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Wilson Marques

ribeirão preto medical school
H指数:37
被引数:7,262

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Neuropathy in Val122Ile Hereditary Transthyretin (ATTR) Amyloidosis: A Multicenter Retrospective Cohort Study

Val122Ile遗传性甲状腺素转运蛋白(ATTR)淀粉样变性中的神经病变:一项多中心回顾性队列研究

2026-09-120
OAAI
VRK1-Related Motor Neuropathy With Upper Motor Neuron Signs and Selective Muscle Involvement

<i>VRK1</i>相关运动神经病变伴上运动神经元体征及选择性肌肉受累

2026-09-110
OA
Late-Onset Tay–Sachs Disease With SMALED-Like Muscle MRI Pattern Despite a Distinct Clinical Phenotype

迟发性Tay–Sachs病具有SMALED样肌肉MRI模式,尽管临床表型独特

2026-09-110
OAAI
Longitudinal Evaluation of Ataxia and Brain Structural Changes in RFC1-Related Disorder

RFC1相关疾病的共济失调及脑结构变化的纵向评估

2025-09-040
OAAI
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD

由于SORD基因突变导致的Charcot-Marie-Tooth疾病的基因型与表型谱

BRAIN
IF11.7
2025-08-013
OAAI
Incidence and associated factors with atrial fibrillation in patients with transthyretin amyloidosis cardiomyopathy: Insights from the multicenter REACT-SP registry

透运甲状腺素蛋白淀粉样变性心肌病患者中房颤的发生率及其相关因素:来自多中心REACT-SP登记研究的见解

2025-06-010
PRE
Clinical and molecular spectrum of TK2-deficiency: a large Brazilian cohort

TK2-deficiency的临床和分子谱: 一个大型巴西队列

2025-03-150
OAAI
EEFSEC deficiency: A selenopathy with early-onset neurodegeneration
2025-01-010
OAAI
Clinical and genetic profiles of patients with hereditary and wild-type transthyretin amyloidosis: the Transthyretin Cardiac Amyloidosis Registry in the state of São Paulo, Brazil (REACT-SP)

遗传性和野生型转甲状腺素蛋白淀粉样变性患者的临床和遗传特征: 巴西圣保罗州的转甲状腺素蛋白心脏淀粉样变性登记处 (REACT-SP)

2024-07-200
OAAI