
18.
Single Admission C-reactive protein Levels as a Sole Predictor of Patient Flow and Clinical Course in a General Internal Medicine Department.
Isr Med Assoc J
; 21(10): 686-691, 2019 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-31599512
19.
Keppen-Lubinsky syndrome is caused by mutations in the inwardly rectifying K+ channel encoded by KCNJ6.
Am J Hum Genet
; 96(2): 295-300, 2015 Feb 05.
Artigo
Inglês
| MEDLINE | ID: mdl-25620207
20.
Sepsis-induced activation of endogenous GLP-1 system is enhanced in type 2 diabetes.
Diabetes Metab Res Rev
; 34(4): e2982, 2018 05.
Artigo
Inglês
| MEDLINE | ID: mdl-29334697