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Brent L. Fogel

university of bologna
H指数:46
被引数:7,453

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Clinical Practice Guidelines for the Diagnosis, Management, and Surveillance of LMNB1-Related Autosomal Dominant Leukodystrophy

LMNB1相关常染色体显性遗传性白质脑病的诊断、管理与监测临床实践指南

2025-10-010
OA
112. BROAD REPETITIVE TRANSCRANIAL MAGNETIC STIMULATION (RTMS) OF THE PRECUNEUS IN ALZHEIMER’S DISEASE: A RATIONALE AND STUDY DESIGN

112. 颞顶小叶后部在阿尔茨海默病中的广泛重复经颅磁刺激(RTMS)治疗:理论基础与研究设计

2025-07-140
PRE
Broad repetitive transcranial magnetic stimulation (rTMS) of the precuneus in Alzheimer's disease: A rationale and study design

阿尔茨海默氏病的前uneus的广泛重复经颅磁刺激 (rTMS): 原理和研究设计

2025-01-010
OAAI
Clinical, Radiological and Pathological Features of a Large American Cohort of Spinocerebellar Ataxia (SCA27B)

脊髓小脑性共济失调 (SCA27B) 的大型美国队列的临床,放射学和病理学特征

2024-09-124
OA
An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (vol 110, pg 105, 2023)

FGF14中的内含子GAA重复扩增导致常染色体显性成年型共济失调SCA27B/ATX-FGF14 (110卷,105页,2023页)

2023-06-0131
OAAI
Toward a Biomarker Panel measured in CNS-originating Extracellular Vesicles for Differential Diagnosis of Parkinson's Disease and Multiple System Atrophy
2023-04-250
PRE
Toward a biomarker panel measured in CNS-originating extracellular vesicles for improved differential diagnosis of Parkinson's disease and multiple system atrophy
2023-03-2012
OAAI
An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14
2023-01-0194
OAAI
eP296-The yield of thorough record review in the Undiagnosed Diseases Network (vol 132, pg S187, 2021)
2021-11-010
PREAI
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

PRKAR1B的变异导致自闭症谱系障碍,失用症和对疼痛不敏感的神经发育障碍

2021-08-0115
OAAI
α-Synuclein in blood exosomes immunoprecipitated using neuronal and oligodendroglial markers distinguishes Parkinson's disease from multiple system atrophy (May, 10.1007/s00401-021-02324-0, 2021)
2021-05-242
OAAI