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GREGORY GRABOWSKI, M.D.

M.D.

NPI: 1174547806Individual

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

35.063485(OH)

Research & Publications (20)

Dose-response relationships for enzyme replacement therapy with imiglucerase/alglucerase in patients with Gaucher disease type 1.
PMID 19265748·Genet Med·2009
8-other
Treatment perspectives for the lysosomal storage diseases.
PMID 18321157·Expert Opin Emerg Drugs·2008
6-review
Phenotype, diagnosis, and treatment of Gaucher's disease.
PMID 19094956·Lancet·2008
8-other
Delivery of lysosomal enzymes for therapeutic use: glucocerebrosidase as an example.
PMID 17076599·Expert Opin Drug Deliv·2006
6-review
Recent clinical progress in Gaucher disease.
PMID 16012266·Curr Opin Pediatr·2005
6-review
Pediatric non-neuronopathic Gaucher disease: presentation, diagnosis and assessment. Consensus statements.
PMID 14677061·Eur J Pediatr·2004
6-review
Gaucher disease: lessons from a decade of therapy.
PMID 15126979·J Pediatr·2004
8-other
Enzyme therapy for lysosomal storage disease: principles, practice, and prospects.
PMID 14527307·Annu Rev Genomics Hum Genet·2003
6-review
Perspectives on gene therapy for lysosomal storage diseases that affect hematopoiesis.
PMID 12901334·Curr Hematol Rep·2003
6-review
Gaucher's disease. Enzyme therapy is not enough.
PMID 11784578·Lancet·2001
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
3333 BURNET AVE, ML 4006
CINCINNATI, OH 45229

Quick Facts

NPI
1174547806
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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