日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

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

儿童迟发型庞贝病:一项针对38名意大利患者的全国性调查结果及针对性诊断算法的提出

Spada, Marco; Gasperini, Serena; Filosto, Massimiliano; Astrea, Guja; Bracci, Beatrice; Bruno, Claudio; Burlina, Alberto; Cavallini, Anna; Concolino, Daniela; Crescitelli, Viola; D'Amico, Adele; Deodato, Federica; Dionisi-Vici, Carlo; Donati, Maria Alice; Fecarotta, Simona; Fischetto, Rita; Fiumara, Agata; Furlan, Francesca; Gragnaniello, Vincenza; Mala, Damiano; Marica, Monica; Menni, Francesca; Pagliardini, Veronica; Panicucci, Claudia; Parenti, Giancarlo; Pession, Andrea; Ricci, Federica; Rovelli, Valentina; Sacchini, Michele; Santorelli, Filippo Maria; Santoro, Lucia; Scarpa, Maurizio; Taurisano, Roberta; Tummolo, Albina; Porta, Francesco

Genetics in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and Clinical Implications

21-羟化酶缺乏引起的先天性肾上腺皮质增生症的遗传学及其临床意义

Concolino, Paola; Falhammar, Henrik

Detection of Clinically Significant BRCA Large Genomic Rearrangements in FFPE Ovarian Cancer Samples: A Comparative NGS Study

在FFPE卵巢癌样本中检测具有临床意义的BRCA大片段基因组重排:一项比较NGS研究

Perrucci, Alessia; De Bonis, Maria; Maneri, Giulia; Ricciardi Tenore, Claudio; Concolino, Paola; Corsi, Matteo; Conca, Alessandra; Evangelista, Jessica; Piermattei, Alessia; Nero, Camilla; Giacò, Luciano; De Paolis, Elisa; Fagotti, Anna; Minucci, Angelo

Effectiveness of steroid intra-articular injections on functioning in children and adolescents affected by juvenile idiopathic arthritis: a systematic review

类固醇关节内注射对幼年特发性关节炎患儿及青少年功能的影响:系统评价

Gallizzi, Romina; Dipasquale, Rosario Francesco; Mendicino, Alessia; Ferrillo, Martina; Longo, Umile Giuseppe; Concolino, Daniela; Ammendolia, Antonio; de Sire, Alessandro

Identification of a False-positive Multiplex Ligationdependent Probe Amplification Result in BRCA1 Using a Copy Number Variation Algorithm Under Development for a Commercial Next-Generation Sequencing-based Homologous Recombination Deficiency Assay

利用正在开发的用于商业化下一代测序同源重组缺陷检测的拷贝数变异算法,识别BRCA1中多重连接依赖性探针扩增的假阳性结果

Concolino, Paola; De Paolis, Elisa; Rinelli, Martina; Maneri, Giulia; Brisighelli, Francesca; Trozzi, Rita; Duranti, Simona; Giacò, Luciano; Piane, Maria; Preziosi, Alessia; Panfili, Arianna; Scambia, Giovanni; Nero, Camilla; De Bonis, Maria; Minucci, Angelo

Challenging Molecular Diagnosis of Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency: Case Series and Novel Variants of CYP21A2 Gene

21-羟化酶缺乏症引起的先天性肾上腺皮质增生症(CAH)的分子诊断面临挑战:病例系列及CYP21A2基因的新变异

Concolino, Paola

Point of care lung ultrasound in preschool children with cystic fibrosis: a case-controlled, prospective, pilot study

囊性纤维化学龄前儿童床旁肺部超声检查:一项病例对照、前瞻性试点研究

Crispino, Antonio Alessandro; Musolino, Anna Maria; Buonsenso, Danilo; Caloiero, Mimma; Concolino, Daniela

Phenotypic presentation of MEN1 c.758delC (p.Ser253Cysfs (*)28) pathogenic variant: a case report

MEN1 c.758delC (p.Ser253Cysfs(*)28)致病变异的表型表现:病例报告

Mancini, Antonio; Concolino, Paola; Vergani, Edoardo; Oliva, Alessandro; Macis, Giuseppe; Traini, Emanuela; Rossi, Esther Diana

Triple Genetic Diagnosis in a Patient with Late-Onset Leukodystrophy and Mild Intellectual Disability

一名患有晚发性脑白质营养不良和轻度智力障碍的患者的三重基因诊断

Pasquetti, Domizia; Gazzellone, Annalisa; Rossi, Salvatore; Orteschi, Daniela; L'Erario, Federica Francesca; Concolino, Paola; Minucci, Angelo; Dionisi-Vici, Carlo; Genuardi, Maurizio; Silvestri, Gabriella; Chiurazzi, Pietro

Screening for lysosomal diseases in a selected pediatric population: the case of Gaucher disease and acid sphingomyelinase deficiency

对特定儿科人群进行溶酶体疾病筛查:以戈谢病和酸性鞘磷脂酶缺乏症为例

Di Rocco, Maja; Vici, Carlo Dionisi; Burlina, Alberto; Venturelli, Francesco; Fiumara, Agata; Fecarotta, Simona; Donati, Maria Alice; Spada, Marco; Concolino, Daniela; Pession, Andrea