Skip to main navigation
Skip to search
Skip to main content
Experts@Minnesota Home
Home
Profiles
Research units
University Assets
Projects and Grants
Research output
Press/Media
Datasets
Activities
Fellowships, Honors, and Prizes
Search by expertise, name or affiliation
Spinal cord disease in hereditary spherocytosis: report of two cases with a hypothesized common mechanism for neurologic and red cell abnormalities
S. R. McCann, H. S. Jacob
Medicine - Hematology, Oncology, Transplant
Research output
:
Contribution to journal
›
Article
›
peer-review
27
Scopus citations
Overview
Fingerprint
Fingerprint
Dive into the research topics of 'Spinal cord disease in hereditary spherocytosis: report of two cases with a hypothesized common mechanism for neurologic and red cell abnormalities'. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Keyphrases
Neurologic
100%
Common Mechanisms
100%
Spinal Cord Diseases
100%
Red Cell Membrane
100%
Hereditary Spherocytosis
100%
Red Cell Abnormalities
100%
Muscular Dystrophy
50%
Nerve Tissue
50%
Similar Individuals
50%
European Literature
50%
Medicine and Dentistry
Spinal Cord Disease
100%
Erythrocyte Membrane
100%
Hereditary Spherocytosis
100%
Muscular Dystrophy
50%
Nerve Tissue
50%
Pharmacology, Toxicology and Pharmaceutical Science
Spinal Cord Disease
100%
Hereditary Spherocytosis
100%
Muscular Dystrophy
50%