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Hypothyroidism in dogs on prednisone - • Search the Neurology Website • Differential diagnosis Muscle & NMJ Nerve Spinal Cord Hereditary ataxias • Molecular & Cellular topics • Pathology & Illustrations • New or newly revised • Neuromuscular Home Page AAA syndrome α-Actinin AARS Aarskog Scott Abdominal muscles A-β-lipoproteinemia Absent muscles ACAD9 Acanthosis Nricans Acetylcholine & ACh Receptors Acetylcholine Receptor Antibodies Disorders Epsilon subunit Myasthenia Gravis Acetylcholinesterase Achalasia Achondroplasia Acid Maltase Aconitase Acromegaly Acromutilation (Ulceromutilation) Acrylamide Actin Actinin Acute Immune neuropathies Motor Neuropathies Myopathies Neuropathies Quadriplegic myopathies Weakness Acyl-Co A dehydrogenase disorders hydroxy long chain medium chain very long chain Multiple deficiency Adenosine receptors Adhalin Adhesion molecules Adrenal Adrenomyeloneuropathy α-Dystroglycan Disorders α-galactosidase AGAT Age: Muscle; Nerve Agrin Alacrimia Alanine-repeat disorders Alcoholic (Ethanol) polyneuropathy Aldolase A deficiency Alexander disease Adult onset Mitochondrial Allgrove syndrome Allodynia All-Trans-Retinoic Acid Allyl coride Alpers-Huttenlocher α-Methylacyl-Co A racemase (AMACR) Almitrine neuropathy Alpers ALS ALS Association Alsin AMACR AMAN Aminoacyl-t RNA synthetase Antibodies Cytoplasmic Mitochondrial -Amino Caproic Acid Amiodarone neuropathy Ammonia AMPDA deficiency Amphiphysin Amyloidosis Amyotrophic Lateral Sclerosis (ALS) Hereditary Sporadic An-α-lipoproteinemia ANCA Andermann Syndrome Andersen disease Andersen periodic paralysis Androgen Receptor Angiogenin Angiotropic lymphoma Anhidrosis Anion exchangers Ankylosing spondylitis ANO10 Anterior interosseus nerve Anterior primary rami Antibodies Acetylcholine Receptor Connective tissue disease Decorin (BJ) Glutamic acid decarboxylase GM1 Ganglioside Hu Jo-1 MAG M-protein Monoclonal Muscle Nerve Polymyositis Polyspecific Striational (Muscle) Sulfatide t RNA Synthetase Tubulin Yo Antibody testing Requisition Form Instructions AP4 proteins Apamin APECED Apoptosis Congenital myopathy Apoptosis Arachnoiditis Argininemia Arm predominance Myopathy Neuropathy Arnold-Chiari Malformation ARS Antibodies Cytoplasmic Mitochondrial Arsenic Arthrogryposis ARVD Asymmetric Neuropathies Myopathies Ataxias Ataxia Telangectasia Ataxia Telangectasia-like Autosomal Dominant Autosomal Recessive Congenital DNA repair defects Episodic Metabolic disorders Multisystem disorders SCA Sensory Treatments X-linked Atetes Disorders Genetics Atlanto-Axial instability α-tocopherol transfer protein (ATTP) ATP ATPase 6 ATPase Disorders Atrial septal defect Atrophy, type 2 muscle fibers Autonomic Disorders Syndromes Cardiac Sweating Hypotension Urinary Sexual Ocular Autophagy Differential diagnosis Excessive General features Pathology AVSF Pathology Axenfeld-Rieger anomaly Axillary nerve Axonal Neuropathies - Immune Transport Axons: Characteristics Azathioprine AZT myopathy , vitamin β-Enolase BAG3 Baltic myoclonus Bariatric surgery Barium Barnes's myopathy Barth syndrome Basal Lamina: Muscle Baseball Basement membrane BCIM Becker Muscular Dystrophy Becker Myotonia Bee stings Behçet Behr syndrome Bell's Palsy Benn acute childhood myositis Bent spine syndrome Betem myopathy β-galactosidase BICD2 Biceps Bickerstaff brainstem encephalitis Biemond Congenital Anesthesia Bilbao & Schmidt Text Index Biochemical-genetic testing Biopsy Muscle Nerve Pictures Quiz Results: Differential diagnosis Biotinidase deficiency BJ (Decorin) antibodies & myopathy Björnstad syndrome Black widow spider toxin Blepharophimosis Bodybuilding Bone morphogenetic proteins Bortezomib (Velcade) Botulism Boucher-Neuhäuser Brachial Amyotrophic Diplegia Brachial Plexopathy Brachial plexus: Innervation Branching Enzyme Brachio-Cervical Inflammatory Myopathy Pathology Broad A-band disease Brody Disease 1-Bromopropane (n-propyl bromide) Brown-Vialetto-van Laere (BVVLS) Brucellosis Brugada BSMA (X-linked) Buckthorn Bulbar weakness Bulbospinal Neuronopathy (X-linked) Bungarotoxins: α; β; κ Burning mouth syndrome Burning feet syndrome Burns & neuropathy C1-C2 instability c9orf72 c20orf7 Cabezas CADASIL (Multi-infarct dementia) Cadherins CADM-140 Cadmium CAGSSS Calcinosis Calciphylaxis Calcium Channels Antibodies Disorders Calmodulin 1 Calpain 3 Camera-Marugo-Cohen Syndrome CAMOS Camptocormia Camurati-Engelmann CANOMAD CANVAS Cap myopathy CAPOS syndrome Carbohydrate Deficient Glycoproteins Carbon disulphide Cardiac Disorders Myopathy Heart only; Hereditary Cardiofaciocutaneous 1 Cardiomyopathy Dilated Hypertrophic Mitochondrial Carey-Fineman-Ziter syndrome Carnitine Carnitine-acylcarnitine translocase Carnitine palmitoyltransferase II Carpal tunnel syndrome Cartilage-Hair hypoplasia Caspr2 Cataract & Facial disorder: HMSN Catecholamines Cavanagh's sensory neuropathy Caveolin-3 CCDD CCFDN CD59 CDG CEDNIK Celiac disease CEMCOX Central Core Central European encephalitis Central Nervous System (CNS) ... 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Becker's muscular dystrophy - pedia The segment of the spinal cord at which the damage occurs determines which parts of the body are affected. Becker muscular dystrophy is an X-linked recessive inherited disorder characterized by slowly progressive muscle weakness of the legs and pelvis.

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