Muscle & Nerve, ISSN 0148-639X, 11/2019
Journal Article
Brain and nerve = Shinkei kenkyu no shinpo, ISSN 1881-6096, 02/2018, Volume 70, Issue 2, pp. 113 - 120
Journal Article
Brain and nerve = Shinkei kenkyu no shinpo, ISSN 1881-6096, 02/2018, Volume 70, Issue 2, p. 113
Recent studies revealed an association between Zika virus infection and a variety of neurological disorders, including microcephaly, meningoencephalitis,...
Guillain-Barre Syndrome - therapy | Animals | Prognosis | Guillain-Barre Syndrome - diagnosis | Humans | Guillain-Barre Syndrome - etiology | Zika Virus | Zika Virus Infection - complications
Guillain-Barre Syndrome - therapy | Animals | Prognosis | Guillain-Barre Syndrome - diagnosis | Humans | Guillain-Barre Syndrome - etiology | Zika Virus | Zika Virus Infection - complications
Journal Article
Brain and nerve = Shinkei kenkyū no shinpo, ISSN 1881-6096, 03/2016, Volume 68, Issue 3, pp. 233 - 241
Journal Article
Brain and Nerve, ISSN 1881-6096, 11/2015, Volume 67, Issue 11, pp. 1377 - 1387
Journal Article
Brain and nerve = Shinkei kenkyu no shinpo, ISSN 1881-6096, 11/2015, Volume 67, Issue 11, p. 1377
From the perspective of neuropathies with an acute onset mimicking that of Guillain-Barré syndrome (GBS), cases with profound sensory and/or autonomic...
Peripheral Nervous System Diseases - diagnosis | Acute Disease | Ganglia, Autonomic - ultrastructure | Humans | Autoimmune Diseases of the Nervous System - pathology | Autonomic Nervous System Diseases - diagnosis | Autonomic Nervous System - ultrastructure | Autoimmune Diseases of the Nervous System - immunology | Animals | Peripheral Nervous System Diseases - pathology | Autonomic Nervous System Diseases - pathology | Ganglia, Autonomic - immunology | Autoimmune Diseases of the Nervous System - diagnosis | Autonomic Nervous System Diseases - immunology
Peripheral Nervous System Diseases - diagnosis | Acute Disease | Ganglia, Autonomic - ultrastructure | Humans | Autoimmune Diseases of the Nervous System - pathology | Autonomic Nervous System Diseases - diagnosis | Autonomic Nervous System - ultrastructure | Autoimmune Diseases of the Nervous System - immunology | Animals | Peripheral Nervous System Diseases - pathology | Autonomic Nervous System Diseases - pathology | Ganglia, Autonomic - immunology | Autoimmune Diseases of the Nervous System - diagnosis | Autonomic Nervous System Diseases - immunology
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 02/2019, Volume 90, Issue 2, pp. 124 - 124
Correspondence to Dr Haruki Koike, Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan;...
neurofascin | amyloid | amyloidosis | pathology | polyglucosan body | lymphoma | biopsy | CIDP | neurolymphomatosis | SURGERY | POLYNEUROPATHY | PSYCHIATRY | CLINICAL NEUROLOGY | Morphology
neurofascin | amyloid | amyloidosis | pathology | polyglucosan body | lymphoma | biopsy | CIDP | neurolymphomatosis | SURGERY | POLYNEUROPATHY | PSYCHIATRY | CLINICAL NEUROLOGY | Morphology
Journal Article
Clinical and Experimental Nephrology, ISSN 1342-1751, 10/2013, Volume 17, Issue 5, pp. 683 - 685
Microscopic polyangiitis (MPA), Churg–Strauss syndrome (CSS), and Wegener’s granulomatosis are anti-neutrophil cytoplasmic antibody (ANCA)-associated...
