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Publications by Brian Hinds
Schnitzler Syndrome Associated With MYD88 L265P Mutation
JAAD Case Reports
Dermatology
Related publications
Response to Ibrutinib of a Refractory IgA Lymphoplasmacytic Lymphoma Carrying the MYD88 L265P Gene Mutation
Mediterranean Journal of Hematology and Infectious Diseases
Infectious Diseases
Hematology
Schnitzler Syndrome
L265P Mutation of the MYD88 Gene Is Frequent in Waldenström’s Macroglobulinemia and Its Absence in Myeloma
PLoS ONE
Multidisciplinary
CCL2 in Schnitzler Syndrome
British Journal of Dermatology
Dermatology
Medicine
IGHV Gene Features and MYD88 L265P Mutation Separate the Three Marginal Zone Lymphoma Entities and Waldenström Macroglobulinemia/Lymphoplasmacytic Lymphomas
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
Hematology
PW03-008 – Mitochondrial Disturbances in Schnitzler Syndrome
Pediatric Rheumatology
Immunology
Pediatrics
Rheumatology
Allergy
Perinatology
Child Health
MYD88 L265P Is a Marker Highly Characteristic Of, but Not Restricted To, Waldenström’s Macroglobulinemia
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
Hematology
A Rare but Fascinating Disorder: Case Collection of Patients With Schnitzler Syndrome
Case Reports in Rheumatology
Digital PCR in Bone Marrow Trephine Biopsies Is Highly Sensitive for MYD88 L265P Detection in Lymphomas With Plasmacytic/Plasmacytoid Differentiation
British Journal of Haematology
Hematology
