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NATHAN DAHL, M.D.
M.D.
Pediatric Hematology & Oncology Physician
NPI: 1760825343IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatric Hematology & Oncology PhysicianPrimary
Pediatrics — Pediatric Hematology-Oncology
Code: 2080P0207X
DR.0056879(CO)
Education
UNIVERSITY OF NEVADA SCHOOL OF MEDICINE
Class of 2013
Research & Publications (20)
Deficient HCO3- transport in an AE1 mutant with normal Cl- transport can be rescued by carbonic anhydrase II presented on an adjacent AE1 protomer.
PMID 12933803·J Biol Chem·2003
7-preclinical
Screening for copy number alterations in loci associated with autism spectrum disorders by two-color multiplex ligation-dependent probe amplification.
PMID 19319887·Am J Med Genet B Neuropsychiatr Genet·2010
8-other
Thrombotic microangiopathy and renal failure exacerbated by epsilon-aminocaproic acid.
PMID 18805613·Am J Kidney Dis·2009
5-case
Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities.
PMID 19499579·Pediatr Blood Cancer·2009
5-case
Mutations in the fatty acid transport protein 4 gene cause the ichthyosis prematurity syndrome.
PMID 19631310·Am J Hum Genet·2009
8-other
N(alpha)-tosyl-L-phenylalanine chloromethyl ketone induces caspase-dependent apoptosis in transformed human B cell lines with transcriptional down-regulation of anti-apoptotic HS1-associated protein X-1.
PMID 19679660·J Biol Chem·2009
8-other
SPIFA-A presentation of the Structured Psychiatric Interview for General Practice.
PMID 19370449·Nord J Psychiatry·2009
4-observational
Posttranscriptional down-regulation of small ribosomal subunit proteins correlates with reduction of 18S rRNA in RPS19 deficiency.
PMID 19454283·FEBS Lett·2009
8-other
Targeted resequencing and analysis of the Diamond-Blackfan anemia disease locus RPS19.
PMID 19587786·PLoS One·2009
8-other
A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population.
PMID 19213037·Am J Med Genet A·2009
8-other
SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.
PMID 19194956·Am J Med Genet B Neuropsychiatr Genet·2009
5-case
Impact of transdermal oxybutynin on work productivity in patients with overactive bladder: results from the MATRIX study.
PMID 19485428·Pharmacoeconomics·2009
8-other
WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.
PMID 19471313·Eur J Hum Genet·2009
8-other
Duchenne muscular dystrophy and idiopathic hyperCKemia in the same family.
PMID 18833644·Eur J Paediatr Neurol·2008
5-case
Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations.
PMID 18513342·J Intern Med·2008
5-case
Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference.
PMID 18671700·Br J Haematol·2008
8-other
A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia.
PMID 18688569·J Hum Genet·2008
8-other
Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure.
PMID 18782852·Hum Mol Genet·2008
8-other
Familial osteochondritis dissecans associated with early osteoarthritis and disproportionate short stature.
PMID 18226555·Osteoarthritis Cartilage·2008
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
- 13123 E 16TH AVE
AURORA, CO 80045 - Phone
- (720) 777-1234
Quick Facts
- NPI
- 1760825343
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 20
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