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1. Full Text Downbeat nystagmus: aetiology and comorbidity in 117 patients
by Wagner, J N and Glaser, M and Brandt, T and Strupp, M
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 06/2008, Volume 79, Issue 6, pp. 672 - 677
Objectives:Downbeat nystagmus (DBN) is the most common form of acquired involuntary ocular oscillation overriding fixation. According to previous studies, the... 
SURGERY | VERTICAL NYSTAGMUS | BILATERAL VESTIBULOPATHY | PSYCHIATRY | FLOCCULUS | HYPOMETABOLISM | ATAXIA | EYE-MOVEMENTS | CLINICAL NEUROLOGY | Vestibular Diseases - complications | Humans | Middle Aged | Male | Multiple System Atrophy - complications | Spinocerebellar Degenerations - diagnosis | Vestibular Diseases - epidemiology | Polyneuropathies - diagnosis | Aged, 80 and over | Adult | Female | Electromyography | Nystagmus, Pathologic - etiology | Retrospective Studies | Multiple System Atrophy - diagnosis | Child | Diagnosis, Differential | Comorbidity | Polyneuropathies - epidemiology | Nystagmus, Pathologic - epidemiology | Electronystagmography | Multiple System Atrophy - epidemiology | Magnetic Resonance Imaging | Spinocerebellar Degenerations - complications | Neurologic Examination | Adolescent | Aged | Vestibular Diseases - diagnosis | Spinocerebellar Degenerations - epidemiology | Causes of | Neurologic manifestations of general diseases | Diagnosis | Research | Nystagmus | Index Medicus
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2. Full Text Etiology of small-fiber neuropathy
by Bednarik, Josef and Vlckova-Moravcova, Eva and Bursova, Sarka and Belobradkova, Jana and Dusek, Ladislav and Sommer, Claudia
Journal of the Peripheral Nervous System, ISSN 1085-9489, 09/2009, Volume 14, Issue 3, pp. 177 - 183
The aim of this study was to evaluate the etiology in a group of 84 patients with painful sensory neuropathy with predominant small-fiber dysfunction (54 men... 
Painful sensory neuropathy | Etiology | Small-fiber neuropathy | Risk factors | DIAGNOSIS | risk factors | small-fiber neuropathy | painful sensory neuropathy | AXONAL POLYNEUROPATHY | IMPAIRED GLUCOSE-TOLERANCE | RISK | SKIN BIOPSY | SENSORY NEUROPATHY | NEUROSCIENCES | CLINICAL NEUROLOGY | etiology | DISEASE | Nerve Fibers - pathology | Sensory Receptor Cells - pathology | Humans | Middle Aged | Risk Factors | Sensation Disorders - etiology | Male | Czech Republic | Polyneuropathies - etiology | Aged, 80 and over | Adult | Female | Aged | Index Medicus
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3. Full Text Neurologic complications of gastric bypass surgery for morbid obesity
by Juhasz-Pocsine, Katalin and Rudnicki, Stacy A and Archer, Robert L and Harik, Sami I
Neurology, ISSN 0028-3878, 05/2007, Volume 68, Issue 21, pp. 1843 - 1850
Background: The number of bariatric procedures is rapidly growing as the prevalence of obesity in the USA is increasing. Such procedures are not without... 
