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- Clinical Trial (66)
- Demography (33)
- Eligibility Determination (17)
- Laboratories (16)
- Pharmacogenetics (15)
- Clinical Trial, Phase III (15)
- Hepatitis B (15)
- Consent Forms (12)
- Vaccination (11)
- Adverse event (10)
- Hepatitis B Vaccines (7)
- On-Study Form (7)
- Physical Examination (6)
- Cohort Studies (6)
- Haemophilus influenzae type b (6)
- Gastroenterology (6)
- Hepatitis A (6)
- Influenza Vaccines (6)
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- Vaccines (5)
- Clinical Trial, Phase I (5)
- Clinical Trial, Phase II (5)
- Follow-Up Studies (5)
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- Diphtheria-Tetanus-acellular Pertussis Vaccines (4)
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- HIV (4)
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- Diphtheria-Tetanus-Pertussis Vaccine (3)
- Pneumococcal Vaccines (3)
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- Diabetes Mellitus, Type 2 (3)
- Internal Medicine (3)
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- Pharmacokinetics (2)
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- Clinical Trial, Phase IV (2)
- Malaria Vaccines (2)
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- Meningococcal Vaccines (2)
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- Neisseria meningitidis (2)
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- Philadelphia Chromosome (1)
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- Randomized Controlled Trial (1)
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- Blood Pressure (1)
- Ventricular Dysfunction, Left (1)
- Simvastatin (1)
- Heart Valve Prosthesis Implantation (1)
- Clinical Chemistry Tests (1)
- Substance-Related Disorders (1)
- Breast Neoplasms (1)
- Streptococcal Vaccines (1)
- Measles-Mumps-Rubella Vaccine (1)
- Pulmonary Disease, Chronic Obstructive (1)
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Itemgroep: t1.visitlog
t1.referenz
1 Itemgroep 9 Data-elementent1.medhist
1 Itemgroep 11 Data-elementent1.weather
1 Itemgroep 21 Data-elementent1.intro
1 Itemgroep 58 Data-elementen Itemgroepen: Patient Information, Subsequent consent, Withdrawal of consent
Itemgroep: welcome, informed, consent
Itemgroep: welcome, informed, consent
Itemgroep: final discussion, criticism
Itemgroep: internal medicine consent
Itemgroep: internal medicine consent
Itemgroepen: Administrative data, Date of Visit/Assessment, PGx Research Consent
Itemgroepen: Administrative data, Date of Visit/Assessment, PGx Research Withdrawal of Consent
Itemgroep: final discussion, criticism
Itemgroep: Study termination
Itemgroepen: Informed Consent for the long-term follow-up, Administrative, Statement by Doctor, Nurse or Project Assistant who conducted the informed consent discussion: