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Francesco Nicita

bambino gesu children's hospital
H指数:31
被引数:2,614

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Novel heterozygous truncating variant in TUBB associated with thrombocytopaenia and neurological abnormalities

TUBB基因新型杂合截断变异与血小板减少症及神经异常的关联

2026-08-130
OA
Developmental trajectory of individuals with Pelizaeus-Merzbacher Disease (PMD)

佩利扎厄斯-默茨巴赫病患者的发展轨迹

2026-05-150
PRE
Efficacy of JAK1/2 inhibitors in AGS genes-related interferonopathies: A multicenter retrospective observational study with treated vs untreated comparison

JAK1/2抑制剂在AGS基因相关干扰素通路病中的疗效:一项治疗与未治疗组比较的多中心回顾性观察研究

2026-03-190
PRE
Megalencephalic leukoencephalopathy with subcortical cysts: a multicenter Italian experience

胼胝体发育不全伴皮质下囊肿:一项意大利多中心研究经验

2026-01-020
PRE
The Impact of POLR3-related Leukodystrophy on Non-Affected Family Members: A Qualitative Study

POLR3相关脑白质营养不良对未受影响的家庭成员的影响:一项定性研究

2025-12-160
OAAI
Astrocytes differentiated from patient iPSCs model the rare leukodystrophy MLC and uncover disease-linked maturation defects and Kir4.1 channel dysfunction

来自患者iPSCs的星形胶质细胞模拟了罕见的髓鞘白质营养不良MLC,并揭示了与疾病相关的成熟缺陷和Kir4.1通道功能障碍。

2025-12-080
OAAI
Infantile-Onset Ascending Hereditary Spastic Paraplegia due to a Homozygous ALS2 Exons 24-25 Deletion: Expanding the Genotypic Spectrum

婴儿期发病的进行性遗传性痉挛性截瘫,由纯合子ALS2外显子24-25缺失引起:扩展基因型谱

2025-11-010
OAAI
Altered Dopamine Metabolism and Response to Treatment with Levodopa/Carbidopa in MCT8 Deficiency

MCT8缺乏症中多巴胺代谢的改变以及对左旋多巴/卡比多巴治疗的反应

2025-10-270
OAAI
A clinical and genotype-phenotype analysis of MACF1 variants

MACF1变异的临床与基因型-表型分析

2025-09-080
PRE
Clinical Characterization of a Multicenter International Cohort of Patients With Aicardi-Goutières Syndrome Homozygous for the RNASEH2B:p.Ala177Thr Variant: Early Clinical Markers of Disease Severity

Aicardi-Goutières综合征患者(RNASEH2B基因p.Ala177Thr变异纯合子)的多中心国际队列的临床特征:疾病严重程度的早期临床标志物

2025-07-250
OAAI
Comprehensive Genotype-Phenotype Analysis in POLR3-Related Disorders

POLR3相关疾病的全面基因型-表型分析

2025-07-180
OAAI
The natural history of variable subtypes in pediatric-onset TUBB4A-related leukodystrophy
2025-03-010
PRE
Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders
2024-06-200
OA
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias

非扩张性脊髓小脑共济失调的极端表型异质性

2023-07-0116
OAAI