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1. Full Text Movement Disorders in Treatable Inborn Errors of Metabolism
by Ebrahimi‐Fakhari, Darius and Van Karnebeek, Clara and Münchau, Alexander
Movement disorders, ISSN 0885-3185, 05/2019, Volume 34, Issue 5, pp. 598 - 613
inborn errors of metabolism | treatment | movement disorders | neurotransmitter disorders | neurogenetics | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Amino Acid Metabolism, Inborn Errors - complications | Niemann-Pick Disease, Type C - therapy | Hepatolenticular Degeneration - therapy | Monosaccharide Transport Proteins - deficiency | Amino Acid Metabolism, Inborn Errors - physiopathology | Humans | Folic Acid Deficiency - therapy | Hepatolenticular Degeneration - physiopathology | Vitamin E Deficiency - therapy | Dystonic Disorders - complications | Brain Diseases, Metabolic - diagnosis | Vitamin E Deficiency - diagnosis | Xanthomatosis, Cerebrotendinous - diagnosis | Basal Ganglia Diseases - diagnosis | Carbohydrate Metabolism, Inborn Errors - therapy | Dystonia - etiology | Carbohydrate Metabolism, Inborn Errors - diagnosis | Parkinsonian Disorders - physiopathology | Chorea - physiopathology | Dystonia - physiopathology | Metabolic Diseases - diagnosis | Ataxia - diagnosis | Carbohydrate Metabolism, Inborn Errors - physiopathology | Metabolism, Inborn Errors - diagnosis | Folic Acid Deficiency - complications | Movement Disorders - physiopathology | Brain Diseases, Metabolic - physiopathology | Basal Ganglia Diseases - therapy | Ataxia - complications | Muscle Spasticity - physiopathology | Xanthomatosis, Cerebrotendinous - complications | Metabolic Diseases - complications | Metabolism, Inborn Errors - complications | Metabolism, Inborn Errors - physiopathology | Brain Diseases, Metabolic - complications | Glutaryl-CoA Dehydrogenase - deficiency | Carbohydrate Metabolism, Inborn Errors - complications | Ataxia - etiology | Hepatolenticular Degeneration - diagnosis | Metabolism, Inborn Errors - therapy | Niemann-Pick Disease, Type C - physiopathology | Parkinsonian Disorders - etiology | Amino Acid Metabolism, Inborn Errors - diagnosis | Brain Diseases, Metabolic - therapy | Xanthomatosis, Cerebrotendinous - therapy | Metabolic Diseases - therapy | Metabolic Diseases - physiopathology | Myoclonus - etiology | Vitamin E Deficiency - complications | Niemann-Pick Disease, Type C - diagnosis | Dystonic Disorders - physiopathology | Dystonic Disorders - therapy | Hepatolenticular Degeneration - complications | Vitamin E Deficiency - physiopathology | Ataxia - physiopathology | Ataxia - therapy | Chorea - etiology | Amino Acid Metabolism, Inborn Errors - therapy | Basal Ganglia Diseases - complications | Folic Acid Deficiency - physiopathology | Myoclonus - physiopathology | Muscle Spasticity - etiology | Dystonic Disorders - diagnosis | Basal Ganglia Diseases - physiopathology | Movement Disorders - etiology | Xanthomatosis, Cerebrotendinous - physiopathology | Folic Acid Deficiency - diagnosis | Niemann-Pick Disease, Type C - complications | Dystonic Disorders - etiology | Metabolism, Inborn errors of | Education | Mortality | Finance | Physiological aspects | Creatine | Movement disorders | Energy metabolism | Inborn errors of metabolism | Lysosomal storage diseases | Metabolism | Autophagy | Morbidity | Quality of life | Phenomenology | Psychiatrists | Differential diagnosis | Children | Phagocytosis | Index Medicus
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2. Full Text Genetic mimics of cerebral palsy
