慢性疾病遗传检测的不确定性

A novel method for thermal noise reduction, enabling measurements of broadband, low-amplitude electron temperature fluctuations using individual radiometer channels.

The Review of scientific instruments·2026

Design of a correlation reflectometer radiometer diagnostic and measurements of the electron density-temperature cross-phase angle in the H-mode pedestal with small edge localized modes at ASDEX Upgrade.

The Review of scientific instruments·2025

System-level recommendations for improved wellness for gynecologic oncologists: A Society of Gynecologic Oncology Review.

Gynecologic oncology·2024

Invasive ductal breast carcinoma metastasis to the cervix: A case review and clinical correlation.

Gynecologic oncology reports·2020

Immature teratoma diagnosed and treated during pregnancy and later complicated by growing teratoma syndrome: A case review with clinical considerations.

Gynecologic oncology reports·2020

Synchronous renal and para-aortic metastasis in a uterine serous carcinoma: A case review and clinical considerations.

Gynecologic oncology reports·2019

Prognostic Value of Blood-Based P-Tau217 Levels for Progression to Cognitive Impairment.

JAMA·2026

Ceperognastat in Early Symptomatic Alzheimer Disease: A Randomized Clinical Trial.

JAMA·2026

Amyloid PET Quantitation and Centiloid Thresholds in the Diagnosis of Alzheimer Disease: An Individual Participant Data Meta-Analysis.

JAMA·2026

Clinicopathologic Evaluation of Amyloid Clearance in Alzheimer Disease.

JAMA·2026

YEARS Algorithm for Diagnosis of Suspected Pulmonary Embolism in Patients With Cancer: A Randomized Clinical Trial.

JAMA·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

相关实验视频

慢性疾病遗传检测的不确定性

相关概念视频

A novel method for thermal noise reduction, enabling measurements of broadband, low-amplitude electron temperature fluctuations using individual radiometer channels.

Design of a correlation reflectometer radiometer diagnostic and measurements of the electron density-temperature cross-phase angle in the H-mode pedestal with small edge localized modes at ASDEX Upgrade.

System-level recommendations for improved wellness for gynecologic oncologists: A Society of Gynecologic Oncology Review.

Invasive ductal breast carcinoma metastasis to the cervix: A case review and clinical correlation.

Immature teratoma diagnosed and treated during pregnancy and later complicated by growing teratoma syndrome: A case review with clinical considerations.

Synchronous renal and para-aortic metastasis in a uterine serous carcinoma: A case review and clinical considerations.

Prognostic Value of Blood-Based P-Tau217 Levels for Progression to Cognitive Impairment.

Ceperognastat in Early Symptomatic Alzheimer Disease: A Randomized Clinical Trial.

Amyloid PET Quantitation and Centiloid Thresholds in the Diagnosis of Alzheimer Disease: An Individual Participant Data Meta-Analysis.

Clinicopathologic Evaluation of Amyloid Clearance in Alzheimer Disease.

YEARS Algorithm for Diagnosis of Suspected Pulmonary Embolism in Patients With Cancer: A Randomized Clinical Trial.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

相关实验视频

慢性疾病遗传检测的不确定性

相关概念视频

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