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ADAM ROSCHER, MD
MD
Psychiatry Physician
NPI: 1376182824Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
A189618(CA)
Research & Publications (20)
Towards a catalytic hydrogenolysis of silicon-silicon bonds: formation of Si-H bonds from disilanes and H2 at platinum.
PMID 19462659·Dalton Trans·2009
8-other
Stability of acylcarnitines and free carnitine in dried blood samples: implications for retrospective diagnosis of inborn errors of metabolism and neonatal screening for carnitine transporter deficiency.
PMID 19323528·Anal Chem·2009
8-other
Loss of function in phenylketonuria is caused by impaired molecular motions and conformational instability.
PMID 18538294·Am J Hum Genet·2008
8-other
X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype.
PMID 18834860·Biochem Biophys Res Commun·2008
8-other
Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung disease.
PMID 18059279·Nat Med·2007
7-preclinical
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessment.
PMID 16835865·Hum Mutat·2006
8-other
Disease manifestations and X inactivation in heterozygous females with Fabry disease.
PMID 16720462·Acta Paediatr Suppl·2006
8-other
Population spectrum of ACADM genotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency.
PMID 15832312·Hum Mutat·2005
8-other
Reduced incidence of severe metabolic crisis or death in children with medium chain acyl-CoA dehydrogenase deficiency homozygous for c.985A>G identified by neonatal screening.
PMID 15896661·Mol Genet Metab·2005
8-other
Mitochondrial targeting signals and mature peptides of 3-methylcrotonyl-CoA carboxylase.
PMID 16023992·Biochem Biophys Res Commun·2005
8-other
Stereoselectivity of the demethylation of nicotine piperidine homologues by Nicotiana plumbaginifolia cell suspension cultures.
PMID 16122770·Phytochemistry·2005
8-other
Role of Pex19p in the targeting of PMP70 to peroxisome.
PMID 16344115·Biochim Biophys Acta·2005
7-preclinical
Rapid second-tier molecular genetic analysis for congenital adrenal hyperplasia attributable to steroid 21-hydroxylase deficiency.
PMID 15608154·Clin Chem·2005
8-other
Nicotine demethylation in Nicotiana cell suspension cultures: N'-formylnornicotine is not involved.
PMID 16139853·Phytochemistry·2005
8-other
Simultaneous quantitative and allele-specific expression analysis with real competitive PCR.
PMID 15128429·BMC Genet·2004
4-observational
Frequencies of inherited organic acidurias and disorders of mitochondrial fatty acid transport and oxidation in Germany.
PMID 14714182·Eur J Pediatr·2004
8-other
Alpha1 antitrypsin and the prevalence and severity of asthma.
PMID 14977698·Arch Dis Child·2004
4-observational
Supervised machine learning techniques for the classification of metabolic disorders in newborns.
PMID 15180934·Bioinformatics·2004
3-trial
Interaction of PEX3 and PEX19 visualized by fluorescence resonance energy transfer (FRET).
PMID 14713233·Adv Exp Med Biol·2003
8-other
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
- 601 Duboce Ave, Suite 250, South Tower
San Francisco, CA 94117 - Phone
- (415) 819-0636
Quick Facts
- NPI
- 1376182824
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 3
- Publications
- 20
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