Biennial and Annual Report on the Rare Diseases Research Activities at the National Institutes of Health FY 2004

Index Terms

Abetalipoproteinemia
Acoustic Neuroma
Acquired Aplastic Anemia
Additional Human Genome Resources
Advanced Sleep Phase Syn
Advanced Sleep Phase Syndrome
Alagille Syndrome
Alcoholic Pancreatitis
Alcohol-Induced Hepatic Fibrosis
Alpha-1 Antitrypsin Deficiency
Alzheimer’s Disease
Amebiasis
Amyloidosis
Amyotrophic Lateral Sclerosis
Anabaptist Diseases
Anthrax
Antiphospholipid Syndrome (APS)
Aripiprazole
Arrhythmogenic Right Ventricular Dysplasia
Asbestosis
Ataxia-telangiectasia
Atomoxetine
Auditory Neuropathy
Autoimmune Diseases
Autoimmune Lymphoproliferative Syndrome
Baclofen
Bartter's Syndrome
Behçet's disease
Bench-to-Bedside Intramural Research Awards
Beta-Sitosterolemia
Bladder Cancer
Botulism
Bronchopulmonary Dysplasia
Brugada’s Syndrome
Bupropion
Cabergoline
Cannabis-Related Disorders
Carcinoma of the Vocal Tract
Childhood Acute Lymphoblastic Leukemia
Childhood-onset Schizophrenia
Cholera
Cholesteryl Ester Storage Disease
Choline Supplementation
Chromosome 18q deletion syndrome
Chronic Fatigue Syndrome
Chronic Granulomatous Disease
Cleft Lip/Cleft Palate
Cocaine
Cocaine Addiction Treatment
Coffin-Lowry Syndrome
Combined Health Information Database
Congenital Central Hypoventilation Syndrome
Congenital Diaphragmatic Hernia
Congenital Disorders of Glycosylation
Congenital Heart Defects
Congenital Heart Disease
Cooley’s Anemia
Craniosynostosis
Creutzfeldt-Jakob Disease
Crohn’s Disease
Crohn’s Diseases
Cryptococcosis
Cystic Fibrosis
Database of the Major Histocompatibility Complex
Dengue
Dentin Dysplasia
Depot Naltrexone
Developmental Disorders
Diagnostic Testing
Diamond-Blackfan Anemia and Other Congenital Bone Marrow Failure Syndromes: Underlying Molecular Mechanisms
DiGeorge Syndrome
Disorders of Vision
Disulfiram
Dopamine Agonists
Drug Addiction
Drug-Drug Interactions
Dysbetalipoproteinemia
Dyssegmental Dysplasia
Ebola
Endocrine Disorders
Enlarged Vestibular Aqueduct (EVA)
Epidermolysis Bullosa
Epilepsy
Epstein Barr Virus
Escherichia coli
Fabry Disease
Familial dysautonomia
Familial Hypobetalipoproteinemia
Fanconi anemia
Fetal Alcohol Syndrome
Fibromyalgia Syndrome
Fibrous Dysplasia of Bone
Gaucher Disease
GBR12909
Genetic Alliance
Genetic Analysis Software
Genetic and Rare Diseases Information Center
Genetic Disorders of Mucociliary Clearance Consortium
Giant-Cell Arteritis
Giardiasis
Glaucoma
Glioblastoma
Glucocorticoid and Corticotropin Releasing Factor (CRF) Antagonists
Graft-Versus-Host Disease
Grants
Growth Hormone Deficiency
Hemophilia
Hepatitis E Virus
Hereditary Cerebellar Ataxia Syndrome of Early Onset
Hereditary Hemorrhagic Telangiectasia
hereditary idiopathic pulmonary fibrosis
Hirschsprung Disease
Histoplasmosis capsulatum
HIV/AIDS and Aging
Homozygous Familial Hypercholesterolemia
Human Genetic Cell Repository
Huntington’s disease
Hypereosinophilic syndrome
Ichthyosis
Idiopathic Lung Fibrosis Clinical Research Network
Idiopathic Pulmonary Fibrosis
Immunology
Inherited Disorders of the Immune System
Irritable Bowel Syndrome
Job’s Syndrome
Juvenile Rheumatoid Arthritis
Kallmann Syndrome
Kaposi’s Sarcoma
Kappa Opioid Antagonists
Klinefelter’s Syndrome
Klippel-Trenaunay-Weber Syndrome
Krabbe Disease
Lecithin Cholesterol Acyltransferase Deficiency
Leishmaniasis
Liddle's Syndrome
