Oleg A Shchelochkov, M.D., MD
Rare Disease / Clinical Research
National Human Genome Research Institute (NHGRI)
IOWA CITY, IA
PI on 1 trialNPI: 1841434537
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Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.
Report missing dataRare diseases treated or studied
Based on trial PI assignments and publication topics.
- Deficiency of adenosine deaminase 2
- X-linked spasticity-intellectual disability-epilepsy syndrome
- Hyper-IgM syndrome type 5
- Adenosine monophosphate deaminase deficiency
- Postaxial acrofacial dysostosis
- Beta-ureidopropionase deficiency
- Phosphoribosylpyrophosphate synthetase superactivity
- Dihydropyrimidinuria
- Pontocerebellar hypoplasia type 2
- Cerebral malformation with epilepsy
- Charcot-Marie-Tooth disease type 1
- Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy
- Hereditary xanthinuria
- X-linked Charcot-Marie-Tooth disease
- X-linked intellectual disability-epilepsy syndrome
- Lesch-Nyhan syndrome
- Sneddon syndrome
- X-linked Charcot-Marie-Tooth disease type 5
- Acrofacial dysostosis
- Pontocerebellar hypoplasia type 1
- Lethal ataxia with deafness and optic atrophy
- X-linked Charcot-Marie-Tooth disease type 1
- Pontocerebellar hypoplasia type 11
- Hereditary spastic paraplegia
- Xanthinuria type I
- Hereditary motor and sensory neuropathy type 5
- Hereditary orotic aciduria
- Adenylosuccinate lyase deficiency
- Pontocerebellar hypoplasia type 5
- Purine nucleoside phosphorylase deficiency