arginine and Symptom Cluster

Topics: Ammonia; Animals; Arginine; Biological Transport; Brain; Cell Membrane; Humans; Hyperammonemia; Hyperinsulinism; Liver; Liver Diseases; Pyruvate Carboxylase Deficiency Disease; Syndrome; Urea; Urologic Diseases; Valproic Acid

Topics: Arginase; Arginine; Cytokines; Deficiency Diseases; Humans; Macrophages; Phosphotransferases; Signal Transduction; Syndrome; T-Lymphocytes

Topics: Arginine; Blood Flow Velocity; Chest Pain; Coronary Circulation; Diagnosis, Differential; Endothelium, Vascular; Female; Hemorheology; Humans; Hyperhomocysteinemia; Inflammation; Male; Microvessels; Myocardial Ischemia; Nitric Oxide; Platelet Activation; Syndrome; Vascular Resistance; Vasodilator Agents

Topics: Anemia, Hemolytic; Anemia, Sickle Cell; Arginine; Biological Availability; Humans; Hypertension, Pulmonary; Nitric Oxide; Prognosis; Pulmonary Wedge Pressure; Syndrome; Vasodilator Agents

Topics: Angioplasty, Balloon, Coronary; Arginine; Clinical Trials as Topic; Coronary Disease; Fibrinolytic Agents; Heparin; Hirudin Therapy; Hirudins; Humans; Myocardial Infarction; Peptide Fragments; Pipecolic Acids; Recombinant Proteins; Sulfonamides; Syndrome; Thrombin; Thrombolytic Therapy

Topics: Anticoagulants; Arginine; Binding Sites; Heparin; Hirudins; Humans; Models, Biological; Pipecolic Acids; Recombinant Proteins; Sulfonamides; Syndrome; Thrombin; Thrombocytopenia; Treatment Outcome

Topics: Adult; Arginine; Arthritis, Juvenile; Body Height; Collagen Type II; Cysteine; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Lumbar Vertebrae; Middle Aged; Mutation; Osteoarthritis; Scoliosis; Syndrome

Topics: Acute Disease; Angioplasty, Balloon, Coronary; Anticoagulants; Arginine; Atrial Fibrillation; Azetidines; Benzylamines; Clinical Trials as Topic; Coronary Disease; Heparin; Hirudins; Humans; Myocardial Infarction; Peptide Fragments; Pipecolic Acids; Recombinant Proteins; Sulfonamides; Syndrome; Thrombin; Thromboembolism; Thrombosis; Venous Thrombosis

Topics: Animals; Apoptosis; Arginine; Cardiovascular Diseases; Cellular Senescence; Endothelium, Vascular; Glycation End Products, Advanced; Humans; Hyperhomocysteinemia; Kidney Diseases; Models, Biological; Oxidative Stress; Syndrome

Topics: Administration, Oral; Anticoagulants; Arginine; Critical Care; Drug Monitoring; Enzyme-Linked Immunosorbent Assay; Heparin; Hirudins; Humans; International Normalized Ratio; Nurse's Role; Nursing Assessment; Partial Thromboplastin Time; Patient Selection; Pipecolic Acids; Platelet Count; Practice Guidelines as Topic; Recombinant Proteins; Risk Factors; Sulfonamides; Syndrome; Thrombocytopenia; Time Factors

Topics: Algorithms; Angioplasty, Balloon, Coronary; Anticoagulants; Arginine; Chondroitin Sulfates; Comorbidity; Dermatan Sulfate; Drug Therapy, Combination; Fibrinolytic Agents; Fondaparinux; Heparin; Heparinoids; Heparitin Sulfate; Hirudins; Humans; Myocardial Infarction; Peptide Fragments; Pipecolic Acids; Polysaccharides; Recombinant Proteins; Sulfonamides; Syndrome; Thrombocytopenia; Vitamin K

Topics: Acute Disease; Angina Pectoris; Angina, Unstable; Angioplasty, Balloon, Coronary; Anticoagulants; Arginine; Fondaparinux; Hemorrhage; Heparin; Heparin, Low-Molecular-Weight; Hirudins; Humans; Models, Molecular; Molecular Structure; Myocardial Ischemia; Peptide Fragments; Pipecolic Acids; Platelet Activation; Polysaccharides; Recombinant Proteins; Sulfonamides; Syndrome; Thrombin; Thrombosis

Topics: Antibodies; Antithrombins; Arginine; Heparin; Humans; Pipecolic Acids; Sulfonamides; Syndrome; Thrombocytopenia; Thrombosis

Topics: Adolescent; Adult; Amino Acid Sequence; Amino Acid Substitution; Arginine; Base Sequence; Cytosine; Epithelial Cells; Female; Genes, Dominant; Humans; Hypertension; Molecular Sequence Data; Mutagenesis, Insertional; Pedigree; Peptide Fragments; Sodium Channels; Syndrome; Water-Electrolyte Imbalance

