Back to Search
DOROTHY GERMAIN, PHARMD
PHARMD
Pharmacist
NPI: 1366728321Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
5302033722(MI)
Research & Publications (20)
Fabry disease: the need to stratify patient populations to better understand the outcome of enzyme replacement therapy.
PMID 17580237·Clin Ther·2007
8-other
[Development of an orphan drug to treat a genetic disease: the paradigm of agalsidase beta].
PMID 17546772·Presse Med·2007
6-review
[Genetics of Fabry disease: diagnostic and therapeutic implications].
PMID 17546762·Presse Med·2007
6-review
Sustained, long-term renal stabilization after 54 months of agalsidase beta therapy in patients with Fabry disease.
PMID 17409312·J Am Soc Nephrol·2007
3-trial
[Gaucher disease: clinical, genetic and therapeutic aspects].
PMID 15261378·Pathol Biol (Paris)·2004
6-review
Arterial remodeling and stiffness in patients with pseudoxanthoma elasticum.
PMID 12649085·Arterioscler Thromb Vasc Biol·2003
8-other
Fabry disease: twenty novel alpha-galactosidase A mutations and genotype-phenotype correlations in classical and variant phenotypes.
PMID 12428061·Mol Med·2002
8-other
Fabry disease: recent advances in enzyme replacement therapy.
PMID 12387706·Expert Opin Investig Drugs·2002
6-review
Patients affected with Fabry disease have an increased incidence of progressive hearing loss and sudden deafness: an investigation of twenty-two hemizygous male patients.
PMID 12377100·BMC Med Genet·2002
8-other
A new phenotype of Fabry disease with intermediate severity between the classical form and the cardiac variant.
PMID 11688386·Contrib Nephrol·2001
5-case
Mutation analysis of the acid beta-glucosidase gene in a patient with type 3 Gaucher disease and neutralizing antibody to alglucerase.
PMID 11600137·Mutat Res·2001
5-case
Co-occurrence and contribution of Fabry disease and Klippel-Trénaunay-Weber syndrome to a patient with atypical skin lesions.
PMID 11531972·Clin Genet·2001
5-case
Identification of a novel de novo mutation (G373D) in the alpha-galactosidase A gene (GLA) in a patient affected with Fabry disease.
PMID 11295840·Hum Mutat·2001
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
- 1181 WALKER AVE NW
GRAND RAPIDS, MI 49504 - Phone
- (616) 458-9640
Quick Facts
- NPI
- 1366728321
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile