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1. Full Text Periodic paralysis
by Fialho, Doreen and Griggs, Robert C and Matthews, Emma
2018, ISBN 9780444640765, Volume 148
muscle excitability | Andersen–Tawil syndrome | thyrotoxic periodic paralysis | hypokalemic periodic paralysis | hyperkalemic periodic paralysis | paradoxic depolarization | gating pore leak | SCN4A | CACNA1S | KCNJ2 | Ion Channels - genetics | Genetic Predisposition to Disease - genetics | Paralyses, Familial Periodic - physiopathology | Mutation - genetics | Humans | Paralyses, Familial Periodic - genetics | Index Medicus
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2. Full Text Thyrotoxic hypokalemic periodic paralysis
by Urbina-Soto, L and Urbina-Soto, L and Hernández-Martínez, P and Ortiz-Flores, F and Hernández, J.L and Hernández, J.L
QJM : monthly journal of the Association of Physicians, ISSN 1460-2725, 12/2018, Volume 111, Issue 12, pp. 887 - 889
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Muscle Weakness - etiology | Diagnosis, Differential | Hypokalemic Periodic Paralysis - etiology | Hyperthyroidism - diagnosis | Humans | Hyperthyroidism - complications | Adult | Hyperthyroidism - drug therapy | Male | Hypokalemic Periodic Paralysis - drug therapy | Adrenergic beta-Antagonists - therapeutic use | Index Medicus
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3. Full Text Thyrotoxic periodic paralysis
by Lin, Shih-Hua
Mayo Clinic proceedings, ISSN 0025-6196, 2005, Volume 80, Issue 1, pp. 99 - 105
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Biological and medical sciences | General aspects | Medical sciences | Hypokalemic Periodic Paralysis - etiology | Thyrotoxicosis - complications | Humans | Phosphates - urine | Hypokalemic Periodic Paralysis - diagnosis | Calcium - urine | Hypokalemic Periodic Paralysis - drug therapy | Hypokalemic Periodic Paralysis - physiopathology | Index Medicus | Abridged Index Medicus
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4. Full Text Thyrotoxic hypokalemic periodic paralysis
by Zayac, A and Shah, R and Shah, M and Umar, J and Bansal, N and Dhamoon, A
QJM : monthly journal of the Association of Physicians, ISSN 1460-2725, 09/2016, Volume 109, Issue 9, pp. 613 - 614
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Methimazole - administration & dosage | Tachycardia, Sinus - etiology | Hypokalemic Periodic Paralysis - metabolism | Thyrotoxicosis - complications | Humans | Thyrotoxicosis - metabolism | Hypokalemic Periodic Paralysis - diagnosis | Male | Thyrotoxicosis - drug therapy | Thyroid Hormones - blood | Adult | Tachycardia, Sinus - diagnosis | Muscle Strength | Hypokalemic Periodic Paralysis - drug therapy | Ultrasonography - methods | Hypokalemic Periodic Paralysis - etiology | Treatment Outcome | Metoprolol - administration & dosage | Tachycardia, Sinus - drug therapy | Antithyroid Agents - administration & dosage | Anti-Arrhythmia Agents - administration & dosage | Thyroid Gland - diagnostic imaging | Thyrotoxicosis - diagnosis | Potassium - administration & dosage | Potassium - blood | Index Medicus
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5. Full Text Clinical Review: Thyrotoxic periodic paralysis: A diagnostic challenge
by Kung, Annie W. C
The journal of clinical endocrinology and metabolism, ISSN 0021-972X, 2006, Volume 91, Issue 7, pp. 2490 - 2495
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Fundamental and applied biological sciences. Psychology | Non tumoral diseases. Target tissue resistance. Benign neoplasms | Vertebrates: endocrinology | Thyroid. Thyroid axis (diseases) | Biological and medical sciences | Endocrinopathies | Medical sciences | Graves Disease - diagnosis | MEDLINE | Potassium - metabolism | Thyrotoxicosis - complications | Humans | Male | Thyrotoxicosis - therapy | Muscular Diseases - etiology | Iodine Radioisotopes - therapeutic use | Exercise | Hypokalemia - drug therapy | Potassium Chloride - administration & dosage | Electromyography | Paralysis - etiology | Antithyroid Agents - therapeutic use | Periodicity | Hypokalemic Periodic Paralysis | Graves Disease - therapy | Thyroidectomy | Thyrotoxicosis - diagnosis | Muscular Diseases - diagnosis | Sodium-Potassium-Exchanging ATPase - metabolism | Paralysis - therapy | Asia | Muscle, Skeletal - physiopathology | Hyperthyroidism - complications | Graves Disease - complications | Hypokalemia - complications | Muscular Diseases - therapy | Paralysis - diagnosis | Thyroid Hormones - physiology | Index Medicus | Abridged Index Medicus
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6. Full Text Review of the Diagnosis and Treatment of Periodic Paralysis