Nephrology | Microscopic polyangiitis | Vasculitis | Medicine & Public Health | Urology/Andrology | ANCA | Neuropathy | Churg–Strauss syndrome | Churg-Strauss syndrome | CHURG-STRAUSS-SYNDROME | UROLOGY & NEPHROLOGY | POLYANGIITIS-ASSOCIATED NEUROPATHY | Peripheral Nervous System Diseases - etiology | Churg-Strauss Syndrome - therapy | Humans | Biomarkers - analysis | Peripheral Nervous System Diseases - therapy | Churg-Strauss Syndrome - pathology | Treatment Outcome | Microscopic Polyangiitis - complications | Peripheral Nervous System - immunology | Peripheral Nervous System - pathology | Churg-Strauss Syndrome - complications | Microscopic Polyangiitis - therapy | Antibodies, Antineutrophil Cytoplasmic - analysis | Microscopic Polyangiitis - immunology | Peripheral Nervous System Diseases - pathology | Churg-Strauss Syndrome - immunology | Microscopic Polyangiitis - pathology | Peripheral Nervous System Diseases - immunology | Viral antibodies | Antibodies | Medical colleges
Nephrology | Microscopic polyangiitis | Vasculitis | Medicine & Public Health | Urology/Andrology | ANCA | Neuropathy | Churg–Strauss syndrome | Churg-Strauss syndrome | CHURG-STRAUSS-SYNDROME | UROLOGY & NEPHROLOGY | POLYANGIITIS-ASSOCIATED NEUROPATHY | Peripheral Nervous System Diseases - etiology | Churg-Strauss Syndrome - therapy | Humans | Biomarkers - analysis | Peripheral Nervous System Diseases - therapy | Churg-Strauss Syndrome - pathology | Treatment Outcome | Microscopic Polyangiitis - complications | Peripheral Nervous System - immunology | Peripheral Nervous System - pathology | Churg-Strauss Syndrome - complications | Microscopic Polyangiitis - therapy | Antibodies, Antineutrophil Cytoplasmic - analysis | Microscopic Polyangiitis - immunology | Peripheral Nervous System Diseases - pathology | Churg-Strauss Syndrome - immunology | Microscopic Polyangiitis - pathology | Peripheral Nervous System Diseases - immunology | Viral antibodies | Antibodies | Medical colleges
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 01/2013, Volume 84, Issue 1, pp. 98 - 106
Although autonomic neuropathy may occur as a secondary consequence of various diseases, other patients without any obvious underlying diseases show profound...
SURGERY | NERVOUS-SYSTEM | ACETYLCHOLINE-RECEPTOR ANTIBODY | ORTHOSTATIC TACHYCARDIA SYNDROME | PSYCHIATRY | GUILLAIN-BARRE-SYNDROME | ACUTE PANAUTONOMIC NEUROPATHY | SENSORY NEUROPATHY | GASTROINTESTINAL MOTOR DYSFUNCTION | CLINICAL NEUROLOGY | INTRAVENOUS IMMUNOGLOBULIN | SELECTIVE CHOLINERGIC DYSAUTONOMIA | ACUTE PANDYSAUTONOMIA | Autonomic Nervous System Diseases - complications | Humans | Sjogren's Syndrome - immunology | Paraneoplastic Syndromes - diagnosis | Sensation Disorders - immunology | Autonomic Nervous System Diseases - diagnosis | Autoimmune Diseases of the Nervous System - complications | Autoimmune Diseases of the Nervous System - immunology | Paraneoplastic Syndromes - complications | Sjogren's Syndrome - diagnosis | Receptors, Cholinergic - immunology | Paraneoplastic Syndromes - immunology | Sensation Disorders - diagnosis | Sjogren's Syndrome - complications | Autoantibodies - adverse effects | Autoimmune Diseases of the Nervous System - diagnosis | Autonomic Nervous System Diseases - immunology | Sensation Disorders - complications | Autonomic neuropathies | Immune response | Research | Index Medicus
SURGERY | NERVOUS-SYSTEM | ACETYLCHOLINE-RECEPTOR ANTIBODY | ORTHOSTATIC TACHYCARDIA SYNDROME | PSYCHIATRY | GUILLAIN-BARRE-SYNDROME | ACUTE PANAUTONOMIC NEUROPATHY | SENSORY NEUROPATHY | GASTROINTESTINAL MOTOR DYSFUNCTION | CLINICAL NEUROLOGY | INTRAVENOUS IMMUNOGLOBULIN | SELECTIVE CHOLINERGIC DYSAUTONOMIA | ACUTE PANDYSAUTONOMIA | Autonomic Nervous System Diseases - complications | Humans | Sjogren's Syndrome - immunology | Paraneoplastic Syndromes - diagnosis | Sensation Disorders - immunology | Autonomic Nervous System Diseases - diagnosis | Autoimmune Diseases of the Nervous System - complications | Autoimmune Diseases of the Nervous System - immunology | Paraneoplastic Syndromes - complications | Sjogren's Syndrome - diagnosis | Receptors, Cholinergic - immunology | Paraneoplastic Syndromes - immunology | Sensation Disorders - diagnosis | Sjogren's Syndrome - complications | Autoantibodies - adverse effects | Autoimmune Diseases of the Nervous System - diagnosis | Autonomic Nervous System Diseases - immunology | Sensation Disorders - complications | Autonomic neuropathies | Immune response | Research | Index Medicus
Journal Article
Nature Reviews Neurology, ISSN 1759-4758, 2019, Volume 15, Issue 7, pp. 387 - 404
Hereditary amyloidogenic transthyretin (ATTRv) amyloidosis with polyneuropathy (also known as familial amyloid polyneuropathy) is a condition with adult onset...
