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VICTOR CRUZ, MD
MD
Psychiatry Physician
NPI: 1285669325Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
4301026837(MI)
Research & Publications (20)
Cortical remapping in amputees and dysmelic patients: a functional MRI study.
PMID 14757926·NeuroRehabilitation·2003
4-observational
Differential gender-related susceptibility to learning and memory deficits in mice submitted to neonatal freezing microgyria model.
PMID 19429188·Brain Res Bull·2009
7-preclinical
Successful treatment of a sinonasal cryptococcal granuloma in a horse.
PMID 19222362·J Am Vet Med Assoc·2009
5-case
Novel SPG3A and SPG4 mutations in dominant spastic paraplegia families.
PMID 18664244·Acta Neurol Scand·2009
8-other
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
PMID 18079167·Brain·2008
4-observational
Results of carotid endarterectomy with pericardial patch angioplasty: rate and predictors of restenosis.
PMID 17980796·Ann Vasc Surg·2007
7-preclinical
A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21.
PMID 17515546·Neurology·2007
5-case
Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
PMID 17322883·Nat Genet·2007
7-preclinical
Assessment of the general knowledge of emergency physicians from the hospitals of the city of Salvador (Brazil) on the care of cardiac arrest patients.
PMID 17221041·Arq Bras Cardiol·2006
8-other
Enhancement of non-dominant hand motor function by anodal transcranial direct current stimulation.
PMID 16808997·Neurosci Lett·2006
8-other
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity.
PMID 16699786·Neurogenetics·2006
8-other
Cerebellar ataxia with spasmodic cough: a new form of dominant ataxia.
PMID 16606768·Arch Neurol·2006
8-other
A novel H101Q mutation causes PKCgamma loss in spinocerebellar ataxia type 14.
PMID 16189624·J Hum Genet·2005
8-other
A population-based study of drug resistance and transmission of tuberculosis in an urban community.
PMID 16158889·Int J Tuberc Lung Dis·2005
8-other
Neuroferritinopathy: missense mutation in FTL causing early-onset bilateral pallidal involvement.
PMID 16116125·Neurology·2005
5-case
[Therapeutic intervention scoring system-28 (TISS-28): directions for application].
PMID 16060311·Rev Esc Enferm USP·2005
8-other
Influence of diet on assimilation and turnover of 13C in the tissues of broiler chickens.
PMID 16050194·Br Poult Sci·2005
4-observational
Ethylene-styrene copolymerization with constrained geometry catalysts: a density functional study.
PMID 15743264·J Chem Phys·2005
8-other
Intestinal adhesion to the abdominal wall after skin closure with octylcyanoacrylate.
PMID 15559358·J Am Assoc Gynecol Laparosc·2004
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 17177 N LAUREL PARK DR, SUITE 131
LIVONIA, MI 48152 - Phone
- (734) 462-3210
Quick Facts
- NPI
- 1285669325
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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