Genetics | Hadassah International

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Mystery of Devastating Pediatric Disease Solved by Hadassah Team

A genetic mutation causing a rare and devastating pediatric neurological disease that has puzzled medical centers around the world has been identified at the Hadassah Medical Organization by Prof. Orly…

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Bone-marrow (transplantation)

Hadassah, Palestinian, and German Triumverate Rescues Children with Severe Immune Defects

Hadassah Genetic Discovery Article Singled Out for Recognition

Hadassah Opens Clinic for Cardiac Genetic Counseling and Treatment

Hadassah Cardiologist is Key Researcher in Identifying Genetic Heart Mutation

Chinese Scientists Visit Hadassah Partners in Psychiatric Research Project

Hadassah Hospital Senior Oncologist Dr. Asher Salmon Rejects Universal BRCA Gene Home Tests Without Analysis of Family History & Genetic Counseling

Hadassah Cures Mumbai Child of Thalassemia, with Help of Cutting-Edge Diagnosis

Hadassah’s Advanced Gene Sequencing Changes the Life of a Family from Uzbekistan

Building Bridges to Peace

The Story of Tasnin: A Mysteriously Sick Little Girl, a Genetic Mutation, and a Cure

Deep Sequencing Analysis Leads to Major Genetic Discoveries at Hadassah

Creating the Medicine of the Future: Hadassah’s Goldyne Savad Institute of Gene Therapy

Cancer Research

New Test Developed at Hadassah Predicts Presence of Harmful BRCA Mutation Which Can Trigger Breast Cancer

Hadassah Physician/Researchers Identify Defective Gene and Halt Paralysis of Babies’ Limbs and Vocal Cords

Hadassah Physician/Researchers Identify Defective Gene and Halt Paralysis of Babies’ Limbs and Vocal Cords

Bone-marrow (transplantation)

Enlivex Successfully Completes First Trial for Treatment of Graft-Versus-Host Disease (GVHD)

Hadassah Researchers Identify Anti-Aging Genes in Community of Orthodox Women

From Improved Diagnosis to Novel Therapies: Advances in Parkinson’s Disease at the Hadassah University Medical Center

Hadassah Medical Center: In the Forefront of Fertility Treatment and Research

Hadassah Researchers Identify Genetic Mutation That Causes Children To Be Born with Brain Atrophy