Professor, Human Genetics, University of Miami School of Medicine
Medical Genetics
Dr. Olaf A. Bodamer, MD
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Olaf Bodamer is an expert in the field of Medical Genetics. He graduated from Baylor College of Medicine. He over the years received 1 awards: "CMS Meaningful Use Stage 1 Certification". Olaf Bodamer is also a published doctor. He has 101 paper published. The most recent paper is: Importance of measuring plasma cholesterol precursors. Olaf Bodamer accepts Medicare.
Publications
- Liver, Pancreas and Kidney Transplantation for the Treatment of Wolcott-Rallison Syndrome.
- Bridging the Gaps Between the Histopathological and Demographic Risk Factors of Preterm Birth in a Unique Miami Inner-City Population.
- Phenylketonuria Scientific Review Conference: State of the science and future research needs.
- Subfertility and growth restriction in a new galactose-1 phosphate uridylyltransferase (GALT) - deficient mouse model.
- Diagnosing lysosomal storage disorders: fabry disease.
- Effects of Creatine Supplementation in Rett Syndrome: A Randomized, Placebo-Controlled Trial.
- Low levels of asymmetric dimethylarginine in children with diabetes mellitus type I compared with healthy children.
- The identification of novel mutations in the biotinidase gene using denaturing high pressure liquid chromatography (dHPLC).
- Transcobalamin II deficiency at birth.
- Screening for X-linked creatine transporter (SLC6A8) deficiency via simultaneous determination of urinary creatine to creatinine ratio by tandem mass-spectrometry.
- Development and evaluation of quality control dried blood spot materials in newborn screening for lysosomal storage disorders.
- Newborn screening for Pompe disease by measuring acid alpha-glucosidase activity using tandem mass spectrometry.
- Heparin cofactor II-thrombin complex: a biomarker of MPS disease.
- Total homocysteine, B-vitamins and genetic polymorphisms in patients with classical phenylketonuria.
- Newborn screening in Fabry disease: what can be achieved with early diagnosis?
- Trisomy 1q42.3-qter and monosomy 21q22.3-qter associated with ear anomaly, facial dysmorphology, psychomotor retardation, and epilepsy: delineation of a new syndrome.
- Manifestation of hawkinsinuria in a patient compound heterozygous for hawkinsinuria and tyrosinemia III.
- Long-term stability of amino acids and acylcarnitines in dried blood spots.
- Evidence for an association between mannose-binding lectin 2 (MBL2) gene polymorphisms and pre-term birth.
- Prenatal and postnatal treatment in cobalamin C defect.
- Central nervous system malformations in oral-facial-digital syndrome, type 1.
- Creatine metabolism in combined methylmalonic aciduria and homocystinuria.
- Mucopolysaccharidosis type II in females: case report and review of literature.
- Use of denaturing HPLC to provide efficient detection of mutations causing familial hypercholesterolemia.
- L-alanine supplementation in late infantile glycogen storage disease type II.
- Denaturing gradient gel electrophoresis for the molecular characterization of six patients with guanidinoacetate methyltransferase deficiency.
- Practical management of combined methylmalonicaciduria and homocystinuria.
- B4GALT1-congenital disorders of glycosylation presents as a non-neurologic glycosylation disorder with hepatointestinal involvement.
- Mutation analysis in 54 propionic acidemia patients.
- The role of enzyme replacement therapy in severe Hunter syndrome-an expert panel consensus.
- Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease.
- Propionic acidemia: neonatal versus selective metabolic screening.
- Early access experience with VPRIV(®): recommendations for 'core data' collection.
- Molecular analysis of guanidinoacetate-n-methyltransferase (GAMT) and creatine transporter (SLC6A8) gene by using denaturing high pressure liquid chromatography (DHPLC...
- Lysosomal storage diseases: diagnostic confirmation and management of presymptomatic individuals.
- Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency.
- Magnetic resonance spectroscopy in patients with Fabry and Gaucher disease.
- Semi-quantitative method for determination of hematocrit in dried blood spots, using data collected in HPLC hemoglobin variant testing.
- Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation.
- Newborn screening for Fabry disease by measuring GLA activity using tandem mass spectrometry.
- Laboratory and genetic evaluation of Gaucher disease.
- Importance of surgical history in diagnosing mucopolysaccharidosis type II (Hunter syndrome): data from the Hunter Outcome Survey.
- Analysis of glucocerebrosidase activity in dry blood spots using tandem mass spectrometry.
- Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters.
- A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia.
- Rapid and accurate denaturating high performance liquid chromatography protocol for the detection of alpha-l-iduronidase mutations causing mucopolysaccharidosis type I.
- Guidelines for the restart of imiglucerase in patients with Gaucher disease: recommendations from the European Working Group on Gaucher disease.