by Pearson, Toni S and Pons, Roser and Ghaoui, Roula and Sue, Carolyn M
Movement disorders, ISSN 0885-3185, 05/2019, Volume 34, Issue 5, pp. 625 - 636
cerebral palsy | inborn errors of metabolism | spasticity | ataxia | dystonia | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Brain - diagnostic imaging | Monosaccharide Transport Proteins - deficiency | Lesch-Nyhan Syndrome - therapy | Spastic Paraplegia, Hereditary - diagnosis | Humans | Movement Disorders - diagnosis | Folic Acid Deficiency - therapy | Lesch-Nyhan Syndrome - genetics | Cerebral Palsy - diagnosis | Multiple Carboxylase Deficiency - genetics | Carbohydrate Metabolism, Inborn Errors - therapy | Brain Diseases, Metabolic, Inborn - genetics | Dyskinesias - genetics | Folic Acid Deficiency - genetics | Multiple Carboxylase Deficiency - physiopathology | Carbohydrate Metabolism, Inborn Errors - diagnosis | Monosaccharide Transport Proteins - genetics | Chorea - physiopathology | Creatine - genetics | Hyperargininemia - physiopathology | Dyskinesias - physiopathology | Dystonia - physiopathology | Pelizaeus-Merzbacher Disease - diagnosis | Plasma Membrane Neurotransmitter Transport Proteins - genetics | Carbohydrate Metabolism, Inborn Errors - physiopathology | Magnetic Resonance Imaging | Hyperargininemia - diagnosis | Movement Disorders - physiopathology | Dyskinesias - diagnosis | Hyperargininemia - genetics | Ataxia Telangiectasia - genetics | Lesch-Nyhan Syndrome - diagnosis | Brain Diseases, Metabolic, Inborn - therapy | Muscle Spasticity - physiopathology | Movement Disorders - genetics | Multiple Carboxylase Deficiency - diagnosis | Multiple Carboxylase Deficiency - therapy | GTP-Binding Protein alpha Subunits, Gi-Go - genetics | Spastic Paraplegia, Hereditary - genetics | Cerebral Palsy - physiopathology | Lesch-Nyhan Syndrome - physiopathology | Mental Retardation, X-Linked - physiopathology | Carbohydrate Metabolism, Inborn Errors - genetics | Brain Diseases, Metabolic, Inborn - diagnosis | Mental Retardation, X-Linked - genetics | Mental Retardation, X-Linked - diagnosis | Hyperargininemia - therapy | Creatine - deficiency | Thyroid Nuclear Factor 1 - genetics | Pelizaeus-Merzbacher Disease - therapy | Spastic Paraplegia, Hereditary - physiopathology | Mental Retardation, X-Linked - therapy | Ataxia Telangiectasia - diagnosis | Ataxia Telangiectasia - physiopathology | Plasma Membrane Neurotransmitter Transport Proteins - deficiency | Ataxia - physiopathology | Ataxia Telangiectasia - therapy | Diagnosis, Differential | Pelizaeus-Merzbacher Disease - genetics | Spastic Paraplegia, Hereditary - therapy | Brain Diseases, Metabolic, Inborn - physiopathology | Folic Acid Deficiency - physiopathology | Dyskinesias - therapy | Movement Disorders - therapy | Pelizaeus-Merzbacher Disease - physiopathology | Folic Acid Deficiency - diagnosis | Adenylyl Cyclases - genetics | Cerebral palsy | Development and progression | Medical genetics | Neuroimaging | Genetic counseling | Etiology | Chorea | Spasticity | Ataxia | Dystonia | Children | Paralysis | Neurodevelopmental disorders | Metabolic disorders | Index Medicus
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3. Full Text Guidelines for the diagnosis and treatment of cobalamin and folate disorders
by Devalia, Vinod and Hamilton, Malcolm S and Molloy, Anne M and British Comm Stand Haematology and British Committee for Standards in Haematology and the British Committee for Standards in Haematology
