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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 Clinicopathologic features of folate-deficiency neuropathy
by Koike, Haruki and Takahashi, Mie and Ohyama, Ken and Hashimoto, Rina and Kawagashira, Yuichi and Iijima, Masahiro and Katsuno, Masahisa and Doi, Hiroshi and Tanaka, Fumiaki and Sobue, Gen
Neurology, ISSN 0028-3878, 03/2015, Volume 84, Issue 10, pp. 1026 - 1033
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Folic Acid Deficiency - diet therapy | Folic Acid - pharmacology | Humans | Middle Aged | Male | Treatment Outcome | Vitamin B 12 Deficiency - physiopathology | Polyneuropathies - physiopathology | Vitamin B Complex - pharmacology | Folic Acid - administration & dosage | Beriberi - physiopathology | Disease Progression | Vitamin B Complex - administration & dosage | Polyneuropathies - chemically induced | Folic Acid Deficiency - complications | Sural Nerve - pathology | Polyneuropathies - pathology | Aged, 80 and over | Adult | Female | Aged | Alcoholism - complications | Folic Acid Deficiency - blood | Folic Acid Deficiency - drug therapy | Index Medicus | Abridged Index Medicus
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4. Full Text MTHFR deficiency or reduced intake of folate or choline in pregnant mice results in impaired short-term memory and increased apoptosis in the hippocampus of wild-type offspring
by Jadavji, N.M and Deng, L and Malysheva, O and Caudill, M.A and Rozen, R
Neuroscience, ISSN 0306-4522, 2015, Volume 300, pp. 1 - 9
Neurology | MTHFR deficiency | apoptosis | short-term memory | maternal folate deficiency | maternal choline deficiency | Maternal choline deficiency | Maternal folate deficiency | Short-term memory | Apoptosis | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Memory Disorders - physiopathology | Maternal Nutritional Physiological Phenomena | Male | Memory, Short-Term - physiology | Choline O-Acetyltransferase - metabolism | Recognition (Psychology) - physiology | Homocystinuria - physiopathology | Psychotic Disorders - physiopathology | Female | Methylenetetrahydrofolate Reductase (NADPH2) - deficiency | Hippocampus - growth & development | Memory Disorders - pathology | Disease Models, Animal | Maze Learning - physiology | Homocysteine - blood | Organ Size | Mice, Transgenic | Hippocampus - pathology | Pregnancy Complications - physiopathology | Folic Acid Deficiency - physiopathology | Pregnancy | Choline Deficiency - physiopathology | Animals | Memory Disorders - etiology | Neurogenesis - physiology | Muscle Spasticity - physiopathology | Apoptosis - physiology | Body Weight - physiology | Hippocampus - physiopathology | Brain | Choline | Folic acid | Index Medicus
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5. Full Text Low maternal vitamin B-12 status is associated with offspring insulin resistance regardless of antenatal micronutrient supplementation in rural Nepal
by Stewart, Christine P and Christian, Parul and Schulze, Kerry J and Arguello, Margia and LeClerq, Steven C and Khatry, Subarna K and West Jr, Keith P
The Journal of nutrition, ISSN 0022-3166, 10/2011, Volume 141, Issue 10, pp. 1912 - 1917
Life Sciences & Biomedicine | Nutrition & Dietetics | Science & Technology | Fundamental and applied biological sciences. Psychology | Feeding. Feeding behavior | Biological and medical sciences | Vertebrates: anatomy and physiology, studies on body, several organs or systems | Folic Acid - therapeutic use | Maternal Nutritional Physiological Phenomena | Prevalence | Folic Acid - adverse effects | Humans | Folic Acid Deficiency - epidemiology | Male | Anemia, Iron-Deficiency - prevention & control | Folic Acid Deficiency - prevention & control | Vitamin B 12 Deficiency - complications | Prenatal Exposure Delayed Effects - blood | Female | Anemia, Iron-Deficiency - complications | Vitamin B 12 Deficiency - epidemiology | Dietary Supplements - adverse effects | Child | Insulin Resistance | Vitamin B 12 Deficiency - physiopathology | Pregnancy Complications - physiopathology | Zinc - adverse effects | Prenatal Exposure Delayed Effects - etiology | Rural Health | Zinc - therapeutic use | Folic Acid Deficiency - physiopathology | Pregnancy | Folic Acid Deficiency - complications | Folic Acid - blood | Iron, Dietary - therapeutic use | Pregnancy Complications - prevention & control | Iron, Dietary - adverse effects | Vitamin B 12 Deficiency - prevention & control | Nepal - epidemiology | Pregnancy Complications - epidemiology | Cohort Studies | Zinc - deficiency | Development and progression | Insulin resistance | Food and nutrition | Pregnant women | Vitamin B12 deficiency | Risk factors | Index Medicus