MALNUTRITION | POLYNEUROPATHY | VERTICAL BANDED GASTROPLASTY | DISORDER | BERIBERI | PERIPHERAL NEUROPATHY | BARIATRIC SURGERY | WERNICKE-KORSAKOFF ENCEPHALOPATHY | DEFICIENCIES | WEIGHT | CLINICAL NEUROLOGY | Brain Diseases, Metabolic - pathology | Postoperative Complications - etiology | Spinal Cord - metabolism | Obesity, Morbid - surgery | Vitamin B 12 Deficiency - etiology | Neurodegenerative Diseases - etiology | Spinal Cord Diseases - physiopathology | Humans | Middle Aged | Male | Peripheral Nervous System Diseases - physiopathology | Wernicke Encephalopathy - physiopathology | Brain - metabolism | Obesity, Morbid - physiopathology | Thiamine Deficiency - etiology | Spinal Cord - pathology | Wernicke Encephalopathy - pathology | Adult | Female | Avitaminosis - pathology | Gastric Bypass - methods | Peripheral Nerves - metabolism | Peripheral Nervous System Diseases - pathology | Copper - deficiency | Postoperative Complications - pathology | Peripheral Nervous System Diseases - etiology | Reoperation | Neurodegenerative Diseases - pathology | Postoperative Complications - physiopathology | Wernicke Encephalopathy - etiology | Brain - physiopathology | Gastric Bypass - adverse effects | Vitamin B 12 Deficiency - physiopathology | Thiamine Deficiency - physiopathology | Peripheral Nerves - pathology | Peripheral Nerves - physiopathology | Avitaminosis - complications | Neurodegenerative Diseases - physiopathology | Spinal Cord Diseases - etiology | Brain Diseases, Metabolic - physiopathology | Dietary Supplements - standards | Avitaminosis - physiopathology | Brain - pathology | Brain Diseases, Metabolic - etiology | Spinal Cord - physiopathology | Spinal Cord Diseases - pathology | Index Medicus | Abridged Index Medicus
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4. Full Text Food-cobalamin malabsorption in elderly patients: Clinical manifestations and treatment
by Andrès, Emmanuel and Affenberger, Stéphane and Vinzio, Stéphane and Kurtz, Jean-Emmanuel and Noel, Esther and Kaltenbach, Georges and Maloisel, Frédéric and Schlienger, Jean-Louis and Blicklé, Jean-Frédéric
The American Journal of Medicine, ISSN 0002-9343, 2005, Volume 118, Issue 10, pp. 1154 - 1159
Approximately 15% of people aged more than 60 years old have a cobalamin (vitamin B12) deficiency, mainly in relation with food-cobalamin malabsorption (FCM).... 
Drugs | Cobalamin deficiency | Atrophic gastritis | Oral cobalamin treatment | Food-cobalamin malabsorption | Elderly patients | elderly patients | HOMOCYSTEINE | food-cobalamin malabsorption | FOLATE-DEFICIENCY | drugs | VITAMIN-B-12 DEFICIENCY | atrophic gastritis | METHYLMALONIC ACID | OPEN-LABEL | PARENTERAL THERAPY | PERNICIOUS-ANEMIA | ORAL COBALAMIN | DIAGNOSING COBALAMIN | MEDICINE, GENERAL & INTERNAL | oral cobalamin treatment | MEGALOBLASTIC-ANEMIA | cobalamin deficiency | Malabsorption Syndromes - diagnosis | Follow-Up Studies | Vitamin B 12 Deficiency - blood | Humans | Hematologic Diseases - drug therapy | Erythrocyte Indices | Male | Polyneuropathies - drug therapy | Paresthesia - etiology | Vitamin B 12 - therapeutic use | Jaundice - drug therapy | Asthenia - drug therapy | Malabsorption Syndromes - blood | Reflex, Abnormal | Cognition Disorders - etiology | Vitamin B 12 Deficiency - complications | Aged, 80 and over | Female | Gastritis, Atrophic - etiology | Retrospective Studies | Malabsorption Syndromes - drug therapy | Gastritis, Atrophic - drug therapy | Confusion - drug therapy | Homocysteine - blood | Edema - drug therapy | Vitamin B 12 - blood | Cognition Disorders - drug therapy | Vitamin B 12 Deficiency - drug therapy | Edema - etiology | Paresthesia - drug therapy | Confusion - etiology | Polyneuropathies - etiology | Asthenia - etiology | Hematologic Diseases - etiology | Aged | Hemoglobins - analysis | Jaundice - etiology | Cohort Studies | Medical examination | Malabsorption syndromes | Aged patients | Dosage and administration | Research | Drug therapy | Vitamin B12 | Risk factors | Diseases | Medical disorders | Older people | Vitamin B | Dietary supplements | Index Medicus | Abridged Index Medicus
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5. Full Text The selective sigma-1 receptor antagonist E-52862 attenuates neuropathic pain of different aetiology in rats
by Gris, Georgia and Portillo-Salido, Enrique and Aubel, Bertrand and Darbaky, Yassine and Deseure, Kristof and Vela, José Miguel and Merlos, Manuel and Zamanillo, Daniel
Scientific Reports, ISSN 2045-2322, 04/2016, Volume 6, Issue 1, pp. 24591 - 24591
E-52862 is a selective sigma R-1 antagonist currently undergoing phase II clinical trials for neuropathic pain and represents a potential first-in-class... 
MECHANICAL ALLODYNIA | NMDA RECEPTOR | CENTRAL SENSITIZATION | ACTIVATION | ALLODYNIA-LIKE BEHAVIOR | MULTIDISCIPLINARY SCIENCES | FORMALIN-INDUCED PAIN | SPINAL-CORD | INFLAMMATORY PAIN | MODEL | MICE ROLE | Peripheral Nerve Injuries - complications | Analgesics - pharmacology | Analgesics - therapeutic use | Pyrazoles - therapeutic use | Morpholines - administration & dosage | Analgesics - administration & dosage | Morpholines - pharmacology | Rats | Male | Receptors, sigma - antagonists & inhibitors | Rats, Sprague-Dawley | Neuralgia - drug therapy | Organoplatinum Compounds - toxicity | Pyrazoles - administration & dosage | Animals | Hyperalgesia - drug therapy | Neuralgia - etiology | Hyperalgesia - etiology | Morpholines - therapeutic use | Diabetic Neuropathies - complications | Pyrazoles - pharmacology | Pain perception | Gabapentin | Streptozocin | Diabetes mellitus | Hypersensitivity | Clinical trials | Morphine | Antagonists | Neuropathy | Polyneuropathy | Cold stimuli | Pain | Oxaliplatin | Drug tolerance | Surgery | Rodents | Index Medicus
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6. Full Text Progressive cranial nerve involvement and grading of facial paralysis in gelsolin amyloidosis
by Pihlamaa, Tiia and Salmi, Tapani and Suominen, Sinikka and Kiuru‐Enari, Sari
Muscle & Nerve, ISSN 0148-639X, 05/2016, Volume 53, Issue 5, pp. 762 - 769
IntroductionHereditary gelsolin amyloidosis (GA) is a rare condition caused by the gelsolin gene mutation. The diagnostic triad includes corneal lattice... 
cranial neuropathy | amyloidosis | gelsolin | bilateral facial paresis | facial paresis grading | Facial paresis grading | Amyloidosis | Gelsolin | Cranial neuropathy | Bilateral facial paresis | GSN GENE | NEUROSCIENCES | FINNISH TYPE FAF | POLYNEUROPATHY TYPE-IV | CLINICAL NEUROLOGY | LATTICE CORNEAL-DYSTROPHY | HEARING-LOSS | NEUROPATHY | FAMILIAL AMYLOIDOSIS | MERETOJAS SYNDROME | HEREDITARY AMYLOIDOSIS | MUTATION | Vestibulocochlear Nerve Diseases - physiopathology | Cutis Laxa - etiology | Humans | Middle Aged | Vestibulocochlear Nerve Diseases - etiology | Oculomotor Nerve Diseases - etiology | Male | Amyloid Neuropathies, Familial - physiopathology | Facial Nerve Diseases - etiology | Hypoglossal Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - physiopathology | Facial Paralysis - physiopathology | Aged, 80 and over | Adult | Female | Electromyography | Amyloidosis - complications | Cranial Nerve Diseases - physiopathology | Hypoglossal Nerve Diseases - etiology | Trigeminal Nerve Diseases - physiopathology | Trigeminal Nerve Diseases - etiology | Amyloid Neuropathies, Familial - complications | Amyloidosis - physiopathology | Neural Conduction | Facial Nerve Diseases - physiopathology | Oculomotor Nerve Diseases - physiopathology | Facial Muscles - physiopathology | Cranial Nerve Diseases - etiology | Corneal Dystrophies, Hereditary - complications | Aged | Facial Paralysis - etiology | Development and progression | Paralysis, Facial | Gene mutations | Wood products | Workshops | Index Medicus
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7. Full Text ID 106 – Pathophysiological classification of polyneuropathies in different aetiologies
by Murtuzova, A and Fuglsang-Frederiksen, A and Tankisi, H
Clinical Neurophysiology, ISSN 1388-2457, 2015, Volume 127, Issue 3, pp. e105 - e105
Objective We aimed in this study to examine aetiologies and pathopysiological classification of patients referred for electrodiagnosis of polyneuropathy (PNP).... 
