Syndrome - Page 3

Molde de látex natural (Hevea brasiliensis) para neovaginoplastia

Adolescent / Humans / Female / Young Adult / Hevea brasiliensis / Patient Satisfaction / Vagina / Adult / Retrospective Studies / Hevea / Equipment Design / Syndrome / Patient Satisfaction / Vagina / Adult / Retrospective Studies / Hevea / Equipment Design / Syndrome

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Cirrhotic cardiomyopathy

Hepatology / Electrocardiography / Humans / Portal hypertension / Liver Cirrhosis / Animals / Calcium Signaling / Liver Transplantation / Fibrosis / Clinical Sciences / Nitric Oxide Synthase / Myocardium / Public health systems and services research / Baroreflex / Nervous System / Cardiomyopathies / Syndrome / Cardiac failure / The American / Animals / Calcium Signaling / Liver Transplantation / Fibrosis / Clinical Sciences / Nitric Oxide Synthase / Myocardium / Public health systems and services research / Baroreflex / Nervous System / Cardiomyopathies / Syndrome / Cardiac failure / The American

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Cirrhotic Cardiomyopathy

Hepatology / Electrocardiography / Humans / Portal hypertension / Liver Cirrhosis / Animals / Calcium Signaling / Liver Transplantation / Fibrosis / Clinical Sciences / Nitric Oxide Synthase / Myocardium / Public health systems and services research / Baroreflex / Nervous System / Cardiomyopathies / Syndrome / Cardiac failure / The American / Animals / Calcium Signaling / Liver Transplantation / Fibrosis / Clinical Sciences / Nitric Oxide Synthase / Myocardium / Public health systems and services research / Baroreflex / Nervous System / Cardiomyopathies / Syndrome / Cardiac failure / The American

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[Tumor necrosis factor receptor associated periodic syndrome (TRAPS). Report of two cases]

Genetics / Rheumatology / Immunology / Inflammation / Adolescent / Biological Sciences / DNA / Osteoporosis / Humans / Child / Mutation / Haplotypes / Female / Male / Alternative splicing / Monoclonal Antibodies / Netherlands / Fever of Unknown Origin / Differential Diagnosis / Pedigree / Phenotype / Ethnic Groups / Skin Diseases / Recurrence / Clinical Sciences / Alendronate / Introns / Middle Aged / Family Health / Adult / Fever / Public health systems and services research / Immunophenotyping / Combination drug therapy / Alternative Splicing / Amino Acid Sequence / Base Sequence / Syndrome / Amyloidosis / immunoglobulin G / Familial Mediterranean Fever / Etanercept / Biological Sciences / DNA / Osteoporosis / Humans / Child / Mutation / Haplotypes / Female / Male / Alternative splicing / Monoclonal Antibodies / Netherlands / Fever of Unknown Origin / Differential Diagnosis / Pedigree / Phenotype / Ethnic Groups / Skin Diseases / Recurrence / Clinical Sciences / Alendronate / Introns / Middle Aged / Family Health / Adult / Fever / Public health systems and services research / Immunophenotyping / Combination drug therapy / Alternative Splicing / Amino Acid Sequence / Base Sequence / Syndrome / Amyloidosis / immunoglobulin G / Familial Mediterranean Fever / Etanercept

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Embolia Cutis Medicamentosa (Nicolau Syndrome) after Endodontic Treatment: A Case Report

Dentistry / Rare diseases / Case Report / Humans / Female / Male / Follow-up studies / Mandible / Maxilla / Aged / Endodontics / Adult / Necrosis / Hypesthesia / Calcium Hydroxide / Thrombosis / Root Canal Filling Materials / Iatrogenic Disease / X ray Computed Tomography / Syndrome / Embolism / Foreign Bodies / Orbit / Chin / Male / Follow-up studies / Mandible / Maxilla / Aged / Endodontics / Adult / Necrosis / Hypesthesia / Calcium Hydroxide / Thrombosis / Root Canal Filling Materials / Iatrogenic Disease / X ray Computed Tomography / Syndrome / Embolism / Foreign Bodies / Orbit / Chin

