Forbes D Porter, M.D.
Rare Disease Specialist
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Bethesda, Maryland
PI on 14 trials
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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.
- Creatine deficiency syndrome
- Batten Disease
- Congenital Malformation Syndrome
- Niemann-Pick disease type C
- Chronic visceral acid sphingomyelinase deficiency
- Primary progressive aphasia
- Semantic dementia
- Desmosterolosis
- Frontotemporal dementia
- CHILD syndrome
- Juvenile CLN3 disease
- Interatrial communication
- Fragile X syndrome
- Lysosomal disease
- Congenital deformities of limbs
- Greenberg dysplasia
- Congenital limb malformation
- Smith-Lemli-Opitz syndrome
- Primary progressive apraxia of speech
- Langerhans cell histiocytosis
- Lipid storage disease
- Non-Langerhans cell histiocytosis
- Genetic congenital limb malformation
- Sphingolipidosis
- CLN3 disease
- KID syndrome
- Congenital ichthyosiform erythroderma
- X-linked creatine transporter deficiency
- Lathosterolosis
Clinical trials (14)
Verify independently
Other specialists for Creatine deficiency syndrome
Peers ranked by clinical-trial PI role, publications, and verification quality.
- Michael Stevenson, MDOklahoma Blood Institute
- Tuan Le, MDOklahoma Blood Institute
- David Hoover, MDICON plc
- Sergej M Ostojic, MD, PhDCenter for Health, Exercise and Sport Sciences
- Morris Schambelan, MD, MDUniversity of California, San Francisco; San Francisco General HospitalCA
- Kathleen Mulligan, PhDUniversity of California, San Francisco; San Francisco General Hospital
- S Andreas, Prof. DrGeorg-August-Universität, Göttingen, Department of Cardiology and Pneumology, Robert-Koch Str. 40, 37075 Göttingen, Germany
- Eduardo Tibirica, MD, PhDNational Institute of Cardiology