Topics: Anticoagulants; Antithrombins; Arginine; Hemostasis; Heparin; Humans; Models, Biological; Pipecolic Acids; Selectins; Sulfonamides; Syndrome; Thrombocytopenia

Topics: Angina, Unstable; Arginine; Coronary Angiography; Fibrinolytic Agents; Heparin; Humans; Metalloendopeptidases; Myocardial Infarction; Pipecolic Acids; Platelet Aggregation Inhibitors; Randomized Controlled Trials as Topic; Sulfonamides; Survival Rate; Syndrome; Thrombolytic Therapy; Tissue Plasminogen Activator

Topics: Acute Disease; Angina, Unstable; Angioplasty, Balloon, Coronary; Animals; Anticoagulants; Antithrombins; Arginine; Azetidines; Benzylamines; Fibrinolytic Agents; Glycine; Hirudin Therapy; Hirudins; Humans; Myocardial Infarction; Peptide Fragments; Pipecolic Acids; Platelet Aggregation Inhibitors; Rabbits; Recombinant Proteins; Sulfonamides; Syndrome; Thrombin; Thromboembolism; Thrombosis; Time Factors

Topics: Arginine; Fatty Acids; Gastrointestinal Diseases; Glutamine; Humans; Nutritional Status; Pectins; Syndrome

Topics: Acidosis; Amino Acids; Ammonia; Animals; Arginine; Brain; Brain Diseases; Chemical and Drug Induced Liver Injury; Citrulline; Dementia; Homeostasis; Humans; Infant, Newborn; Liver; Lysine; Metabolism, Inborn Errors; Ornithine Carbamoyltransferase; Phosphotransferases; Succinates; Syndrome; Urea; Urease

Topics: Angina Pectoris; Arginine; Blood Pressure; Coronary Angiography; Cyclic GMP; Endothelin-1; Endothelium, Vascular; Female; Forearm; Humans; Infusions, Intravenous; Insulin; Male; Middle Aged; Nitric Oxide; Regional Blood Flow; Syndrome

Topics: Abnormalities, Multiple; Adolescent; Adult; Amino Acid Substitution; Arginine; Child; Child, Preschool; Facial Paralysis; Female; Fibrosis; Histidine; Humans; Infant; Male; Mutation; Ophthalmoplegia; Peripheral Nervous System Diseases; Syndrome; Tubulin; Young Adult

Topics: Arginine; Chromatography, High Pressure Liquid; Creatine; Guanidinoacetate N-Methyltransferase; Humans; Syndrome; Tandem Mass Spectrometry

Topics: Arginine; Cell Nucleolus; Frameshift Mutation; HMGB1 Protein; Humans; Intrinsically Disordered Proteins; Phase Transition; Syndrome

Topics: Adolescent; Amino Acid Substitution; Antigens, CD; Arginine; China; Female; Glutamine; Heterozygote; Humans; Hyperandrogenism; Insulin Resistance; Metabolic Syndrome; Mutation, Missense; Protein-Tyrosine Kinases; Receptor, Insulin; Syndrome

Topics: Amino Acid Substitution; Arginine; Autoimmune Diseases; cdc42 GTP-Binding Protein; Cysteine; Humans; Inflammation; Lipoylation; Mutation, Missense; Palmitic Acid; Syndrome

Topics: Aged; Arginine; Cerebrovascular Circulation; Cerebrovascular Disorders; Cranial Irradiation; Humans; Male; Middle Aged; Migraine Disorders; Radiation Injuries; Stroke; Syndrome

Topics: Arginine; Biomarkers; Coronary Disease; Humans; Odds Ratio; Recurrence; Risk Factors; ROC Curve; Syndrome

Topics: Amino Acid Substitution; Animals; Arginine; Child; Developmental Disabilities; Drinking; Epilepsy; Humans; Hyperglycemia; Male; Models, Molecular; Mutation, Missense; Potassium Channels, Inwardly Rectifying; Proline; Rats; Rats, Wistar; Syndrome

Topics: Anticoagulants; Antithrombins; Arginine; Carcinoma, Squamous Cell; Drug Substitution; Female; Heparin; Humans; International Normalized Ratio; Mandibular Neoplasms; Middle Aged; Mouth Mucosa; Pipecolic Acids; Prothrombin Time; Sulfonamides; Syndrome; Thrombocytopenia; Thrombosis; Treatment Failure; Warfarin

Topics: Aged; Ammonia; Arginine; Biomarkers; Carnitine; Combined Modality Therapy; Decontamination; Female; Humans; Hyperammonemia; Immunosuppressive Agents; Lung Transplantation; Male; Middle Aged; Missouri; Phenylacetates; Protective Agents; Renal Dialysis; Retrospective Studies; Sodium Benzoate; Syndrome; Time Factors; Treatment Outcome; Up-Regulation