- Low creatinine: the diagnostic clue for a treatable neurologic disorder.
- Introduction of a novel prototype bioartificial liver support system utilizing small human hepatocytes in rotary culture.
- Diagnostic work-up and management of patients with isolated methylmalonic acidurias in European metabolic centres.
- Methylation status in females with rett syndrome.
- Metabolic changes in the normal ageing brain: consistent findings from short and long echo time proton spectroscopy.
- Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy.
- Methods for a prompt and reliable laboratory diagnosis of Pompe disease: report from an international consensus meeting.
- Comparison of tetrahydrofuran and ethyl acetate as extraction solvents for urinary organic acid analysis.
- Severe speech delay as the presenting symptom of guanidinoacetate methyltransferase deficiency.
- Expanded newborn screening in Europe 2007.
- Screening for leukemia- and clone-specific markers at birth in children with T-cell precursor ALL suggests a predominantly postnatal origin.
- Prevalence of congenital adrenal hyperplasia among sudden infant death in the Czech Republic and Austria.
- Glucose and leucine kinetics in idiopathic ketotic hypoglycaemia.
- Influence of hematocrit and localisation of punch in dried blood spots on levels of amino acids and acylcarnitines measured by tandem mass spectrometry.
- Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency.
- Use of denaturing HPLC to provide efficient detection of mutations causing guanidinoacetate methyltransferase deficiency.
- Familial complex chromosomal rearrangement resulting in a recombinant chromosome.
- Variant Gaucher disease characterized by dysmorphic features, absence of cardiovascular involvement, laryngospasm, and compound heterozygosity for a novel mutation (D4...
- Diagnosing lysosomal storage disorders: mucopolysaccharidosis type i.
- Microarray-based detection of mannose-binding lectin 2 (MBL2) polymorphisms in a routine clinical setting.
- Lack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome?
- Utilization of cornstarch in glycogen storage disease type Ia.
- Reversibility of cirrhotic regenerative liver nodules upon NTBC treatment in a child with tyrosinaemia type I.
- Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism.
- Homocystinuria due to cystathionine beta-synthase deficiency: novel biochemical findings and treatment efficacy.
- Hypoketotic hypofattyacidaemic hypoinsulinaemic hypoglycaemia in a child with hemihypertrophy? A new syndrome.
- Characterization of seven novel mutations in seven patients with GAMT deficiency.
- Recurrent acroparaesthesia during febrile infections.
- Fabry disease defined.
- Nuclear magnetic resonance spectroscopy in glutaryl-CoA dehydrogenase deficiency.
- Rapid analysis of total plasma homocysteine by tandem mass spectrometry.
- Intermittent maple syrup disease.
- Medicine in Germany.
- H2-breath tests--importance of adequate storage of breath samples.
- Assessment of energy expenditure in metabolic disorders.
- Diagnosing Lysosomal Storage Disorders: Mucopolysaccharidosis Type II.
- Measurement of glucose turnover--implications for the study of inborn errors of metabolism.
- Dietary treatment in late-onset acid maltase deficiency.
- Protein turnover in critically ill children.
- Stable isotope studies in inborn errors of metabolism--implications and conclusions.
- Leucine and glucose kinetics in glycogen storage disease type IIIa.
- Increased resting energy expenditure in glycogen storage disease type Ia.
- Effects of fish oil supplementation on apolipoprotein B100 production and lipoprotein metabolism in normolipidaemic males.
- Importance of measuring plasma cholesterol precursors.
- Sublingual therapy for cobalamin deficiency.
- Psychiatric symptoms of inherited metabolic disease.
- Protein, glucose and energy metabolism in Gaucher disease type I.
- Deletion (9) (p13.1 p21.1).
- Resting energy expenditure in disorders of propionate metabolism.
- Measurement of carbon dioxide production in very low birth weight babies.
- The effects of l-alanine supplementation in late-onset glycogen storage disease type II.
- Subdural hematomas and glutaric aciduria type I.
- Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria.
Doctors Specialties
- Clinical Genetics
- Medical Biochemical Genetics
- Medical Genetics
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Blue Card PPO
- Blue Care HMO
- BlueDental Choice
- NetworkBlue
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- LocalPlus
- Open Access Plus
- Employer Group PPO
- Choice Care PPO
- Preferred PPO
- Select HMO
- MultiPlan PPO
- PHCS Network PPO
- Choice Plus POS
- Navigate HMO
- Neighborhood Health Partnership
Awards
- CMS Meaningful Use Stage 1 Certification
Education
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Baylor College of Medicine -
Ruprecht Karl University Faculty of Medicine
Hospital
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University of Miami Hospital
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1487958146 |
| Last Name Of The Provider | BODAMER |
| First Name Of The Provider | OLAF |
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