SALIVARY-GLAND BIOPSY | LIVER-TRANSPLANTATION | WILD-TYPE TRANSTHYRETIN | FAMILIAL AMYLOIDOSIS | LONG-TERM SURVIVAL | PRACTICE PARAMETER EVALUATION | LATE-ONSET | SYMMETRIC POLYNEUROPATHY ROLE | PORTUGUESE PATIENTS | CLINICAL NEUROLOGY | APOLIPOPROTEIN-A-I
SALIVARY-GLAND BIOPSY | LIVER-TRANSPLANTATION | WILD-TYPE TRANSTHYRETIN | FAMILIAL AMYLOIDOSIS | LONG-TERM SURVIVAL | PRACTICE PARAMETER EVALUATION | LATE-ONSET | SYMMETRIC POLYNEUROPATHY ROLE | PORTUGUESE PATIENTS | CLINICAL NEUROLOGY | APOLIPOPROTEIN-A-I
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2016, Volume 15, Issue 11, pp. 1129 - 1137
Summary Background Polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome is a rare cause of demyelinating neuropathy, with...
Neurology | PERIPHERAL NEUROPATHY | VEGF | CLINICAL NEUROLOGY | JAPAN | Thalidomide - adverse effects | Dexamethasone - administration & dosage | Double-Blind Method | Outcome Assessment (Health Care) | Anti-Inflammatory Agents - pharmacology | Humans | Middle Aged | Vascular Endothelial Growth Factor A - blood | Angiogenesis Inhibitors - pharmacology | Male | Thalidomide - administration & dosage | Thalidomide - pharmacology | POEMS Syndrome - drug therapy | Angiogenesis Inhibitors - administration & dosage | Dexamethasone - pharmacology | POEMS Syndrome - blood | Adult | Anti-Inflammatory Agents - administration & dosage | Female | Aged | Vascular Endothelial Growth Factor A - drug effects | Drug Therapy, Combination | Medical colleges | Neurosciences | Endothelial growth factors | Stem cells | Clinical trials | Transplantation | Skin | Research institutes | Proteins | Drug dosages | Blood | Multiple myeloma
Neurology | PERIPHERAL NEUROPATHY | VEGF | CLINICAL NEUROLOGY | JAPAN | Thalidomide - adverse effects | Dexamethasone - administration & dosage | Double-Blind Method | Outcome Assessment (Health Care) | Anti-Inflammatory Agents - pharmacology | Humans | Middle Aged | Vascular Endothelial Growth Factor A - blood | Angiogenesis Inhibitors - pharmacology | Male | Thalidomide - administration & dosage | Thalidomide - pharmacology | POEMS Syndrome - drug therapy | Angiogenesis Inhibitors - administration & dosage | Dexamethasone - pharmacology | POEMS Syndrome - blood | Adult | Anti-Inflammatory Agents - administration & dosage | Female | Aged | Vascular Endothelial Growth Factor A - drug effects | Drug Therapy, Combination | Medical colleges | Neurosciences | Endothelial growth factors | Stem cells | Clinical trials | Transplantation | Skin | Research institutes | Proteins | Drug dosages | Blood | Multiple myeloma
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 01/2018, Volume 13, Issue 1, pp. 6 - 17
Hereditary ATTR (ATTRm) amyloidosis (also called transthyretin-type familial amyloid polyneuropathy [ATTR-FAP]) is an autosomal-dominant, adult-onset, rare...