by Statland, Jeffrey M and Fontaine, Bertrand and Hanna, Michael G and Johnson, Nicholas E and Kissel, John T and Sansone, Valeria A and Shieh, Perry B and Tawil, Rabi N and Trivedi, Jaya and Cannon, Stephen C and Griggs, Robert C
Muscle & nerve, ISSN 0148-639X, 04/2018, Volume 57, Issue 4, pp. 522 - 530
treatment | periodic paralyses | review | acetazolamide | Andersen‐Tawil syndrome | channelopathies | dichlorphenamide | Andersen-Tawil syndrome | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Care and treatment | Gene mutations | Therapeutics | Muscles | Diuretics | Paralysis | Diagnosis | Genetic screening | Homeopathy | Materia medica and therapeutics | Calcium | Heredity | Skeletal muscle | Sodium | Carbonic anhydrase | Mutation | Potassium | Neuromuscular system | Index Medicus | Invited Reviews | Invited Review
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7. Full Text A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis
by Wu, Fenfen and Mi, Wentao and Burns, Dennis K and Fu, Yu and Gray, Hillery F and Struyk, Arie F and Cannon, Stephen C
The Journal of clinical investigation, ISSN 0021-9738, 10/2011, Volume 121, Issue 10, pp. 4082 - 4094
Isometric Contraction - drug effects | Humans | Hypokalemic Periodic Paralysis - genetics | Male | Sodium Channels - physiology | Hypokalemic Periodic Paralysis - physiopathology | Mice, Mutant Strains | Isometric Contraction - genetics | Female | Isometric Contraction - physiology | Ouabain - pharmacology | Disease Models, Animal | Insulin - pharmacology | Mutagenesis, Site-Directed | Mutant Proteins - genetics | NAV1.4 Voltage-Gated Sodium Channel | Glucose - pharmacology | Mutant Proteins - physiology | Potassium - pharmacology | Gene Knock-In Techniques | Homozygote | Phenotype | Animals | Sodium Channels - chemistry | Mutant Proteins - chemistry | Mice | Sodium Channels - genetics | Amino Acid Substitution | Sodium channels | Familial periodic paralysis | Gene mutations | Physiological aspects | Development and progression | Genetic aspects | Research | Index Medicus | Abridged Index Medicus
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8. Full Text Hypokalaemia periodic paralysis
by Stapleton, Liam J
Scottish medical journal, ISSN 0036-9330, 2/2018, Volume 63, Issue 1, pp. 28 - 31
Hypokalaemic period paralysis | Channelopathy | Periodic paralysis | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Hypokalemic Periodic Paralysis - blood | Diagnosis, Differential | Hypokalemic Periodic Paralysis - diet therapy | Hypokalemic Periodic Paralysis - etiology | Humans | Potassium, Dietary - therapeutic use | Adult | Male | Potassium - blood | Treatment Outcome | Diet, Carbohydrate-Restricted | Hypokalemic Periodic Paralysis - physiopathology | Index Medicus
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9. Full Text Treatment for periodic paralysis
by Sansone, Valeria and Meola, G and Links, T. P and Panzeri, M and Rose, M. R
Cochrane database of systematic reviews, ISSN 1469-493X, 2008, Volume 2010, Issue 1, pp. CD005045 - CD005045
BETA-ADRENERGIC TREATMENT | PARAMYOTONIA-CONGENITA | ALPHA-SUBUNIT | ANDERSEN-TAWIL-SYNDROME | MYOTONIA-CONGENITA | MUSCLE SODIUM-CHANNEL | GENE SCN4A | ACETAZOLAMIDE | MUTATIONS | WEAKNESS | Pinacidil | Muscle Diseases | Mexiletine treatment | Paralysis, Hyperkalemic Periodic | Acetazolamide | Hypokalemic Periodic Paralysis | Randomized Controlled Trials as Topic | Neurology | Carbonic Anhydrase Inhibitors | Dichlorphenamide | Anabolic steroid treatment | Periodic paralysis | Hypokalaemic periodic paralysis | Hyperkalaemic periodic paralysis | Muscle disease | Medicine General & Introductory Medical Sciences | Testosterone analogue treatment | Dichlorphenamide treatment | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Pinacidil - therapeutic use | Dichlorphenamide - therapeutic use | Humans | Paralysis, Hyperkalemic Periodic - drug therapy | Acetazolamide - therapeutic use | Hypokalemic Periodic Paralysis - drug therapy | Carbonic Anhydrase Inhibitors - therapeutic use | Index Medicus
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10. Full Text Structural basis for gating pore current in periodic paralysis
by Jiang, Daohua and El-Din, Tamer M. Gamal and Ing, Christopher and Lu, Peilong and Pomes, Regis and Zheng, Ning and Catterall, William A
Nature (London), ISSN 0028-0836, 05/2018, Volume 557, Issue 7706, pp. 590 - 594
