Clinical Presentation - Page 2

Internal Hernia as a Complication of Laparoscopic Roux-en-Y Gastric Bypass

Bariatric Surgery / Humans / Female / Male / Acute respiratory distress syndrome / Ct Scan / Obesity Surgery / Clinical Sciences / Middle Aged / Intestinal Obstruction / Adult / Public health systems and services research / Retrospective Studies / Gastric Bypass / Clinical Presentation / Abdominal Pain / Laparoscopy / Ct Scan / Obesity Surgery / Clinical Sciences / Middle Aged / Intestinal Obstruction / Adult / Public health systems and services research / Retrospective Studies / Gastric Bypass / Clinical Presentation / Abdominal Pain / Laparoscopy

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Factores de riesgo cardiovascular y estilo de vida asociados a la aparición prematura de infarto agudo de miocardio

Acute Myocardial Infarction / Risk factors / Risk Factors / Clinical Presentation

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Intramedullary non-specific inflammatory lesion of thoracic spine: A case report

Magnetic Resonance Imaging / Inflammation / Case Report / Humans / Female / Spinal Cord / Specification Tests / Differential Diagnosis / Clinical Sciences / Aged / Clinical Presentation / Spinal Cord / Specification Tests / Differential Diagnosis / Clinical Sciences / Aged / Clinical Presentation

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Endocarditis infecciosa: análisis retrospectivo en el Hospital Nacional Arzobispo

Infective Endocarditis / Clinical Presentation

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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ-oxidation

Nursing / Pediatrics / Treatment Outcome / Mitochondria / Pediatric nursing / Adolescent / Liver diseases / High Frequency / Heart Failure / Pregnancy / Humans / Child / Liver Cirrhosis / Liver / Mutation / Female / Male / Hypoglycemia / Fatty Acid Oxidation / Infant / Follow-up studies / Netherlands / Differential Diagnosis / HELLP Syndrome / Phenotype / Clinical Sciences / Newborn Infant / L-carnitine / Questionnaires / Optometry and Ophthalmology / Public health systems and services research / Survival Rate / Fatty Acid / Health surveys / Multienzyme complexes / Cardiomyopathies / Status Epilepticus / Base Sequence / Human Fibroblasts / Clinical Presentation / Clinical Signs / Antiepileptic Drug / Archivos Argentinos De Pediatria / Brain Damage / Age of Onset / Adolescent / Liver diseases / High Frequency / Heart Failure / Pregnancy / Humans / Child / Liver Cirrhosis / Liver / Mutation / Female / Male / Hypoglycemia / Fatty Acid Oxidation / Infant / Follow-up studies / Netherlands / Differential Diagnosis / HELLP Syndrome / Phenotype / Clinical Sciences / Newborn Infant / L-carnitine / Questionnaires / Optometry and Ophthalmology / Public health systems and services research / Survival Rate / Fatty Acid / Health surveys / Multienzyme complexes / Cardiomyopathies / Status Epilepticus / Base Sequence / Human Fibroblasts / Clinical Presentation / Clinical Signs / Antiepileptic Drug / Archivos Argentinos De Pediatria / Brain Damage / Age of Onset

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Erupciones de tipo micosis fungoide inducidas por carbamazepina

Polymorphism / Inflammatory disease / Malignant Lymphoma / Actas / Clinical Presentation / Mycosis Fungoides

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Human disease classification in the postgenomic era: A complex systems approach to human pathobiology

Genomics / Systems Biology / Complex System / Humans / Disease / Molecular systems biology / Human Disease / Clinical Presentation / Molecular systems biology / Human Disease / Clinical Presentation

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Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency

Mitochondria / Humans / Fatty acids / Mutation / Male / Fatty Acid Oxidation / Phenotype / Enzyme / Clinical Sciences / L-carnitine / Spectrum / Prognosis / Multienzyme complexes / Cardiomyopathies / Human Fibroblasts / Clinical Presentation / Rhabdomyolysis / Fatty Acid Oxidation / Phenotype / Enzyme / Clinical Sciences / L-carnitine / Spectrum / Prognosis / Multienzyme complexes / Cardiomyopathies / Human Fibroblasts / Clinical Presentation / Rhabdomyolysis

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Habitual Physical Activity in Mitochondrial Disease

Physical Activity / Exercise therapy / Multidisciplinary / Humans / Mutation / Habits / Female / Male / Risk factors / Phenotype / PLoS one / Mitochondrial Diseases / Neuromuscular Disease / Genotype / Adult / Risk Factors / Clinical Presentation / Control Group / Motor activity / Habits / Female / Male / Risk factors / Phenotype / PLoS one / Mitochondrial Diseases / Neuromuscular Disease / Genotype / Adult / Risk Factors / Clinical Presentation / Control Group / Motor activity

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Aromatic L-Amino Acid Decarboxylase Deficiency Is a Cause of Long-Fasting Hypoglycemia