Carpal tunnel syndrome | Amyloidosis neuropathy | Tafamidis | Red-flag symptom clusters | Cardiomyopathy | Hereditary ATTR amyloidosis | Disease-modifying agent | Familial amyloid polyneuropathy | Liver transplantation | MEDICINE, RESEARCH & EXPERIMENTAL | ATTR AMYLOIDOSIS | LIVER-TRANSPLANTATION | AUTONOMIC DYSFUNCTION | LONG-TERM SURVIVAL | CARPAL-TUNNEL-SYNDROME | AGE-OF-ONSET | VARIANT TRANSTHYRETIN | WORLD TRANSPLANT REGISTRY | BIOCHEMICAL FINDINGS | GENETICS & HEREDITY | CHOROID-PLEXUS | Care and treatment | Algorithms | Polyneuropathies | Gene mutations | Liver | Immunotherapy | Transplantation of organs, tissues, etc | Genetic aspects | Amyloidosis | Diagnosis | Health aspects | Donation of organs, tissues, etc
Carpal tunnel syndrome | Amyloidosis neuropathy | Tafamidis | Red-flag symptom clusters | Cardiomyopathy | Hereditary ATTR amyloidosis | Disease-modifying agent | Familial amyloid polyneuropathy | Liver transplantation | MEDICINE, RESEARCH & EXPERIMENTAL | ATTR AMYLOIDOSIS | LIVER-TRANSPLANTATION | AUTONOMIC DYSFUNCTION | LONG-TERM SURVIVAL | CARPAL-TUNNEL-SYNDROME | AGE-OF-ONSET | VARIANT TRANSTHYRETIN | WORLD TRANSPLANT REGISTRY | BIOCHEMICAL FINDINGS | GENETICS & HEREDITY | CHOROID-PLEXUS | Care and treatment | Algorithms | Polyneuropathies | Gene mutations | Liver | Immunotherapy | Transplantation of organs, tissues, etc | Genetic aspects | Amyloidosis | Diagnosis | Health aspects | Donation of organs, tissues, etc
Journal Article
Clinical and Experimental Neuroimmunology, ISSN 1759-1961, 02/2018, Volume 9, Issue 1, pp. 35 - 46
Chronic inflammatory demyelinating polyneuropathy (CIDP) is a form of chronic neuropathy characterized by demyelination due to immune‐mediated processes. In...
chronic inflammatory demyelinating polyneuropathy | Schwann cell | node of Ranvier | neurofascin 155 | contactin 1 | Viral antibodies | Autoimmunity | Antibodies | Polyneuropathies
chronic inflammatory demyelinating polyneuropathy | Schwann cell | node of Ranvier | neurofascin 155 | contactin 1 | Viral antibodies | Autoimmunity | Antibodies | Polyneuropathies
Journal Article
Journal of Gastroenterology, ISSN 0944-1174, 2/2018, Volume 53, Issue 2, pp. 258 - 268
Although tolvaptan is an effective treatment for hepatic edema, there are no established criteria for assessment of the therapeutic effect. The present study...
