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PAMELA MCGRANN, M.D.
M.D.
NPI: 1356311898Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
34027(MN)
Research & Publications (5)
Ornithine transcarbamylase deficiency presenting as encephalopathy during adulthood following bariatric surgery.
PMID 17210820·Arch Neurol·2007
5-case
Phase II trial of pirfenidone in adults with neurofibromatosis type 1.
PMID 17035676·Neurology·2006
3-trial
A case of mosaic supernumerary ring chromosome 15 with two copies of the segment 15p11.1-q14.
PMID 16830338·Am J Med Genet A·2006
5-case
Lack of evidence for an association between neurofibromatosis and pulmonary fibrosis.
PMID 16236898·Chest·2005
8-other
Nonmosaic smallest duplication of 12q24.31-qter: the first reported case.
PMID 15216553·Am J Med Genet A·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
- 801 BROADWAY N
FARGO, ND 58102 - Phone
- (701) 234-2000
Quick Facts
- NPI
- 1356311898
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 5
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