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Francesca Nardecchia

Sapienza University of Rome
H指数:18
被引数:932

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Current management of biotinidase deficiency following newborn screening in Italy: evidence from a clinical nationwide survey

意大利新生儿筛查后生物素酶缺乏症的当前管理:来自全国临床调查的证据

2026-09-010
PRE
Transition in inherited metabolic diseases: the dietitians, pediatricians and adult physicians' point of view: the results of an Italian survey

遗传代谢病中的过渡期:营养师、儿科医生和成人科医生的观点:一项意大利调查的结果

2025-05-220
OA
Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18)

DEGS1基因的缺失检测应作为诊断少突胶质细胞减少性脑白质营养不良(HLD18)流程的一部分。

2025-05-070
OA
Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome

MRPS36的双等位基因变体导致Leigh综合征的新形式

2024-04-300
PRE
The recurrent pathogenic Pro890Leu substitution in CLTC causes a generalized defect in synaptic transmission in Caenorhabditis elegans

CLTC中反复出现的致病性Pro890Leu取代导致秀丽隐杆线虫突触传递的普遍缺陷

2023-05-311
OAAI
Expanded Newborn Screening in Italy Using Tandem Mass Spectrometry: Two Years of National Experience
2022-08-0925
OAAI