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BENJAMIN SCHRANK, MD, PHD
MD, PHD
Radiation Oncology Physician
NPI: 1679109664IndividualAccepts Medicare
Specialties, Licenses & Credentials
Radiation Oncology PhysicianPrimary
Radiology — Radiation Oncology
Code: 2085R0001X
V8391(TX)
CMS Specialties
PrimaryRADIATION ONCOLOGY
Education
COLUMBIA UNIVERSITY COLLEGE OF PHYSICIANS AND SURGEONS
Class of 2020
Research & Publications (17)
Socioeconomic burden of amyotrophic lateral sclerosis, myasthenia gravis and facioscapulohumeral muscular dystrophy.
PMID 19629566·J Neurol·2010
4-observational
Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome.
PMID 19503089·Nat Genet·2009
8-other
[Mental health service user involvement in therapeutic and service delivery decisions: professional service staff appear optimistic].
PMID 17987541·Psychiatr Prax·2008
8-other
Site-specific effects of PECAM-1 on atherosclerosis in LDL receptor-deficient mice.
PMID 18669884·Arterioscler Thromb Vasc Biol·2008
7-preclinical
[Bipolar disorder and manic-depressive disorder on the Internet].
PMID 17640501·Neuropsychiatr·2007
8-other
[The "Gretchen question" for psychiatry--the importance of religion and spirituality in psychiatric treatment].
PMID 18082105·Neuropsychiatr·2007
6-review
[Unjustly neglected: siblings of people with a schizophrenic psychosis].
PMID 17915182·Neuropsychiatr·2007
8-other
Mildly affected patients with spinal muscular atrophy are partially protected by an increased SMN2 copy number.
PMID 16508748·Hum Genet·2006
8-other
High dose vitamin E therapy in amyotrophic lateral sclerosis as add-on therapy to riluzole: results of a placebo-controlled double-blind study.
PMID 15517433·J Neural Transm (Vienna)·2005
3-trial
Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutation.
PMID 10976646·Ann Neurol·2000
5-case
Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III.
PMID 10655542·Hum Mol Genet·2000
7-preclinical
The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy.
PMID 10655541·Hum Mol Genet·2000
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
- 1515 HOLCOMBE BLVD, 77030-4009
HOUSTON, TX 77030 - Phone
- (713) 792-6161
Quick Facts
- NPI
- 1679109664
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 6
- Publications
- 17
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