Lipoprotein Lipase Deficiency
Liver Neoplasms
Lobeline
Long QT Syndrome
Lowe Oculocerebrorenal Syndrome
Lyme Disease
Lymphangioleiomyomatosis
Lymphedema
Lysosomal storage disorders
Malaria Genetics and Genomics
Marfan Syndrome
McCune-Albright Syndrome
Mercy Medical Airlift
Metabolic Disorders
Methamphetamine Addiction Treatment
Methylmalonic Acidemia and Related Disorders
Microphthalmia Syndromes
Modafinil
Mold-Related Health Effects
Mucolipidosis
Mucopolysaccharidosis
Multiple Endocrine Neoplasia Type 1
Muscular Dystrophies
Muscular Dystrophy
Myelodysplastic Syndromes
Myeloproliferative Disorders
Myositis
Narcolepsy
National Coalition for Health Professional Education in Genetics
National Council of La Raza’s Institute for Hispanic Health
Neurofibromatosis
Neurological Disorders
NHLBI Clinical Proteomics Programs
NHLBI Lung Tissue Resource
Niemann-Pick disease type C (NP-C)
Niemann-Pick Type C Disease
Non-Hodgkin’s Lymphoma
Nonsyndromic Deafness
Novel Approaches to Enhance Animal Stem Cell Research
Olfactory Function
Ondansetron
Opiate Addiction Treatment
Osteogenesis Imperfecta
Ovarian Cancer
Paroxysmal Nocturnal Hemoglobinuria
Pathogenesis of SARS Lung Disease
Pediatric Bipolar Disorder
Pediatric Mechanical Circulatory Support
Pendred Syndrome
Periventricular leukomalacia
Persistent Pulmonary Hypertension of the Newborn
Pertussis
Plague
Polycystic Kidney Disease
Polydactyly Syndromes
Polyglutamine Protein Inhibition of Proteosomes in Neurodegenerative Diseases
Primary Ciliary Dyskinesia
Primary Pulmonary Hypertension
Programs for Genomic Applications (PGAs) for Heart, Lung, and Blood Research
Programs of Excellence in Gene Therapy
Proteus Syndrome
Pseudoxanthoma Elasticum
pulmonary alveolar proteinosis
Pulmonary Vascular Disease
Q fever
Quetiapine
Rapid-onset dystonia parkinsonism
Rare Disease Research Initiatives
Rare Diseases Biospecimen Repositories
Rare Diseases Clinical Research Network
Rare Diseases: Exploratory and Developmental Research Grant
Rare Liver Diseases Consortium
Rare Thrombotic Diseases Consortium
Research Support
Reserpine
Resistance to Thyroid Hormone
Retinal degeneration
Retinitis Pigmentosa and Related Disorders
Rieger Syndrome
RPR
Sarcoidosis
Sarcoma
SARS Coronavirus Resource
Schwartz-Jampel Syndrome
Scleroderma
Selegiline
Severe Acute Respiratory Syndrome
Severe Combined Immunodeficiency
Sickle Cell Anemia
Sickle Cell Disease
Smallpox
Smith-Lemli-Opitz Syndrome
Spinal Bulbar Muscular Atrophy
Spinocerebellar ataxia type I
Squamous Cell Carcinomas of the Head and Neck
Stickler Syndrome
Streptoccus Group B
Streptococcal Group A Invasive Disease
Streptococcus pnemoniae
Suicide
Supravalvular Aortic Stenosis
syncope
Systemic Lupus Erythematosus
Tangier Disease
Temporomandibular Muscle and Joint Disorders
Thalassemia Clinical Research Network
The Human Genetic Map
Three-Dimensional Structure Database
Thrombotic Thrombocytopenic Purpura
Tiagabine
Tickborne Encephalitis Virus
Topiramate
Toxoplasmosis
Transmissible Spongiform Encephalopathies
Trans-NIH Rare Diseases Research Working Group
Trimethylaminuria
Tyrosinemia
Unstable DNA Repeats in Neurodegenerative Disorders
Usher Syndrome
Vanoxerine
Vasculitis Clinical Research Consortium
ventricular arrhythmias
Waardenburg Syndrome (WS)
Wegener’s Granulomatosis
West Nile Virus
William’s Syndrome

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Last Reviewed: July 22, 2005