نتائج البحث

A Prospective Study of Pembrolizumab Combining Chemotherapy in Advanced NSCLC Patients With EGFR Exon 21 Point Mutation.

• Source: A Phase II Study of Pembrolizumab Plus Platinum and Pemetrexed as First Line Therapy in Advanced Non-squamous Non-small Cell Lung Cancer Patients With EGFR Exon 21 Point

تفاصيل العنوان

Safety and Efficacy Study of A0001 in Patients With the A3243G Mitochondrial DNA Point Mutation

• Authors : Thomas Sciascia, MD/Chief Medical Officer and VP Clinical Operations and Regulatory Affairs

• Source: A Phase 2a, Double Blind, Randomized, Placebo-controlled, 28 Day, Two-arm, Parallel Group Study of A0001 in Patients With the A3243G Mitochondrial DNA Point

تفاصيل العنوان

Helicobacter Pylori Eradication Study

• Authors : Kim Ji Hyun, Clinical Professor

• Source: Helicobacter Pylori Eradication Rates of Concomitant Therapy and Tailored Therapy Based on 23S Ribosomal RNA Point Mutations Associated With Clarithromycin Resistance: A

تفاصيل العنوان

Trans-auricular Nerve Stimulation as an Innovative Approach to the Treatment of Pain in Pediatric Patients Suffering From Sickle Cell Disease

• Authors : Anna Woodbury, Associate Professor

• Source: Trans-auricular Nerve Stimulation as an Innovative Approach to the Treatment of Pain in Pediatric Patients Suffering From Sickle Cell Disease

تفاصيل العنوان

OMT-28 in Patients With Primary Mitochondrial Disease (PMD) (PMD-OPTION) (PMD-OPTION)

• Source: A Phase 2a Safety, Tolerability, and Pharmacodynamic Study of OMT-28 in PMD Patients With Myopathy and/or Cardiomyopathy and Inflammation (PMD-OPTION)

تفاصيل العنوان

Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders (DANNIgene)

• Authors : URC-CIC Paris Descartes Necker Cochin

• Source: Evaluation of the Diagnostic Performance of Non-Invasive Prenatal Diagnosis for Single Gene DisordersPacault M, Verebi C, Champion M, Orhant L, Perrier A, Girodon E, Leturcq F, Vidaud D, Ferec

تفاصيل العنوان

Detection and Prognostic Value of Recurrent XPO1 Mutations of Patients With Classical Hodgkin Lymphoma (XPO1)

• Source: Prevalence, Kinetic and Prognostic Value of XPO1 E571K Mutation Detection in Plasma Cell-free DNA From Patients Xith Classical Hodgkin LymphomaCamus V, Viennot M,

تفاصيل العنوان

Molecular Analysis of Thoracic Malignancies

• Source: Molecular Analysis of Thoracic Malignancies

تفاصيل العنوان

Newborn Screening for Spinal Muscular Atrophy (SMA-NBS)

• Authors : Novartis Gene Therapies; Hoffmann-La Roche; Oxford University Hospitals NHS Trust

• Source: Population-based New-Born Screening of Spinal Muscular Atrophy to Evaluate the Uptake and Feasibility in the UK Context

تفاصيل العنوان

Study of Erlotinib (Tarceva®) in Combination With OSI-906 in Patients With Advanced Non-small Cell Lung Cancer (NSCLC) With Activating Mutations of the Epidermal Growth Factor Receptor (EGFR) Gene

• Source: A Randomized, Double-Blind, Phase 2 Study of Erlotinib (Tarceva®) in Combination With OSI-906 or Placebo in Chemonaive Patients With Advanced NSCLC With Activating Mutations of the Epidermal Growth

تفاصيل العنوان