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KARI CASAS, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1497723662IndividualAccepts Medicare
Specialties, Licenses & Credentials
Adolescent Medicine (Internal Medicine) Physician
Internal Medicine — Adolescent Medicine
Code: 207RA0000X
M3490(TX)
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
M3490(TX)12657(ND)
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
M3490(TX)
CMS Specialties
PrimaryMEDICAL GENETICS AND GENOMICS
Additional
PEDIATRIC MEDICINE
Education
UNIVERSITY OF NORTH DAKOTA SCHOOL OF MEDICINE
Class of 1998
Research & Publications (11)
De novo mutation in POLG leads to haplotype insufficiency and Alpers syndrome.
PMID 19501198·Mitochondrion·2009
5-case
De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.
PMID 18203189·Am J Med Genet A·2008
5-case
Chromosome 2q37 deletion: clinical and molecular aspects.
PMID 17910077·Am J Med Genet C Semin Med Genet·2007
6-review
Mitochondrial myopathy, sideroblastic anemia, and lactic acidosis: an autosomal recessive syndrome in Persian Jews caused by a mutation in the PUS1 gene.
PMID 15971356·J Child Neurol·2005
5-case
Aspartate 120 of Escherichia coli methylenetetrahydrofolate reductase: evidence for major roles in folate binding and catalysis and a minor role in flavin reactivity.
PMID 15865426·Biochemistry·2005
8-other
Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals.
PMID 15386475·Am J Med Genet A·2004
5-case
Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA).
PMID 15108122·Am J Hum Genet·2004
8-other
Gene responsible for mitochondrial myopathy and sideroblastic anemia (MSA) maps to chromosome 12q24.33.
PMID 15103716·Am J Med Genet A·2004
5-case
Clinical, radiological, and chondro-osseous findings in opsismodysplasia: survey of a series of 12 unreported cases.
PMID 12624139·J Med Genet·2003
5-case
Functional genomics of Down syndrome: a multidisciplinary approach.
PMID 11771739·J Neural Transm Suppl·2001
6-review
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) 234-2431
Quick Facts
- NPI
- 1497723662
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 1
- Years in Practice
- 28
- Publications
- 11
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