Neurology | Polyneuropathies | Analysis
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8. Full Text Testicular vasculitis: Findings differentiating isolated disease from systemic disease in 72 patients
by Hernández-Rodríguez, José and Tan, Carmela D and Koening, Curry L and Khasnis, Atul and Rodríguez, E. René and Hoffman, Gary S
Medicine, ISSN 0025-7974, 03/2012, Volume 91, Issue 2, pp. 75 - 85
Testicular vasculitis (TV) may be part of systemic (testicular) vasculitis (STV) or may exist as single-organ/isolated (testicular) vasculitis (ITV). In the... 
NECROTIZING GRANULOMATOUS VASCULITIS | ISOLATED POLYARTERITIS-NODOSA | MEDICINE, GENERAL & INTERNAL | UROGENITAL MANIFESTATIONS | SYSTEMIC VASCULITIS | PAIN | PERIARTERITIS-NODOSA | ORCHITIS | TESTIS | TUMOR | THROMBOANGIITIS-OBLITERANS | Arthralgia - etiology | Blood Sedimentation | Glucocorticoids - therapeutic use | Angiography | Humans | Middle Aged | Child, Preschool | Fatigue - etiology | Male | Systemic Vasculitis - therapy | Testis - diagnostic imaging | Young Adult | Ultrasonography | Pain - etiology | Adult | Glomerulonephritis - etiology | Child | Anemia - etiology | Systemic Vasculitis - diagnosis | Testis - blood supply | Vasculitis - therapy | Testicular Diseases - diagnosis | Magnetic Resonance Angiography | Orchiectomy | Biopsy, Fine-Needle | Edema - etiology | Testicular Diseases - therapy | Testis - pathology | Polyneuropathies - etiology | Vasculitis - diagnosis | Weight Loss | Adolescent | Fever - etiology | Aged | Hemoglobins - analysis | Usage | Corticosteroids | Medical case management | Surgery | Patient outcomes | Blood vessels | Dosage and administration | Methods | Index Medicus | Abridged Index Medicus
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9. Full Text Impact of etiology and duration of pain on pharmacological treatment effects in painful polyneuropathy
by Sindrup, S. H and Holbech, J and Demant, D and Finnerup, N. B and Bach, F. W and Jensen, T. S
European Journal of Pain, ISSN 1090-3801, 09/2017, Volume 21, Issue 8, pp. 1443 - 1450
BackgroundThe pharmacological treatments for painful polyneuropathy have not changed much for more than a decade, and less than half of the patients obtain... 
