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2 studies found for:    "Familial encephalopathy with neuroserpin inclusion bodies"
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Study Details
Participant Details
Identifiers
Dates
Rank Status Study
1 Enrolling by invitation Genetic Disease Gene Identification
Conditions: Congenital Vertical Talus;   Familial Encephalopathy With Neuroserpin Inclusion Bodies;   Idiopathic Generalised Epilepsy;   Familial Dementia;   X-Linked Mental Retardation
Intervention:
2 Completed Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion Bodies
Conditions: Familial Dementia With Neuroserpin Inclusion Bodies;   Nervous System Heredodegenerative Disorder
Intervention:

Indicates status has not been verified in more than two years