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NATHAN BLAU, MD
MD
Cardiovascular Disease Physician
NPI: 1508137555IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
GFE34173(CA)
Education
R FRANKLIN UNIVERSITY OF MED & SCI/CHICAGO MEDICAL SCHOOL
Class of 1972
Research & Publications (20)
Optimizing the use of sapropterin (BH(4)) in the management of phenylketonuria.
PMID 19208488·Mol Genet Metab·2009
6-review
The metabolic and molecular bases of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.
PMID 15171997·Mol Genet Metab·2004
6-review
Cerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome: a new phenotype.
PMID 12963755·Neurology·2003
5-case
Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPS.
PMID 10874306·Hum Mutat·2000
5-case
Genotype-predicted tetrahydrobiopterin (BH4)-responsiveness and molecular genetics in Croatian patients with phenylalanine hydroxylase (PAH) deficiency.
PMID 19394257·Mol Genet Metab·2009
3-trial
Sepiapterin reductase deficiency in a 2-year-old girl with incomplete response to treatment during short-term follow-up.
PMID 19130291·J Inherit Metab Dis·2009
5-case
Effect of BH(4) supplementation on phenylalanine tolerance.
PMID 19067227·J Inherit Metab Dis·2009
8-other
Pharmacokinetics of tetrahydrobiopterin following oral loadings with three single dosages in patients with phenylketonuria.
PMID 19016342·J Inherit Metab Dis·2009
2-rct
Disease-causing mutations improving the branch site and polypyrimidine tract: pseudoexon activation of LINE-2 and antisense Alu lacking the poly(T)-tail.
PMID 19280650·Hum Mutat·2009
5-case
Outcome and long-term follow-up of 36 patients with tetrahydrobiopterin deficiency.
PMID 18060820·Mol Genet Metab·2008
5-case
A milk-free diet downregulates folate receptor autoimmunity in cerebral folate deficiency syndrome.
PMID 18355335·Dev Med Child Neurol·2008
3-trial
Defining tetrahydrobiopterin (BH4)-responsiveness in PKU.
PMID 18327672·J Inherit Metab Dis·2008
8-other
Autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia: evidence of a phenotypic continuum between dominant and recessive forms.
PMID 18276179·Mol Genet Metab·2008
5-case
Atypical presentation of distal renal tubular acidosis in two siblings.
PMID 18386070·Pediatr Nephrol·2008
5-case
Mitochondrial diseases associated with cerebral folate deficiency.
PMID 18413591·Neurology·2008
8-other
Mutations in human monoamine-related neurotransmitter pathway genes.
PMID 18444257·Hum Mutat·2008
6-review
Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.
PMID 17935162·Hum Mutat·2008
4-observational
Tetrahydrobiopterin shows chaperone activity for tyrosine hydroxylase.
PMID 18419768·J Neurochem·2008
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
- 335 KATHERINE AVE # T
SALINAS, CA 93901 - Phone
- (831) 751-6222
Quick Facts
- NPI
- 1508137555
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 54
- Publications
- 20
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