12 studies found for:    neural tube defects | NIH
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Study Details
Participant Details
Identifiers
Dates
Rank Status Study
1 Completed Genetic Analysis of Neural Tube and Orofacial Cleft Defects in the Irish Population
Conditions: Neural Tube Defects (NTDs);   Facial Cleft Defect
Intervention:
2 Unknown  Study of Genetic Risk Factors for Spina Bifida and Anencephaly
Conditions: Spina Bifida;   Anencephaly
Intervention: Other: No Intervention
3 Completed Follow-up Study of Late Effects of Periconceptional Folic Acid in Mothers and Offspring in the Community Intervention Program Population: The Chinese Children and Families Study
Conditions: Pediatric Leukemia;   Other Pediatric Cancers
Intervention:
4 Completed Influence of Genetics on Vitamin Metabolism in Pregnant Women
Conditions: Pregnancy;   Birth Defects
Intervention:
5 Active, not recruiting Psychosocial Adjustment of Adolescents With Spina Bifida
Condition: Spina Bifida
Intervention:
6 Withdrawn Nerve Rerouting Treatment for Neurogenic Bladder in Spina Bifida
Condition: Spina Bifida
Intervention: Procedure: Nerve Rerouting
7 Recruiting Mutations in Genes Associated With Pentalogy of Cantrell or Non-Muscle Myosin II Syndromes
Conditions: Inborn Genetic Diseases;   Pentalogy of Cantrell
Intervention:
8 Enrolling by invitation dbGaP Protocol: Genetic Variants Associated With Pentalogy of Cantrell
Condition: Pentalogy of Cantrell
Intervention:
9 Recruiting A Prospective Natural History Study of Patients With Syringomyelia
Conditions: Syringomyelia;   Arnold Chiari Deformity
Intervention:
10 Recruiting Genetic Analysis of the Chiari I Malformation
Conditions: Syringomyelia;   Type I Arnold Chiari Malformation
Intervention:
11 Completed Establishing the Physiology of Syringomyelia
Conditions: Arnold Chiari Deformity;   Hydrocephalus;   Syringomyelia
Intervention:
12 Recruiting UAB HRFD Core Center: Core A: The Hepato/Renal Fibrocystic Diseases Translational Resource
Conditions: Hepato/Renal Fibrocystic Disease;   Autosomal Recessive Polycystic Kidney Disease;   Joubert Syndrome;   Bardet Biedl Syndrome;   Meckel-Gruber Syndrome;   Congenital Hepatic Fibrosis;   Caroli Syndrome;   Oro-Facial-Digital Syndrome Type I;   Nephronophthisis;   Glomerulocystic Kidney Disease
Intervention:

Indicates status has not been verified in more than two years