Commentary: J Rare Disord Diagn Ther (1-2)
Multielement Examination of Single Red Platelets
Author(s): Amin Haq
DOI: 10.36648/2380-7245.10.1.146
Commentary: J Rare Disord Diagn Ther (1-2)
Examination of Gene Mutation Attributes and it's Connection with Prognosis in Patients
Author(s): Haiping Zhang
DOI: 10.36648/2380-7245.10.6.147
Commentary: J Rare Disord Diagn Ther (1-2)
Cryopreserved Allogenic Bone Marrow Relocate inside Paediatric Population
Author(s): Kimberlee Hanna
DOI: 10.36648/2380-7245.10.1.148
Perspective Article: J Rare Disord Diagn Ther (1-2)
Advancements in Precision Medicine: From Rare Diseases to Complex Syndromes
Author(s): Klein Haneveld
DOI: 10.36648/2380-7245.10.1.149
Perspective Article: J Rare Disord Diagn Ther (1-2)
The Role of FEM1B in a Rare Syndromic Neurodevelopmental Disorder
Author(s): Brook Meyer
DOI: 10.36648/2380-7245.10.1.150
Opinion Article: J Rare Disord Diagn Ther (1-2)
Genomic Sequencing's Impact on Rare Disease Diagnosis
Author(s): Sandra Cooper
DOI: 10.36648/2380-7245.10.1.154
Opinion Article: J Rare Disord Diagn Ther (1-2)
Cushing's Syndrome: Causes, Symptoms, Diagnosis, and Treatment
Author(s): Gul Ilhan
DOI: 10.36648/2380-7245.10.1.152
Opinion Article: J Rare Disord Diagn Ther (1-2)
Rare Muscular Disorder Research and Treatment
Author(s): Hanns Lochmüller
DOI: 10.36648/2380-7245.10.1.153
Perspective Article: J Rare Disord Diagn Ther (1-2)
Adolescent Health and Well-being in Sickle Cell Disease
Author(s): Marcos Bezerra
DOI: 10.36648/2380-7245.10.1.152
Case Report: J Rare Disord Diagn Ther (1-2)
Splenic, Hepatic and Gastric Sarcoidosis: Case Study
Author(s): Nawal Lagdali*, Camelia Berhili, Maryeme Kadiri, Fatima Zahra Habib, Imane Benelbarhdadi, Mohamed Borahma and Fatima Zahra Ajana
DOI: 10.36648/2380-7245.10.1.145