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Francesca Menni

Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico di Milano
H指数:21
被引数:1,589

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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
Perceived severity and parental distress after positive expanded newborn screening: parent–clinician concordance and dyadic processes

阳性扩展新生儿筛查后的感知严重程度与父母痛苦:父母-临床医生一致性及伴侣过程

2026-04-290
OAAI
Late-onset Pompe’s disease in pediatrics: results from an Italian national survey on 38 patients and proposal of a targeted diagnostic algorithm

儿科迟发性庞贝病:来自一项意大利全国性调查的38例患者的结果及针对性诊断算法的提出

2025-11-280
OAAI
Expanded Newborn Screening in Italy: The First Report of Lombardy Region

意大利扩大新生儿筛查:伦巴第大区的首次报告

2025-09-290
OAAI
The PHOX2B c.428A>G missense variant affects post-transcriptional regulation and may explain the absence of neural crest-derived tumors in congenital central hypoventilation syndrome

PHOX2B基因c.428A>G错义变异影响转录后调控,并可能解释先天性中枢性低通气综合征中神经嵴源性肿瘤的缺失。

2025-09-290
OAAI
Expanded Newborn Screening in Italy: The First Report of Lombardy Region

意大利扩展新生儿筛查:伦巴第大区首份报告

2025-08-210
PRE
Correction: Berardo et al. Expanded Newborn Screening in Italy: The First Report of Lombardy Region. Int. J. Neonatal Screen. 2025, 11, 31

更正:Berardo等人. 意大利新生儿筛查扩展:伦巴第地区的首次报告。Int. J. Neonatal Screen. 2025, 11, 31

2025-07-220
OAAI
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome
2024-05-063
OAAI
A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy
2023-07-196
PRE
PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations
2021-07-029
OAAI
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy
2018-02-0866
OAAI