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MITCHELL SCHWARTZ, M.D.
M.D.
Specialist
NPI: 1326041625Individual
Specialties, Licenses & Credentials
Research & Publications (20)
A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria.
PMID 19526370·Eur J Pediatr·2010
5-case
The role of human demographic history in determining the distribution and frequency of transferase-deficient galactosaemia mutations.
PMID 19639008·Heredity (Edinb)·2010
8-other
Testicular adrenal rest tumours in boys, adolescents and adult men with congenital adrenal hyperplasia may be associated with the CYP21A2 mutation.
PMID 19531083·Int J Androl·2010
8-other
Thymic involution, a co-morbidity factor in amyotrophic lateral sclerosis.
PMID 19650830·J Cell Mol Med·2010
7-preclinical
Dysregulation of kisspeptin and neurogenesis at adolescence link inborn immune deficits to the late onset of abnormal sensorimotor gating in congenital psychological disorders.
PMID 19636313·Mol Psychiatry·2010
7-preclinical
Pelvic cake kidney with a solitary ureter and bilateral congenital absence of the vas deferens.
PMID 19628269·Urology·2010
5-case
Clinical evaluation of stereotactic target localization using 3-Tesla MRI for radiosurgery planning.
PMID 19515512·Int J Radiat Oncol Biol Phys·2010
8-other
A comparison of postoperative complications in open versus robotic cystectomy.
PMID 19560255·Eur Urol·2010
4-observational
Genetic testing in familial AD and FTD: mutation and phenotype spectrum in a Danish cohort.
PMID 19659892·Clin Genet·2009
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 372 DORSET ST
SOUTH BURLINGTON, VT 05403 - Phone
- (802) 660-8808
Quick Facts
- NPI
- 1326041625
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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