CONTROLLED-TRIAL | PREDICTOR | DOUBLE-BLIND | PHENOTYPE | IMIPRAMINE | ANESTHESIOLOGY | PERIPHERAL NEUROPATHIC PAIN | DIABETIC-NEUROPATHY | NEUROSCIENCES | DORSAL-HORN | CLINICAL NEUROLOGY | Imipramine - therapeutic use | Carbamazepine - analogs & derivatives | Pregabalin - therapeutic use | Humans | Middle Aged | Anticonvulsants - therapeutic use | Carbamazepine - therapeutic use | Male | Polyneuropathies - drug therapy | Diabetic Neuropathies - drug therapy | Venlafaxine Hydrochloride - therapeutic use | Neuralgia - drug therapy | Antidepressive Agents - therapeutic use | Polyneuropathies - etiology | Time Factors | Neuralgia - etiology | Adult | Female | Aged | Retrospective Studies | Diabetic Neuropathies - complications | Index Medicus
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10. Full Text Frequency of Fabry disease in patients with small‐fibre neuropathy of unknown aetiology: a pilot study
by Tanislav, C and Kaps, M and Rolfs, A and Böttcher, T and Lackner, K and Paschke, E and Mascher, H and Laue, M and Blaes, F
European Journal of Neurology, ISSN 1351-5101, 04/2011, Volume 18, Issue 4, pp. 631 - 636
Background:  Early occurrence of small‐fibre neuropathy (SFN) is a common feature of Fabry disease (FD) – an X‐linked storage disorder caused by reduced... 
Fabry disease | neuropathic pain | small‐fibre neuropathy | enzyme replacement therapy | biomarkers | Biomarkers | Enzyme replacement therapy | Small-fibre neuropathy | Neuropathic pain | DIAGNOSIS | INVOLVEMENT | SKIN BIOPSY | PREVALENCE | OUTCOME SURVEY | NEUROSCIENCES | MASS-SPECTROMETRY | CLINICAL NEUROLOGY | GLOBOTRIAOSYLSPHINGOSINE | CLINICAL-MANIFESTATIONS | small-fibre neuropathy | AGALSIDASE-ALPHA | Immunohistochemistry | alpha-Galactosidase - genetics | Fabry Disease - epidemiology | Fabry Disease - genetics | alpha-Galactosidase - analysis | Humans | Middle Aged | Fabry Disease - complications | Male | Pilot Projects | DNA Mutational Analysis | Mass Spectrometry | Polyneuropathies - genetics | Adult | Female | Aged | Mutation | Medicine, Experimental | Medical colleges | Enzymes | Medical research | Anopheles | Index Medicus
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11. Full Text Case report of severe Cushing's syndrome in medullary thyroid cancer complicated by functional diabetes insipidus, aortic dissection, jejunal intussusception, and paraneoplastic dysautonomia: Remission with sorafenib without reduction in cortisol concentration
by Hammami, Muhammad M and Duaiji, Najla and Mutairi, Ghazi and Aklabi, Sabah and Qattan, Nasser and Abouzied, Mohei El-Din M and Sous, Mohamed W
BMC Cancer, ISSN 1471-2407, 09/2015, Volume 15, Issue 1, pp. 624 - 624
Background: Normalization of cortisol concentration by multikinase inhibitors have been reported in three patients with medullary thyroid cancer-related... 