Topics: Alanine; Animals; Arginine; Arrhythmias, Cardiac; Calcium; Calcium Channels, L-Type; Calcium Channels, N-Type; Calcium Channels, R-Type; Cation Transport Proteins; Cognition Disorders; Genotype; Glutamic Acid; Glycine; GTP-Binding Proteins; Ion Channel Gating; Kinetics; Membrane Potentials; Mutation; Phenotype; Rats; Syndrome; Valine; Xenopus

Topics: Adult; Arginine; Arginine Vasopressin; DNA Mutational Analysis; Exons; Humans; Hyponatremia; Inappropriate ADH Syndrome; Kidney Diseases; Male; Mutation; Mutation, Missense; Receptors, Vasopressin; Seizures; Syndrome

Topics: Abnormalities, Multiple; Adolescent; Adult; Amino Acid Substitution; Arginine; Child; Child Behavior Disorders; Communication; Humans; Male; Mediator Complex; Mental Retardation, X-Linked; Receptors, Thyroid Hormone; Social Behavior Disorders; Socialization; Syndrome; Tryptophan; Young Adult

Topics: Amino Acid Substitution; Anesthetics, Inhalation; Arginine; Carnitine O-Palmitoyltransferase; Child, Preschool; Cysteine; Female; Genetic Predisposition to Disease; Halothane; Heterozygote; Humans; Malignant Hyperthermia; Metabolism, Inborn Errors; Mutation; Neuromuscular Depolarizing Agents; Risk Factors; Succinylcholine; Syndrome

Topics: 3' Untranslated Regions; Abnormalities, Multiple; Adenine; Arginine; Cleft Lip; Cleft Palate; Cohort Studies; Cytosine; Exons; Female; Genetic Variation; Genotype; Guanine; Heterozygote; Homozygote; Humans; India; Interferon Regulatory Factors; Introns; Male; Open Reading Frames; Point Mutation; Sequence Analysis, DNA; Serine; Syndrome; Thymine

Topics: Arginine; Brain; Brain Diseases; Cerebellum; Cysteine; Diffuse Cerebral Sclerosis of Schilder; Diffusion Magnetic Resonance Imaging; Disease Progression; DNA Polymerase gamma; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Electroencephalography; Energy Metabolism; Epilepsy; Glycine; Humans; Magnetic Resonance Angiography; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mitochondrial Diseases; Mutation; Neocortex; Sensitivity and Specificity; Spinocerebellar Ataxias; Stroke; Syndrome; Thalamus; Tomography, X-Ray Computed

Topics: Acrocephalosyndactylia; Adenoviridae; Alkaline Phosphatase; Animals; Arginine; Biomarkers; Cell Differentiation; Cell Proliferation; Cells, Cultured; Coculture Techniques; Coloring Agents; Core Binding Factor Alpha 1 Subunit; Craniofacial Dysostosis; Craniosynostoses; Cysteine; Dura Mater; Genetic Vectors; Mice; Osteoblasts; Osteogenesis; Osteopontin; Phenylalanine; Point Mutation; Receptor, Fibroblast Growth Factor, Type 2; Syndrome; Tetrazolium Salts; Thiazoles

Topics: Alleles; Animals; Arginine; Argininosuccinate Synthase; Blotting, Western; Cell Movement; Cerebellum; Citrullinemia; Developmental Disabilities; Disease Models, Animal; Female; Growth Disorders; Humans; Hyperammonemia; Immunoenzyme Techniques; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Mutant Strains; Mutation, Missense; Nitric Oxide; Phenotype; Sodium Benzoate; Syndrome

Topics: Amino Acid Metabolism, Inborn Errors; Animals; Animals, Suckling; Arginase; Arginine; B-Lymphocytes; Growth Hormone; Hair Diseases; Hypoglycemia; Insulin-Like Growth Factor I; Mechanistic Target of Rapamycin Complex 1; Mice; Mice, Knockout; Multiprotein Complexes; Muscular Diseases; Protein Serine-Threonine Kinases; Proteins; Signal Transduction; Syndrome; TOR Serine-Threonine Kinases

Topics: Abnormalities, Multiple; Arginine; Child; Child, Preschool; Egypt; Female; Founder Effect; Heterozygote; Humans; Lamin Type A; Leucine; Mandible; Mutation, Missense; Pedigree; Polymorphism, Restriction Fragment Length; Progeria; Protein Stability; Syndrome

Topics: Aged; Arginine; Female; Fondaparinux; Heparin; Humans; Immunoenzyme Techniques; Inflammation; Pipecolic Acids; Platelet Factor 4; Polysaccharides; Sulfonamides; Syndrome; Thrombocytopenia; Treatment Outcome

