John Nicholas Whitaker - Birmingham AL Robert David Kachelhofer - Birmingham AL Beverly Ann Layton - Birmingham AL Edwin Luther Bradley - Birmingham AL Sheila Loughran Burgard - Lake Bluff IL Anthony Thomas Reder - Oak Park IL Wendy Jean Morrison - Vancouver, CA Guojun Zhao - Vancouver, CA Donald Winston Paty - Vancouver, CA
Assignee:
UAB Research Foundation - Birmingham AL
International Classification:
G01N 3353 G01N 33566 G01N 33567 G01N 33536
US Classification:
435 71
Abstract:
The present invention provides a method of determining the status of a multiple sclerosis patient, i. e. , predicting the transition from a status of relapsing-remitting to a progressive phase of multiple sclerosis, comprising the step of measuring the levels of urinary myelin basic protein-like material in the patient. The present invention also provides a method of determining the amount of lesions and total lesion area of a multiple sclerosis patient, comprising the step of measuring the levels of urinary myelin basic protein-like material in the patient. Further provided is a method of monitoring myelination in a developing child, comprising the step of: measuring the levels of myelin basic protein-like material in the urine of said child.
P-Cresol Sulfate, A Component Of Urinary Myelin Basic Protein-Like Material, As A Correlate Of Multiple Sclerosis Status
John Nicholas Whitaker - Birmingham AL Robert David Kachelhofer - Birmingham AL Edwin Luther Bradley - Birmingham AL Sheila Loughran Burgard - Lake Bluff IL Beverly Ann Layton - Birmingham AL Anthony Thomas Reder - Oak Park IL Wendy Jean Morrision - Vancouver, CA Guojun Zhao - Burnaby, CA Donald Winston Paty - Vancouver, CA Ligong Cao - Birmingham AL Lori Coward - Birmingham AL Patricia L. Jackson - Moody AL Marion Kirk - Birmingham AL
Assignee:
UAB Research Foundation - Birmingham AL
International Classification:
G01N 3353 G01N 33566 G01N 33567 G01N 33536
US Classification:
435 71
Abstract:
The present invention provides a method of determining the status of a multiple sclerosis patient, i. e. , predicting the transition from a status of relapsing-remitting to a progressive phase of multiple sclerosis, comprising the step of measuring the amount of urinary p-cresol sulfate in the patient. The present invention also provides a method of determining the amount of lesions and total lesion area of a multiple sclerosis patient, comprising the step of measuring the amount of urinary p-cresol sulfate in the patient. Further provided is a method of monitoring myelination in a developing child, comprising the step of: measuring the amount of p-cresol sulfate in the urine of said child.