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | NAV1.4 Voltage-Gated Sodium Channel - chemistry | NAV1.4 Voltage-Gated Sodium Channel - genetics | Hypokalemic Periodic Paralysis - metabolism | Humans | Hypokalemic Periodic Paralysis - genetics | Paralyses, Familial Periodic - metabolism | Electric Conductivity | Guanidine - metabolism | NAV1.4 Voltage-Gated Sodium Channel - metabolism | Sodium - metabolism | Molecular Dynamics Simulation | Thermodynamics | Ion Channel Gating - genetics | Mutation | Binding Sites | Paralyses, Familial Periodic - genetics | Sodium channels | Familial periodic paralysis | Gene mutations | Causes of | Genetic aspects | Models | Observations | Health aspects | Electric potential | Calcium | Computer simulation | Channel gating | Calcium channels (voltage-gated) | Muscles | Molecular dynamics | Ions | Hydrophobicity | Molecular chains | Skeletal muscle | Molecular modelling | Sodium | Sodium channels (voltage-gated) | Cations | Paralysis | Variation | Potassium | Crystal structure | Index Medicus
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11. Full Text Proximal Muscle Weakness With Overlying Hypokalemic Periodic Paralysis in Sjögren Syndrome: Report of 6 Cases
by Paliwal, Vimal K and Rai, Anmol Singh and Kumar, Surendra and Verma, Ritu and Agarwal, Vikas
Journal of clinical rheumatology, ISSN 1076-1608, 01/2020, Volume 26, Issue 1, pp. 24 - 27
Life Sciences & Biomedicine | Rheumatology | Science & Technology | Muscle Weakness - etiology | Sodium Bicarbonate - therapeutic use | Diagnosis, Differential | Acidosis, Renal Tubular - complications | Muscle Weakness - diagnosis | Autoantibodies - blood | Humans | Sjogren's Syndrome - physiopathology | Acidosis, Renal Tubular - diagnosis | Sjogren's Syndrome - immunology | Male | Treatment Outcome | Acidosis, Renal Tubular - blood | Hypokalemic Periodic Paralysis - complications | Calcium-Regulating Hormones and Agents - therapeutic use | Hypokalemic Periodic Paralysis - physiopathology | Calcium - therapeutic use | Muscle Weakness - drug therapy | Potassium - therapeutic use | Adult | Female | Hypokalemic Periodic Paralysis - immunology | Electromyography - methods | Sjogren's Syndrome - complications | Index Medicus
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12. Full Text A calcium channel mutant mouse model of hypokalemic periodic paralysis
by Wu, Fenfen and Mi, Wentao and Hernández-Ochoa, Erick O and Burns, Dennis K and Fu, Yu and Gray, Hillery F and Struyk, Arie F and Schneider, Martin F and Cannon, Stephen C
The Journal of clinical investigation, ISSN 0021-9738, 12/2012, Volume 122, Issue 12, pp. 4580 - 4591
Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Electric Stimulation | Excitation Contraction Coupling | Humans | Hypokalemic Periodic Paralysis - genetics | Male | Glucose | Mice, 129 Strain | Muscle Fibers, Skeletal - metabolism | Mutation, Missense | Muscle Weakness - genetics | Action Potentials | Female | Muscle Fibers, Skeletal - physiology | Disease Models, Animal | Hypokalemic Periodic Paralysis - pathology | Hypokalemic Periodic Paralysis - chemically induced | Lysosomal Storage Diseases - genetics | Insulin | Phenotype | Animals | Calcium Channels, L-Type - genetics | Muscle Contraction | Analysis of Variance | Muscle, Skeletal - physiopathology | Muscle Fibers, Skeletal - pathology | Mice | Calcium Channels, L-Type - metabolism | Muscle, Skeletal - pathology | Muscular Diseases - genetics | In Vitro Techniques | Calcium channels | Familial periodic paralysis | Care and treatment | Gene mutations | Models | Diagnosis | Properties | Identification and classification | Index Medicus | Abridged Index Medicus | Channel pores | Sodium channels | Animal models | Channel gating | Calcium channels (voltage-gated) | Excitability | Tubules | Skeletal muscle | Missense mutation | Membrane potential | Paralysis | Potassium | Myopathy
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13. Full Text Mutations in Potassium Channel Kir2.6 Cause Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis
by Ryan, Devon P and Dias da Silva, Magnus R and Soong, Tuck Wah and Fontaine, Bertrand and Donaldson, Matt R and Kung, Annie W.C and Jongjaroenprasert, Wallaya and Liang, Mui Cheng and Khoo, Daphne H.C and Cheah, Jin Seng and Ho, Su Chin and Bernstein, Harold S and Maciel, Rui M.B and Brown, Robert H and Ptáček, Louis J
Cell (Cambridge), ISSN 0092-8674, 2010, Volume 140, Issue 1, pp. 88 - 98
PROTEINS | HUMDISEASE | SIGNALING | Amino Acid Sequence | Genetic Predisposition to Disease | Hypokalemic Periodic Paralysis - metabolism | Humans | Hypokalemic Periodic Paralysis - genetics | Molecular Sequence Data | Potassium Channels, Inwardly Rectifying - genetics | Potassium Channels, Inwardly Rectifying - chemistry | Triiodothyronine - metabolism | DNA Mutational Analysis | Base Sequence | Transcription, Genetic | Electrophysiological Phenomena | Mutation | Potassium Channels, Inwardly Rectifying - metabolism | Index Medicus
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