Topics: Acute Disease; Anticoagulants; Arginine; Catheterization; Catheterization, Central Venous; Coated Materials, Biocompatible; Female; Heparin; Humans; Middle Aged; Pipecolic Acids; Pulmonary Embolism; Radionuclide Imaging; Sulfonamides; Syndrome; Thrombocytopenia; Thromboembolism; Tomography, X-Ray Computed; Ultrasonography

Topics: Adult; Arginine; B-Lymphocytes; CD40 Ligand; Child, Preschool; Consanguinity; Cytidine Deaminase; DNA Mutational Analysis; Female; Histidine; Humans; Hypergammaglobulinemia; Immunoglobulin Class Switching; Immunoglobulin M; Infant; Japan; Male; Middle Aged; Mutation; Siblings; Somatic Hypermutation, Immunoglobulin; Syndrome

Topics: Angioplasty, Balloon, Coronary; Anticoagulants; Arginine; Cardiac Catheterization; Coronary Stenosis; Coronary Thrombosis; Follow-Up Studies; Heparin; Humans; Male; Middle Aged; Myocardial Infarction; Pipecolic Acids; Radiography; Risk Assessment; Sulfonamides; Syndrome; Thrombocytopenia; Treatment Outcome

Topics: Arginine; Aspartic Acid; Biomedical Research; Confusion; Drug Therapy; Electroconvulsive Therapy; Flavin Mononucleotide; Geriatrics; Intracranial Arteriosclerosis; Memory; Mental Disorders; Nucleotides; RNA; Syndrome

Topics: Adolescent; Arginine; Base Sequence; Biopsy; DNA; Eunuchism; Fertility; Gene Amplification; Genitalia, Male; Humans; Isoleucine; Luteinizing Hormone, beta Subunit; Male; Mutation; Osmolar Concentration; Polymerase Chain Reaction; Syndrome; Testis; Testosterone; Threonine; Tryptophan

Topics: Adolescent; Age Factors; Arginine; Blood Pressure; Body Constitution; Body Mass Index; Body Weight; Female; Genotype; Heterozygote; Humans; Hypertension; Male; Obesity; Polymorphism, Genetic; Receptors, Adrenergic, beta-3; Sex Factors; Syndrome; Tryptophan

Topics: Arginine; Bone and Bones; Craniosynostoses; Facies; Female; Genes, Dominant; History, 20th Century; Humans; Infant, Newborn; Mutation; Penetrance; Proline; Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Syndrome; Tomography, X-Ray Computed

Topics: Arginine; Cardiomyopathies; Chromosomes, Human, X; Fatal Outcome; Glutarates; Glycine; Humans; Infant, Newborn; Male; Muscular Diseases; Mutation; Mutation, Missense; Pedigree; Syndrome

Topics: Arginine; Female; Humans; Hypogonadism; Male; Mental Retardation, X-Linked; Obesity; Pedigree; Point Mutation; Syndrome

Topics: 5' Untranslated Regions; Abnormalities, Multiple; Anodontia; Arginine; Base Sequence; Cleft Lip; Cleft Palate; DNA; DNA Primers; DNA-Binding Proteins; Electrophoresis, Polyacrylamide Gel; Exons; Family Health; Female; Genes, Dominant; Glycine; Heterozygote; Humans; Interferon Regulatory Factors; Male; Molecular Sequence Data; Mouth Abnormalities; Mutation; Pedigree; Penetrance; Phenotype; Promoter Regions, Genetic; Protein Structure, Tertiary; Sequence Analysis, DNA; Syndrome; Transcription Factors; Turkey

Topics: Adenine; Adolescent; Adult; Amino Acid Substitution; Arginine; Child; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 11; Cranial Nerves; Female; Fibrosis; Genes, Recessive; Genetic Variation; Glutamine; Guanine; Humans; Kinesins; Male; Mobius Syndrome; Mutation; Nerve Tissue Proteins; Oculomotor Muscles; Ophthalmoplegia; Pedigree; Phenotype; Scoliosis; Syndrome

Topics: Abnormalities, Multiple; Adenosine Triphosphatases; Amino Acid Substitution; Arginine; Bone and Bones; Child; Cytosine; Diarrhea; DNA Helicases; Glutamine; Growth Disorders; Guanine; Humans; Joint Dislocations; Limb Deformities, Congenital; Male; Mutation; Mutation, Missense; Palate; Patella; Radius; RecQ Helicases; Rothmund-Thomson Syndrome; Syndrome; Thymine

Topics: Adolescent; Amino Acid Substitution; Arginine; Child; Child, Preschool; Craniosynostoses; Craniotomy; Female; Heterozygote; Humans; Intracranial Hypertension; Male; Point Mutation; Proline; Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Reoperation; Retrospective Studies; Syndrome

Topics: Arginine; Child; DNA Mutational Analysis; Female; Glycine; Humans; Infant; Lamin Type A; Lamins; Male; Muscle Proteins; Muscle Weakness; Muscular Dystrophies; Mutation; Neck Muscles; Selenoproteins; Syndrome

