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MARY CHAMPION, PHD
PHD
Clinical Psychologist
NPI: 1902926736Individual
Specialties, Licenses & Credentials
Clinical PsychologistPrimary
Psychologist — Clinical
Code: 103TC0700X
P2726(TN)
Research & Publications (20)
Congenital disorders of glycosylation: a rare cause of nephrotic syndrome.
PMID 19474279·Nephrol Dial Transplant·2009
5-case
ESX-1 secreted virulence factors are recognized by multiple cytosolic AAA ATPases in pathogenic mycobacteria.
PMID 19682254·Mol Microbiol·2009
8-other
Analysis of transfusion reactions associated with prestorage-pooled platelet components.
PMID 19389029·Transfusion·2009
8-other
Commentary: doing time in maximum security--the pains of separation.
PMID 19535557·J Am Acad Psychiatry Law·2009
8-other
Comparative genomic characterization of Francisella tularensis strains belonging to low and high virulence subspecies.
PMID 19478886·PLoS Pathog·2009
4-observational
Muscle MRI findings in siblings with juvenile-onset acid maltase deficiency (Pompe disease).
PMID 18434155·Neuromuscul Disord·2008
5-case
Mitochondrial disorders and general anaesthesia: a case series and review.
PMID 18285393·Br J Anaesth·2008
6-review
Management of blood shortages in a tertiary care academic medical center: the Yale-New Haven Hospital frozen blood reserve.
PMID 18631164·Transfusion·2008
6-review
Hepatocyte transplantation followed by auxiliary liver transplantation--a novel treatment for ornithine transcarbamylase deficiency.
PMID 18211511·Am J Transplant·2008
5-case
The birth prevalence of PKU in populations of European, South Asian and sub-Saharan African ancestry living in South East England.
PMID 18184144·Ann Hum Genet·2008
8-other
A novel starch for the treatment of glycogen storage diseases.
PMID 17514432·J Inherit Metab Dis·2007
2-rct
Auxiliary liver transplantation for propionic acidemia: a 10-year follow-up.
PMID 17697263·Am J Transplant·2007
5-case
High frequency of missense mutations in glycogen storage disease type VI.
PMID 17705025·J Inherit Metab Dis·2007
5-case
Recommendations on chronic constipation (including constipation associated with irritable bowel syndrome) treatment.
PMID 17464377·Can J Gastroenterol·2007
6-review
Clinical, enzymatic and molecular characterization of nine new patients with malonyl-coenzyme A decarboxylase deficiency.
PMID 17186413·J Inherit Metab Dis·2007
5-case
Commentary: seclusion and restraint in corrections a time for change.
PMID 18086732·J Am Acad Psychiatry Law·2007
8-other
C-terminal signal sequence promotes virulence factor secretion in Mycobacterium tuberculosis.
PMID 16973880·Science·2006
8-other
Refining the diagnosis of mitochondrial HMG-CoA synthase deficiency.
PMID 16601895·J Inherit Metab Dis·2006
5-case
Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5'-phosphate oxidase.
PMID 15772097·Hum Mol Genet·2005
7-preclinical
Characteristic mass spectral fragments of the organophosphorus agent FP-biotin and FP-biotinylated peptides from trypsin and bovine albumin (Tyr410).
PMID 16125664·Anal Biochem·2005
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2018 WESTERN AVENUE
KNOXVILLE, TN 37921 - Phone
- (865) 544-0406
Quick Facts
- NPI
- 1902926736
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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