British journal of haematology, ISSN 0007-1048, 08/2014, Volume 166, Issue 4, pp. 496 - 513
holotranscobalamin | methylmalonic acid | folate | cobalamin | intrinsic factor antibody | Cobalamin | Holotranscobalamin | Intrinsic factor antibody | Methylmalonic acid | Folate | Life Sciences & Biomedicine | Hematology | Science & Technology | Hematologic and hematopoietic diseases | Biological and medical sciences | Medical sciences | Tumors | Diagnosis, Differential | Folic Acid - therapeutic use | Folic Acid Deficiency - etiology | Vitamin B 12 Deficiency - etiology | Vitamin B 12 Deficiency - diagnosis | Humans | Folic Acid Deficiency - diagnosis | Biomarkers - blood | Vitamin B 12 Deficiency - drug therapy | Folic Acid Deficiency - drug therapy | Hydroxocobalamin - therapeutic use | Practice guidelines (Medicine) | Folic acid | Index Medicus
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4. Full Text Screening and Diagnosis of Micronutrient Deficiencies Before and After Bariatric Surgery
by Gudzune, Kimberly A and Huizinga, Mary M and Chang, Hsien-Yen and Asamoah, Vivian and Gadgil, Meghana and Clark, Jeanne M
Obesity surgery, ISSN 0960-8923, 10/2013, Volume 23, Issue 10, pp. 1581 - 1589
Vitamin D deficiency | Medicine & Public Health | Surgery | Bariatric surgery | Iron deficiency | Vitamin B12 deficiency | Folate deficiency | Life Sciences & Biomedicine | Science & Technology | United States - epidemiology | Prevalence | Obesity, Morbid - surgery | Vitamin B 12 Deficiency - blood | Humans | Mass Screening - statistics & numerical data | Micronutrients - deficiency | Male | Time Factors | Vitamin D Deficiency - blood | Iron - deficiency | Adult | Female | Micronutrients - blood | Folic Acid Deficiency - blood | Iron - blood | Maryland - epidemiology | Vitamin B 12 Deficiency - diagnosis | Mass Screening - standards | Postoperative Period | Gastric Bypass - adverse effects | Vitamin D Deficiency - diagnosis | Folic Acid Deficiency - diagnosis | Obesity, Morbid - blood | Obesity, Morbid - epidemiology | Practice Guidelines as Topic | Preoperative Period | Obesity | Vitamin deficiency | Gastrointestinal surgery | Nutrition | Medical screening | Index Medicus | folate deficiency | bariatric surgery | iron deficiency | vitamin B12 deficiency | vitamin D deficiency
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5. Full Text Micronutrient deficiencies in patients with chronic atrophic autoimmune gastritis: A review
by Federica Cavalcoli Alessandra Zilli Dario Conte Sara
World journal of gastroenterology : WJG, ISSN 1007-9327, 2017, Volume 23, Issue 4, pp. 563 - 572
Calcium | Vitamin D | Chronic atrophic autoimmune gastritis | Vitamin C | Malabsorption | Iron | Vitamin B12 | Nutritional deficiency | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Vitamin B 12 Deficiency - diagnosis | Humans | Autoimmune Diseases - complications | Micronutrients - deficiency | Ascorbic Acid Deficiency - diagnosis | Autoimmune Diseases - diagnosis | Anemia, Megaloblastic - complications | Gastritis, Atrophic - complications | Anemia, Pernicious - complications | Ascorbic Acid Deficiency - complications | Gastritis, Atrophic - diagnosis | Anemia, Pernicious - diagnosis | Calcium - deficiency | Folic Acid Deficiency - complications | Anemia, Megaloblastic - diagnosis | Vitamin B 12 Deficiency - complications | Folic Acid Deficiency - diagnosis | Chronic Disease | Osteoporosis - physiopathology | Hydrogen-Ion Concentration | Index Medicus
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