Molecular Laboratory, HIBM Research Group (HRG)
Medical Genetics
Dr. Daniel K. Darvish, MD
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Daniel K. Darvish, MD practices Medical Genetics. He studied medicine at George Washington University School of Medicine. George Washington University School of Medicine has a rank of 67 in research and a 0 in primary care Daniel K. Darvish, MD is also a published doctor. He has 14 publication published. The most recent publication is: Hypertensive encephalopathy in an old man.
Publications
- Novel GNE Mutations in Autosomal Recessive Hereditary Inclusion Body Myopathy Patients.
- Prevalence of GNE p.M712T and hereditary inclusion body myopathy (HIBM) in Sangesar population of Northern Iran.
- Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.
- Single nucleotide polymorphisms in the dystroglycan gene do not correlate with disease severity in hereditary inclusion body myopathy.
- Limb-girdle muscular dystrophy in the United States.
- Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine.
- Validation of GNE:p.M712T identification by melting curve analysis.
- A case of hereditary inclusion body myopathy: 1 patient, 2 novel mutations.
- MTHFR C677T genotype frequency in patients of Middle Eastern descent as determined by real-time PCR and melting curve analysis.
- Preclinical assessment of wt GNE gene plasmid for management of hereditary inclusion body myopathy 2 (HIBM2).
- Novel GNE mutations in hereditary inclusion body myopathy patients of non-Middle Eastern descent.
- Wolman disease (LIPA p.G87V) genotype frequency in people of Iranian-Jewish ancestry.
- Hypertensive encephalopathy in an old man.
Schools
George Washington University School of Medicine And Health Sciences
Doctors Specialties
- Internal Medicine
- Medical Genetics
Accepted Insurances
Education
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Olive View - UCLA Medical Center -
George Washington University School of Medicine
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