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C1 inhibitor deficiency: consensus document

Immunology / Adolescent / Genetic Engineering / Pregnancy / Humans / Child / Female / Animals / Clinical / Male / Adult / Dental Care / Emergencies / Gastrointestinal Tract / Angioedema / New Products / Syndrome / Child / Female / Animals / Clinical / Male / Adult / Dental Care / Emergencies / Gastrointestinal Tract / Angioedema / New Products / Syndrome

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Mouse autosomal trisomy: two’s company, three’s a crowd

Genetics / Down Syndrome / Biological Sciences / Pregnancy / Humans / Mice / Female / Animals / Male / Pregnancy Loss / Trisomy 21 / Syndrome / Mice / Female / Animals / Male / Pregnancy Loss / Trisomy 21 / Syndrome

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Brain-derived neurotrophic factor gene val66met polymorphism and executive functioning in patients with bipolar disorder Polimorfismo do gene do fator neurotrófico derivado do cérebro val66met e função executiva em pacientes com transtorno bipolar

Engineering / Genetics / Demography / Physics / Chemistry / Bipolar Disorder / Polymorphism / Cognition / Biology / Cognitive Dissonance / Brazil / Adolescent / Medicine / Multidisciplinary / Executive Function / Brain / Humans / Female / Male / Obsessive Compulsive Disorder / American / Endothelial dysfunction / Vasoconstriction / Phenotype / PLoS one / Cognitive Performance / Clinical Sciences / Middle Aged / Gene Polymorphism / Genotype / Wisconsin Card Sorting Test / Adult / Methionine / Genetic Polymorphism / Reproducibility of Results / European Continental Ancestry Group / Amino Acid Substitution Rates / Syndrome / Neurosciences / Middle Cerebral Artery / Allele Frequency / Cognition disorders / Magnetic resonance angiography / Bipolar Disorder / Polymorphism / Cognition / Biology / Cognitive Dissonance / Brazil / Adolescent / Medicine / Multidisciplinary / Executive Function / Brain / Humans / Female / Male / Obsessive Compulsive Disorder / American / Endothelial dysfunction / Vasoconstriction / Phenotype / PLoS one / Cognitive Performance / Clinical Sciences / Middle Aged / Gene Polymorphism / Genotype / Wisconsin Card Sorting Test / Adult / Methionine / Genetic Polymorphism / Reproducibility of Results / European Continental Ancestry Group / Amino Acid Substitution Rates / Syndrome / Neurosciences / Middle Cerebral Artery / Allele Frequency / Cognition disorders / Magnetic resonance angiography

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Familial Syndromic Esophageal Atresia Maps to 2p23-p24

Biological Sciences / Humans / Mice / Female / Animals / Male / Netherlands / Pedigree / Phenotype / Molecular cloning / Fluorescent in situ hybridization / Base Sequence / Syndrome / The American / Male / Netherlands / Pedigree / Phenotype / Molecular cloning / Fluorescent in situ hybridization / Base Sequence / Syndrome / The American

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Serum Complement C3/C4 Ratio, a Novel Marker for Recurrent Cardiovascular Events

Survival Analysis / Finland / Humans / Female / Male / Follow-up studies / Risk factors / Recurrence / Aged / Middle Aged / Myocardial Infarction / Coronary heart disease / Analysis of Variance / Biological markers / Risk Factors / Sensitivity and Specificity / Syndrome / Proportional Hazards Models / Logistic Models / Cerebral Infarction / Follow-up studies / Risk factors / Recurrence / Aged / Middle Aged / Myocardial Infarction / Coronary heart disease / Analysis of Variance / Biological markers / Risk Factors / Sensitivity and Specificity / Syndrome / Proportional Hazards Models / Logistic Models / Cerebral Infarction

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Jerusalem Syndrome or Paranoid Schizophrenia?

