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MIRIAM SCHWARTZ, M.D.
M.D.
Geriatric Medicine (Family Medicine) Physician
NPI: 1841482809Individual
Specialties, Licenses & Credentials
Geriatric Medicine (Family Medicine) PhysicianPrimary
Family Medicine — Geriatric Medicine
Code: 207QG0300X
A92198(CA)
Research & Publications (20)
Type 2 diabetes mellitus in childhood: obesity and insulin resistance.
PMID 18806081·J Am Osteopath Assoc·2008
6-review
Medical toxicology and public health--update on research and activities at the Centers for Disease Control and Prevention, and the Agency for Toxic Substances and Disease Registry.
PMID 18072150·J Med Toxicol·2007
8-other
Deletion of exon 16 of the dystrophin gene is not associated with disease.
PMID 17226814·Hum Mutat·2007
5-case
Development and validation of a chronic copper biotic ligand model for Ceriodaphnia dubia.
PMID 17673307·Aquat Toxicol·2007
4-observational
The promise and the potential consequences of the global transport of mycorrhizal fungal inoculum.
PMID 16643296·Ecol Lett·2006
8-other
How conservation scientists can help develop social capital for biodiversity.
PMID 17002774·Conserv Biol·2006
8-other
LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype.
PMID 15883334·Neurology·2005
8-other
Improved molecular diagnosis of dystrophin gene mutations using the multiplex ligation-dependent probe amplification method.
PMID 15684864·Genet Test·2004
3-trial
No evidence for paternal inheritance of mtDNA in patients with sporadic mtDNA mutations.
PMID 14759640·J Neurol Sci·2004
4-observational
Influence of natural organic matter source on acute copper, lead, and cadmium toxicity to rainbow trout (Oncorhynchus mykiss).
PMID 15648764·Environ Toxicol Chem·2004
4-observational
New patterns of inheritance in mitochondrial disease.
PMID 14521902·Biochem Biophys Res Commun·2003
6-review
Pelvic cake kidney with a solitary ureter and bilateral congenital absence of the vas deferens.
PMID 19628269·Urology·2010
5-case
Thymic involution, a co-morbidity factor in amyotrophic lateral sclerosis.
PMID 19650830·J Cell Mol Med·2010
7-preclinical
The role of human demographic history in determining the distribution and frequency of transferase-deficient galactosaemia mutations.
PMID 19639008·Heredity (Edinb)·2010
8-other
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
A comparison of postoperative complications in open versus robotic cystectomy.
PMID 19560255·Eur Urol·2010
4-observational
A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria.
PMID 19526370·Eur J Pediatr·2010
5-case
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 516 NIZHONI BLVD
GALLUP, NM 87301 - Phone
- (505) 722-1000
Quick Facts
- NPI
- 1841482809
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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