Associate Professor, Pediatrics, Medical College of Wisconsin
Medical Genetics
Dr. David P. Dimmock, MD
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David P. Dimmock, MD practices Medical Genetics. He went to Baylor College of Medicine. David Dimmock is also published. He has 46 publications published. The lastest publication: "Potentially diagnostic electron paramagnetic resonance spectra elucidate the underlying mechanism of mitochondrial dysfunction in the deoxyguanosine kinase deficient r...' David Dimmock is registered with Medicare and accepts Medicare payments.
Publications
- Necrotizing Enterocolitis Is Not Associated With Sequence Variants in Antioxidant Response Genes in Premature Infants.
- Potentially diagnostic electron paramagnetic resonance spectra elucidate the underlying mechanism of mitochondrial dysfunction in the deoxyguanosine kinase deficient r...
- Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis.
- Successful immune tolerance induction to enzyme replacement therapy in CRIM-negative infantile Pompe disease.
- Guidelines for investigating causality of sequence variants in human disease.
- Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.
- Clinical decisions. Screening an asymptomatic person for genetic risk.
- Good laboratory practice for clinical next-generation sequencing informatics pipelines.
- SIGIRR genetic variants in premature infants with necrotizing enterocolitis.
- Long-term safety and efficacy of sapropterin: The PKUDOS registry experience.
- A novel FOXF1 mutation associated with alveolar capillary dysplasia and coexisting colobomas and hemihyperplasia.
- Ethical Issues in DNA Sequencing in the Neonate.
- Anti-Oxidant Response Genes sequence variants and BPD susceptibility in VLBW infants.
- Hypertrophic Cardiomyopathy: A New Mutation Illustrates the Need for Family-Centered Care.
- Long-term developmental progression in infants and young children taking sapropterin for phenylketonuria: a two-year analysis of safety and efficacy.
- In the absence of evidentiary harm, existing societal norms regarding parental authority should prevail.
- Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
- Practice patterns of mitochondrial disease physicians in North America. Part 2: treatment, care and management.
- Reduced Mitochondrial DNA Content and Heterozygous Nuclear Gene Mutations in Patients With Acute Liver Failure.
- Feasibility of adjunct therapeutic hypothermia treatment for hyperammonemia and encephalopathy due to urea cycle disorders and organic acidemias.
- Genomics in clinical practice: lessons from the front lines.
- Practice patterns of mitochondrial disease physicians in North America. Part 1: Diagnostic and clinical challenges.
- Whole genome sequencing: a considered approach to clinical implementation.
- Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes.
- Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study.
- Assuring the quality of next-generation sequencing in clinical laboratory practice.
- Recessive deoxyguanosine kinase deficiency causes juvenile onset mitochondrial myopathy.
- A personal perspective on returning secondary results of clinical genome sequencing.
- A timely arrival for genomic medicine.
- The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia.
- Abnormal neurological features predict poor survival and should preclude liver transplantation in patients with deoxyguanosine kinase deficiency.
- Correction of hyperbilirubinemia in gunn rats using clinically relevant low doses of helper-dependent adenoviral vectors.
- Quantitative evaluation of the mitochondrial DNA depletion syndrome.
- A novel c.592-4_c.592-3delTT mutation in DGUOK gene causes exon skipping.
- Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutations.
- Novel human pathological mutations. Gene symbol: ASS1. Disease: Citrullinaemia.
- De novo mutations in POLG presenting with acute liver failure or encephalopathy.
- Simultaneous detection of mitochondrial DNA depletion and single-exon deletion in the deoxyguanosine gene using array-based comparative genomic hybridisation.
- Citrin deficiency, a perplexing global disorder.
- Utility of oligonucleotide array-based comparative genomic hybridization for detection of target gene deletions.
- Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.
- Citrin deficiency: a novel cause of failure to thrive that responds to a high-protein, low-carbohydrate diet.
- Whole exome and whole genome sequencing.
- Next-generation Sequencing Facilitates the Diagnosis in a Child With Twinkle Mutations Causing Cholestatic Liver Failure.
- Real-time quantitative PCR analysis of mitochondrial DNA content.
Schools
St Georges Hospital Medical School
St Josephs Hospital
Baylor College Of Medicine
Doctors Specialties
- Medical Genetics
- Pediatrics
Accepted Insurances
- Choice Plus POS II
- Anthem Blue Cross Blue Shield HMO
- Anthem Blue Cross Blue Shield PPO
- Blue Preferred Plus POS
- Blue Card PPO
- Blue Cross Blue Shield of Illinois PPO
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Commercial Insurance Company
- CoreSource
- Choice Care PPO
- Medicare MCR
- Molina
- MultiPlan
- Pekin Insurance
- Principal Life
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
- Wisconsin Physicians Service
Education
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Baylor College of Medicine -
St Joseph's Hospital and Medical Center -
St. George's Hospital Medical School
Hospital
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Children's Hospital of Wisconsin -
Froedtert Memorial Lutheran Hospital
Drug Facts
| NPI NUMBER | 1275796419 | |
| NPPES Provider LastName | DIMMOCK | |
| NPPES Provider FirstName | DAVID | |
| NPPES Provider ZIPCode | 532264874 | |
| NPPES Provider State | WI | |
| Specialty Description | Pediatric Medicine | |
| Total Claim Count | 12.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1275796419 |
| Last Name Of The Provider | DIMMOCK |
| First Name Of The Provider | DAVID |
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