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6. Full Text High folic acid consumption leads to pseudo-MTHFR deficiency, altered lipid metabolism, and liver injury in mice
by Christensen, Karen E and Mikael, Leonie G and Leung, Kit-Yi and Lévesque, Nancy and Deng, Liyuan and Wu, Qing and Malysheva, Olga V and Best, Ana and Caudill, Marie A and Greene, Nicholas D.E and Rozen, Rima
The American journal of clinical nutrition, ISSN 0002-9165, 03/2015, Volume 101, Issue 3, pp. 646 - 658
Methylenetetrahydrofolate reductase | Lipid metabolism | Liver | Choline metabolism | Folic acid | Life Sciences & Biomedicine | Nutrition & Dietetics | Science & Technology | Liver - pathology | Enzyme Inhibitors - poisoning | Folic Acid - poisoning | Non-alcoholic Fatty Liver Disease - etiology | Homocystinuria - etiology | Male | Methylenetetrahydrofolate Reductase (NADPH2) - metabolism | Homocystinuria - metabolism | Liver - physiopathology | Homocystinuria - physiopathology | Psychotic Disorders - physiopathology | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Mice, Mutant Strains | Psychotic Disorders - pathology | Lipogenesis | Methylenetetrahydrofolate Reductase (NADPH2) - deficiency | Dietary Supplements - poisoning | Methylenetetrahydrofolate Reductase (NADPH2) - antagonists & inhibitors | Specific Pathogen-Free Organisms | Liver - metabolism | Gene Expression Regulation | Organ Size | Lipid Metabolism | Muscle Spasticity - metabolism | Muscle Spasticity - pathology | Homocystinuria - pathology | Muscle Spasticity - etiology | Psychotic Disorders - metabolism | Animals | Heterozygote | Mice, Inbred BALB C | Muscle Spasticity - physiopathology | Mutation | Methylation | Psychotic Disorders - etiology | Liver diseases | Metabolism | Health aspects | Risk factors | Lipids | Vitamin B | Rodents | Index Medicus | Abridged Index Medicus
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7. Full Text Maternal anemia and risk of adverse birth and health outcomes in low- and middle-income countries: Systematic review and meta-analysis
by Rahman, Md Mizanur and Abe, Sarah Krull and Rahman, Md Shafiur and Kanda, Mikiko and Narita, Saki and Bilano, Ver and Ota, Erika and Gilmour, Stuart and Shibuya, Kenji
The American journal of clinical nutrition, ISSN 0002-9165, 02/2016, Volume 103, Issue 2, pp. 495 - 504
Population-attributable fraction | Maternal anemia | Low- and middle-income countries | Birth and health outcomes | Meta-analysis | Life Sciences & Biomedicine | Nutrition & Dietetics | Science & Technology | Maternal Nutritional Physiological Phenomena | Prevalence | Anemia, Iron-Deficiency - physiopathology | Infant Mortality | Anemia - epidemiology | Humans | Folic Acid Deficiency - epidemiology | Infant | Male | Anemia - physiopathology | Fetal Growth Retardation - etiology | Perinatal Mortality | Adult | Female | Infant, Newborn | Risk Factors | Fetal Growth Retardation - epidemiology | Pregnancy Complications - physiopathology | Premature Birth - epidemiology | Premature Birth - etiology | Folic Acid Deficiency - physiopathology | Pregnancy | Anemia, Iron-Deficiency - epidemiology | Avitaminosis - physiopathology | Avitaminosis - epidemiology | Developing Countries | Pregnancy Complications - epidemiology | Complications and side effects | Anemia | Pregnant women | Patient outcomes | Infants | Health aspects | Risk factors | Maternal & child health | Mortality | Systematic review | Developing countries--LDCs | Index Medicus | Abridged Index Medicus
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