Topics: Abnormalities, Multiple; Adolescent; Adult; Arginine; Bile Ducts, Intrahepatic; Body Height; Bone and Bones; Cardiovascular Abnormalities; Child; Child, Preschool; Cholestasis; Endocrine System; Female; Fibrosis; Follow-Up Studies; Growth Disorders; Growth Hormone; Humans; Intellectual Disability; Male; Ornithine; Osteoporosis; Syndrome; Testis

Topics: Acrocephalosyndactylia; Adolescent; Amino Acid Substitution; Arginine; Child, Preschool; Ear; Hearing Loss, Sensorineural; Humans; Intellectual Disability; Intracranial Pressure; Mutation; Nuclear Proteins; Pedigree; Proline; Receptor, Fibroblast Growth Factor, Type 3; Repetitive Sequences, Nucleic Acid; Syndrome; Synostosis; Twist-Related Protein 1

Topics: Abnormalities, Multiple; Arginine; Cleft Lip; Cleft Palate; DNA-Binding Proteins; Ectodermal Dysplasia; Female; Genes, Tumor Suppressor; Genotype; Humans; Immunohistochemistry; Infant, Newborn; Male; Mutation, Missense; Phenotype; Phosphoproteins; Proline; Skin; Syndrome; Trans-Activators; Transcription Factors; Tumor Suppressor Proteins

Topics: Acrocephalosyndactylia; Adenine; Adolescent; Arginine; Child, Preschool; Craniofacial Dysostosis; Craniosynostoses; Cysteine; Cytosine; DNA Transposable Elements; Female; Follow-Up Studies; Guanine; Humans; Male; Mutation; Receptor, Fibroblast Growth Factor, Type 2; Sequence Deletion; Serine; Syndrome; Thymine; Treatment Outcome; Tryptophan; Twist-Related Protein 1

Topics: Alanine Transaminase; Amino Acid Transport Systems, Basic; Arginine; Aspartate Aminotransferases; Child, Preschool; Citrulline; Diet, Protein-Restricted; Hepatitis; Humans; Hyperammonemia; Liver; Male; Metabolism, Inborn Errors; Mitochondrial Membrane Transport Proteins; Ornithine; Proteins; Syndrome

Topics: Abnormalities, Multiple; Adult; Arginine; Child; Ectodermal Dysplasia; Female; Genes, Tumor Suppressor; Humans; Limb Deformities, Congenital; Male; Middle Aged; Mutation, Missense; Phenotype; Syndrome; Tooth Abnormalities; Transcriptional Activation

Topics: Alleles; Amino Acid Sequence; Amino Acid Substitution; Arginine; Codon, Terminator; Cold Temperature; Cytokines; Humans; Hyperhidrosis; Ligands; Male; Middle Aged; Molecular Sequence Data; Mutation; Receptor, Ciliary Neurotrophic Factor; Sweating; Syndrome

Topics: Arginine; Diagnosis, Differential; Electrolytes; Female; Humans; Hyperkalemia; Hypertension; Middle Aged; Nitric Oxide; Pseudohypoaldosteronism; Syndrome

Topics: Amino Acid Substitution; Arginine; Family; Female; Genetic Diseases, X-Linked; Humans; Intellectual Disability; Male; Mediator Complex; Muscle Hypotonia; Mutation; Pedigree; Receptors, Thyroid Hormone; Syndrome; Tryptophan

Topics: Arginine; Cleft Lip; Cleft Palate; Cohort Studies; Environment; Exons; Genes, Dominant; Genetic Predisposition to Disease; Genotype; Humans; Interferon Regulatory Factors; Leg; Lip; Mutation; Phenotype; Polymorphism, Single Nucleotide; Syndrome

Topics: Amino Acid Substitution; Arginine; Chi-Square Distribution; Cranial Sutures; Craniosynostoses; Facial Asymmetry; Female; Humans; Imaging, Three-Dimensional; Infant; Male; Mutation, Missense; Proline; Receptor, Fibroblast Growth Factor, Type 3; Severity of Illness Index; Sex Ratio; Statistics, Nonparametric; Syndrome; Tomography, X-Ray Computed

Topics: Abnormalities, Multiple; Adult; Arginine; Child, Preschool; Cleft Lip; Cleft Palate; DNA-Binding Proteins; Ectodermal Dysplasia; Female; Fingers; Genotype; Glutamine; Humans; Infant; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Syndrome; Trans-Activators; Transcription Factors; Tumor Suppressor Proteins; Urination Disorders

Topics: Abnormalities, Multiple; Adult; Amino Acid Substitution; Anal Canal; Arginine; Asian People; Female; Homeodomain Proteins; Humans; Korea; Male; Mutation; Pedigree; Rectum; Sacrum; Syndrome; Transcription Factors; Tryptophan

