Dr. Owen Murray Rennert M.D.
Pediatrician
10 CENTER DRIVE NIH BETHESDA MD, 20892About
Dr. Owen Rennert is a pediatrician practicing in BETHESDA, MD. Dr. Rennert is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Rennert diagnoses and treats infections, injuries, diseases and other disorders in children. Pediatricians typically work with infants, children, teenagers and young adults up to age 21. They practice medical care as well as preventative health care. Dr. Rennert can oversee and manage the physical, mental and emotional health of their patients.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Polyamine distribution in cellular compartments of blood and in aging erythrocytes.
- Severe skeletal complications in Japanese patients with type 1 Gaucher disease.
- Polymorphisms in the coding exons of the human luteinizing hormone receptor gene. Mutations in brief no. 124. Online.
- Case report on SHORT syndrome.
- Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutation.
- Congenital adrenal hyperplasia: molecular genetics and alternative approaches to treatment.
- Update on the genetics and pathophysiology of type I diabetes mellitus.
- Neurochemical abnormality in I-cell disease: chemical analysis and a possible importance of beta-galactosidase deficiency.
- Neurochemical abnormality in I-cell disease: chemical analysis and a possible importance of beta-galactosidase deficiency.
- Luteinizing hormone receptor mutations in disorders of sexual development and cancer.
- Serotypes and antibiotic susceptibilities of Pseudomonas aeruginosa isolates from single sputa of cystic fibrosis patients.
- Serotypes and antibiotic susceptibilities of Pseudomonas aeruginosa isolates from single sputa of cystic fibrosis patients.
- Effects of enzyme replacement therapy in thirteen Japanese paediatric patients with Gaucher disease.
- Gitelman's syndrome (familial hypokalemia-hypomagnesemia).
- Penicillamine in prevention of symptomatic Wilson's disease: 8 year follow up in two sibs.
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