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VALERIE HOWELL, D.O.

D.O.

Anesthesiology Physician

NPI: 1578839569IndividualAccepts Medicare

Specialties, Licenses & Credentials

Anesthesiology PhysicianPrimary

Anesthesiology

Code: 207L00000X

5101019921(MI)

CMS Specialties

PrimaryANESTHESIOLOGY

Education

MICHIGAN STATE UNIVERSITY COLLEGE OF OSTEOPATHIC MEDICINE

Class of 2012

Research & Publications (19)

A targeted deleterious allele of the splicing factor SCNM1 in the mouse.
PMID 18791226·Genetics·2008
7-preclinical
Evidence for a direct role of the disease modifier SCNM1 in splicing.
PMID 17656373·Hum Mol Genet·2007
7-preclinical
HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours.
PMID 12960210·J Med Genet·2003
8-other
Accuracy of combined protein gene product 9.5 and parafibromin markers for immunohistochemical diagnosis of parathyroid carcinoma.
PMID 19017757·J Clin Endocrinol Metab·2009
4-observational
Lung cancer, caring for the caregivers. A qualitative study of providing pro-active social support targeted to the carers of patients with lung cancer.
PMID 18477717·Palliat Med·2008
8-other
Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.
PMID 17065424·J Mol Diagn·2006
8-other
Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasias.
PMID 16931959·Am J Surg Pathol·2006
8-other
[Prophylactic parathyroidectomy for familial parathyroid carcinoma].
PMID 16418876·Chirurg·2006
8-other
Gene expression of parathyroid tumors: molecular subclassification and identification of the potential malignant phenotype.
PMID 15492263·Cancer Res·2004
8-other
A molecular diagnosis of hyperparathyroidism-jaw tumor syndrome in an adolescent with recurrent kidney stones.
PMID 15480389·J Pediatr·2004
5-case
Carrier screening for Canavan disease in Australia.
PMID 15243987·J Inherit Metab Dis·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046109·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046107·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046105·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046102·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046098·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046094·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046050·Hum Genet·2004
8-other
A genetic screening programme for Tay-Sachs disease and cystic fibrosis for Australian Jewish high school students.
PMID 12676918·J Med Genet·2003
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
1500 EAST MEDICAL CENTER DRIVE, 1H247 UNIVERSITY HOSPITAL
ANN ARBOR, MI 48109

Location

Practice Location

1500 EAST MEDICAL CENTER DRIVE, ANN ARBOR, MI
(734) 936-4280

Quick Facts

NPI
1578839569
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
14
Publications
19

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