Topics: Arginine; Blood Platelets; GATA1 Transcription Factor; Genes, X-Linked; Glutamine; Humans; Mutation; Syndrome; Terminology as Topic; Thalassemia; Thrombocytopenia

Topics: Abnormalities, Multiple; Arginine; Base Sequence; Cell Line; Cell Proliferation; Child; Child, Preschool; Codon; DNA Mutational Analysis; Guanosine Diphosphate; Humans; Hydrolysis; Infant; Infant, Newborn; Lysine; Molecular Sequence Data; Mutant Proteins; Mutation; Proto-Oncogene Proteins p21(ras); Syndrome

Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Arginine; Case-Control Studies; Conserved Sequence; Diseases in Twins; DNA Helicases; DNA-Binding Proteins; Female; Genes, Dominant; Genetic Variation; Humans; Male; Molecular Sequence Data; Mosaicism; Mutation, Missense; Pedigree; Sequence Analysis, DNA; Sequence Homology, Amino Acid; Siblings; Syndrome; Twins, Monozygotic

Topics: Adult; Arginine; Carcinoma, Hepatocellular; Citrulline; Female; Glutamine; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver Neoplasms; Ornithine; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Polymorphism, Single-Stranded Conformational; Syndrome

Topics: Acanthosis Nigricans; Adolescent; Arginine; C-Peptide; Diabetes Complications; Diabetes Mellitus; Glucose Tolerance Test; Humans; Insulin Resistance; Islets of Langerhans; Male; Proinsulin; Receptor, Insulin; Syndrome

Topics: Amino Acid Sequence; Androgens; Arginine; Base Sequence; Cell Line; Disorders of Sex Development; DNA Primers; Humans; Leucine; Male; Molecular Sequence Data; Protein Binding; Receptors, Androgen; Syndrome; Transfection

Topics: Animals; Arginine; Base Sequence; Chromosomes, Human, Pair 11; Disorders of Sex Development; DNA-Binding Proteins; Exons; Female; Gene Deletion; Genes, Tumor Suppressor; Gonadal Dysgenesis; Hernia, Diaphragmatic; Heterozygote; Histidine; Homozygote; Humans; Infant, Newborn; Kidney Glomerulus; Mice; Mice, Transgenic; Molecular Sequence Data; Ovary; Point Mutation; Syndrome; Transcription Factors; WT1 Proteins

Topics: Arginine; Disorders of Sex Development; Exons; Histidine; Humans; Male; Mutation; Receptors, Androgen; Syndrome

Topics: Animals; Arginine; Blood Pressure; Cardiac Output; Dogs; Endotoxins; Escherichia coli Infections; Hemodynamics; Nitric Oxide; omega-N-Methylarginine; Oxygen Consumption; Syndrome; Vascular Resistance

Topics: Androgen-Insensitivity Syndrome; Androgens; Arginine; Base Sequence; Cells, Cultured; Child, Preschool; DNA; Exons; Female; Fibroblasts; Histidine; Hot Temperature; Humans; Infant; Male; Molecular Sequence Data; Pedigree; Point Mutation; Receptors, Androgen; Restriction Mapping; Syndrome

Topics: Animals; Arginine; Behavior, Animal; Cosyntropin; Enzyme Inhibitors; Grooming; Male; NG-Nitroarginine Methyl Ester; Nitric Oxide; Nitric Oxide Synthase; Penile Erection; Rats; Rats, Wistar; Syndrome; Yawning

Topics: Animals; Arginine; Capillary Permeability; Female; Interleukin-2; Kidney; Mice; Mice, Inbred C3H; NG-Nitroarginine Methyl Ester; Nitric Oxide; Pleural Effusion; Pulmonary Edema; Survival Analysis; Syndrome

Topics: Adult; Antithrombin III; Antithrombins; Arginine; Cerebral Infarction; Dementia; Factor V; Female; Fibrinogen; Humans; Male; Migraine Disorders; Peptide Hydrolases; Pipecolic Acids; Sneddon Syndrome; Sulfonamides; Syndrome

Topics: Aged; Angioplasty, Balloon, Coronary; Arginine; Coronary Angiography; Coronary Disease; Female; Heparin; Humans; Myocardial Infarction; Pipecolic Acids; Platelet Aggregation Inhibitors; Stents; Sulfonamides; Syndrome; Thrombocytopenia; Thrombosis

Topics: Adult; Alleles; Arginine; Diabetes Mellitus, Type 2; DNA; DNA Primers; Exons; Female; Finland; Gene Frequency; Genetic Predisposition to Disease; Humans; Insulin Resistance; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Receptors, Adrenergic, beta; Receptors, Adrenergic, beta-3; Syndrome; Tryptophan

Topics: Arginine; Brain; Creatine; Humans; Liver; Magnetic Resonance Spectroscopy; Metabolic Diseases; Muscle, Skeletal; Syndrome

