Detalles de la búsqueda
1.
The white lupin trehalase gene LaTRE1 regulates cluster root formation and function under phosphorus deficiency.
Plant Physiol
; 2024 May 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-38805210
2.
Metal deposits associated with brain atrophy in the deep gray matter nucleus in Wilson's disease.
Cereb Cortex
; 33(15): 9223-9232, 2023 07 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-37365842
3.
Soilborne bacterium Klebsiella pneumoniae promotes cluster root formation in white lupin through ethylene mediation.
New Phytol
; 237(4): 1320-1332, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36336781
4.
Study on different pathogenic factors in different disease stages of patients with Wilson disease.
Neurol Sci
; 42(9): 3749-3756, 2021 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-33443665
5.
Regional morphometric abnormalities and clinical relevance in Wilson's disease.
Mov Disord
; 34(4): 545-554, 2019 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30817852
6.
A study of neurite orientation dispersion and density imaging in wilson's disease.
J Magn Reson Imaging
; 48(2): 423-430, 2018 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29251804
7.
Characterizing brain mineral deposition in patients with Wilson disease using susceptibility-weighted imaging.
Neurol India
; 62(4): 362-6, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-25237939
8.
Symptom aggravation after withdrawal of metal chelating agent therapy in patients with Wilson's disease.
Brain Behav
; 13(9): e3170, 2023 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-37491953
9.
[Insulin-like growth factor-1 gene therapy improves the levels of mRNA and protein of endothelial nitric oxide synthase in aging related erectile dysfunction in rats].
Zhonghua Yi Xue Za Zhi
; 92(2): 128-30, 2012 Jan 10.
Artículo
en Zh
| MEDLINE | ID: mdl-22490699
10.
Higher expression of mRNA and protein of insulin-like growth factor binding protein-3 in old rat penile tissues: implications for erectile dysfunction.
J Sex Med
; 8(8): 2181-90, 2011 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-21595839
11.
[Values of serum copper and serum free copper in the diagnosis and monitoring of Wilson's disease and its carriers].
Zhonghua Yi Xue Za Zhi
; 91(39): 2757-60, 2011 Oct 25.
Artículo
en Zh
| MEDLINE | ID: mdl-22322054
12.
Whole brain volume and cortical thickness abnormalities in Wilson's disease: a clinical correlation study.
Brain Imaging Behav
; 15(4): 1778-1787, 2021 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-33052506
13.
Observation on the changes of clinical symptoms, blood and brain copper deposition in Wilson disease patients treated with dimercaptosuccinic acid for 2 years.
J Clin Neurosci
; 81: 448-454, 2020 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-33222961
14.
A study of susceptibility-weighted imaging in patients with Wilson disease during the treatment of metal chelator.
J Neurol
; 267(6): 1643-1650, 2020 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-32060651
15.
Co-occurrence of ATXN3 and ATXN2 repeat expansions in Chinese ataxia patients with slow saccades.
Mol Genet Genomic Med
; 7(6): e663, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30920184
16.
Adult-onset mitochondrial encephalopathy in association with the MT-ND3 T10158C mutation exhibits unique characteristics: A case report.
World J Clin Cases
; 7(9): 1066-1072, 2019 May 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-31123680
17.
Injury factors and pathological features of toxic milk mice during different disease stages.
Brain Behav
; 9(12): e01459, 2019 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-31742933
18.
[Update of gene therapy for aging-related erectile dysfunction].
Zhonghua Nan Ke Xue
; 14(10): 931-4, 2008 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-19157108
19.
The asymmetry of neural symptoms in Wilson's disease patients detecting by diffusion tensor imaging, resting-state functional MRI, and susceptibility-weighted imaging.
Brain Behav
; 8(5): e00930, 2018 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29761003
20.
Muscle MRI findings in a one-year-old girl with merosin-deficient congenital muscular dystrophy type 1A due to LAMA2 mutation: A case report.
Biomed Rep
; 7(2): 193-196, 2017 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-28804634