Cognitive Science / Neurology / Magnetic Resonance Imaging / Treatment Outcome / Adolescent / Movement disorders / Dopamine / Cerebrospinal Fluid / Brain / Pregnancy / Humans / Child / Hemodynamics / Female / Inborn errors of metabolism / Male / Young Adult / Infant / Follow-up studies / Amniotic Fluid / Differential Diagnosis / Pedigree / Levodopa / Child Neurology / Clinical Sciences / Newborn Infant / European / Longitudinal Studies / Pyridoxine / Adult / Consanguinity / Retrospective Studies / Neuropediatrics / Combination drug therapy / Amino Acid Profile / Biogenic amines / Autosomal Recessive / Clinical Presentation / Neurosciences / Nervous System Diseases / Age of Onset / Movement Disorder / Bromocriptine / Serotonin Uptake Inhibitors / Founder Effect / Medical Treatment / Movement disorders / Dopamine / Cerebrospinal Fluid / Brain / Pregnancy / Humans / Child / Hemodynamics / Female / Inborn errors of metabolism / Male / Young Adult / Infant / Follow-up studies / Amniotic Fluid / Differential Diagnosis / Pedigree / Levodopa / Child Neurology / Clinical Sciences / Newborn Infant / European / Longitudinal Studies / Pyridoxine / Adult / Consanguinity / Retrospective Studies / Neuropediatrics / Combination drug therapy / Amino Acid Profile / Biogenic amines / Autosomal Recessive / Clinical Presentation / Neurosciences / Nervous System Diseases / Age of Onset / Movement Disorder / Bromocriptine / Serotonin Uptake Inhibitors / Founder Effect / Medical Treatment

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Functional correlates of Apolipoprotein E genotype in Frontotemporal Lobar Degeneration

Genetics / Cognitive Science / Dementia / Memory / Humans / Glucose Metabolism / Brain Ischemia / Risk factors / Aged / Middle Aged / Genotype / Single Photon Emission Computed Tomography / Adult / Long Term Memory / Brain Structure / Risk Factors / Parahippocampal Gyrus / Brain Function / Clinical Presentation / Cross Sectional Studies / Alzheimer Disease / Neurosciences / Glucose Metabolism / Brain Ischemia / Risk factors / Aged / Middle Aged / Genotype / Single Photon Emission Computed Tomography / Adult / Long Term Memory / Brain Structure / Risk Factors / Parahippocampal Gyrus / Brain Function / Clinical Presentation / Cross Sectional Studies / Alzheimer Disease / Neurosciences

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Aromatic-L-amino-acid decarboxylase, a pyridoxal phosphate-dependent enzyme, is a beta-cell autoantigen

Adolescent / Multidisciplinary / Serotonin / Dopamine / Humans / Female / Animals / Alternative splicing / Enzyme / Rats / Amino Acid Profile / Alternative Splicing / Amino Acid Sequence / Base Sequence / Type 2 Diabetes Mellitus / Clinical Presentation / Recombinant Proteins / Syndrome / Gonads / Full Length Movies / Glutamate decarboxylase / islets of Langerhans / Autoantigens / Female / Animals / Alternative splicing / Enzyme / Rats / Amino Acid Profile / Alternative Splicing / Amino Acid Sequence / Base Sequence / Type 2 Diabetes Mellitus / Clinical Presentation / Recombinant Proteins / Syndrome / Gonads / Full Length Movies / Glutamate decarboxylase / islets of Langerhans / Autoantigens

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Unusual insidious spinal accessory nerve palsy: a case report

Case Report / Anatomical Variation / Clinical Presentation / Clinical Signs / Conservative treatment / Medical Case Reports

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Superior Vena Cava Syndrome Due to Thrombotic Occlusion in a Thrombophilic Renal Transplant Recipient: A Case Report

Kidney transplantation / Renal transplantation / Case Report / Humans / Female / Thromboembolism / Anticoagulants / Middle Aged / Warfarin / Central Venous Catheter / Clinical Presentation / Chronic Kidney Failure / SUPERIOR VENA CAVA / Thromboembolism / Anticoagulants / Middle Aged / Warfarin / Central Venous Catheter / Clinical Presentation / Chronic Kidney Failure / SUPERIOR VENA CAVA

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Clinical features of facioscapulohumeral muscular dystrophy 2

Cognitive Science / Neurology / Adolescent / Humans / Child / Muscular Dystrophy / Female / Male / Gender Difference / DNA methylation / Young Adult / Infant / Disease Severity / Phenotype / Chromatin structure / Clinical Sciences / Newborn Infant / Middle Aged / Family Health / Genotype / Adult / Clinical Assessment / Cross sectional Study / Clinical Presentation / Cross Sectional Studies / Neurosciences / Clinical evaluation / Cohort Studies / Muscular Dystrophy / Female / Male / Gender Difference / DNA methylation / Young Adult / Infant / Disease Severity / Phenotype / Chromatin structure / Clinical Sciences / Newborn Infant / Middle Aged / Family Health / Genotype / Adult / Clinical Assessment / Cross sectional Study / Clinical Presentation / Cross Sectional Studies / Neurosciences / Clinical evaluation / Cohort Studies

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Pyruvate dehydrogenase E1 alpha deficiency in a family: Different clinical presentation in two siblings

Humans / Female / Male / Clinical Sciences / Acidosis / Clinical Presentation

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