Topics: Arginine; Base Sequence; Chromosomes, Human, Pair 11; Consanguinity; DNA; Female; Genes, Recessive; Genetic Linkage; Genetics, Population; Haplotypes; Hearing Loss, Sensorineural; Humans; Male; Middle East; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Syndrome; Tryptophan; Vestibular Diseases; Vision Disorders

Topics: Arginine; Body Mass Index; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genotype; Glucose Tolerance Test; Humans; Insulin; Insulin Resistance; Male; Mexican Americans; Middle Aged; Mutation; Obesity; Receptors, Adrenergic, beta; Receptors, Adrenergic, beta-3; Syndrome; Texas; Tryptophan

Topics: Amino Acid Substitution; Arginine; Child; Female; Glycine; Hearing Disorders; Humans; Piebaldism; Point Mutation; Pregnancy; Proto-Oncogene Mas; Proto-Oncogene Proteins c-kit; Syndrome

Topics: Aged; Anticoagulants; Antithrombins; Arginine; Carotid Arteries; Carotid Stenosis; Catheterization; Cerebrovascular Disorders; Femoral Artery; Follow-Up Studies; Heparin; Humans; Male; Paresis; Pipecolic Acids; Platelet Aggregation Inhibitors; Recurrence; Stents; Sulfonamides; Syndrome; Thrombocytopenia; Thrombosis

Topics: Abnormalities, Multiple; Adolescent; Arginine; Craniosynostoses; DNA Mutational Analysis; Female; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Infant; Male; Pedigree; Point Mutation; Proline; Protein-Tyrosine Kinases; Radiography; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Syndrome

Topics: Adult; Arginine; Craniosynostoses; Female; Humans; Infant; Proline; Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Syndrome

Topics: Animals; Arginine; Dose-Response Relationship, Drug; Endorphins; GABA Modulators; Nitric Oxide; Pain; Pain Measurement; Penicillin G; Rats; Spinal Cord; Syndrome

Topics: Adult; Arginine; Bartter Syndrome; Carrier Proteins; Chromosome Aberrations; Chromosome Disorders; Codon; Cysteine; DNA Mutational Analysis; Electrolytes; Exons; Female; Genes, Recessive; Humans; Kidney Function Tests; Male; Mutation, Missense; Pedigree; Sodium Chloride Symporters; Symporters; Syndrome

Topics: Alleles; Amino Acid Substitution; Arginine; Asian People; China; Genes, Recessive; Germ-Line Mutation; Glutamine; Humans; Mucopolysaccharidosis VI; Mutation, Missense; N-Acetylgalactosamine-4-Sulfatase; Syndrome; Taiwan

Topics: Adult; Aged; Arginine; Biomarkers; Cardiovascular Diseases; Chromatography, High Pressure Liquid; Citrulline; Female; Humans; Hyperglycemia; Hyperlipidemias; Hypertension; Male; Mass Spectrometry; Middle Aged; Nitric Oxide; Obesity; Risk Factors; Syndrome

Topics: Adolescent; Adult; Arginine; Breath Tests; Child; Ciliary Motility Disorders; Cystic Fibrosis; Female; Humans; Infusions, Intravenous; Male; Nitric Oxide; Syndrome

Topics: Acute Disease; Arginine; Case-Control Studies; Humans; Nitric Oxide; Prospective Studies; Sickle Cell Trait; Syndrome; Vascular Diseases

Topics: Adult; Arginine; Biological Transport; Carrier Proteins; Chromosomes, Human, Pair 7; Disease Progression; DNA Mutational Analysis; Evoked Potentials, Auditory, Brain Stem; Female; Goiter; Hearing Loss, Sensorineural; Histidine; Humans; Magnetic Resonance Imaging; Membrane Transport Proteins; Mutation, Missense; Sulfate Transporters; Syndrome; Time Factors; Vestibular Aqueduct

Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Arginine; Carrier Proteins; Child; Endolymphatic Duct; Endolymphatic Sac; Female; Goiter; Hearing Loss, Sensorineural; Heterozygote; Histidine; Homozygote; Humans; Iodides; Iodine; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Mutation; Mutation, Missense; Phenotype; RNA Splicing; Sequence Analysis, DNA; Sulfate Transporters; Syndrome; Thyroglobulin; Vestibular Aqueduct

Topics: Adult; Arginine; Child, Preschool; Craniosynostoses; Facies; Family Health; Female; Humans; Klippel-Feil Syndrome; Male; Mutation; Pedigree; Point Mutation; Proline; Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Shoulder; Syndrome

Topics: Acute Disease; Adolescent; Anemia, Sickle Cell; Arginine; Breath Tests; Child; Citrulline; Forced Expiratory Volume; Genotype; Humans; Lung Diseases; Nitrates; Nitric Oxide; Nitric Oxide Synthase; Nitric Oxide Synthase Type I; Nitrites; Polymorphism, Genetic; Syndrome; Trinucleotide Repeats; Vital Capacity