Tolvaptan | Medicine & Public Health | Colorectal Surgery | Hepatology | Gastroenterology | Abdominal Surgery | Hepatic edema | Body weight loss | Cutoff value | Surgical Oncology | Clinical findings | KIDNEY-DISEASE | MANAGEMENT | EFFICACY | PHARMACOLOGICAL ACTION | POST HOC ANALYSIS | HEPATORENAL-SYNDROME | REFRACTORY ASCITES | LIVER-CIRRHOSIS PATIENTS | DECOMPENSATED HEART-FAILURE | QUALITY-OF-LIFE | GASTROENTEROLOGY & HEPATOLOGY | Antidiuretic Hormone Receptor Antagonists - pharmacology | Tolvaptan - therapeutic use | Humans | Middle Aged | Male | Weight Loss - drug effects | Tolvaptan - administration & dosage | Dose-Response Relationship, Drug | Young Adult | Antidiuretic Hormone Receptor Antagonists - administration & dosage | Aged, 80 and over | Adult | Female | Retrospective Studies | Severity of Illness Index | Liver Cirrhosis - drug therapy | Reproducibility of Results | Tolvaptan - pharmacology | Treatment Outcome | Edema - drug therapy | Antidiuretic Hormone Receptor Antagonists - therapeutic use | ROC Curve | Aged | Edema - physiopathology | Liver Cirrhosis - physiopathology | Medical research | Dropsy | Edema | Care and treatment | Analysis | Body weight | Medicine, Experimental | Liver
Tolvaptan | Medicine & Public Health | Colorectal Surgery | Hepatology | Gastroenterology | Abdominal Surgery | Hepatic edema | Body weight loss | Cutoff value | Surgical Oncology | Clinical findings | KIDNEY-DISEASE | MANAGEMENT | EFFICACY | PHARMACOLOGICAL ACTION | POST HOC ANALYSIS | HEPATORENAL-SYNDROME | REFRACTORY ASCITES | LIVER-CIRRHOSIS PATIENTS | DECOMPENSATED HEART-FAILURE | QUALITY-OF-LIFE | GASTROENTEROLOGY & HEPATOLOGY | Antidiuretic Hormone Receptor Antagonists - pharmacology | Tolvaptan - therapeutic use | Humans | Middle Aged | Male | Weight Loss - drug effects | Tolvaptan - administration & dosage | Dose-Response Relationship, Drug | Young Adult | Antidiuretic Hormone Receptor Antagonists - administration & dosage | Aged, 80 and over | Adult | Female | Retrospective Studies | Severity of Illness Index | Liver Cirrhosis - drug therapy | Reproducibility of Results | Tolvaptan - pharmacology | Treatment Outcome | Edema - drug therapy | Antidiuretic Hormone Receptor Antagonists - therapeutic use | ROC Curve | Aged | Edema - physiopathology | Liver Cirrhosis - physiopathology | Medical research | Dropsy | Edema | Care and treatment | Analysis | Body weight | Medicine, Experimental | Liver
Journal Article
15.
Full Text
Ultrastructure in transthyretin amyloidosis: From pathophysiology to therapeutic insights
Biomedicines, ISSN 2227-9059, 03/2019, Volume 7, Issue 1, p. 11
Transthyretin (TTR) amyloidosis is caused by systemic deposition of wild-type or variant amyloidogenic TTR (ATTRwt and ATTRv, respectively). ATTRwt amyloidosis...
Oligomers | Pathology | Therapy | Angiopathy | Tafamidis | Pathogenesis | Schwann cell | Protein misfolding disease | Diflunisal | Electron microscopy | angiopathy | pathogenesis | pathology | oligomers | therapy | diflunisal | electron microscopy | protein misfolding disease | tafamidis
Oligomers | Pathology | Therapy | Angiopathy | Tafamidis | Pathogenesis | Schwann cell | Protein misfolding disease | Diflunisal | Electron microscopy | angiopathy | pathogenesis | pathology | oligomers | therapy | diflunisal | electron microscopy | protein misfolding disease | tafamidis
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 03/2018, Volume 71, Issue 11, pp. A1756 - A1756
[...]its diagnosis rate in Japan is less than 1%. hFH is caused by mutations of FH genes such as LDL-receptor (LDLR), apolipoprotein B-100 (APOB), proprotein...
