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DANIEL ROSENBLATT, M.D.
M.D.
Internal Medicine Physician
NPI: 1295078707Individual
Specialties, Licenses & Credentials
Hospice and Palliative Medicine (Family Medicine) Physician
Family Medicine — Hospice and Palliative Medicine
Code: 207QH0002X
T6467(TX)
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
EMC0001414(MI)53193(TN)
Hospice and Palliative Medicine (Internal Medicine) Physician
Internal Medicine — Hospice and Palliative Medicine
Code: 207RH0002X
TM2022-1477(NM)EMC0001414(MI)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Processing of alkylcobalamins in mammalian cells: A role for the MMACHC (cblC) gene product.
PMID 19447654·Mol Genet Metab·2009
7-preclinical
Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations.
PMID 19370762·Hum Mutat·2009
4-observational
Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism.
PMID 19058814·J Pediatr·2009
5-case
Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism.
PMID 19136951·Nat Genet·2009
8-other
Epigenetic modification of the gene for the vitamin B(12) chaperone MMACHC can result in increased tumorigenicity and methionine dependence.
PMID 19200761·Mol Genet Metab·2009
8-other
Transcobalamin (TC) deficiency--potential cause of bone marrow failure in childhood.
PMID 18956254·J Inherit Metab Dis·2008
5-case
Gene identification for the cblD defect of vitamin B12 metabolism.
PMID 18385497·N Engl J Med·2008
8-other
Neonatal vitamin B12 deficiency secondary to maternal subclinical pernicious anemia: identification by expanded newborn screening.
PMID 18410783·J Pediatr·2008
5-case
Late-onset combined homocystinuria and methylmalonic aciduria (cblC) and neuropsychiatric disturbance.
PMID 17853453·Am J Med Genet A·2007
5-case
The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption.
PMID 17446347·Blood·2007
8-other
Mitochondrial vitamin B12-binding proteins in patients with inborn errors of cobalamin metabolism.
PMID 17011224·Mol Genet Metab·2007
8-other
Polymorphic background of methionine synthase reductase modulates the phenotype of a disease-causing mutation.
PMID 17554763·Hum Mutat·2007
8-other
Atypical methylmalonic aciduria: frequency of mutations in the methylmalonyl CoA epimerase gene (MCEE).
PMID 17823972·Hum Mutat·2007
8-other
A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria.
PMID 16752391·Hum Mutat·2006
5-case
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
PMID 16311595·Nat Genet·2006
8-other
Mutation and biochemical analysis of patients belonging to the cblB complementation class of vitamin B12-dependent methylmalonic aciduria.
PMID 16410054·Mol Genet Metab·2006
8-other
Impact of cblB mutations on the function of ATP:cob(I)alamin adenosyltransferase in disorders of vitamin B12 metabolism.
PMID 16439175·Mol Genet Metab·2006
8-other
Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria.
PMID 16697227·Mol Genet Metab·2006
8-other
Combined methylmalonic aciduria and homocystinuria (cblC): phenotype-genotype correlations and ethnic-specific observations.
PMID 16714133·Mol Genet Metab·2006
8-other
Parallel changes in metabolite and expression profiles in crooked-tail mutant and folate-reduced wild-type mice.
PMID 17050573·Hum Mol Genet·2006
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 250 Monroe Ave NW Ste 400
Grand Rapids, MI 49503 - Phone
- (616) 432-2989
Quick Facts
- NPI
- 1295078707
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 6
- Locations
- 3
- Publications
- 20
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