Israel / Delusions / Travel / Humans / Differential Diagnosis / Religion and psychology / Public health systems and services research / Psychiatric Services / Psychiatric / Syndrome / Religion and psychology / Public health systems and services research / Psychiatric Services / Psychiatric / Syndrome

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Is developmental dyslexia a disconnection syndrome?

Phonetics / Dyslexia / Developmental dyslexia / Brain / Humans / Male / Single Photon Emission Computed Tomography / Adult / Short Term Memory / Neural pathways / Reference Values / Syndrome / Male / Single Photon Emission Computed Tomography / Adult / Short Term Memory / Neural pathways / Reference Values / Syndrome

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Universal grammar in the frontotemporal dementia spectrum

Psychology / Cognitive Science / Semantics / Dementia / Aphasia / Working Memory / Language Impairment / Neurodegenerative Diseases / Temporal Lobe / Humans / Sentence Comprehension / Cerebral Cortex / Universal grammar / Differential Diagnosis / Aged / Middle Aged / Spectrum / Analysis of Variance / Frontotemporal Dementia / Neuropsychologia / Basal ganglia / Reference Values / Alzheimer Disease / Syndrome / Neurosciences / Frontal Lobe / Case Control Studies / Working Memory / Language Impairment / Neurodegenerative Diseases / Temporal Lobe / Humans / Sentence Comprehension / Cerebral Cortex / Universal grammar / Differential Diagnosis / Aged / Middle Aged / Spectrum / Analysis of Variance / Frontotemporal Dementia / Neuropsychologia / Basal ganglia / Reference Values / Alzheimer Disease / Syndrome / Neurosciences / Frontal Lobe / Case Control Studies

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Global developmental delay, osteopenia and ectodermal defect: A new syndrome

Genetics / Social Problems / Intellectual Disability / Brain development / Biopsy / Mental Retardation / Brain / Humans / Child / Genetic Testing / Female / Male / Developmental disabilities / Central Nervous System / Siblings / Skin / Melanocytes / Developmental delay / Syndrome / Sweat glands / Keratins / Mental Retardation / Brain / Humans / Child / Genetic Testing / Female / Male / Developmental disabilities / Central Nervous System / Siblings / Skin / Melanocytes / Developmental delay / Syndrome / Sweat glands / Keratins

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Endothelial NO Synthase Polymorphisms and Postural Tachycardia Syndrome

Genetics / Polymorphism / Adolescent / Cardiovascular disease / Humans / Hypertension / Blood Pressure / Nitric oxide / Female / Male / Heart rate / Threonine / D-Aspartic Acid / Posture / Norepinephrine / Clinical Sciences / Middle Aged / Genotype / Adult / Blood Flow / Genetic Polymorphism / Enzyme activity / Cysteine / Syndrome / Glutamic Acid / Confidence Interval / Tachycardia / Case Control Studies / Hypertension / Blood Pressure / Nitric oxide / Female / Male / Heart rate / Threonine / D-Aspartic Acid / Posture / Norepinephrine / Clinical Sciences / Middle Aged / Genotype / Adult / Blood Flow / Genetic Polymorphism / Enzyme activity / Cysteine / Syndrome / Glutamic Acid / Confidence Interval / Tachycardia / Case Control Studies

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Pulmonary Nontuberculous Mycobacterial Disease

Prospective studies / Humans / Mutation / Smoking / Female / Male / American / Risk factors / Phenotype / Aged / Middle Aged / Sex Factors / Scoliosis / Thinness / Risk Factors / Body Height / Syndrome / Prospective Study / Case Control Studies / Male / American / Risk factors / Phenotype / Aged / Middle Aged / Sex Factors / Scoliosis / Thinness / Risk Factors / Body Height / Syndrome / Prospective Study / Case Control Studies

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