Topics: Adult; Arginine; Bromocriptine; Child; Dwarfism; Female; Glucose; Growth Hormone; Humans; Kinetics; Male; Somatostatin; Syndrome; Thyroxine; Triiodothyronine

Topics: Arginine; Blood Glucose; Cyclic AMP; Female; Glucagon; Growth Hormone; Humans; Hypertension; Insulin; Mandelic Acids; Metanephrine; Middle Aged; Propranolol; Receptors, Adrenergic; Receptors, Adrenergic, beta; Syndrome; Vascular Diseases

Topics: Adenoma, Islet Cell; Aged; Alanine; Anemia; Arginine; Chromatography, Gel; Erythema; Glossitis; Glucagon; Glucose Tolerance Test; Glycosuria, Renal; Humans; Hypoglycemia; Insulin; Male; Nicotinic Acids; Pancreatic Neoplasms; Somatostatin; Syndrome

Topics: Adult; Anthropometry; Arginine; Clomiphene; Estrogens; Eunuchism; Female; Follicle Stimulating Hormone; Gonadotropin-Releasing Hormone; Growth Hormone; Humans; Hypogonadism; Insulin; Luteinizing Hormone; Olfaction Disorders; Physical Examination; Radioimmunoassay; Syndrome; Thyrotropin

Topics: Aged; Amino Acids; Arginine; Blood Glucose; Female; Glucagon; Glucose; Glucose Tolerance Test; Humans; Insulin; Male; Middle Aged; Pancreatic Neoplasms; Somatostatin; Syndrome

Topics: Abnormalities, Multiple; Arginine; Child; Consanguinity; Electromyography; Eyelid Diseases; Female; Genes, Recessive; Growth Hormone; Humans; Insulin; Muscular Dystrophies; Pedigree; Syndrome

Topics: Arginine; Base Sequence; Codon; Cystine; Deoxyribonucleases, Type II Site-Specific; DNA; Drug Resistance; Genetic Linkage; Humans; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Proto-Oncogene Proteins; Receptors, Thyroid Hormone; Syndrome; Thyroid Hormones; Triiodothyronine

Topics: Adenoma, Islet Cell; Arginine; Diagnostic Errors; Glucagon; Glucagonoma; Humans; Lymphatic Metastasis; Male; Middle Aged; Pancreatic Neoplasms; Skin Diseases; Syndrome

Topics: Amino Acids; Ammonia; Arginine; Aspartic Acid; Child; Female; Glutamates; Glutamic Acid; Humans; Intellectual Disability; Male; Movement Disorders; Polyamines; Syndrome; Urea

Topics: Acromegaly; Adolescent; Arginine; Child; Growth; Growth Hormone; Humans; Insulin; Radioimmunoassay; Radioligand Assay; Receptors, Somatotropin; Recombinant Proteins; Syndrome

Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Child, Preschool; Citrulline; Creatine; Female; Humans; Lysine; Male; Ornithine; Orotic Acid; Syndrome

Topics: Ammonia; Animals; Arginine; Blood Pressure; Cardiac Output; Dogs; Evoked Potentials, Visual; Glycine; Halothane; Hemodynamics; Humans; Infusions, Parenteral; Male; Prostatectomy; Syndrome

Topics: Amino Acids; Ammonia; Arginine; Ataxia; Blood Urea Nitrogen; Child, Preschool; Chromatography, Paper; Cystine; Electroencephalography; Epilepsy, Tonic-Clonic; Female; Hair; Humans; Intellectual Disability; Metabolism, Inborn Errors; Stress, Mechanical; Succinates; Syndrome

Topics: Animals; Arginine; Carcinoma, Squamous Cell; Centrifugation; Chromatography, Gel; Cytoplasm; Microsomes; Neoplasm Proteins; Neoplasms, Experimental; Protein Binding; Rats; Syndrome

Topics: Adult; Aged; Alcoholism; Arginine; Blood Glucose; Fatty Liver; Female; Glucose Tolerance Test; Growth Hormone; Humans; Insulin; Insulin Secretion; Liver Cirrhosis; Male; Middle Aged; Potassium; Potassium Chloride; Potassium Deficiency; Potassium Isotopes; Radioimmunoassay; Syndrome

Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Diet Therapy; Growth Disorders; Humans; Intellectual Disability; Intestinal Absorption; Kidney Concentrating Ability; Lysine; Male; Protein Biosynthesis; Syndrome; Urea

Topics: Child, Preschool; Erythrocytes; Female; Histiocytes; Humans; Infant; Lymphatic Diseases; Lymphocytes; Male; Phagocytosis; Podophyllotoxin; Syndrome; Teniposide