Hypercholesterolemia | Mutation | Low density lipoprotein | Abnormalities
Hypercholesterolemia | Mutation | Low density lipoprotein | Abnormalities
Journal Article
Orphanet journal of rare diseases, ISSN 1750-1172, 05/2019, Volume 14, Issue 1, pp. 111 - 1
Journal Article
2013, ISBN 9780444529022, Volume 115
Recent progress in serological screening of paraneoplastic antibodies and in diagnostic imaging techniques to detect malignancies has enabled a broadening of...
chronic inflammatory demyelinating polyneuropathy | vasculitis | paraneoplastic neuropathy | sensory neuronopathy | neuropathy | Guillain–Barré syndrome | vasculitic neuropathy | autonomic neuropathy | chronic intestinal pseudo-obstruction | paraneoplastic syndrome | Chronic intestinal pseudo-obstruction | Vasculitis | Vasculitic neuropathy | Paraneoplastic syndrome | Neuropathy | Autonomic neuropathy | Paraneoplastic neuropathy | Sensory neuronopathy | Chronic inflammatory demyelinating polyneuropathy | Guillain-Barré syndrome | Paraneoplastic Polyneuropathy - therapy | Paraneoplastic Polyneuropathy - classification | Humans | Paraneoplastic Polyneuropathy - diagnosis
chronic inflammatory demyelinating polyneuropathy | vasculitis | paraneoplastic neuropathy | sensory neuronopathy | neuropathy | Guillain–Barré syndrome | vasculitic neuropathy | autonomic neuropathy | chronic intestinal pseudo-obstruction | paraneoplastic syndrome | Chronic intestinal pseudo-obstruction | Vasculitis | Vasculitic neuropathy | Paraneoplastic syndrome | Neuropathy | Autonomic neuropathy | Paraneoplastic neuropathy | Sensory neuronopathy | Chronic inflammatory demyelinating polyneuropathy | Guillain-Barré syndrome | Paraneoplastic Polyneuropathy - therapy | Paraneoplastic Polyneuropathy - classification | Humans | Paraneoplastic Polyneuropathy - diagnosis
Book Chapter
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 06/2017, Volume 88, Issue 6, pp. 465 - 473
ObjectiveTo investigate the morphological features of chronic inflammatory demyelinating polyneuropathy (CIDP) with autoantibodies directed against paranodal...
AUTOANTIBODIES | SURGERY | PSYCHIATRY | NEUROFASCIN | IGG4 | CIDP | CLINICAL NEUROLOGY | PERIPHERAL-NERVE | DEFICIENCY NEUROPATHY | IVIG RESPONSIVENESS | POEMS SYNDROME | POLYRADICULONEUROPATHY | CLINICOPATHOLOGICAL FEATURES | Ranvier's Nodes - immunology | Neuroglia - pathology | Humans | Middle Aged | Male | Cell Adhesion Molecules - immunology | Schwann Cells - immunology | Young Adult | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - immunology | Sural Nerve - immunology | Sural Nerve - pathology | Neuroglia - immunology | Adult | Autoantibodies - analysis | Female | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - pathology | Myelin Sheath - immunology | Myelin Sheath - pathology | Schwann Cells - pathology | Nerve Growth Factors - immunology | Microscopy, Electron | Contactin 1 - immunology | Biopsy | Axons - pathology | Adolescent | Aged | Ranvier's Nodes - pathology | Axons - immunology | Viral antibodies | Complications and side effects | Usage | Guillain-Barre syndrome | Antibodies | Dosage and administration | Electron microscopy | Dissection | Risk factors
AUTOANTIBODIES | SURGERY | PSYCHIATRY | NEUROFASCIN | IGG4 | CIDP | CLINICAL NEUROLOGY | PERIPHERAL-NERVE | DEFICIENCY NEUROPATHY | IVIG RESPONSIVENESS | POEMS SYNDROME | POLYRADICULONEUROPATHY | CLINICOPATHOLOGICAL FEATURES | Ranvier's Nodes - immunology | Neuroglia - pathology | Humans | Middle Aged | Male | Cell Adhesion Molecules - immunology | Schwann Cells - immunology | Young Adult | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - immunology | Sural Nerve - immunology | Sural Nerve - pathology | Neuroglia - immunology | Adult | Autoantibodies - analysis | Female | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - pathology | Myelin Sheath - immunology | Myelin Sheath - pathology | Schwann Cells - pathology | Nerve Growth Factors - immunology | Microscopy, Electron | Contactin 1 - immunology | Biopsy | Axons - pathology | Adolescent | Aged | Ranvier's Nodes - pathology | Axons - immunology | Viral antibodies | Complications and side effects | Usage | Guillain-Barre syndrome | Antibodies | Dosage and administration | Electron microscopy | Dissection | Risk factors
Journal Article