METASTASIS | PROGESTERONE | ONCOLOGY | EATON MYASTHENIC SYNDROME | PROCALCITONIN | RECEPTOR | PATIENT | VANDETANIB | ADRENOCORTICOTROPIC HORMONE-SYNDROME | SECRETION | CARCINOMA | Niacinamide - analogs & derivatives | Intussusception - etiology | Diabetes Insipidus - etiology | Humans | Primary Dysautonomias - etiology | Niacinamide - therapeutic use | Phenylurea Compounds - therapeutic use | Thyroid Neoplasms - complications | Carcinoma, Medullary - complications | Cushing Syndrome - etiology | Male | Antineoplastic Agents - therapeutic use | Aortic Aneurysm - etiology | Jejunal Diseases - etiology | Paraneoplastic Polyneuropathy - etiology | Carcinoma, Medullary - drug therapy | Thyroid Neoplasms - drug therapy | Fatal Outcome | Adult | Hydrocortisone - blood | Aneurysm, Dissecting - etiology | Cushing Syndrome - drug therapy | Diagnosis | Research | Drug therapy | Risk factors | Cushing syndrome | Viral antibodies | CT imaging | Medical equipment and supplies industry | Medical test kit industry | Diabetes insipidus | Antibodies | Progesterone | Metastasis | Index Medicus
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12. Full Text Idiopathic Small Fiber Neuropathy: Phenotype, Etiologies, and the Search for Fabry Disease
by Samuelsson, Kristin and Kostulas, Konstantinos and Vrethem, Magnus and Rolfs, Arndt and Press, Rayomand and Närsjukvården i centrala Östergötland and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Avdelningen för neurovetenskap and Neurologiska kliniken and Östergötlands Läns Landsting and Hälsouniversitetet
Journal of Clinical Neurology, ISSN 1738-6586, 04/2014, Volume 10, Issue 2, pp. 108 - 118
The etiology of small fiber neuropathy (SFN) often remains unclear. Since SFN may be the only symptom of late-onset Fabry disease, it may be underdiagnosed in... 
Fabry Disease | small fiber neuropathy | Etiology | Impaired glucose tolerance | Idiopathic | Fabry disease | Small fiber neuropathy | NERVE-FIBERS | impaired glucose tolerance | IMPAIRED GLUCOSE-TOLERANCE | SKIN BIOPSY | SENSORY NEUROPATHY | CLINICAL NEUROLOGY | etiology | CRYPTOGENIC POLYNEUROPATHY | GENE | idiopathic | PERIPHERAL NEUROPATHY | MUTATIONS | ENZYME REPLACEMENT THERAPY | ALPHA-GALACTOSIDASE | Original | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | etiology; Fabry disease; idiopathic; impaired glucose tolerance; small fiber neuropathy | MEDICIN
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13. Full Text Natural history of transthyretin Val30Met familial amyloid polyneuropathy: Analysis of late-onset cases from non-endemic areas
by Koike, Haruki and Tanaka, Fumiaki and Hashimoto, Rina and Tomita, Minoru and Kawagashira, Yuichi and Iijima, Masahiro and Fujitake, Junko and Kawanami, Toru and Kato, Takeo and Yamamoto, Masahiko and Sobue, Gen
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 02/2012, Volume 83, Issue 2, pp. 152 - 158
Objective The objective of this study was to elucidate the natural history of late-onset transthyretin Val30Met-associated familial amyloid polyneuropathy (FAP... 
SURGERY | LIVER-TRANSPLANTATION | PROGNOSTIC-FACTORS | PSYCHIATRY | DEPOSITION | CARDIAC AMYLOIDOSIS | IDENTIFICATION | CLINICAL NEUROLOGY | ATTR VAL30MET | GENETIC FEATURES | FAP | ENDEMIC FOCUS | JAPAN | Prealbumin - genetics | Follow-Up Studies | Humans | Middle Aged | Cardiomegaly - etiology | Sensation Disorders - etiology | Male | Nervous System Diseases - genetics | Cause of Death | Pacemaker, Artificial | Amyloid Neuropathies, Familial - physiopathology | Endemic Diseases | Amyloid - metabolism | Ultrasonography | Pain - etiology | Female | Nervous System Diseases - physiopathology | Retrospective Studies | Heart - physiopathology | Neural Conduction - genetics | Amyloid Neuropathies, Familial - genetics | Japan | Cardiomegaly - diagnostic imaging | Amyloid Neuropathies, Familial - complications | Neural Conduction - physiology | Disease Progression | Action Potentials - physiology | Heart Diseases - etiology | Neurologic Examination | Heart Diseases - therapy | Age of Onset | Aged | Case studies | Polyneuropathies | Development and progression | Index Medicus
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